House of Lords

Tuesday 17th January 2012 Lords Chamber

Tuesday, 17 January 2012.

14:30

Prayers—read by the Lord Bishop of Chichester.

Housing: Managing Agents

Tuesday 17th January 2012 Lords Chamber

Question

14:36

Asked By

[Baroness Gardner of Parkes]

To ask Her Majesty’s Government whether they will introduce regulations or a code of practice to set standards for managing agents for leasehold blocks of flats.

[Baroness Gardner of Parkes]

My Lords, I beg leave to ask the Question standing in my name on the Order Paper and declare my interest as a leaseholder.

[The Parliamentary Under-Secretary of State, Department for Communities and Local Government (Baroness Hanham)]

My Lords, there are already two codes of practice in force that can be used in evidence in a court or tribunal: the Service Charge Residential Management Code, which is published by the Royal Institution of Chartered Surveyors, and Private Retirement Housing: Code of Practice, which is published by the Association of Retirement Housing Managers. The Government recognise that problems caused by the actions of managing agents can cause leaseholders real inconvenience and distress. Landlords and managing agents must obey the law and should act in a socially responsible manner. While we have no plans for a wide-ranging review of leasehold law, we are keeping a close watching brief and will not rule out making changes.

[Baroness Gardner of Parkes]

Can the Minister tell me what rights leaseholders have to be assured that managing agents carry out regular assessments of property condition and arrange necessary repairs for works in blocks of flats? Are the agents responsible for ensuring that any work done is carried out to a satisfactory standard?

[Baroness Hanham]

My Lords, managing agents are employed by the freeholders, although leaseholders have rights as to what they are being charged for and the work that is being done. We believe that any managing agent acting on behalf of a landlord owes a duty of care to leaseholders. Reasonable steps should be taken to ensure that all work is done properly and safely. Leaseholders of course have a right to challenge the management of their blocks and the people who are doing it through the leasehold valuation tribunal.

[Lord Best]

My Lords, I declare my interest as chairman of the council of The Property Ombudsman, which listens to complaints against managing agents. Although the Minister is probably against regulation of this sector, does she agree that it would be a good idea if it was compulsory for all managing agents to belong to an ombudsman scheme that can resolve disputes between residents and managing agents without the need to go to court?

[Baroness Hanham]

My Lords, I do not think that we would want to compel managing agents to do that, but I agree that it would be very helpful if they would voluntarily ensure that they are members of the ombudsman scheme, which is very valuable in terms of leaseholders being sure that they are getting and can get proper access to advice.

[Lord Lea of Crondall]

My Lords, does the Minister agree that the words “regulation” and “overregulation” should be used with some care, while acknowledging, as the noble Baroness has done, that in practical terms redress through an ombudsman or some other route should be made a lot easier? I speak as having been chair of a residents association of a block of 24 flats over some years. The accounts are almost impenetrable and it is difficult to get stuff done according to the lease. You do not get an answer to the telephone. If you need a plumber, you can use only a named plumber who is never available, et cetera. We all know the litany.

[Baroness Hanham]

My Lords, I acknowledge that it is probably not very easy, but I do not acknowledge that there are no routes for dissatisfied leaseholders. They have access to the lease valuation tribunal if they have concerns, particularly about charges. They also can go to LEASE if they are concerned about the way in which their property is being managed. It requires at least one person in the property to be in charge of the residents and how they feel in order to make sure that they follow the routes that are already open to them.

[Lord Shipley]

My Lords, is the Minister aware of the report published last year which showed that some leaseholders were paying far too much in property insurance to managing agents and that, as a consequence, regulation would most certainly help? In addition, might it be for government to promote the right to manage to leaseholders groups in blocks of flats, so that they themselves can reduce the costs that they have to bear?

[Baroness Hanham]

My Lords, the matter of commission is already being investigated as there have been many complaints about it. As I understand it, the commission of, for example, insurance would not appear on the service charge but could form another charge that the leaseholders have to pay. I think that most leaseholders need to have a tenants association within their blocks of flats or wherever they live to ensure that they do have some muscle with poor managing agents and that they can then use the routes that are, as I said, there for them.

Eurozone Crisis

Tuesday 17th January 2012 Lords Chamber

Question

14:42

Asked By

[Lord Barnett]

To ask Her Majesty’s Government whether HM Treasury is developing contingency plans for use in the event of a Eurozone collapse.

[The Commercial Secretary to the Treasury (Lord Sassoon)]

My Lords, as my right honourable friend the Chancellor of the Exchequer made clear in the Autumn Statement, the Government, including of course the Treasury, are undertaking extensive contingency planning to deal with all potential outcomes of the euro crisis.

[Lord Barnett]

Thanks for that very informative reply. I hope that there will never be a need to use the contingency reserve, because, as the Chancellor has said, it would be devastating for the UK economy if there was a collapse in the eurozone. We already have a near recession—if not an actual one—forecast without such a collapse. I gather that the Government are more amenable to the new draft treaty that has been promoted for the next summit. In those circumstances, and given the risk of jeopardising the slightest chance of preventing that collapse, would he not agree that it would be very foolish to veto that summit as well?

[Lord Sassoon]

My Lords, first of all I welcome the compliment paid to my Answer by the noble Lord, Lord Barnett. He asked me a yes or no Question. I gave him a very full Answer and some extra things he did not ask about, so I am glad that he appreciates that. I am not going to speculate on our negotiating position because this is all very fast moving. All I can reiterate is that we are working very hard with our European partners to see a resolution of all aspects of the crisis. They have invited us to be at the table to discuss the arrangements that the eurozone countries are making among themselves and we are active and positive participants when we are invited to be there, as we are at those discussions.

[Lord Higgins]

My Lords, does the Minister agree that it is very much easier, technically, for a country to join the single currency than to leave it? Does he accept that the contingency plans which he mentioned—and which are welcome—need to be designed to ensure that, for anyone leaving, the process is completed as soon as possible? It is not just a question of having the notes and coins available but of having an extensive programme, including provision for exchange controls. I welcome my noble friend’s reply but stress that this is a very complex question.

[Lord Sassoon]

My noble friend makes some interesting and relevant points. I shall not speculate on what precise aspects the Government are looking at in their exercises but, as he points out, none of this, under a range of scenarios, would be at all simple.

[Lord Campbell-Savours]

Has the Treasury carried out internally an inquiry into the level of exposure of British banks to banks within the eurozone that might collapse?

[Lord Sassoon]

My Lords, of course the FSA, in the course of its normal work, continually examines the exposure of the financial sector to a whole range of issues, including to the eurozone. The Europe-wide stress tests which were done, and done again, and finally done on a much better basis, looked at that matter last year.

[Lord Forsyth of Drumlean]

Will my noble friend confirm that in these contingency plans there is no question of the Government providing money for eurozone states to bail them out while the underlying problem of lack of competitiveness within the euro remains unresolved and unaddressed?

[Lord Sassoon]

My Lords, of course I can confirm to my noble friend that we work extremely hard to make sure that the competitiveness of the EU and the eurozone is not lost in the discussions. It is encouraging—they are only early signs, but they are encouraging—that in the Merkel-Sarkozy discussions on 10 January there was specific reference to growth-enhancing policies for prioritising EU spend towards growth and competitiveness. We look forward to the letter which I think they are likely to write to President Van Rompuy ahead of the next Council meeting.

[Lord Grenfell]

My Lords—

[Lord Pearson of Rannoch]

My Lords—

[The Chancellor of the Duchy of Lancaster (Lord Strathclyde)]

My Lords, there is plenty of time. Shall we hear from the noble Lord, Lord Grenfell, and then perhaps from the noble Lord, Lord Pearson?

[Lord Grenfell]

My Lords, given the unrest on the Conservative Benches in the other place, I was tempted to ask whether the Prime Minister had contingency plans for the full recovery and strengthening of the eurozone, but I have a more serious point to make. Does the Minister agree with me that it is extraordinary that the rating agencies disclaim all responsibility for the impact on borrowing costs of their downgradings when a Government like Italy’s are doing their best to solve their problems, and when an institution such as the European Financial Stability Facility—which was downgraded yesterday by Standard & Poor’s—is trying to maintain its lending capacity in advance of the creation of the new ESM, which will take some time? Do these unaccountable agencies just not care whether the impact of what they do is likely to hamper and jeopardise the eurozone recovery?

[Lord Sassoon]

My Lords, the credit rating agencies have a useful and important part to play in the good working of the financial markets. Your Lordships produced a report in committee on aspects of the regulation of the credit rating agencies on which we had a good debate before Christmas. There are issues about the performance of the credit rating agencies in respect of the financial crisis, but their record generally on sovereign ratings has been perfectly acceptable in most people’s judgment. However, I am not going to comment on their individual judgments in the past couple of weeks.

[Lord Pearson of Rannoch]

My Lords, is it not now clear that there are really only two ways forward—either full fiscal union, which does not look as though it will be accepted by the peoples of Europe, or a return to national currencies? On the latter alternative, have the Government seen the research from Bank of America Merrill Lynch which suggests that an orderly return to national currencies need not be nearly as traumatic as the political class would have us believe?

[Lord Sassoon]

My Lords, there is a whole range of views about the effect of the eurozone breaking down in any way. All I can say is that 40 per cent of our trade goes to Europe, and we want to see a strengthened and healthy eurozone. That is fundamentally in the interests of the UK. A crisis in the eurozone presents the most imminent threat to growth in this country.

[Lord Peston]

My Lords—

[Lord Newby]

My Lords, if there is a collapse in the eurozone—

[Lord Strathclyde]

My Lords, there is plenty of time to hear the noble Lord, Lord Peston. Can we hear first from my noble friend Lord Newby, and then from the noble Lord, Lord Peston?

[Lord Newby]

My Lords, does the Minister agree that if there is a collapse in the eurozone, it is highly likely that the IMF will be asked to play a larger role that it has done up to now? What is the Government’s thinking about making further resources available to the IMF in those circumstances?

[Lord Sassoon]

I am happy to try to clarify the Government’s position. It is very clear that the Government see the IMF’s role as supporting individual countries and not currencies. That has always been its role. If the IMF puts forward a case, as it may well do, for an increase in its resources, and if there is a strong case, the UK will support the IMF in increasing resources as required, as it has always done in the past.

[Lord Peston]

My Lords, using the immortal words of the noble Lord, Lord Henley, will the Minister give me a lesson in economics and explain why the Government still do not forthrightly support the maintenance of the euro? What possible benefit is there to us in the Government seeming to drag their heels when dealing with this matter?

[Lord Sassoon]

My Lords, as I have repeatedly made clear this afternoon and on other occasions, the UK Government want to see a strong and dynamic eurozone and European economy. But it is for the eurozone countries to take the lead in supporting the euro as a currency.

[Lord Lawson of Blaby]

My Lords, there is only one thing as worrying as the collapse of the eurozone, and that is the continuation of the eurozone. It has been demonstrated to be fundamentally flawed and is the cause of all these problems. Is the noble Lord, Lord Campbell-Savours, not right that at the heart of the thing that we need to address is the risk of a banking meltdown? Will the Minister give an undertaking that should it prove necessary for the United Kingdom Government to rescue any British banks, they will do so on much tougher terms than the ludicrously soft terms on which the previous Administration went in to save banks?

[Lord Sassoon]

My Lords, we have a lot to learn about the softness with which the previous Administration went about a lot of things. One of the key lessons for this crisis is that we must stick to a deficit reduction programme that is firm and fair, and keep this country isolated from the worst of the problems that are all around us.

Education: Careers Advice

Tuesday 17th January 2012 Lords Chamber

Question

14:52

Asked By

[Lord Roberts of Llandudno]

To ask Her Majesty’s Government what plans they have to improve careers guidance for under-25s.

[The Parliamentary Under-Secretary of State, Department for Business, Innovation and Skills (Baroness Wilcox)]

My Lords, in April the National Careers Service will be launched in England. It will provide high-quality information and advice on careers, online and by telephone. For those aged 18 and over, it will provide a face-to-face service in the community. From September all secondary schools in England will have a legal duty to secure access to careers guidance for pupils aged 14 to 16. Subject to consultation, this duty will be extended to 16 to 18 year-olds in schools and in further education.

[Lord Roberts of Llandudno]

I am grateful for the references to England and I only hope that we speak to Wales, Scotland and Northern Ireland as well. I appreciate that careers advisers in the new development will be independent. Are we certain they are going to be trained at the top level and that the interviews they conduct will not just be online or by computer but be face-to-face discussions with the youngsters, who are often among the 1 million unemployed? In respect of the face-to-face discussions, do we realise that only 7 per cent of young people know the meaning of apprenticeships? What are the Government going to do to make apprenticeships far more widely known about and better accepted?

[Baroness Wilcox]

The National Careers Service is being put together to answer pretty well everything that the noble Lord, Lord Roberts of Llandudno, has just suggested. We know that the careers advice that has been given up until now has been very patchy, and neither parents nor children have understood what their choices are. We hope that the training and monitoring that we will do will make absolutely sure that schools will get the right advice for children in their area.

[Lord Young of Norwood Green]

My Lords, having visited a comprehensive school this morning and talked to the lower sixth form, never have I been more reminded of the importance of careers guidance when young people begin to make choices about further education and careers. Is the Minister worried about the comments by the president of the Institute of Career Guidance? He said:

“In reality, the National Careers Service is an illusion, and not a very imaginatively branded one either, and is a clear misrepresentation with regard to careers services for young people … The likely reality is that hundreds of thousands, and possibly millions, of young people will never get access to personalised impartial career guidance”—

I stress those words—

“having to rely on the national telephone helpline or website and school staff”.

I do not expect the Minister to agree with that, but I would expect her to assure the House that there will be a review of the current approach to careers guidance and to ensure that the right level of personalised careers guidance is available to young people.

[Baroness Wilcox]

We take this issue very seriously. We are putting new money towards it and ensuring that the youth contract will provide nearly 500,000 new opportunities for young people, including apprenticeships and work experience placements. The important thing as far as we are concerned, and our aim, is to get every unemployed young person earning or learning again. We do not think that careers advice has been good in the past and we think it can be improved upon. We are using the original Connexions system to help us to provide a better outcome than we have had thus far. With 1 million youngsters out of work, we know how important this is.

[Baroness Deech]

Does the Minister appreciate that the cuts in legal aid proposed by the Government will devastate the career prospects of young people, many of them from ethnic minorities, who wish to become lawyers? The possibility of earning a living with legal aid in interesting areas such as immigration and family law has been wrecked, not to mention tuition fees.

[Baroness Wilcox]

We are giving schools the power to decide in their area what is going to be right for the children in their schools. This is a very empowering thing to do. We have enormous confidence in our schoolteachers. We believe that our schools should be given this opportunity. Perhaps the noble Baroness would like to speak further on this to me. We will ensure that every opportunity is available to our children.

[Lord Mawhinney]

My Lords, in her Answer my noble friend referred to the service thus far as “patchy”. Many of us who have been privileged to be Members of Parliament over the past 30 years would not be nearly so generous as she has been. What are the radical changes that are planned that give my noble friend confidence about this bright new tomorrow?

[Baroness Wilcox]

Local authorities deliver both universal careers guidance and targeted support for vulnerable young people under the Connexions brand, and there is widespread evidence that a lack of focus on careers guidance led to provision of variable quality, which is what I was referring to. That is why we have decided to end the Connexions area-based grant that the noble Lord is referring to. Local authorities retain the responsibility to help young people not in education, employment or training to re-engage. We are concerned about children at every level: children in schools, and children who have just left school and are wandering the streets with no training and no work to go to. Do not worry, we are really on top of this, and any advice that the noble Lord can give me, I am happy to have.

[Lord Taylor of Blackburn]

My Lords, the noble Lord, Lord Roberts of Llandudno, mentioned the independence of these advisers. Will they really be independent or will they just be yet more teachers who find themselves with a little spare time in their timetable and are given this job to do?

[Baroness Wilcox]

That sounds a bit like the careers guidance when I was at school all those years ago. No, the whole point is that these are going to be specially trained careers advisers. They will be external to the schools. It will not just be—forgive me—the teacher who maybe has time to go to the library for the couple of rows of books that we used to get pointed towards. This is real careers advice; we need it now, and we are determined to provide it.

Planning: Naseby Wind Farm

Tuesday 17th January 2012 Lords Chamber

Question

14:59

Asked By

[Lord Naseby]

To ask Her Majesty’s Government whether the Secretary of State will intervene in the decision to build a wind farm overlooking the site of the Battle of Naseby.

[Lord Naseby]

My Lords, I beg leave to ask the Question standing in my name on the Order Paper. In doing so, I declare an interest as the patron of the Naseby Battlefield Project.

[The Parliamentary Under-Secretary of State, Department for Communities and Local Government (Baroness Hanham)]

My Lords, I assume—I hope correctly—that my noble friend’s Question relates to the proposed wind farm at Kelmarsh, which has been the subject of a recent planning appeal. In that case, the decision has been made by a planning inspector acting on behalf of the Secretary of State and is final unless it is challenged in the High Court. The period in which a High Court challenge can take place has not yet expired, so I cannot comment on this case.

[Lord Naseby]

My Lords, is it not extraordinary that our precious battlefield sites of Hastings, Bosworth, Culloden and Naseby can be spoilt by wind farms, especially when planning guidance PPS5, introduced less than a year ago by the present Government, specifically mentions the need to protect the setting of a heritage site? How can one inspector ignore PPS5 on the—in my judgment—spurious grounds that wind farms are limited by time as their life is only 25 years? Will the Minister think again and come with me to the viewpoint, which is funded by the Heritage Lottery Fund, and see the impact that six windmills will have from Colonel Oakey and Prince Rupert’s viewpoints? Surely the Secretary of State needs to recognise that we do not have the funds to challenge in the High Court. However, the Secretary of State has the right to call in at any point, and I ask my noble friend to convey that to him.

[Baroness Hanham]

My Lords, I hear very clearly what the noble Lord has said. As I said, I cannot comment on the particular matter that he raises. All I would say is that there are two issues here. One is the Planning Inspectorate, which, as noble Lords will know, is independent. The planning inspector makes a decision on behalf of the Secretary of State, but he or she takes that decision in the light of his or her own views. The protection of areas of a special nature is covered by the national planning policy framework and the expectation is that they will be protected.

[Lord Jones]

My Lords, surely the Government will move towards a rethink, bearing in mind the huge importance that that battlefield held for future parliamentary democracy. Is it not the case that on that battlefield the King lost an army and Parliament assumed dominance? It was there that Cromwell’s cavalry, on the second charge only, was able to smash through the royalist army. It was there that Colonel Oakey’s enfilading of the royalist infantry ensured that the parliamentary forces succeeded. Is this battlefield not quintessentially the middle English countryside, adjacent as it is to the sleepy charm of Naseby village and being the haunt of buzzard and skylark?

[Baroness Hanham]

My Lords, on the back of that history lesson and exposition, I do not think I can say anything more, other than that I hear what noble Lords have said.

[Lord Brooke of Sutton Mandeville]

My Lords—

[Baroness Parminter]

My Lords—

[The Chancellor of the Duchy of Lancaster (Lord Strathclyde)]

My Lords, I feel we should hear from my noble friend Lady Parminter.

[Baroness Parminter]

Thank you. My Lords, does the Minister think that the opportunity to make revisions to the national planning policy framework should be used to make clear the importance of the landscape setting of historical assets in contributing to our understanding of a sense of place and who we are from the ideas and events that have shaped our country?

[Baroness Hanham]

My Lords, the national planning policy framework will be coming into existence in the next weeks or months. We are looking to the protection of areas of natural beauty as the noble Baroness has indicated.

[Lord Lea of Crondall]

My Lords, the noble Lord, Lord Naseby, mentioned Culloden. Are there any plans for a wind farm at Bannockburn?

[Baroness Hanham]

My Lords, that would be a matter for the local community to decide when they put together the local plan on which ultimate decisions will be made.

[Lord Brooke of Sutton Mandeville]

My Lords, does my noble friend recall that the royalist centre at the Battle of Naseby was led by that great soldier Sir Jacob Astley, who subsequently surrendered the last royalist army in the field with the words which have a lasting relevance to the political scene: “Gentlemen, you have beaten us, now go fall out among yourselves”?

[Baroness Hanham]

My Lords, I merely thank my noble friend for adding to the history lesson which we have all much enjoyed.

[Lord Cormack]

My Lords, my noble friend said that the inspector makes a decision on behalf of the Secretary of State. Can that really be right? Does not the inspector make a recommendation and the Secretary of State makes the ultimate decision?

[Baroness Hanham]

My Lords, as I understand it, the initial recommendation by the planning inspector is made on behalf of the Secretary of State. If that is incorrect, I will come back to the noble Lord.

Consumer Insurance (Disclosure and Representations) Bill [HL]

Tuesday 17th January 2012 Lords Chamber

Third Reading

15:06

Bill passed and sent to the Commons.

Welfare Reform Bill

Tuesday 17th January 2012 Lords Chamber

Report (4th Day)

15:07

Clause 69 : Ending of discretionary payments

Amendment 50ZA

Moved by

[Baroness Lister of Burtersett]

50ZA: Clause 69, page 54, line 8, at end insert—
“( ) Where amounts are re-allocated to local authorities as described in subsection (5), the Secretary of State must publish the following information annually for five years following the first re-allocation—
(a) the amount of money which has been re-allocated from the Consolidated Fund in each local authority; and(b) an annual report accounting for the expenditure of these amounts in each local authority area.”

[Baroness Lister of Burtersett]

My Lords, like Amendment 50 debated last week, this amendment is designed to minimise the adverse effects likely to result from the abolition of the discretionary Social Fund—

[Baroness Anelay of St Johns]

My Lords, in order to be of assistance to the noble Baroness, who is seeking to move a very important amendment, may I suggest that those leaving the Chamber do not pass in front of speakers? That is not the habit of this House. May they please leave the Chamber by another route, so that we may hear from the noble Baroness?

[Baroness Lister of Burtersett]

Thank you.

The amendment is about accountability. Considerable concern was raised in Grand Committee about the accountability of local authorities for the moneys devolved to them when the discretionary Social Fund is abolished. The amendment has been drafted with the help of Family Action, to which I am grateful, so as to put into effect the recommendation of the Communities and Local Government Committee report Localisation issues in welfare reform. While the CLG Committee accepted the Government’s case against ring-fencing the money, its report said that this,

“may carry some risks at a time of difficult financial circumstances for councils”.

The committee therefore recommended that,

“central government identifies clearly the amounts that are being allocated to local authorities, and collects information about their use, until the new arrangements have bedded in—we suggest a period of five years. … This would provide some reassurance about the effectiveness of the new system in helping those in need”.

Ministers have been giving out mixed messages on this issue. I hope that means that they are genuinely trying to find a way of answering the concerns about lack of accountability that have been raised in a number of quarters. One ministerial response has been to rely on the ballot box, even though the people affected are those least likely to vote, and also to contend that it is sufficient to set out the purpose of the funding in a settlement letter.

However, a chink of light emerged in the Government’s response to the call for evidence, when they said that the settlement letter, mentioned last week by the Minister, the noble Lord, Lord De Mauley,

“may be supplemented with a requirement to report on how the funding has been used”.

The CLG Committee observed:

“This would fall some way short of the accountability mechanisms suggested by some stakeholders”.

Nevertheless, if the Minister now committed the Government to imposing such a requirement, we would be satisfied.

Last week, the noble Lord, Lord De Mauley, spoke about supplementing the planned review of a cross-section of local authorities in order to collect more information on how the money is spent. While I welcome the spirit in which this very small concession was offered, I fear that it falls short, not just of what we believe is necessary but of what the Government themselves hinted at in their response to the committee’s evidence.

We are still awaiting an answer to some astute questioning in Grand Committee from the noble Lord, Lord German, about how the Government will meet their obligations of stewardship for the money allocated to local authorities in England. As the noble Lord stated very powerfully, this is a question of accountability to Parliament. How can such accountability be ensured if local authorities are not required to report on how they spend the money allocated to them?

The purpose of Amendment 50ZB is to allay the fears voiced by voluntary organisations such as Family Action, Women’s Aid and Platform 51 that local authorities might impose a local or residence condition as a way of rationing assistance when allocating social housing. Again, I am grateful to Family Action for help with drafting this amendment. Given the pressures on local authorities, it is quite conceivable that some at least might seek to impose a local connection test—that is, confine help to people who already have a local connection with the area. In Committee, I tabled a general amendment to prevent such a test. This amendment is drafted more tightly to ensure that such a test is not applied to people fleeing domestic violence—or, more accurately, people who have fled domestic violence—young people leaving local authority care, people who are homeless or who have been homeless within the previous 12 months and people leaving institutional residential care such as a hospital, prison or a young offenders’ institution. In other words, this amendment is designed to safeguard the interests of groups who are likely not to have a local connection.

As the voluntary sector consortium headed by Family Action points out,

“These groups of people are much less likely than others to be able to demonstrate local connection. Without crucial assistance from a Community Care Grant to buy essential items such as cooking equipment and bedding, they may struggle to set up and maintain a home. This puts them at risk of reoffending or moving back into temporary or institutional accommodation, which is far more costly and means they lose their newly-found independence”.

The consortium is particularly concerned that, without a clear legal prohibition on requiring a local residence connection, women who have experienced domestic violence will be discouraged from moving elsewhere to flee their violent partner, or will return to their partner because they are unable to provide basic household items such as a cooker to prepare cheap healthy food for themselves and their children. The consortium’s concerns were echoed in the impact report published last week by the Office of the Children’s Commissioner for England, which looked at the impact of the legislation in relation to children’s rights. When questioned on this matter in the House of Commons, the Secretary of State assured Members that local authorities had a moral duty. Welcome as this recognition is, I fear that if a woman who has fled domestic violence or an ex-prisoner cites a moral duty to their local authority they will not get very far. Surely if the Government believe that a moral duty holds, they should translate it into a statutory duty.

The Minister, the noble Lord, Lord Freud, did not address these issues in Committee but kindly wrote to me afterwards. However, he simply set out in his letter the local connection provisions on homelessness contained in the Housing Act 1996. I shall not spell those out now, but they protect a person from being denied any assistance anywhere because of a lack of local connection. If the Minister is saying that the same rule will apply here, then I welcome it, but does it not need to be written into the legislation? As I understand it, the Housing Act 1996 does not apply to the legislation we are discussing here. If the Minister were to offer to bring forward his own amendment at Third Reading to give effect to the Housing Act provisions on local connection, I would happily withdraw the amendment as unnecessary. As an absolute minimum, can the Minister assure the House that the settlement letter will spell out that local authorities should follow the same provisions as in the housing legislation?

It seems to me that the aims of these two amendments are not that far from what the Government themselves wish to achieve. I hope therefore that the Minister might be willing either to accept them or to agree to bring forward his own amendments at Third Reading. I beg to move.

15:15

[Baroness Meacher]

My Lords, I will speak briefly to Amendment 50ZA and will refer to Amendment 50ZC. I very much applaud the aims of the noble Baroness, Lady Lister, in seeking to have publication of information about the allocations of money to local authorities for the purposes envisaged. She presented her case very powerfully as always.

I want to thank the Bill team for a most helpful conversation. I understand that the £36 million allocated for crisis loans could be spent by local authorities on grants or payments in kind as well as loans. I find that very encouraging. I for one am very suspicious of loans for people attempting to live on the breadline—they can build up even greater problems for the future—other than when provided for budgeting purposes, which I know is very much what the Minister has in mind. If, for example, households receive half their monthly income half way through the month as a loan only to be repaid at the end of the month, that would go some way to ameliorate what would otherwise, for me anyway, be a highly risky set of proposals.

Amendment 50ZA, tabled by the noble Baroness, Lady Lister, would provide information on whether the funds had been spent by local authorities on the purposes for which the Government are allocating them—we all understand that is what they are being allocated for. I have some concerns that, even if the Minister concedes this amendment, it remains true that there is no statutory requirement for local authorities to provide some form of assistance to households in crisis. Many Social Fund crisis loans are sought because mothers, often single mothers, have no cash for the electricity meter—apparently, this is really the dominant issue confronting people who seek these loans—with several days to go before getting any more benefit and, of course, the children are cold and the mother cannot even make a hot meal for them without some form of electricity. I understand that the idea of the settlement letter is to spell out the purposes for which the £36 million should be used. I applaud that. I also understand that the DWP plans to follow up a representative sample of local authorities after one year to find out how they have spent the money.

My concern is that over time the settlement letter might be redrafted—heaven forbid that Ministers even change from time to time—and, if local authorities report after one year that unfortunately the £36 million had to be spent on other matters, it seems to me that there is no way of ensuring that these households in crisis actually have funds allocated to those needs. That is actually my concern. We need to know that there will continue to be a system for dealing with these household crises, particularly for families with children. We do not want these children disadvantaged.

I understand the logic of making the £178 million for community care grants and crisis payments available to local authorities, which are no doubt closely involved with many of these families—certainly, if they are not involved, they should be. The aim, as I understand it, is that these funds need to be brought together with other forms of assistance for these families in order to generate greater value for money. At the moment, the Social Fund is a national system that operates at arm’s length from other services. I recognise that this has some disadvantages. The concern is that every local authority is likely to respond differently to this challenge. How can we be sure that households in crisis will have somewhere to go for help, as I have already said? The Government are already committed to the settlement letter and review after 12 months, again as I have already alluded to. I welcome those commitments very strongly. They are a start, but they are a weak provision in this very important area of policy.

I hope that the Minister will take seriously the need for a more robust system to underwrite what I understand to be the Government's intentions. The amendment tabled by the noble Baroness, Lady Lister, is one option, but whether or not the Minister accepts Amendment 50ZA, perhaps he will consider incorporating in regulations the requirement that the funds envisaged for resolving household crises are indeed allocated to that purpose. I understand that how local authorities want to do that is a matter for them, but I think that ensuring that the funds are focused on that issue merits a sentence in the regulations. That would certainly make a much stronger support for the provision and give an assurance to the House that we have not lost it.

I would be very grateful for the Minister's serious consideration of the amendment. I should mention that I will not move Amendment 50ZC at this stage.

[Lord Kirkwood of Kirkhope]

My Lords, I make a brief intervention to support the amendments, as I did in Committee. Clause 69 is very important for a relatively small but very vulnerable group of people. The discretionary Social Fund has been part of the furniture, if you like, of social security for a long time, and during the period that it has been deployed, people have been able to take advantage of it to save the public purse considerable sums. One of the main purposes behind the discretionary Social Fund is to prevent people being institutionalised in various ways, and it has done that very successfully. There is cross-party agreement that reform of the Social Fund is long overdue, but to abolish or decentralise it like this raises many questions, which remain unanswered. I hope that the Minister will take the opportunity to try to assuage the concerns that some of us continue to have.

First, the process that will now unfold is less than clear to me. Reading the penultimate subsection of Clause 69, I think that an affirmative resolution will be required to give effect to the power that the Government are seeking in the clause, but I should like reassurance about our ability to have ongoing discussion about how the Social Fund Commissioner’s assets and the apparatus that we have in place at the moment will be dismantled in a way that makes sense, and that the allocation formula for the disbursement of these moneys is carefully considered and consulted on, because the discretionary Social Fund spend obviously has a very spatial dimension to it because some communities need it much more than others. We need to be careful about how we make that decision in the first instance. That is another reason why Parliament, by virtue of affirmative resolution or statutory instrument, must be continuously approached for advice and reassurance. The sample of local authorities being lined up for the welcome review process needs to be carefully considered because of the point I have just made: the decentralisation process will affect some dramatically differently from others.

I still have serious misgivings about this. If we are going to do this, we need to be really careful that we are getting it correct in the first instance and that the client group who have relied on discretionary payments from the Social Fund in crisis situations are not left wanting, completely abandoned and without access to liquid cash in circumstances where they find it difficult to survive.

[Lord Boswell of Aynho]

My Lords, I wish to raise briefly the question of whether to centralise payments to people in extreme difficulty or whether to leave that to the discretion of local authorities or, as was originally suggested prior to the First World War, friendly societies, or others. That idea has subsisted for at least 100 years and I think it will continue. I am generally supportive of the localism agenda and I can see material benefits in devolving this opportunity to local authorities. However, the amendments raise two issues that need a little reflection.

The wider question, which has been touched on by a number of noble Lords, is whether this money, which was intended for people in severe difficulties, will continue, albeit with local administration, to be applied to such people in general. I think that on the whole the Government are facing in the right direction here, but I look forward to the Minister’s assurances on it.

The specific twist that I want to add was prompted by something that the noble Baroness, Lady Lister, said about whether there should be a local connection. Clearly there is the subtext that there could be some discrimination in favour of the local boy or girl against someone from outside, someone who was felt to be in some sense the architect of their own distress or someone in some way morally unworthy. I do not want to go on about that now, but we can see the argument developing.

I should like the Minister to consider—and it may be helpful to him to do so—the fact that since the passage of the Housing Act some 16 years ago, we have had all the equality duties, including the public sector equality duty. Certainly local authorities, in exercising the discretion being offered them, will have to operate within the framework of that duty. I wonder whether that is indeed helpful in obtaining the assurances that I think we want with regard to making sure not only that the money goes where it is intended to go but that it goes to the people who need it most within that category of difficulty, rather than being siphoned off to people who are more acceptable or who come more within the interest of the local authority concerned.

[Baroness Sherlock]

My Lords, I want to speak in favour of all these amendments and to ask a question about Amendment 50ZB. When we discussed the Social Fund on our previous day on Report, I raised the fact that the Office of the Children’s Commissioner had published the Child Rights Impact Assessment of the Welfare Reform Bill. I understand that at that point the Minister had not had the opportunity to read the assessment in any detail, but I wonder whether he has had the chance to read it since then and, if so, whether he can assure the House about the line that says:

“In failing to guarantee that crisis support is available for children fleeing an abusive home with their parent/carer, the clauses abolishing the Social Fund fail to take all appropriate legislative measures to protect children from domestic abuse and we therefore believe they are in breach of Article 19”,

of the UN Convention on the Rights of the Child. That goes to the heart of the point which the noble Lord, Lord Boswell, has just raised. People might have a very good reason to cross boundaries. If one were fleeing domestic violence, that would be a good reason not to move to the neighbouring street, as I am sure the noble Lord would accept. How can the Government guarantee that local authorities will give appropriate support to children and families in that circumstance, and how can they prove that the UK will discharge its responsibilities under this convention?

[Lord Newton of Braintree]

My Lords, I speak as a heretic who is even now probably having his burning at the stake prepared by the Secretary of State for Local Government, my right honourable friend Eric Pickles, because I believe in ring-fencing. I have always thought it daft that Governments make available for a specific purpose money that is then spent by other people on something else. The Government get the blame for not having provided the money and everyone else gets the credit when anything good happens. I do not think that is sensible. However, it is a brick wall against which I do not propose to bang my head this afternoon.

The suggestion of the noble Baroness, Lady Lister—that if local authorities are going to have this money, they should at least be required to account for it—is a good one. I am slightly scarred by my experience as chairman—although I am no longer—of Help the Hospices; the previous Government allegedly made £50 million available but no one ever found it. It disappeared into thin air. I do not want to see that happen here. I do not want to see it spent on swimming pools, or campaigns, or many other good causes, when it is intended for people with severe disabilities.

15:30

There is an irony here which the noble Baroness, Lady Lister, will appreciate. Nearly 25 years ago, when we were introducing the Social Fund, I was the villain. She pursued me up hill and down dale. Now I am the hero whose achievement is to be safeguarded. I hope she may reflect on that.

This transfer is probably sensible. The needs of very seriously disabled people require a discretionary, judgmental element in the help that is provided. This cannot be met by benefit rates, which are inevitably restricted and generalised, so I am not opposed to this. The noble Baroness knows that I declined to sign her earlier amendment on the basis that all such money intended for disabled people—not just the Social Fund money—should be, if not ring-fenced, then protected to some extent. I cleave to that view.

It is sensible to have at least this requirement for local authorities to say what their allocation has been and what they have done with it, in line with whatever protestations Ministers have made. It does not cost the Government anything significant. It does not blow a further hole in the finances. It is reasonable, sensible, proportionate and justified, and I hope we shall get a positive response.

[Lord Blair of Boughton]

My Lords, like other speakers I support Amendment 50ZB. Very few police officers have not come across the fleeing mother with her children. There is no more desperate person imaginable. However, that is not the point I want to make. My point relates to a longer-term issue, and is about making sure that this funding goes towards the long-term prevention of crime. The connection between criminality and having been in care, between criminality and homelessness, and between criminality and having been already in prison is so clear that money spent here and accounted for by the local authorities, as the noble Lord, Lord Newton, has just said, is money well spent. This money should be spent on this, and to have it spent on other things would be a great shame.

[Lord German]

My Lords, to concur with the noble Lord’s last sentence, this is a matter of accountability. I refer to Amendment 50ZA, which applies only to England. Members of the House of Lords will be very familiar with the fact that other parts of the United Kingdom will receive this money, and I would like some confirmation from the Minister on the arrangements that are to be made for Scotland and Wales. If, as I understand it, this money is to be transferred by means of the Barnett formula, the amendment will apply only to England. I wonder how it is possible to seek accountability for money that has been given by this Parliament for the services that are so vital for people within the current arrangements for the Social Fund. This is not an anti-devolution to local government statement, but the lines of accountability here do need to be judged. If we are devolving the power for that accountability to the Welsh and Scottish Governments, we need to state that now, and noble Lords need to understand that this is a further devolution of responsibility. Many noble Lords may accept this, or like it, or find it an attractive proposition, but the Government’s intention in this respect is as yet unclear to me.

[Baroness Hayter of Kentish Town]

My Lords, I am not sure whether the noble Lord, Lord German, is for or against the amendment, but all the other speakers have clearly supported these amendments. This is quite sensible, because the amendments all set out to ensure that vulnerable people can continue to access support once the Social Fund has been devolved, to whomsoever.

The first amendment in the group implements a recommendation of the Select Committee in another place. It would provide some reassurance about the effectiveness of the new system of helping those in need, and clearer information to local voters about whether their local authority is choosing to spend less than the allocated amount. It does nothing to restrict local discretion in how to implement the Social Fund replacement scheme; it merely places a requirement on the local authority, as has been said, to account for it. I think that all noble Lords who spoke would support that, and I feel sure that this is an aim that the Minister, similarly, will support.

The second amendment in the group, as was spelled out, would ensure that the use of local connection rules cannot prevent, for example, care leavers, the homeless, those fleeing domestic violence—the noble Lord, Lord Blair, spoke about them—and those leaving institutional residential care accessing Social Fund-type support. It is true that it ties the hands of local authorities a little, but only to ensure that groups that might be very much in need of support are not left with nowhere else to turn. As we heard, for many women fleeing domestic violence, community care grants are vital in helping them to set up a new home and perhaps buy a cot, a bed or a cooker. Given that many women need to enter refuges or other homes away from their former partners, they will often be unable to meet local connection rules.

We know that, among people who use the discretionary Social Fund, one in eight is leaving some sort of institutional care; nearly one in 10 is leaving prison; and one in five has at some time experienced homelessness. I work in Camden with people who have alcohol problems. There are a lot of train stations in Camden, so a lot of people arrive on our doorstep. At the time we help them with their drink problem, they will not be in the same area where they have lived and worked for perhaps 30 years.

Although I understand that the noble Baroness, Lady Meacher, will not press her amendment, I urge the Minister to consider it. We know that although universal credit budgeting loans could be available for rent in advance, crisis loans will be abolished before the introduction of universal credit, and it could be some time before the new system is set up and reliable. We know from our experience of many new IT systems that even the best laid plans occasionally go wrong. We have had many assurances from the noble Lord, Lord Freud, about the robust nature of the system being put in place, but it would be prudent to ensure that a national safety net remains while we wait for him—we hope—to be proved right on this occasion. I said “prudent” but it is probably vital that we continue to guarantee national access to community care loans and crisis loans until the universal credit system is set up. Once national systems have been devolved, the accountability that my noble friend spoke of, as well as the local connection rules, will be an essential part of helping these vulnerable groups. We are happy to support all three amendments in this group.

[Lord De Mauley]

My Lords, when we discussed the Social Fund last week, I hope I was able to offer reassurance in two key areas. First, I informed noble Lords that we would extend the 2014-15 review of a cross-section of local authorities to include information about the way they have used their funding for the new local provision. Perhaps I may return to that in a moment.

I was also able to assure your Lordships that the settlement letter that noble Lords referred to today that will accompany the funding will set out what the funding is to be used for and will describe the outcome that must be achieved—although, for reasons I explained, not the method that should be used to achieve the outcome. After further consideration of the issue, and following questions from noble Lords, I am able to explain what the settlement letter will contain. The letter will set out what the funding is to be used for, the underlying principles, and describe the outcome that must be achieved. It will say that the funding is to concentrate resources on those facing greatest difficulty in managing their income, and to enable a more flexible response to unavoidable need. The letter will make explicit that the funding is to provide a replacement provision for community care grants and general living expenses crisis loans.

The letter will go on to explain that community care grants were awarded for a range of expenses, including household equipment, and were intended to support vulnerable people to return to or remain in the community or to ease exceptional pressure on families. They were also intended to assist with certain travel expenses. It will also explain that crisis loans were made to meet immediate short-term needs in an emergency or as a consequence of a disaster when a person had insufficient resources to prevent a serious risk to the health and safety of themselves or their family. As I said in our discussion of Amendment 50 last week, I assure your Lordships that we are equally committed to ensuring that this funding goes to help the most vulnerable.

Amendment 50ZA would require the Secretary of State to publish information on the amount of money given annually to each local authority. I can assure your Lordships that we already plan to publish this information on the DWP website. On community care grant budgets, noble Lords might like to be aware that work has been done since Committee to make the funding distribution fairer by changing the funding allocation methodology.

It is each local authority’s responsibility to decide what type of support it provides with these funds. We have already been made aware of a variety of innovative ways in which local authorities plan to use this money, such as furniture re-use schemes, working with credit unions, investing in existing projects or joining up with other organisations in the area. For example, the fieldwork undertaken by the department shows that rural local authorities had very different ideas from those of urban authorities, and would embrace the freedom to design and establish local provision that suits the particular challenges they face.

Some benefit recipients cannot even afford the delivery of free goods from support schemes. During the fieldwork, the department was made aware of the fact that a local authority in Yorkshire is considering using some of the new funding to pay the delivery fees charged by an existing provider for the delivery of free goods to benefit recipients and other low income groups. This demonstrates the benefit of tailoring support to the local area. This initiative is particularly useful in a rural area, as it would have been far more expensive for people to arrange their own deliveries than in an urban area. This service would help people on the lowest incomes to receive free household goods that they might otherwise be simply unable to access.

Another example of innovative thinking came from a local authority in the Greater Manchester area, which said that it would use the funding to expand the local credit union, as this already provides household goods to people on low incomes. Expanding the scheme would increase access to affordable credit for those on low incomes and reduce the reliance on high-cost and illegal lenders. Yet another different approach to the new provision is that of a local authority in the south-west, which has been looking at how commissioning services would boost the local economy, providing new skills and routes back into employment and out of poverty.

As I hope is evident from these examples, giving local authorities the responsibility for deciding what the new local provision will look like allows for innovative new schemes that are tailored to the local area.

[Lord Kirkwood of Kirkhope]

These examples are very helpful, as is the further fleshing-out of the content of the letter to local authorities, but what is the arbitration process, supposing local authorities deliberately and in bad faith pay no attention to the contents of the letter that the Minister is proposing to send?

[Lord De Mauley]

Perhaps I might come to that as I proceed. Amendment 50ZA would also require the Secretary of State to publish an annual report accounting for the expenditure of this funding. As each local authority will be delivering different types of support, requiring the Secretary of State to report on a large number and variety of schemes—some of which, as I have explained, would be combined with existing services—would, I suggest, be impractical as well as costly. It would lead to expenditure on administration when local authorities will, in any event, be required to account to their communities for their spending and services.

There will be a large variety in the size of awards to local authorities, as the amount of funding each will receive will be based on the equivalent Social Fund spend at the point of transition. Therefore, while some local authorities will receive large amounts, others will receive less than £10,000. It would be far too onerous to require these authorities to report in detail on how the funding is spent. It would make no sense to enforce the same reporting requirements on such a wide range of local authorities receiving such differing amounts. However, as I said in the debate on Amendment 50, the department will conduct a review in 2014-15, obtaining appropriate information from a representative cross-section of local authorities, in order to help inform future funding levels. I am not talking about a small sample. An analogous exercise conducted last year covered 50 local authorities, so we are talking about quite a substantial exercise. Following the helpful contributions of noble Lords in Committee, I have made a commitment that this exercise will be extended to provide more information about the way in which local authorities have used the funding.

Amendment 50ZB seeks to ensure that certain particularly vulnerable groups of people are not rendered ineligible for support on the basis of a test of local residence or connections. We have discussed this issue with local authorities, which are, of course, as noble Lords will be well aware, already very familiar with the issue. In fact, it is not really a Social Fund-specific issue at all because local authorities already deal with boundary issues in the delivery of other services, such as housing and homelessness. Local authorities already have many duties to provide assistance to vulnerable people under existing legislation and frequently co-operate with other local authorities in doing so. We believe that local authorities should be given the freedom to set their own eligibility criteria to enable them to tailor the new provision to their local area.

Furthermore, we will encourage local authorities to link support across boundaries. Indeed, several authorities have mentioned to us in discussions that they were already planning to establish collaborative working relationships. Wandsworth, Hammersmith and Fulham and Kensington and Chelsea, for example, already work together to provide some joint services and have said that they will look to see how they can join up for this new local provision. Bristol is also looking at working with neighbouring authorities. Each of the groups referred to in Amendment 50ZB already receives assistance from local authorities and the Government. As my noble friend Lord Boswell mentioned, local authorities already have a number of existing responsibilities in relation to the provision of emergency and longer-term accommodation. They have particular responsibilities in respect of those with a priority need, such as those who are vulnerable because of age, mental illness or disability and those with dependent children.

The noble Baroness, Lady Lister, referred to Section 199 of the Housing Act 1996, which sets out what constitutes a local connection in relation to people who are homeless. There is also statutory guidance for local authorities from the Department for Communities and Local Government to which local authorities must have regard. The effect is that those with no local connection receive help from the local authority to which they apply; those with a local connection to a particular area receive help from the authority responsible for that area unless they are at risk of violence if they return there. A local authority housing a vulnerable person would be in a good position to provide help through the new local provision—for example, by providing furnishing for the accommodation it arranges. This is a more holistic approach for local authorities to adopt and such an approach would also be beneficial for local authorities delivering support to those fleeing domestic violence. Local authorities can use the new local provision alongside existing support.

The noble Baroness, Lady Lister, challenged me as to how the other groups in the amendment are covered by duties and responsibilities. Local authorities already have a duty to house someone fleeing from domestic violence. They will be able to use the new provision to continue to provide support further down the line—for example, helping to furnish new accommodation that has been provided to someone who has fled domestic violence. As regards young people leaving local authority care, local authorities have a duty to safeguard and promote the welfare of a child who has been a looked-after child, including providing maintenance, and have such duties until the child is 21. Local authorities also already have duties to support disabled people or those who are destitute. They must make arrangements for promoting the welfare of those with a disability or mental disorder, including assessing the welfare needs of a person leaving hospital having received in-patient treatment for a mental disorder.

The National Health Service and Community Care Act 1990 requires local authorities to prepare a plan for the provision of community care services in consultation with relevant bodies and to assess the needs of people who may be in need of these services. Local authorities are already required by multiple legislative duties to provide support to the most vulnerable people in their area and they have a great deal of experience of doing so. They will be able to use this experience to deliver the new local provision in a way that will best suit the people in their local area. Therefore, I suggest that there is no specific need for local connection eligibility rules to be published.

The noble Baroness, Lady Sherlock, asked about the Children’s Commissioner’s report. I have read the report, published last week, which suggests that certain changes made by the Bill could lead to breach of the UN Convention on the Rights of the Child. The Government are satisfied that the Bill is compatible with their human rights obligations, including those under the UN Convention on the Rights of the Child.

The safeguards to which I have referred will ensure that the money intended for vulnerable people goes to vulnerable people. The most discretionary support will be better tailored to people’s needs when it is delivered locally. The new local provision and the national provision of payments on account will complement each other and, taken as a whole, they will provide more effective and better targeted support. For these reasons, I urge noble Lords not to press their amendments.

[Lord Wigley]

Does the Minister intend to respond to the point raised by the noble Lord, Lord German, with regard to the interplay with devolved authorities? It is a material question that was raised in Committee. My understanding in Committee was different from the understanding of the noble Lord, Lord German. If the Minister cannot respond now, perhaps he will write to interested parties in order to provide clarity on the matter.

[Lord De Mauley]

I am grateful to the noble Lord. I will write to him.

[Baroness Meacher]

Can the Minister also respond to the point raised by the noble Lord, Lord Kirkwood, which I also raised, on the real assurance—the teeth, if you like—that the Government will need in emergencies to make sure, without specifying how it is spent, that the money is spent on those in greatest need? I would be grateful for a response from the Minister.

[Lord De Mauley]

My Lords, I hoped that I had emphasised that point. A great deal of work has been done with local authorities explaining the proposal and the intentions behind it. We have encountered considerable enthusiasm for the principle. We have put a lot of effort into helping and educating local authorities which will be making the decisions. I hoped that I had emphasised the importance of that point. I am agreeing with the noble Baroness but I do not think that I can go very much further than I have gone.

[Baroness Sherlock]

I am obviously being very slow. What will the Government do if a local authority spends the money on a swimming pool?

[Lord De Mauley]

My Lords, the local authority will not spend the money on a swimming pool.

[Baroness Lister of Burtersett]

My Lords, I thank all noble Lords who have contributed to the debate. They have added some powerful arguments and questioning. In response to the noble Lord, Lord Newton, I should say that it is better to go from zero to hero than the other way round.

I thank the Minister who, I feel, is inching gradually in the direction that we have been trying to push him. He has again reassured us that the Government share the concern across the House that the money that is allocated to local authorities should be used for the purposes intended. It was helpful to have more information about what will be in the settlement letter. However, I have heard nothing today to reassure me that the money will necessarily be spent on what is intended. We should think of the context. Local authorities are under huge pressure. Apart from anything else, they will have to be responsible for council tax benefit, with a cut of 10 per cent in the money available for it. How tempting it might be for them to say, “Oh, let us use a bit of the Social Fund money to top up council tax benefit”.

How can the noble Lord say with such assurance that the money will not be used on a swimming pool, a road or anything else? Without the information that this amendment would provide, I am afraid that the Government simply cannot give that assurance. I am very disappointed that the noble Lord has not felt able to go further in meeting the spirit of these amendments even if not the letter of them. I do not think that he has dealt adequately with the questions and comments made by noble Lords.

We have the example of the supporting people budget. When the ring-fence was removed, immediately many local authorities started spending the money on other things. That was with an existing budget. This is a new budget, which will be even more tempting for local authorities. I hope that the Government will reflect further on this issue. We will certainly reflect further but, for the moment, I beg leave to withdraw the amendment.

Amendment 50ZA withdrawn.

Amendments 50ZB and 50ZC not moved.

Clause 74 : State pension credit: capital limit

Amendment 50ZD not moved.

Clause 76 : Personal independence payment

Amendment 50ZE

Tabled by

[Baroness Campbell of Surbiton]

50ZE: Clause 76, page 56, line 8, leave out “personal independence payment” and insert “personal disability costs payment”

[Baroness Grey-Thompson]

My Lords, the noble Baroness, Lady Campbell of Surbiton, is unfortunately unwell today. Currently, she is watching the Report stage of the Welfare Reform Bill from her hospital bed. She has asked that Amendment 50ZE is not moved and I would ask your Lordships’ House to agree to this request. I am sure that your Lordships’ House would also want to send best wishes to the noble Baroness for a speedy return to the Chamber.

Amendment 50ZE not moved.

Amendments 50ZF and 50ZG not moved.

Amendment 50ZGA

Moved by

[Baroness Meacher]

50ZGA: Clause 76, page 56, line 17, at end insert—
“(4) A person is not entitled to personal independence payment unless the person is aged 18 or over.”

[Baroness Meacher]

My Lords, in moving Amendment 50ZGA, I shall speak also to Amendment 56ZC, the purpose of which is to allow disabled children aged 16 and 17 to continue to qualify for DLA for children instead of PIP until they reach the age of 18. It would mean that they would not have to go through the PIP assessment process until they reach an adult age. It would also simplify the benefits system by aligning PIP with universal credit.

I thank the Minister for sparing time to discuss this amendment at the end of a long day, which was at the end of a long week. I should offer him my apologies because last week I was jetlagged, tired and not very well, and I did not always get all my little ducks in a row. But I understand that 16 and 17 year-olds applying for PIP would not have to go through an income assessment. However, they would have to undertake a capability assessment. The point of this amendment is to sort out some issues of principle and consistency in relation to 16 and 17 year-olds. When I met the Minister, we did not touch on these issues and I should be interested to know his response today.

I understand that this amendment would bring the Bill into line with the United Nations Convention on the Rights of the Child, which defines a child as,

“every human being below the age of eighteen years”.

More particularly—in my view more importantly—this amendment would deal with the adverse consequences of these clauses for the young people affected. In other words, if disabled 16 and 17 year-olds would benefit from being treated as adults, frankly, that would be good enough for me but the fact is that they will not.

16:00

In terms of consistency, the Government plan to raise the age of participation in education or training to 17 in 2012 and 18 in 2015, but the introduction of PIP from 2013 will treat 16 and 17 year-olds as working-age adults. Does it make any sense to treat these young people as children with respect to education and as adults when it comes to claiming benefits?

Another important point is that Clause 4 of the Welfare Reform Bill sets out the basic conditions of entitlement to universal credit, one of which is that the person will be,

“at least 18 years old”.

I understand that regulations will provide for some exceptions for that. I also understand that some children aged 16 and 17 may claim ESA and thus universal credit. But the basic assumption of the new universal credit system will be that children will be treated as dependents of their parents, and therefore not generally expected to claim universal credit in their own right, until they reach the age of 18.

In our discussion, the Minister defended the decision to transfer 16 and 17 year-olds to PIP on the grounds that they would only need to undertake the capability assessment and not the income assessment. That is fine. My question to the Minister is: why is it necessary to create this anomaly between the age limit for universal credit and the age limit for PIP? I look forward to hearing his explanation. In my experience, the Minister always has very good explanations for everything that the Government do, but I have difficulty imagining what the explanation for this one is, unless it is a straight conflict between the Treasury’s determination to cut £18 billion from the welfare and benefits bill and the DWP’s aspiration to create a much simpler system—an aspiration which noble Lords across this House support.

The treatment of 16 and 17 year-olds under the PIP system rather than the DLA system will also impact upon their entitlement to disability additions. As noble Lords will know, universal credit includes disability additions to provide extra help for both children and adults with disabilities. However, the gateways to this additional support differ for the two groups. Children aged 16 and 17 will, other than in some exceptional circumstances, count as part of their parents’ household. The disability additions for children who are part of their parents’ household will be based upon DLA. Even if these 16 and 17 year-olds are part of their parents’ household, along with younger children—and in almost every case 16 and 17 year-old disabled children will be a part of their parents’ household—they will not be treated as such. Again, is there any logic behind this provision?

A separate point is that the PIP assessment tool envisaged for 16 and 17 year-olds is not appropriate for children, albeit that the PIP assessment tool is more sensitive to mental health disabilities than the DLA assessment—I will return to that point, which is an important one. The Children’s Society points out that children and young people need a system designed to take into account their developmental needs and circumstances, including the importance of social networks and friendships. PIP questions are narrower than those for the DLA assessment. The DLA assessment itself includes reference to reasonable amounts of social activity and the support needed to take part in that. There is no question that friendship and the ability to get out and about are essential for children and perhaps even more essential for 16 and 17 year-olds than for any other age group whatever.

Despite concerns about the applicability of the PIP assessment tool to 16 and 17 year-olds, disabled children will be one of the first groups to trial the new assessment system when they turn 16. Is this not likely to lead to large numbers of unfair or inappropriate decisions? I understand from the CAB service that the numbers affected will be some 50,000 16 and 17 year-olds currently receiving DLA, plus the flow of future youngsters into that age group. I hope that the Minister will take this point seriously.

On mental health issues, the Minister is well aware of the concerns about the efficacy of face-to-face assessments for adults. Some improvements have undoubtedly been made, but those involved in the improvements recognise that there is still a long way to go to achieve an adequate level of reliability. Mind reinforces the point, stating that,

“although we recognise that there is a more explicit reference to mental health in the criteria for PIP than DLA, we are very concerned that many people currently receiving DLA for mental health problems will struggle to access the new benefit”.

Although a smaller proportion of mentally disabled people will lose benefit as a result of the shift from DLA to PIP, considerable numbers of both physically and mentally disabled people will lose out, as the Minister will be aware.

Before concluding these comments, I applaud the Minister’s commitment to improving assessments for people with mental health problems. He has been dedicated to that task and very real improvements have been, and are being, made. I think that this House will want to recognise that.

The amendment would achieve three things: it would align universal credit with PIP and the Government’s plans in other parts of the system to treat 16 and 17 year-olds as still being part of their parents’ household; secondly, it would safeguard young people from being assessed using an inappropriate tool, albeit that more explicit reference is made to mental health in the criteria; and, thirdly, it would further simplify the system. I look forward to the Minister’s response to these points. I beg to move.

[Baroness Finlay of Llandaff]

My Lords, the noble Lord, Lord Patel, and I have amendments in this group. Our noble friend Lady Meacher has spoken most eloquently to the specific problems for these age groups. This is Report stage, and we are well aware that there has already been much debate about young people who have to transition between children’s services and those for adults. However, I remind the Minister that, coming from a medical background, we have tabled our amendment because of the specific problems for those who fall ill suddenly or who are severely ill. As they transition for all their care in the medical sense, they transition also for all their life events and social interactions. They struggle to move to a degree of independent adulthood and are faced with a whole range of problems that those who are more settled either in the security of childhood or, later on, in an adult framework might not encounter so acutely. For that reason, we ask the Government to allow them to be considered separately should it be appropriate.

[Lord McKenzie of Luton]

My Lords, we have strong sympathy with these amendments, spoken to so effectively by the noble Baronesses, Lady Meacher and Lady Finlay. We had a bit of a canter around this issue in Committee, focusing particularly on 16 to 24 year-olds. I took from that debate, and the Minister may take the opportunity to confirm or deny it, that there is potentially scope within the Bill for a regulation not to require 16 year-olds inevitably to move towards PIP. If that is not the case, it is important that we clarify it, because it impacts on how we approach the amendment.

A number of questions have been posed which I should like to emphasise. The first is whether the Minister contends that the PIP assessment as currently constructed is fit. Does he believe that it would be appropriate for most 16 year-olds? The assertion is that it is not. Another issue is the extent to which there is alignment of ages for a range of things—the UN convention certainly, but care generally and education and training. Would it not be better if that alignment were brought into effect also for the purposes of the PIP and the DLA cut-off?

When somebody aged 15 is about to become 16, that is the point at which things change on the DLA journey and we move into a somewhat different regime. If somebody reaches that once PIP is up and running, do they inevitably have to apply and go through the PIP process at that point, or is there an opportunity for them to remain within DLA or perhaps migrate at a subsequent point? Otherwise, there is a real risk that these young people will the first to test the new PIP arrangements. What is the technical position there? Does somebody who wishes to make their first claim after the age of 16 have the route only to PIP and not to DLA? Would somebody currently claiming DLA necessarily be denied the opportunity to continue with that until, perhaps, the migration plan has run its course? I thought part of the noble Lord’s response to our Committee debates was that you could deal with this in part by the way people in the DLA system migrated towards PIP. One way of dealing with some of the issues that have been very validly raised in this amendment would be to use that flexibility, if it exists. If not, it seems doubly important to lock into the 18 year-old cut-off point, which is being pressed.

[Lord Freud]

My Lords, I welcome these amendments tabled by the noble Baroness, Lady Meacher, and the noble Lord, Lord Patel. They allow me just to go through how the Government intend to introduce PIP successfully for young disabled people from the age of 16. Clearly, the central question is whether 16 or 18 is the right age. In one sense, all ages are a little arbitrary here. Adulthood is defined at different ages in different contexts. The key to the decision to start PIP at 16 was based around the assessment criteria and at what stage people fit in with those, in terms of the activities that they can undergo and how we can look at them. When we looked at it with a range of experts, we concluded that you would normally expect individuals without disabilities to be able to carry out these activities independently from the age of 16. For example, you would expect a 16 year-old to be able to wash and dress themselves, to communicate with others, to plan, and to follow and make a journey. It is the age at which, currently, you expect individuals to be able to be employed full-time. There is a general expectation that they have the capabilities of adults.

The group looked at whether you would expect even younger people—I had better use that word now, rather than adults or children—to fit this assessment. They concluded that children go through several developmental stages under the age of 16, and they do that at uneven speeds. So, there was a cut-off in developmental terms between the two stages, for the purposes of this test, at 16. The other way of looking at this is that it is about trying to move people into adulthood and independence. A lot of these youngsters are living in their households but need to move to independence. Having their own independent help and their own funding in PIP at that age matches their aspirations to move into adulthood, and allows them to make their own decisions about aspects of their lives.

This is an area where, as we described in our policy document, we have set out our intentions and outlined the key principles that we have debated and agreed with stakeholders. We have set up a subgroup of the PIP implementation development group specifically to help and inform the design and testing of the new system in relation to disabled young adults. Together with the focus group work and the interviews that we have held with disabled young people, their appointees and representatives, this is the process that we have under way to get the system right. One of the most important areas where we are using the development group is around the question of how we look at the process of moving people into the 16 category and how we signpost, communicate and get awareness of the changes and then join up the support for disabled young adults and their families.

Clearly, this is not the only testing that disabled youngsters undergo in this phase of their lives. There are a number of assessments as they move from childhood to adulthood. We will ensure that all young people claiming PIP or moving on to it at age 16 have the appropriate support to allow them fully to express their needs. We know it is important that they have a parent, an advocate or a friend to accompany them to that face-to-face consultation. We are not changing anything in terms of DLA in this area. We are changing a lot of things by moving DLA to PIP, and we will be discussing some of them, but in this area we are sticking with the same age as the existing DLA arrangements.

There was an anomaly that the noble Baroness, Lady Meacher, tried to pin me down on and defied me to find a good explanation for. I have been challenged and I shall do my best. On the point about the difference between the universal credit at 18 and PIP at 16, the blunt answer is that these are different benefits for different purposes. It is important that we do not think of PIP as an income supplement; that is not what it is, and nor is it for someone who is out of work. PIP is a payment to people who are disabled who will always need extra money to live because their costs of living are higher, and we will pay it regardless of whether people are in work or out of work. That is why it is a different argument. By giving PIP earlier, we are giving youngsters their independent funding to run their own lives from that point—not from the point when they are meant to be in the workforce and fully independent—when, if they do not have a job, they will need an income supplement. That is the difference. I hope that I have risen to the challenge; I am sure that the noble Baroness will say that I have not, but I have done my best.

We are working closely with the Department for Education to explore evidence gathered so that we can have a single assessment for an education, health and care plan that can be used to support a personal independence payment claim. We are trying to get rid of all the multiple assessments.

[Baroness Meacher]

Does the Minister accept that there are a lot of people who are very worried about this shift? The reality is that many of them who might have been entitled to DLA will not be entitled to PIP and will therefore lose out. They will also lose out on the disability additions. There is quite a big financial consequence here.

[Lord Freud]

I accept that there are concerns but one has to stand back. We are spending £12 billion on PIP in real terms, which is the same as the spending in 2009-10. The talk about a big cut refers to a big cut of a projection—the 20 per cent. I want to reinforce that point. In this House we should not get carried away with the simplicity of the big cut. It is not a big cut. With PIP we are trying to direct scarce resources, at a very difficult time, to the people who need them most. That is the purpose of it.

One of the other things that is happening—and is probably the biggest difference in emphasis between DLA and PIP—is that PIP is trying to take account of people with mental health problems in a way that DLA finds much harder. That is why the assessments and activities that are looked at are very different. Therefore, PIP is different and there are changes. Some people will lose out but they are the people who need the money less. That is the point of making the adjustment. However, the overall sum remains that £12 billion.

To pick up the point of the noble Lord, Lord McKenzie, we have the power and flexibility to treat 16 year-olds differently. This includes different assessment processes during the migration period. We are working actively now with children’s groups to make sure that we have the right migration strategy for youngsters and to finalise it. We will publish that approach. It is not a settled matter, which was, I think, the noble Lord’s real question. We are working very hard to get it right.

Let me deal with some of the amendments. Amendments 57, 58, 50ZGA and 56ZC would prevent our abolishing DLA for those aged 18, and potentially limit our flexibility by imposing statutory duties that would be less able to respond to change, especially as we refine and improve processes as a result of feedback and our experiences. It is very important that we have that flexibility. One of the things that we will discuss later this evening is feedback and the amount of research that we will carry out on a continuous basis. Clearly we want to incorporate that into how we apply PIP, particularly for youngsters.

This is very technical but I need to make it clear that the Government consider Amendment 56ZC to be consequential on Amendment 50ZGA; and, separately, Amendment 58 to be directly consequential on Amendment 57. I do not want any misunderstandings later, although the noble Baroness, Lady Hollis, is not in her seat at the moment to give me a piece of her mind. Given the reassurances that I have given the noble Baroness, and the technical limitations that the amendments of the noble Baroness, Lady Finlay, would impose, I hope she will withdraw her amendment.

[Baroness Finlay of Llandaff]

If the amendments which the noble Lord, Lord Patel, and I have tabled would be more restrictive, does the Minister now have more powers to make regulations to exercise discretion in relation to people of different ages? Does this discretion remain wider by not including our amendments where an age group is highlighted?

[Lord Freud]

This is a framework Bill. There is a lot of potential flexibility as we set up the regulations, particularly in this migration period, as we move into them. This flexibility would be denied by these amendments.

[Baroness Meacher]

I thank the noble Baroness, Lady Finlay, and the noble Lord, Lord McKenzie, for contributing to this short debate. This amendment was tabled very late and others have not had a chance to catch up with the thrust of the argument. I thank the Minister for his reply, although I doubt that the considerable number of people who will be losing out as a result of this provision will be very reassured by his response. I do, of course, understand—at least in general terms—the thrust of the Government’s commitment to focus resources on those most severely disabled. I beg leave to withdraw the amendment.

Amendment 50ZGA withdrawn.

Clause 77 : Daily Living Component

Amendment 50ZGB

Moved by

[Baroness Grey-Thompson]

50ZGB: Clause 77, page 56, line 18, at end insert—
“( ) A person is entitled to the daily living component at the basic rate if—
(a) the person’s ability to carry out daily living activities is limited by the person’s physical or mental condition; and(b) the person meets the required period condition.”

[Baroness Grey-Thompson]

My Lords, the amendment is designed to complement broader plans for social care and links to the Dilnot review of care funding. The Dilnot review examined care costs and how best to manage our demographic change. It concluded that universal disability benefits for people of all ages should continue as now. Dilnot was referring to DLA. The rationale for his recommendation was that DLA helps many disabled people avoid formal social services. It acts as a form of low-level needs management. However, Government plans include abolishing the low-rate care DLA payments of £19.55 per week, which 652,000 disabled people aged 16 to 64 currently receive.

Despite ignoring the Dilnot recommendation, the DWP has not provided a cost-benefit analysis of what this abolition could mean for care services. Charities and individual disabled people have, however, indicated that reduced access to DLA will increase dependency on social care services funded by councils. About one in eight of the disabled people who completed a Disability Alliance survey suggested they would be more likely to need a council-funded care home placement as, without DLA, families would no longer be able to manage needs. This leaves councils funding a much more expensive service. The lack of information being provided on this issue, despite the clear recommendation of the Dilnot review, can leave us with no choice but to assume it has not yet been fully analysed.

The Minister has suggested that providing a basic level of help is unaffordable, but we must also take into account the further costs of the two million medical notes from the NHS which disabled people who are forced to undergo the new assessment process will have to provide. This is not a cost-free policy. What about the analysis of the cost of potentially avoidable NHS use following the abolition of low-rate care payments? Disability and ill health do not just disappear, and the costs and needs of disabled people will be exacerbated. I suspect that there is an unfortunate silo approach being operated. Disabled people will suffer first and then their families, followed quickly by the NHS and councils.

The DWP has been pressed on these issues since plans emerged in 2010. It is unacceptable that these legitimate questions on the policy costs remain unanswered. I also believe the amendment is essential to help mitigate the risks of the current government proposals to disabled people, their families, the NHS and councils.

Figures published just yesterday suggest that of the 652,000 disabled people receiving low-rate care, about a quarter of a million may be able to access daily living payments under PIP. The statistics suggest an increase of 166,000 in the numbers receiving enhanced daily living payments, compared to DLA high-rate care, and an increase of 89,000 in standard daily living payments, compared to middle-rate care DLA. However, this means that 400,000 disabled people will lose support.

My amendment aims to secure basic support for just some of those 400,000 disabled people. The amendment will not simply carry over the same people and the same rules. I realise that the Government need to ensure a new approach. The amendment allows them to retain the right to establish the level of basic need at which disabled people would be entitled to support, as well as levels of payments. The DWP has not yet published the payment levels that disabled people can expect under PIP, but it could examine different payment levels. I beg to move.

16:30

[Baroness Wilkins]

My Lords, I strongly support the amendment, which has the support of many disability organisations and thousands of disabled people and their families who face losing help under the Government’s plans.

The noble Baroness, Lady Grey-Thompson, has already outlined the numbers of people affected by the Government’s proposals. These people are not fakers and scroungers. Of current low-rate care claimants, DWP statistics show that 20,000 are blind, 57,000 have learning disabilities, 94,000 have arthritis, and more than 100,000 experience psychosis or psychoneurosis. These are some of the people affected, and these conditions are clearly not fake. These are the people who the Government suggest should lose support.

Disabled people have told the Government exactly what losing low-rate care could mean. Examples include people who categorically state the clear health and social care consequences of cutting DLA, as the noble Baroness, Lady Grey-Thompson, outlined. I shall cite examples of people who have commented. One said:

“If DLA was reduced or removed then I would be unable to attend doctors and hospital appointments due to the cost of getting to and from them, and my health would be severely put at risk due to not having enough money to either keep myself warm and/or fed”.

Another said:

“We would be in crisis—end of story … my son would start self-harming again”,

and that even,

“prescriptions would be out of the question”.

The amendment could help prevent an explosion of avoidable NHS and social care needs, as the noble Baroness said. Will those needs of the disabled people who are losing help be met elsewhere? I fear that no support may be available from any other public service for many of the 400,000 who will lose all their DLA. The past decade has seen a shrinking of council social care service provision through the tightening of eligibility criteria. More than 80 per cent of councils in England now help only people with critical or substantial needs. The people losing DLA may very well not be able to access care services until crises develop. This leaves families, friends and neighbours to care for them. We already have one of the highest economic inactivity rates due to informal care provision. By not accepting this amendment the Government risk ignoring the impact on carers—especially on women aged between 46 and 64 who are more likely to have to take up caring responsibilities in lieu of formal services or benefit provision.

In proposing to abolish low-rate care provision, the department appears to fail to understand or, worse, to wilfully ignore the genuine needs of disabled people and carers. The amendment would help the Government ensure that they did not simply end the lifeline of DLA for disabled people and families who are unable to access alternative help until they receive expensive NHS treatment or residential care. Accepting the amendment and devising a fairer way to share the burden of the proposed dramatic cut in DLA resources would also help the Government ensure that they do not permanently undermine disabled people and the trust and confidence of carers. I hope that the Government really mean what they have said—that we are all in this together.

[Lord McKenzie of Luton]

My Lords, I will speak just briefly on this. It seems to me that the importance of this amendment has been heightened by the documentation we got just yesterday from the DWP, which emphasised that half a million people are going to miss out under the new system compared with the current arrangements. In passing, I might say that it would have been more helpful had we had that documentation a little earlier so we could have studied it in more detail, although clearly the noble Baroness, Lady Grey-Thompson, has delved into it more deeply than I have had the chance to do.

There must be an onus on the Government to undertake some sort of assessment of the consequences for those half a million people who are not going to be able to benefit under the new system. Some of the consequences have been spelt out, such as extra pressure on social services and the health service. We know there will be loss of income tax and national insurance because DLA helps many people to stay in work or to work longer than they otherwise would. All those consequences are quite apart from the worst feature which is the human cost for people who are going to miss out who had been able to rely on funding and not just at the lower rate. It may be that most of those who fall out of the system are currently on the lower rate of DLA, but that certainly is not the case for all of them.

It seems to me that this approach reinforces the perception that is too prevalent that if you claim these benefits then somehow you are not worthy and you do not really deserve them. Half a million people will come out of the system under these proposals. What are the consequences for them? What assessment have the Government undertaken of their needs as a consequence of falling out of the system? Have they or will they look at the sort of proposal that this amendment covers so that there is some basis for bringing some redress for those people who, on any analysis, are bound to suffer as a result of these proposed changes?

[Lord Wigley]

My Lords, before the Minister gets up—I am sorry I did not get in before the noble Lord on the Opposition Front Bench, who beat me to it—I want to say a few words in support of Amendment 50ZGB moved by the noble Baroness, Lady Grey-Thompson. It provides a basic rate of daily-living payment to minimise the number of disabled people who might otherwise be totally deprived of such focused help. Listening to Radio 4 this morning and hearing the Minister from the House of Commons acknowledging that 500,000 people could be hit by these changes really brought home to everyone the significance of what we are talking about. The ending of lower-rate DLA will leave people with needs arising from their disability but without the means to pay for them.

The point was made earlier by the Minister—and I understand his point—that the day-to-day costs of living are covered separately from the additional costs of disability. The implication is that people who would be in the lower group do not have additional costs of disability, but we all know from experience that they do and they are going to be losing out as a direct result. If the Government’s intention is that so many people who have previously been recognised and acknowledged as having needs will no longer be helped to meet those needs, let them say so. I think it is a very retrograde step.

[Baroness Howe of Idlicote]

My Lords, I had also meant to rise to speak a bit earlier. I, too, very much support what has been said about those amendments. We have all been absolutely flooded with e-mails about the situation of many of the people with disabilities we are talking about, who are fearful about their future and about how they are going to be affected. What has really impressed me is the details they give of their own lives and just what they need the extra money for—things that you and I would not even think about. It is not just support to get out of the house and to get to the shops or extra money for a car because there is no other way of getting about, but support for very basic extra things to make it possible to use saucepans and things like that.

I appreciate the actions that have already been taken, but I hope that serious thought will be given to those half a million people who will still suffer as a result. I am sure that the Minister will do everything he can to ensure that those in real need are approached with a flexible mind, but, nevertheless, some will fall between the new systems that are being devised, so I support the amendment and hope that serious consideration will be given to it.

[Lord Brooke of Sutton Mandeville]

My Lords, I hesitate to intervene, but are things said subsequent to the Minister sitting down clarifications of what had been said before? If not, are they in order?

[Lord Freud]

My Lords, I start by picking up the point that the lower rate is being thrown out so everyone on the lower rate will no longer get DLA or PIP. That is absolutely not the structure of what is happening. We are looking at the needs of people from the ground up and designing a support mechanism in PIP to look after people who have disability needs. Clearly, anyone who needs support, on the grounds of a rigorous and consistent assessment, will get it. Many of those people will get more. In fact, we think that the proportion of people who will be in the group with the greatest need, in the highest group, will rise under PIP compared to those in the standard group.

The difference between PIP and DLA is that we are trying to strip out the complexity of all the different rates and boil it back down to eight rates—by the time you take the two components on the two different rate levels. The amendment replicates the complexity of the structure of DLA and moves it back up from eight to 11 components, making it more difficult to administer coherently.

I pick up the specific point made by the noble Baroness, Lady Grey-Thompson, on the Dilnot review, and reassure her that the DLA reform proposals published in April 2011 were shared with Andrew Dilnot’s review of long-term care funding, which was published a couple of months later in July. Andrew Dilnot said that universal disability benefits should continue, based on need and not on means. We are doing PIP exactly on those grounds—it is not means-tested but based on needs. He did not say that that benefit should go on unreformed.

We have designed the PIP assessment criteria to take broader account of the impact of disabilities than simply care and mobility, which are still of course very important factors. In our most recent draft of the assessment criteria—I remind noble Lords that we are still consulting on this process; this is work in progress and we are still listening very hard to the responses that we are getting—care and support needs feature very strongly. If someone needs attention with things such as washing, bathing, going to the toilet, dealing with medication, cooking food and eating, that is taken into account. We have amended the draft assessment criteria so that they now include supervision, whereas before they just considered whether someone needed assistance and prompting.

16:45

Finally, I should make it clear that the constituent parts of the current DLA cooking test have, in effect, been retained in the first activity relating to preparing food and drink. Therefore, again, individuals’ needs in relation to this are taken into account.

It is clear that by moving to a two-tier structure we are not withdrawing support from those who require levels of support which we would expect to be covered by the criteria for entitlement to the lowest-rate care component of DLA. We are moving to fairer, more transparent and more objective criteria against which to assess people.

I apologise to the noble Lord, Lord McKenzie, if I did not give him enough time regarding the thresholds. In future, I shall try to make information available a bit earlier, as I know that there is much to absorb. This is a huge Bill and there is a great deal of information on it, so I acknowledge that getting that information out on a timely basis is important. On the assessment of the thresholds, we have now launched a further formal consultation to gather views from disabled people and their organisations, particularly on the weightings and the entitlement thresholds. This consultation will run for 15 weeks, during which time we aim to get all the information we can, and it will end on 30 April.

Of course I understand the noble Baroness’s concerns, but these amendments would not restore the DLA status quo and they fail to address the more fundamental questions of how, and for whom, support is prioritised. I repeat that we are trying to make sure that the scarce resources that we have go to the people who need them most. We know that under these changes there will be shifts in provision. Some people will receive less support—

[Baroness Browning]

I am sorry to interrupt my noble friend. On the point about scarce resources, I think we all understand the financial situation and the imperative to reduce the deficit. However, if people who are currently on the lower rate of DLA lose it—a point made earlier in the debate—they will not just carry on with life as it is. If we accept that these people do not claim DLA without a need for it, then we accept that they have a genuine disability and that the lower rate of DLA is factored into their weekly budget. If it is then decided that their case is not as important as someone else’s and that that person might need the DLA, that is going to have an impact. Earlier, the point was made that if you take away the lower rate of DLA from a lot of people with a wide range of disabilities, there will be consequences for their health and well-being, which will translate into a financial cost on the public sector. Will my noble friend consider undertaking a cost-benefit analysis of that consequence?

[Lord Freud]

My Lords, I have two answers to that question. The first is that people who need the support because of a disability may happen to be on the lower rate of DLA today but that does not mean that they will not be entitled to the standard rate in the future. My noble friend gave an example of people who are really dependent on that funding. I would expect in those circumstances that it would continue. Indeed, I would regard PIP to be a failure if it did not do that. Secondly, we will be monitoring that really closely. As I have discussed, later this evening I will present an amendment to make sure that we properly monitor what happens in this area and make sure that PIP does what it should be doing, which is to stop people ending up in the situation that my noble friend is so concerned about.

I must point out that if we move to a three-tier system on the daily living component, the implications are that the caseload would be larger—possibly larger than that under DLA—and spending would increase rather than decrease against the original and revised forecast under the personal independence payment. We cannot possibly quantify such expenditure implications, mainly because we have not yet set the rates at which benefit is paid, but the implications are there. I want the House to be under no illusions that they would be anything but significant.

Before I ask the noble Baroness to withdraw her amendments, I would like to confirm that the Government see Amendments 50ZGH and 50ZJA as directly consequential upon Amendment 50ZGB. On that note, I beg the noble Baroness to withdraw the amendment.

[Baroness Grey-Thompson]

My Lords, I thank the Minister for his response. I have to say that I am disappointed. I am also concerned and gravely worried for a huge number of disabled people. The tiny spark I take out of his comment is that he says he is listening. That is positive. However, there are lots of ways in which spending will increase if we push disabled people into poverty or do not give them the right support they need. We will be making massive, long-term mistakes for the rest of those disabled people’s lives. It is not a small number of people. It could be up to 500,000 disabled people—half a million disabled people could be affected by this.

I am keen to keep pressing the Minister to ensure that the outcomes of disabled people losing the lower rate of care will be monitored throughout the rollout of the PIP assessment because, whatever way you look at the maths, there will be people who lose out. It is a big mistake to see this as a deadweight expenditure. You only have to look at our postboxes or e-mail inboxes —in the past two days, I have had nearly 600 emails from different disabled people saying they are terrified of the changes that are going to happen.

It is really important that the assessment process properly records whether losing DLA has a negative impact on the health of disabled people or their ability to work. We have a long way to go on this. Very reluctantly, I beg leave to withdraw the amendment.

Amendment 50ZGB withdrawn.

Amendment 50ZGH not moved.

Amendment 50ZH

Moved by

[Baroness Grey-Thompson]

50ZH: Clause 77, page 56, line 21, after “condition” insert “and the social, practical and environmental barriers they face as a disabled person living with that condition”

[Baroness Grey-Thompson]

My Lords, the issue of the social model of disability was discussed at some great length in Committee and the noble Baroness, Lady Campbell, spoke very eloquently on it. Despite the Government’s commitment to the social model of disability, their other commitment on this issue—to provide an objective assessment—works in opposition to this aim.

The idea of an objective assessment is to ensure that people with the same functionality receive the same level of PIP. This looks only at the person’s functionality, and not at the barriers faced by that person within society. A benefit which was based on the social model of disability would look at the barriers that individuals face, not just at their functionality. Despite their stated intention to bring in a more active and enabling benefit that supports disabled people to overcome the barriers they face to lead full and independent lives, it actually takes less account of the individual barriers people face—because different people face different barriers.

The DLA has been criticised and no one would argue that it could not be improved on. However, DLA takes into account to some extent an individual's circumstances and uses—again to some extent—the social model of disability. It is claimed that, by making the criteria simpler, PIP will use the social model. However, it seems to rely much more on the medical model and appears to be going backwards in terms of taking into account someone's costs in surmounting their barriers. The charity Scope has made it clear that it considers that the Government are introducing a tick-box style medical assessment that will not help them achieve the aims they have set out to achieve.

The stated aim is to provide a more active and enabling benefit that supports disabled people to overcome the barriers they face to leading a full and independent life, yet nowhere in the assessment process is there any space for looking at the barriers that an individual faces. Disabled people face a multitude of barriers to participation and independence, many of which come as a direct result of social, practical and environmental factors. Making the test more objective and simpler will inevitably lead to a greater focus on the medical model, which will work against the stated aims and purpose.

Richard Hawkes, chief executive of the disability charity Scope, said:

“We recognise that Disability Living Allowance needs reforming and we fully support the government's ambitions to create a more active and enabling benefit. However, we are concerned that the new assessment the government is planning to use is flawed because it doesn't take into consideration all the barriers that disabled people face in daily life. Without understanding the extent of barriers people face, the government has no hope to overcome them and genuinely enable people to take part in daily life”.

At a time of limited resources, it is crucial to ensure that support is targeted as effectively and accurately as possible. This will not happen using the proposed assessment. To ensure effective targeting, the assessment process for PIP claimants must accurately measure the extra costs that individuals incur, based on an understanding of the variables that affect those costs. I beg to move.

[Baroness Browning]

My Lords, this is the first time I have contributed on Report. I declare my interest as vice-president of the National Autistic Society, patron of Research Autism and as the named carer of an autistic adult man in receipt of DLA. I am concerned about this part of the Bill and support the amendment and the detail with which it outlines what I believe are shortcomings, despite my noble friend's best efforts to identify how the assessment will affect people on the autistic spectrum.

In 1990, the House of Commons sent to this Chamber the Autism Bill, which became an Act of Parliament. It was passed as a result of a Private Member's Bill introduced by the right honourable Cheryl Gillan MP. It was supported by all parties in both Houses and was enacted in 2010 by the coalition Government. I tabled a Question for Written Answer just before Christmas asking whether the Welfare Reform Bill that is before us was compliant with the Autism Act. It is worth remembering that no other Act of Parliament has been passed that is specific to a condition. Certain medical conditions are mentioned in other Acts, but the reason for both Houses agreeing to pass the Autism Act, which is now on the statute book, was that autism is different. I make no apology—I know I bang on about it quite a lot—for drawing the attention of the House to the fact that an Act of Parliament was needed because autism is so different.

There are many aspects to the Bill, including the amendment we are now debating, which have a specific read-across to the autistic spectrum. Some years ago in another place I introduced the first debate in Parliament on Asperger's syndrome. It was not well understood then. It is far better understood now, which is a great relief to me and many others. Even so, parents and people with Asperger’s syndrome still struggle to get access to services, benefits and independent living, and to take their place in society as they would wish. The Autism Act was passed in recognition of that. I have to say to my noble friend that I was very disappointed when the reply to my Question for Written Answer in relation to this piece of legislation said that this was a matter for the relevant services by local authorities and NHS bodies and was not the subject matter of the Welfare Reform Bill.

Under the Autism Act, there is now a statutory responsibility on health and social services to implement the autism strategy which will require them to work with partners; for example, local authority housing departments. The Health Minister will be in a strong position to call to account local authorities and health authorities that do not implement this strategy. I know it is not the subject of this clause but if you are going to say that people under 35 will have restrictions placed on them as to where and with whom they live, that is a total contravention of what local authorities are being asked to do to implement the Autism Act. Equally, in the assessments for people on the autism spectrum, Asperger’s syndrome is not “autism-lite”.

Some years ago the National Autistic Society produced a report on autism called Ignored or Ineligible?. It is a 10 year-old report but sadly a lot of it is still relevant today, especially for those trying to get support for people on the autism spectrum, particularly those at the end of the spectrum who are more able—people with higher than average IQs. The anomaly about this condition is that you can have people with Masters degrees who cannot cope with some of the day-to-day detail of looking after themselves. The House has put on the statute book the Autism Act because autism is so different. The amendment before us picks up on some of those defects in the assessment.

I had time to read the case study—unfortunately it was number 13—in the information that my noble friend published yesterday, which related to a young man with autism and how his assessment had been carried out. Yes, he scored highly and one would take a lot of comfort from that. But I want to bring my noble friend back to the situation of what is sometimes regarded as quirky behaviour—sometimes threatening or challenging behaviour—but in the main non-threatening behaviour; odd behaviour, yes, with the inability to do certain things sometimes but able to do much more difficult things at other times. It is a very strange and complex condition. Therefore, in an assessment process, it is absolutely essential that people are viewed as individuals in the way in which their condition affects their day-to-day lives, whether it is their medical condition, the way they live socially or their housing conditions. It is that sort of complex condition. It is sometimes associated with other things such as learning disabilities and/or mental health issues as well, which makes it much more specialised in terms of understanding the behaviour that is presented.

I do not want to focus on my own situation but, as I am sure noble Lords can imagine, as a mum I am pretty worried. I want to take this opportunity to say on behalf of other mums—if I do not say it, who is going to say it for them?—that when you have a child who is born with a lifelong disability and you know they are going to die with that disability, as a parent your relationship with that child is very different from your relationship with other children you may have. When they are little children, you agonise about things like education. As they get older, life skills and whether they can cope for themselves become far more important to you than whether they ever got a GCSE. As they and you get older, your waking moments are haunted by how they will cope when you are no longer there to support and help them. I think that most parents of disabled children—whatever the nature of their disability —would understand that. Therefore, when you feel after many years that you have them in what I would describe as a stable situation—and how important, particularly for autism, stability is—it is so worrying when you suddenly look into the future and find that actually it is not stable at all. It is not stable for you—as you are growing older with goodness knows how many years left—and you see that it is not stable for them.

I have every respect for the amount of time my noble friend has put into autism. I am totally in favour of what he is trying to do to get more autistic people into work, because there are many who could work if they were given the right support and back-up to do it. I fully support that. But Asperger’s syndrome and those people on one end of the spectrum of autistic spectrum disorders are not “autism-lite”. I mentioned the report Ignored or Ineligible?. It showed that for people between 20 and 30 the suicide rate was 8 per cent. The reason it was 8 per cent was that the people on that spectrum try like mad to be part of society and try to be like everybody else. However, there comes a point at which, for many of them, they give up that struggle. I am very concerned that if they are not assessed as individuals, with all the quirkiness and strangeness of this very complex condition, we will go back to people on the more able end of the autistic spectrum being either ignored or ineligible, with all that that means. That is why I support the amendment tonight.

[Baroness Thomas of Winchester]

My Lords, that was a most moving contribution from the noble Baroness. I think we were all very touched by it. I declare an interest at this point, as I receive DLA.

There is a real fear among so many disabled people who have contacted us that the migration to PIP is going to be like a horrid game of musical chairs, because they all know that the Government want a 20 per cent cut, wherever that comes. They all think that when the music stops, they will be the one without a chair. They also know that DLA, for all its faults, has the lowest incidence of fraud, and many of them say they feel demonised in the press for being scroungers. Would it not be nice if some of the screaming headlines in tabloid newspapers were about the way in which many people receiving DLA are able to live independently, contributing hugely to society in many different ways, rather than the other way around?

On the low level of DLA fraud, we have to acknowledge that my noble friend, coming to this whole subject with a fresh eye, reckons not that the wrong people are claiming the benefit but perhaps that the net has so small a mesh that it tends to pick up everyone who has any level of disability rather than picking up only those with the greatest need. Therefore, his argument goes, you do not have to resort to fraud in order to get DLA; it is so loosely drawn that almost anyone can get it if they know how to fill in a long and complex form in the right way. Taxpayers are entitled at this point to ask why medical reports are looked at in only around half the cases, which I for one find quite inexplicable, but we will come to that in our debate on a later amendment.

However, it is the phrase

“those with the greatest need”

that is most worrying. It could mean many things and is most closely associated with those who are entitled to means-tested benefits, which we know is not the case for PIP, and long may this last. Among the arguments that the Minister deployed when he rejected this amendment in Grand Committee were that it was too widely drawn; would be too expensive; would lead to too long an assessment, which would be too intrusive; and too complex. The noble Baroness, Lady Campbell, countered this by saying that the proposed points-based tick box descriptors approach will not capture enough information about the barriers and costs faced by disabled people on a daily basis. Both are right, which is why this issue is so difficult. It would be almost impossible to translate this amendment into a points-based assessment in a meaningful way, although in an ideal world that is exactly what is required.

I wonder whether there is any way in which the sense of this admirable amendment, or elements of it, could somehow be incorporated into the assessment process. I shall be most interested in my noble friend’s reply.

[Baroness Wilkins]

My Lords, I support the amendment, which seeks to ensure that the assessment for the new entitlement is fit for purpose and fulfils the Government’s commitment to the social model of disability. As has already been noted, DLA occupies a unique space in the welfare benefits system as it recognises that disabled people face a plethora of extra, often prohibitive, costs as a result of living in our society with a condition or impairment.

We should all warmly welcome the Government’s repeated commitment to the social model of disability, for which, as many of your Lordships know, disabled people have fought long and hard. At the heart of the social model is the recognition that it is our society, not just their bodies, that disables people with health conditions and impairments. However, I fear that the proposed assessment for the new entitlement does not reflect this commitment. Despite the Government’s assurances in Grand Committee, the Minister admitted that the proposed test,

“is not a full social model assessment; it is not intended to be”.—[Official Report, 14/11/11; col. GC 199.]

I ask the Minister in his response to clarify to the House and disabled people why such a commitment was ever made in the first place.

The second draft of the PIP assessment criteria includes some small improvements from the first. However, it does not go nearly far enough. By assuming that a medical assessment will capture social and environmental barriers to independence, the Government risk homogenising the diverse difficulties that disabled people face in their everyday lives. The new threshold document makes many mentions of extra costs and barriers, but only a few of these will be captured by an assessment that looks exclusively at impairment.

It is with this in mind that I support the amendment of the noble Baroness, Lady Grey-Thompson. The assessment for the new entitlement must consider the real social, practical and environmental barriers faced by disabled people with impairments living in our society. I, along with disability charities such as Scope, disabled people’s organisations and disabled people across the country, voice great concern that the Government are reneging on their commitment to the social model of disability. Doing so would undo decades of campaigning for and progress towards a better and more equal society.

[Baroness Hollins]

My Lords, I thank the noble Baroness, Lady Browning, for her honest and enlightening contribution. I speak as a doctor and as a mother; I have two adult children who are in receipt of disability living allowance.

I wish to talk about the medical approach to disability. As a doctor, I have often been accused of being very “medical model”, usually by disabled people. The medical model to disability is reductionist. Many doctors and other health professionals do not understand the social model; they do not understand the social, practical and environmental barriers that people with physical and mental impairments face. I support the amendment, but it would require skilled and sensitive assessments to be available and they would need to be delivered by people who understand the social model.

17:15

[The Countess of Mar]

My Lords, I, too, support the noble Baroness, Lady Grey-Thompson, in her amendment. I read the whole of the information sent to us yesterday and I was pleased to see that ME/CFS, in which I am interested, was raised in two examples, and that the difference between the two conditions was shown. I am concerned not just for people with ME but for those who can almost function normally and will not meet the criteria for getting DLA. For example, there are those who, because they have an endocrine problem, cannot cope with the cold. They need extra heating and clothes. If they are working, they are probably on a minimum salary because they are not very well. Therefore, they need extra money. They might also need extra clothing.

If they are incontinent, they may need to be able to change their clothing regularly. They may need incontinence pads, which—as everyone knows from questions in the House—are extremely difficult to get from the National Health Service. My mother-in-law, who died a few years ago, could not go out of the house because she was worried about wetting herself in public. If she could have afforded incontinence pads, she would have been fine. She was not going to tell her children or her daughter-in-law about her problem and we had to extricate the information from her to find out why she was not going out. Such people get confined to their homes and become desocialised, and it is very difficult to get them back into society. We must take all these things into consideration—not just whether they can cook or wash themselves—when we think about what they need to keep functioning on a relatively normal basis.

[Baroness Howe of Idlicote]

My Lords, I shall speak briefly on this amendment. The comments of the noble Baroness, Lady Browning, about her personal experience of the whole range of autism reminded me just how this range has developed over the years. When I first got involved with the autistic movement many years ago, it really was just one thing; but since then, many different branches and forms of behaviour have been identified. The fact that all these extra aspects have to be borne in mind re-emphasises the whole question of whether the clause is fit for purpose. In particular, the Asperger’s syndrome comment was very apt. I hope the Minister will be able to persuade us that there will be a thorough method of assessment by people who understand the range of problems that we are talking about as well as—as my noble friend Lady Mar said—the detailed and different ways in which extra help is used and needed for such people to have a basic ability to lead a normal life.

[Lord Freud]

My Lords, let me start by referring to the moving speech made by my noble friend Lady Browning. I confess to a real concern about autism generally and I am very proud that my maiden speech was on the Autism Bill. I have undertaken a number of initiatives in the autism area because we do not look after people with autism and Asperger’s properly. I also strongly believe that it would not take a huge effort to make sure that we look after those people much better. As my noble friend knows, there is currently a major initiative to try to ramp up the number of such people who have and keep jobs. Currently only around 15 per cent have jobs, which is ludicrous, and I am determined to double that figure.

As part of that concern for this particular group, we wish to make sure that this assessment takes people with autism and with Asperger’s properly into account. I am hopeful that PIP will do a better job than DLA, and, furthermore, that we will make sure that we have the right processes in place to look after this group. As we refine processes during the next consultation period, which we are running until the end of April, one of the things that I want to make absolutely sure of is that we have the right measures in place for autism. I know that everyone in this Chamber feels similarly on this issue, and feels very strongly that we should get this right for that particular group.

I shall now turn to the more technical aspects of this issue—that is, looking at what we are doing with the PIP and its assessment. Is it a medical assessment, as the noble Baroness suggested? It absolutely is not. In fact, as I said in Committee, our approach is—and this is rather a mouthful—akin to the biopsychosocial model. I shall try to draw this out a bit—I do not mean in time: I shall try to draw the themes out. A medical assessment would be something like the industrial injuries disablement benefit, where there is a direct correlation between the injury sustained and its severity and the amount of benefit or compensation received. Nor will the PIP assessment focus on the functional limitations of the individual in the way that the work capability assessment does. Instead, it will assess how the individual’s health condition or impairment impacts on his or her everyday life by looking at their ability to carry out a series of key and holistic activities, all of which are essential for participation and independent living. In such an approach, the type of condition or impairment an individual has is of limited relevance.

It is not, however, a full social model assessment. I accept that. That is something that many noble Lords and disability organisations would like, but I have to point out that it was not our intention to develop it in this way. As a department, we do support the social model. As the noble Baroness, Lady Wilkins, said, we are on record as supporting it. While we want to ensure that the PIP assessment better reflects it than previous assessments, that does not mean that the full social model is relevant for assessment, although it is relevant for some things. I sent round a rather interesting piece of analysis to many noble Lords in the Committee, called Models of Sickness and Disability, which showed the differences between the models, explaining the medical model, the reaction of the social model against the pure medical model and the synthesis of the biopsychosocial model. The summary of the biopsychosocial model in the analysis is that:

“Sickness and disability are best overcome by an appropriate combination of healthcare, rehabilitation, personal effort and social/work adjustments”.

There is a coherent theory behind this assessment.

[Baroness Browning]

Will my noble friend confirm whether, when people on the autistic spectrum are assessed, there will be somebody present as part of that assessment who is expert in cognitive specialisms?

[Lord Freud]

People will be able to bring anyone with them to the assessment, whether it is a parent, adviser or anyone else. For the WCA, the person doing the assessment can call in that support where they need it. We are now entering the consultation phase on the PIP assessment. Wrapping in that support will be one of the elements that we will look at. I accept that the assessor needs to understand how those factors reduce the ability of the person in front of them to run their lives.

[Baroness Browning]

It has been suggested—I hope that this is an opportunity for my noble friend to put this straight—that the assessor will be able to call somebody on the telephone in making the cognitive assessment. I hope that he is able to assure me tonight that that is not the case.

[Lord Freud]

Clearly, the system will be elaborated and developed, and we are at an early stage. Although the WCA is a very different test from the PIP assessment, one of the useful lessons that we have drawn from Professor Harrington’s recommendations for it is that mental health champions are available on site for assessors. That is the way in which that test has developed, and there are some valuable lessons there for when we look at how we elaborate the PIP assessment.

If we were to go with the full social model assessment along the lines suggested by Scope, looking at the full range of factors that potentially cause barriers and cost, it would require a very long, intrusive and costly assessment, putting significant cost burdens on the state and, more importantly, very large burdens on the individuals involved. They would also inevitably require much more regular assessment, as the social factors that would be taken into consideration would change more regularly than the impact of a health condition or impairment. You might, for instance, get to the ludicrous position where every time a local bus service changed, you would have to do a reassessment on that model. In meeting after meeting with noble Lords, I have been left under no illusion that having too many reassessments is one of the things that they dislike the most. We will try to provide later on some reassurance that there will be decent gaps wherever possible between reassessments.

The situation could go very dramatically the other way and lead inevitably to inconsistency, with factors considered varying from person to person and affected by local factors or service provision. With PIP, we are looking at something that is universal and where entitlement is based on the same criteria wherever individuals are and whatever their circumstances. This discussion carries echoes of our ring-fencing debate earlier today in relation to the Social Fund. If we move to a kind of local needs-testing, which is what the amendment implies, it would be at odds with how we deliver a national benefit. Clearly, we could do something else. We could localise it as a benefit, but then it would be a very different benefit. I suspect that many noble Lords would be very concerned about moving in that direction.

Most importantly, we think that a social-model approach would be more subjective. Benefit entitlement needs to be based on clearly defined and transparent criteria which we need to be able to set down in legislation and apply to individuals consistently, whatever their circumstances and wherever they are in the country. If you cannot do that there would be a level of unfairness and uncertainty, high levels of appeals and a system in disrepute. Under the type of assessment proposed, it would be harder to define the criteria that individuals would be assessed against and less clear whether they had met the thresholds for entitlement.

Finally, we do not think that an assessment along these lines would allow us to control expenditure and keep that benefit spend sustainable, making sure that it goes where it is needed most. I do not think that I can really reach a figure on how much it might cost, but our estimate is that it would be very substantial.

Although the social model approach is superficially attractive—and I emphasise that we support it in many ways—we have decided that it is not the right way to go with this assessment. We have not gone for the medical model; we have gone for the biopsychosocial model. That model has now garnered very significant academic support, as those noble Lords to whom I sent that very interesting piece of research will recognise. It recognises the diverse range of biological, psychological and social factors that impact upon an individual and cause variation in need. We think that approach—of looking at activities and outcomes—matches the requirement.

17:30

[The Countess of Mar]

My Lords, I wonder whether the Minister can answer a question for me. I made a particular point about people having very special needs such as extra heating and incontinence pads, for example. If they are leading a fairly normal life but would be restricted to their homes because they cannot pay for things, will this be taken into account in the PIP assessment? I could not see it anywhere when I read the details. How are these facts going to be elicited when the person is being assessed? People do not fit into boxes—everyone is an individual. It seems that the noble Lord is trying to make people fit into boxes when they do not.

[Lord Freud]

We are very much trying not to make people fit into boxes. We are not saying, “Because you have that condition, that’s your relevant position”. We are trying to look at people as individuals. Clearly, you go through all these criteria very carefully and reach a judgment. It is almost impossible for me to say whether a particular person would hit the assessment criteria or not. You just have to go through it and see. However, we clearly expect someone to get a payment who has genuine needs for coping with life because of their disability. That is what it is designed for. I cannot answer the specific question, but I can tell the noble Baroness the principle—where that person needs that support as a result of their disability, they should get it.

When we develop an assessment for PIP, we have to balance a range of factors. A complete model should include all the perspectives and important interactions between an individual, their health and the environment. That is what the biopsychosocial model does. There are limitations in considering only a single perspective, and this is a much more holistic approach.

I do not accept the criticism that our proposals do not truly reflect the extra costs faced by disabled people. As I have tried to explain, it would not be feasible to assess the actual costs without something hugely intrusive to disabled people and very complicated. We therefore have to assess other factors as a proxy for these costs. We are using “care” and “mobility” in DLA, which we do not think are broad enough. So, in our draft assessment criteria we have a range of everyday activities for PIP that we believe are a good proxy for the impact of impairments, the overall level of disabled people’s needs and the extra disability-related costs. We will go on refining those; we will not just stop when we finish the consultation in April.

The proposals have taken into account many of the key drivers of cost that Scope and others are obviously concerned about. For example, individuals who have difficulty getting out are likely to have higher utility bills, while those who need support planning a journey and moving about are likely to have higher transport costs. The proxies and associated criteria should therefore allow us to prioritise spend on those who face the greatest challenge and expense. In answer to my noble friend Lady Thomas’s point on the tick-box assessment, the proposals, which have been around since May, are very much not a tick-box approach; they are trying to look at people’s functional capability.

We have changed the assessment very considerably as a result of the enormous amount of engagement that we have with disabled people and their organisations. We will go on doing that. However, if we had fundamentally to revisit our approach in the way in which the amendment would require, we would have to go back to the drawing broad, spend more time developing and testing, and have greater consultation. It would push back the start of PIP by at least a year and reduce savings over the reassessment period by £1.4 billion. This is, I think, the priciest amendment yet.

[Baroness Hollis of Heigham]

You wait.

[Lord Freud]

This is about doing the right thing for people and focusing money on them; it is not about playing silly games—by which I mean that we are not playing silly games here and we are determined to get this right. We are consulting widely and know that we have the right approach with the model that we are using. I understand the noble Baroness’s position, but we do not think that the Bill should specify that the assessment should consider social and environmental factors. That approach would be inappropriate and unworkable, because we need the assessment to be straightforward, objective and consistent. We would lose £1.4 billion of savings. For that combination of reasons, these amendments are not acceptable to the Government. Just for the avoidance of any doubt whatever, I confirm that the Government see Amendments 50ZJ to 50ZQ and Amendments 51A and 52A as directly consequential upon Amendment 50ZH. On that basis, I urge the noble Baroness to withdraw her amendment.

[Baroness Grey-Thompson]

I thank the Minister for his response. It is nice to know that, even for a short time, I might hold a record in your Lordships’ Chamber for tabling the priciest amendments. I also thank the noble Baronesses who have brought much personal and moving experience to this debate.

I apologise to your Lordships; in introducing the amendment, I did not declare that I am a recipient of DLA, although I am fairly unlikely to be on PIP. I realise that to many the social model turns into a philosophical debate but I felt that it was important to raise it again, as—

[Lord Freud]

My Lords, I feel that I should interrupt. I think that when the noble Baroness looks at the PIP assessment, she will find that she is on PIP—without doing an assessment myself.

[Baroness Grey-Thompson]

I thank the Minister and accept that I did not just go through an assessment process.

I feel that it is important to raise this issue again as a gentle reminder that the social model is written by disabled people using their experience. The noble Countess, Lady Mar, made the important point that you cannot fit disabled people into boxes. I tend to think that we are a little more like Venn diagrams. It is obvious to me that if the Minister were truly committed to helping disabled people, the full social model would be used. I recognise that there is a balance between costs and how far we want to go to help disabled people.

I share the Minister’s view on autism but I would like to widen the issue and hope that we will take all disabled people’s experiences into account. I look forward to seeing the refined process that he mentioned.

There is one point on which I agree with the Minister: the biopsycho model is interesting. However, that is as far as I can go. If we looked at the definition of “interesting”, he and I would probably differ considerably. Perhaps we could save that exciting debate for another time. I beg leave to withdraw the amendment.

Amendment 50ZH withdrawn.

Amendments 50ZJ to 50ZJA not moved.

Clause 78 : Mobility component

Amendments 50ZK and 50ZL not moved.

Clause 79 : Ability to carry out daily living activities or mobility activities

Amendments 50ZM to 50ZQ not moved.

Amendment 50ZR

Moved by

[Baroness Grey-Thompson]

50ZR: Clause 79, page 58, line 4, at end insert “including a requirement for the decision maker to collect evidence from the claimant’s own health care professionals as a part of the decision making process”

[Baroness Grey-Thompson]

My Lords, there is a great deal of evidence that decisions are frequently inaccurate when made on the basis of reports from face-to-face assessments on their own without being informed by evidence from the claimants and healthcare professionals. The purpose of the amendment is to ensure that in all cases, as a part of the decision-making process to decide eligibility to PIP, evidence is collected by the DWP from the claimants’ own healthcare and other care professionals. If sufficient evidence is collected to decide entitlement to PIP, it should not be necessary to have a face-to-face assessment.

There have been ongoing problems with the assessments for ESA. Recent figures published by DWP show that nearly one-third—29 per cent—of those in the work-related group were originally found fit for work and had to appeal to be placed in the right group. Even more worrying, a staggering 60 per cent of those who won their appeal had been awarded no points at all in their initial face-to-face assessment, and at least 15 points are needed to be awarded ESA. These are not borderline decisions.

Why are so many decisions going wrong? The assessment reports frequently contain a partial or inaccurate account of what the claimant has said. The reports done by the healthcare professional are meant to record accurately what the claimant says about the effect of their condition. The second half of the report is where, on the basis of what the claimant has said and their observations, the healthcare professional comes to their own decision about the level of the claimant’s functionality. However, welfare rights workers have consistently reported over the years that many of the reports contain a partial or inaccurate account of what the claimant has consistently reported is the impact of their impairment on their everyday life. Regular feedback from welfare rights workers, who are dealing with these reports every day, is that although there have been some improvements, such as in the reconsideration process, there are still considerable problems with the accuracy of these reports. It has not been solved and will not be while relying on these assessments on their own.

The healthcare professional doing the assessment sees the claimant for only a relatively short time on one day, which may well be a good day. They are unlikely to be a specialist in the condition and know the likely effects or how they vary, and will not have access to all the medical records and the tests that have been done establishing the level of seriousness of that condition. DWP and Atos now recognise the value of medical evidence from the claimants’ own doctors—this is a really valid point—which was acknowledged by Dr Crawford, clinical director of Atos, in evidence to the Work and Pensions Select Committee. Healthcare professionals working for Atos also acknowledged that when a sample group was interviewed in a survey for DWP.

17:45

The following is an extract from that DWP report, and it demonstrates that Atos healthcare professionals themselves believe that medical evidence from the claimants’ own healthcare professionals should make the assessment process more accurate:

“GPs’ reports were particularly well received because they tended to know the claimant so well. Some HCPs felt that would help to contextualise what they observed on a single appointment … In addition, it was felt that greater access to medical evidence ahead of the face-to-face WCA might improve the quality of decision-making by providing a more rounded picture of the customer’s condition than was really possible in a one-off assessment: ‘It can be very difficult sometimes when you’re assessing somebody in a short space of time as to whether what they’re telling you and whether all your examination findings, whether they all tie together. It can be very difficult, and I think if you had some supporting evidence from a health practitioner, it would make your decision making a lot more robust’”.

So Atos healthcare professionals themselves are saying that their decisions about the level of functionality would be more robust if medical evidence were collected, yet the DWP collects evidence for ESA only when it is likely that there will be no assessment.

Unsurprisingly, in view of all this, the deciding factor in tribunals overturning decisions is frequently evidence from the claimant’s own doctor or healthcare professional. The Government say that they are committed to getting the right decision first time, yet the following is an extract from guidance sent to GPs:

“DWP may ask you to complete a factual ESA113 report on your patient. You can complete this form from your medical records … DWP will only ask you to complete an ESA113 if it could result in us confirming your patient’s benefit on claim evidence alone, without need for a face to face assessment”.

Despite evidence from all sides—welfare rights workers and claimants, the tribunal service and the Atos healthcare professionals themselves—that decision-making in the assessment would be much more likely to be right first time if medical evidence were collected, the only concession is to encourage claimants to send in their own medical evidence. Not getting it right first time will cost money as well as create stress for the claimant. The numbers of ESA appeals are mounting, as are their costs. We do not want PIP appeals to follow a similar trajectory. It clearly makes sense to get this right.

In addition to the costs of appeal, people are too often called in for face-to-face assessments when they should not be. One claimant had recently had a spinal operation. The HCP was shocked that she had been called in for an assessment; he sent her back home immediately and commented that she should not have been asked to leave her house. The stress for the claimant was obviously dreadful but the cost of that face-to-face assessment was also wasted.

The Government estimate that the cost of implementing the changes to DLA, including implementing the new assessment regime, will total £675 million, yet a large number of people receiving DLA could be placed on to the new benefit by a combination of their own evidence in their application together with evidence from their own healthcare professionals, without recourse to a face-to-face consultation or assessment. This is particularly true for those with a lifelong condition or with long-term degenerative conditions, and for those currently receiving the higher rates of benefit.

If there is recognition that medical evidence from claimants’ own healthcare professionals is needed to make the assessment process more accurate, the onus must not be placed on the claimant to collect that evidence. Claimants are often charged for medical reports, and while advisers are sometimes able to negotiate with the doctor to drop the charge where a claimant is going to tribunal, doctors who charge will not make that concession in the case of every claim. The charge is often £30 or £35 and sometimes more. Citizens Advice reported one case where the consultant initially wanted to charge £200 an hour. If someone is living on the basic ESA of £67 a week, or even on the ESA main rate of £94, they cannot afford to pay this amount of money to claim PIP. It must be DWP’s responsibility to collect the evidence that is needed for an accurate assessment.

It is vital that the assessment process for PIP includes a requirement for the decision-maker to collect evidence from the claimant’s own healthcare professionals as a core part of the decision-making process. Without that requirement, there is a danger that there will be a two-tier system, with the poorest and most vulnerable claimants unable to afford to pay for the evidence themselves and, as a result, at risk of receiving a less reliable decision. I beg to move.

[Baroness Thomas of Winchester]

My Lords, the importance of this amendment, and of collecting evidence from a person’s healthcare professionals, cannot be overstated. Some of us are shocked that not all medical reports are looked at presently under DLA; I think only around half are.

Turning to the assessments, I, too, was very interested in the finding by Citizens Advice that welfare rights workers report that the WCAs often present a distorted picture of what a claimant has said. In case noble Lords have forgotten that report, it said that 37 clients were asked to examine their reports and establish how accurately they reflected what they had said and done in their assessments. Sixteen were found to be very inaccurate. We know from experience that if you hear two people speaking to each other and one of them tells you afterwards what they said all over again, it often does not match your recollection of what they said at all. I note that in relation to PIP we are told:

“Individuals or professionals who support the customer on a regular basis will be able to provide evidence to support their claim”.

Who will ask these people to provide evidence? Will it be written evidence? If it is not from a healthcare professional, who else might it be from? The finding of Citizens Advice in connection with the WCA alarms me a great deal about the quality of some of the Atos healthcare professionals who are currently carrying out the assessments. I fervently hope that those doing the PIP assessments will be of a higher calibre altogether.

[Baroness Meacher]

My Lords, I support Amendment 50ZR, tabled by the noble Baroness, Lady Grey-Thompson, and to which I have added my name. The noble Baroness has made the case comprehensively so I will be brief. She referred to the alarming error rate in benefits decisions. At the same time, I am aware that steps are being taken to improve the accuracy of those decisions.

Here I want to make sure that we do not forget the particular problems of people with learning difficulties and mental health problems, who may not adequately convey their limitations in a face-to-face assessment. These groups have to spend their lives concealing their symptoms. They are embarrassed by them, and the last thing they want to do is to spell them out. They are acutely aware of the stigma associated with those symptoms. The Government are ensuring that claimants can take someone along to their assessment. There is no doubt that that will help and in some cases lead to appropriate outcomes. However, for many having a companion simply will not be enough. The companion cannot conduct the interview and the pressure on these individuals to conceal their problems is very difficult to overcome in these one-off assessment interviews.

There are also people for whom the very idea of one of these assessments is completely unacceptable. The obvious example is of people with agoraphobia, for whom just going out of the house can present real problems, as can getting on a bus or whatever it is. It is a real problem for this particular group. These people would benefit massively from having a psychiatric assessment at the start of the process, which would eliminate the need for them to go through all the distress of having to do something that they find completely intolerable. It is very fashionable to knock medical assessments but, having worked in mental health for a quarter of a century, in my experience psychiatric assessments are bio-psycho-social assessments. I think that was the term that the Minister used. They do look at the biological, the social, the genetic and every other aspect of someone’s functioning.

Also, any self-respecting psychiatrist will not do an assessment in a single sitting. They expect to assess someone over a period of time. They will bring in the views of social workers, nurses and others who have seen someone over a period. There is no way that a one-to-one assessment by someone who may be a nurse but not a psychiatric nurse—even if they call in someone who might be a psychiatric nurse but does not know the patient—can meet the need to make sure that someone is properly assessed, gets the benefits to which they are entitled and does not get benefits to which they are not entitled. It works both ways. This is an important issue.

Other examples include people with a psychosis whose symptoms are not controlled by medication. Many people’s symptoms are controlled but some people’s, tragically, are not. Those people should be able to have a medical—a bio-psycho-social—assessment and, on the basis of that assessment showing that such a person may not be able to function at all, it should be sufficient. I would have thought that the Government would accept that view.

There are physical diagnoses to which the same sort of arguments would apply. For example, those undergoing treatment for cancer, who again have uncontrolled and uncontrollable symptoms, would fall into this category. I referred to this group in connection with an earlier set of amendments. An early medical certificate for those people would avoid enormous distress and the gross injustice of requiring them to do things that none of us would wish them to do if we saw them face-to-face.

I understand the issue of medical fees, which has been referred to. GPs will not tolerate an inundation of requests for medical assessments without a fee. One of my daughters is a GP. I discussed it with her and she was not impressed by the idea. I am also aware that the Government have introduced an important new element in that the claimant can seek a report from their favoured clinician, who could be anybody—it might not be a doctor. This is helpful but it raises the issue, which has already been raised, of a two-tier system. Some people may be able to afford such a thing; others may not. It is a great step forward and I wish to acknowledge that, but it does not detract from the importance of this amendment. I look forward to hearing the Minister’s response.

[Baroness Browning]

My Lords, I am sorry to come in on Asperger’s syndrome again. I know that the Government involved people on the autistic spectrum in some trials that they carried out over the summer. I just wanted to encourage my noble friend to take the feedback from some of the people who took part in that, in a mock PIP assessment. Because the spectrum, particularly at the more able end, includes people who may be very articulate, on a good day it may be quite difficult to see that this is a communication disorder. On the other hand, you could have an assessment in which, even with the benefit of someone in support in the same room, the person on the autistic spectrum may have some difficulty in answering any question themselves as they struggle to put the words together or to make eye contact with the assessor.

On this group of amendments, I would encourage my noble friend to be aware of the variation in how people can present. However confident they may appear, it will inevitably be a very stressful situation for them to be in a room, answering questions from someone they are unfamiliar with. However they present, there will be stress behind it. I just reiterate something that I asked my noble friend a little earlier. I ask him to make absolutely sure that the people doing these assessments have not just mugged up on what autism or any other disability is from some book, but really understand and have a working knowledge of the disciplines in which they are assessing people. I will leave it at that.

18:00

[Lord Addington]

The amendment on which mine is the lead name also refers to the autistic spectrum. When the noble Baroness is in the Chamber with us, I always feel as though you are definitely on the end of the passing movement, as opposed to being the play-maker. The noble Baroness knows exactly what she is talking about. At my conference, someone who was talking in a meeting about autism said, “You must understand that autism is a three-dimensional spectrum”. Does that phrase not start to explain why the diversity of people and their reactions are incredibly difficult to understand and always will be? I wish I had thought of that expression myself. The great diversity of needs and different types of behaviour mean that you must have some specific training.

When I was approached to put down this amendment, I had a conversation with the NAS. I want to use it as an example of the fact that you always need a certain degree of knowledge to make this type of assessment. I remember that, in years gone by, when the noble Baroness, Lady Hollis, spoke for the then Government, our exchanges on the subject of the initial interview process went on and on and developed almost into a ritual dance. “Can we have specific knowledge?”, we would ask the Government. “No, but we will give them lots of training”, they would reply. We have got better, because we always do, but it remains the case that unless you have someone who actually understands the condition which they are assessing and reporting on, they will make mistakes.

The noble Baroness, Lady Grey-Thompson, has already pointed out that mistakes cost “blood and gold” for everybody concerned. You burn up time; you burn up money; you cause suffering. Getting more expertise into assessment, either by taking a better history, or by making sure you have the right person there at the right time, will make life a lot easier and will probably save money in the long term or, indeed, in the medium term. The Minister has been moving forward, although he is pushing water uphill with certain concerns here. I stress that I am looking for clarification on where he is moving to and his thoughts on where this expertise is going to be dragged in. If you have a problem, empower people to say that there is a problem and that someone who understands it needs to be brought in. If you can do that, you will take huge steps forward. You will not get it right all the time but you will get it right more often.

If the Minister can give us some encouragement and some firm guidelines about what is going to happen to encourage people to get it right—not just to get the numbers through—I will be a very much happier man at the end of this.

[Lord Touhig]

My Lords, I do not intend to detain the House long, because Amendments 50B, 50C and 50D were debated at some length in Committee. I attempted to withdraw Amendment 50A yesterday, but the gremlins crept in and the only thing that has been withdrawn is my name—the amendment still appears on the Marshalled List.

With Amendment 50B, the noble Lord, Lord Addington, has once again made a very powerful case in support of the need for properly trained assessors. In particular, all assessors should have an understanding of and training in autism if they are to recognise and understand the complex cases they will have to deal with. It has been said a number of times—I make no apology for repeating it here, because it is important—that when you have seen one person with autism, you have seen one person with autism. This is why the training is so important. A knowledge of autism and possessing the right skills to assess the needs of an autistic person are essential in making any decision about the appropriate level of financial support that that person might need. I believe that the Minister accepts this point of view.

Following the Committee stage, a number of other noble Lords and I had a very useful meeting with the Minister and his colleague Maria Miller MP, and we are grateful for that opportunity to exchange views in a less formal situation. One point from that discussion, which was touched on today by the noble Baroness, Lady Browning, did concern me—the point about the qualifications of the person carrying out the initial assessment. One of the Minister’s officials told us at that meeting that the initial assessments would be carried out by an occupational therapist. Will this be the case? That seems a very narrow skill base from which to draw the expertise for any kind of wider assessment, and it leaves me, for one, with the impression that the assessment is aimed primarily at getting people into work and not at trying to understand and support them if they are not able to work. Such a situation would fly in the face of the well-argued case that assessors should have specific training in all mental, intellectual and cognitive disorders, as advocated by the amendment. I hope the Minister can allay my fears.

I turn to Amendments 50C and 50D, in my name and that of my noble friends Lady Healy of Primrose Hill and Lord Wigley. The amendments concern face-to-face assessment and would, if accepted, exempt certain categories of people from the process of continuous reassessment where sufficient medical and other expert evidence existed to demonstrate that their condition would not improve. I return again to my concerns about people with autism. Autism can be summed up in this way: autism is for life. Any reassessment must accept this fact before progress can be made. The Minister made it clear, at Second Reading and in Committee, that the Government did not believe that a face-to-face assessment would be the right course to follow in all cases.

At our meeting, both the Minister and his colleague, Maria Miller MP, gave a strong impression that the Government would support a tiered approach to assessment in such cases, as advocated by the National Autistic Society and others. In practice, this tiered approach would allow for written assessment from professionals to be considered and a decision to be made, on that basis, about whether a face-to-face assessment was appropriate or necessary. I will not test the patience of the House any longer. I look forward to the Minister’s response and hope he will have something positive to say about a tiered assessment.

[Lord Kirkwood of Kirkhope]

This is an important debate because existing relevant medical evidence is absolutely essential to getting this test—and the whole process—delivered as accurately and as sweetly as it possibly can be. This is true in two separate directions. First, getting access to and active consideration of existing relevant medical evidence will make the examination—if an examination is needed—much more satisfactory for all concerned. As has already been said, it will reduce appeals—and it will minimise costs for that reason if for no other.

It has a second important function which I hope the Minister will be able to spend some time on. If the Minister could help us understand better how desktop assessments can obviate face-to-face assessments, he could diminish the fear factor that clearly exists, rightly or wrongly, about what will face people who might be invited to these face-to-face tests in future, and that would be enormously helpful. I am aware, having followed this for some time, that the DLA provisions which we put in the primary legislation in 1992 were, in some respects, too prescriptive. I understand perfectly that assurances can be made and put into regulations and put into medical contracts as well.

I am in the market for voting for this amendment if we do not get the kind of response that I hope for. However, there are ways of delivering the assurances that are being sought by our correspondents and the disability community. It would be helpful if the Minister could say a word about the contract. I understand that the contract is out to tender and it is too early to say who is interested, but people are drawing conclusions from the Atos Healthcare experience. I do not think that that experience would necessarily be repeated in the future if the terms of the contract are drawn sufficiently clearly. In that contract, if not in regulations or primary legislation, we should be saying clearly that on cause shown, if there is heavyweight medical evidence that can be addressed at a desktop level, those are circumstances where it should almost be a default that people will not be subjected—if that is the right verb—to these assessments.

I share a concern about the quality and experience of the assessors. I have a capacity issue as well as a quality issue about that. It does not matter if you get the best contract in the world and the most enthusiastic prime contractors who come in and promise, hand on heart, to do the best they can. The professionals with the right qualifications and experience to do this work may not be out there. If that is the case then we need to be very careful. There is not enough emphasis in the United Kingdom on this kind of medicine, and we should be promoting with our medical colleagues a far higher degree of interest in and development of the specialist skills that medical professionals need to do these jobs in order to make this process a success.

I have here a case history that caught my imagination. A 25 year-old young man is undergoing his first major reassessment of his problems as an adult. His assessments will involve MR scans, examination by neurologists, neurogeneticists, neurophysiotherapists and a specialised occupational therapist. He has scattered neuromotor difficulties. Although I trained as a pharmacist a long time ago, I could not even find on the internet what neuromotor difficulties actually amount to, but it is clearly a serious condition that is being addressed by experts at a tertiary, if not international, level by a centre of excellence in a region in the United Kingdom. The young man has written to say that he is now fearful that he will have to address the circumstances of these tests. It would be completely daft and stone mad that we cannot say something now that is clear. There may be technicalities with the legislation, and perhaps I could be persuaded that such provisions should not be in primary legislation, but we absolutely need some clear, copper-bottomed assurances from the Minister that a person in those circumstances would not face such difficulties.

I hope that the Minister will understand that this is an important amendment and that he will take as much time as he can to tell us as much as he knows about how these processes will work and where in the legislative process—whether by regulation or primary legislation—we can be assured that we will get some protection for the kind of young person to whom I alluded.

[The Countess of Mar]

My Lords, I have difficulty with Amendment 50ZR. I fully endorse the fact that medical evidence is needed, but some people with ME have not seen a doctor in years, simply because there is no treatment for them. If the department is expected to depend a lot on medical evidence for corroboration of the illness, I do not know how people with ME are going to cope. That really disturbs me and the issue needs to be examined.

I fully support the amendment of the noble Lord, Lord Addington, on training. People with ME have cognitive difficulties as well as all their other problems, and these are not very well understood. I give him my heartfelt support, and I hope that the noble Lord will take on board the fact that some people cannot get current medical evidence to corroborate their illness.

[Lord Wigley]

My Lords, I shall speak briefly because time is pressing. We went into this issue in some detail in Committee and I warmly support the amendment of the noble Lord, Lord Addington, which was better than the one we originally considered. The noble Lord, Lord Touhig, referred to the tiered approach, and I very much hope that the Minister can confirm that the tiered approach that has been pressed upon him by those involved with autism will be central to this matter.

I also hope that he can take the main thrust of the amendment of the noble Lord, Lord Addington, whereby expertise needs to be brought on board. Earlier today, the Minister emphasised the need to make sure that those with greater disabilities get the support they need and that those with lesser disabilities get less. That approach is dependent upon knowing exactly what the conditions are. When we consider people in the spectrum associated with autism and Asperger’s we need to know the individual challenges they have. If the wording of this amendment is inappropriate, so be it. However, there needs to be an approach that brings that expertise on board, otherwise we are failing to do what the Minister says he wants to do.

18:15

[Baroness Hollins]

My Lords, I shall speak briefly in support of this amendment and Amendment 50B. I spoke at length in Committee in support of the requirement for the decision-maker to collect evidence from the claimant’s own health professional, and I do not intend to repeat myself. However, I should like to make a specific point about the requirement in Amendment 50B that,

“persons approved by the Secretary of State to undertake assessments have specific training in all mental, intellectual and cognitive disorders”.

This is because it is necessary to state that specialist skills are required in assessing someone with autism, learning disability or mental illness, and I know that it is intended that such expertise should be provided. However, most medical doctors do not have these skills. Indeed, Professor Steve Field, when writing about the NHS Future Forum in connection with the Health and Social Care Bill, pointed out in his most recent papers that it is of some sadness and regret that most doctors do not have training in these specialties, particularly those relating to learning disability and autism.

The other point I should make is that in psychiatry these are also specialist skills and not all psychiatrists have them. All will be good at assessing mental illness, but not all will have expertise in assessing people with learning disability or autism. That requires additional or different specialist training. I wish just to draw that to the Minister’s attention.

[Baroness Hayter of Kentish Town]

My Lords, these amendments would improve the assessment process for the new PIP and allay the fears of many people with disabilities that the poor experience of the ESA assessments, where around 40 per cent have been successfully appealed, is not replicated under the new benefits system.

Amendment 50B relates to the training of those undertaking face-to-face assessments to ensure that they have knowledge of mental, intellectual and cognitive disorders, clear guidance about when to access more specialist advice, and a guarantee that such advice will be available. In Committee, we received some encouragement from the Minister who stated:

“Assessors will be required to have a broad training in disability analysis as well as training on specific impairments … we intend to ensure that they have sufficient training in mental, intellectual and cognitive impairments … and will stipulate this in our contracts”.—[Official Report, 16/11/11; col. GC 263.]

Perhaps the Minister could let us know what budget has been set aside for such training.

Amendments 50C and 50D would exempt certain people from a face-to-face assessment where sufficient evidence is available via other means. This would actually save money for the Government. I hope that the Treasury is listening. Implementing face-to-face assessments was to have cost about £675 million. The amendments would reduce the costs by removing from the process claimants for whom a face-to-face assessment is clearly unnecessary. This would help those with lifelong or degenerative conditions, for whom a face-to-face assessment could be stressful. For example, about half those with MS or Parkinson’s are receiving the highest level of DLA. Putting them through an expensive and stressful face-to-face test seems unnecessary.

Again, we received some assurance in Committee. The Minister stated that,

“where there is already sufficient evidence on which to make a decision … we completely agree … a face-to-face consultation should not be required”.

I hope that the flexibility would be there for that. However, he also argued that other than for those with a terminal illness,

“we do not agree that there should be different rules or processes for different groups of people … on the basis of impairment type”.—[Official Report, 16/11/11; col. GC 261.]

Yet, if the Minister is prepared to accept that those with a terminal illness should not be subject to unnecessary assessment, surely the same argument could be applied to those with degenerative conditions where there is no hope of improvement. We look forward to any assurances the Minister can give that unnecessary face-to-face assessments will not be necessary.

If he is not persuaded by me, perhaps he will be persuaded by someone of his own political background—the Mayor of London, Boris Johnson. I have never quoted from one of his speeches before. He writes:

“Evidence from the individuals GP and/or a consultant will provide an accurate assessment of need. It would be difficult for a healthcare professional in a one-off meeting to elicit a comprehensive response about the daily reality for each claimant. Face-to-face meetings … could prove … inappropriate for an individual who may have difficulty with social contacts, such as those with autism, or for those with an intellectual or mental health disability”.

This brings me to the first amendment in this group which would ensure that the assessment process always takes account of evidence from the claimant’s old healthcare professional. It builds on the experience of the work capability assessment for ESA and is to help the Government to avoid history repeating itself. Unfortunately, in this case, it would be as tragedy not farce. The problem with the current proposals is that they put the onus on the claimant to collect the medical evidence and also to have the knowledge that would be helpful to provide this. As we have seen with ESA assessments, it is exactly this that often leads to unnecessary duplication as a case is assessed and then reassessed in the light of the evidence from the GP or professional. The initial failure to consider such evidence has contributed to the very high and expensive success rates.

In Committee the Minister argued that while medical evidence could be of use, he felt that it was not necessary to gather evidence in every case. He said:

“In some cases what the claimant has already told us … will be sufficient. In other cases, information … might be likely to add only limited value”.—[Official Report, 16/11/11; col. GC 261.]

Surely it would be better to err on the side of caution, given the widespread inaccuracy of the ESA assessments and the need to ensure that the personal independence payments do not follow the same route. Medical evidence is bound to assist the decision-maker in far more cases than those in which it proves unnecessary.

This is a modest amendment. It seeks to ensure that the introduction of personal independence payments proceeds smoothly and more importantly to ensure that the right benefit is paid to the right people. I hope the Minister will accept this. Certainly it would have our full support.

[Lord Freud]

My Lords, I could summarise my speech in about three sentences. I am in agreement with virtually everything said in the Chamber. I hope that after my three sentences I will be able to provide assurances. My only point of real disagreement is that I do not want it to be mandatory—in primary legislation. This is in regard to the point made by my noble friend Lord Kirkwood that it reduces flexibility and we are much better off setting it up in regulations and guides and in the contracts. That is our proposed approach but fundamentally we are absorbing all the valuable points made on this group. I will try now with some speed to go through those assurances. I ask noble Lords to stop me with the precise assurance they want if I am not making the assurance well enough.

Amendment 50A was semi-withdrawn by the noble Lord, Lord Touhig, but I will try to deal with it because it is a building block. People being assessed can bring in someone with them—a relation, a friend or a professional—to help them. That is really important in the group we spent a lot of time on this afternoon relating to autism and Asperger’s. When people are over-bright their relation can make the point about the reality and the over-anxiety of the person being assessed. That would be an active role in the process.

I turn now to Amendment 50B. Clearly, we need to make sure that assessors have all the appropriate training to interpret the evidence that they are provided with. I have to make the point that it is not a medical assessment PIP. It does not ask the assessor to diagnose a condition or to recommend treatment options. It is different. It looks at how the conditions or impairments affect individuals’ everyday lives. That is a different skill set from that involved in treatment. There is not quite the same level of need for specialist skills but it is our intention that assessors will have a broad training in disability analysis as well as training in mental, intellectual and cognitive impairments. That level of training will be stipulated in our contracts with any providers and we will be responsible for signing off the training syllabuses. There will be occasions when assessors need more specialist support in the course of making these assessments. We will ensure that they have access to and support from individuals who have the in-depth knowledge that the noble Baroness, Lady Meacher, mentioned with regard to mental health conditions.

[Baroness Browning]

I am sorry to interrupt again. Can my noble friend give us any hope that when an assessment is called there will be any publication of the qualifications and background of the assessors so that the people being assessed at least have some view of what their expertise actually is?

[Lord Freud]

It is a nice idea. I do not think I will make an utter commitment to it here and now but it is a cute idea and maybe we should put it in the contract. I will take it away and think about it.

We do not think that we should prescribe this in the Bill or even in regulations because it is important that assessors have an understanding of the limits of their knowledge so they know when to bring in the expert advice. I think the noble Baroness, Lady Healy, got that absolutely right.

I will now go on to Amendments 50C, 50D and 50ZR. We know that individuals can have a wealth of material, knowledge and evidence that will help in the assessment process and we need to get the right material and evidence from them at the right time and we need to encourage that evidence to come forward. We will not create a two-tier system where the poorest and the most vulnerable have less chance of receiving benefit because they cannot afford to pay for the evidence. We are going to make sure that does not happen.

I want to pick up the very valuable point raised by the noble Countess, Lady Mar. If we have a mandatory process to involve the individual’s health professionals it may very well be an entirely nugatory and expensive process in the many situations where the GP is not up to date with what is happening. That is the inflexibility of having something in the Bill which adds nothing except cost. If someone who has a learning disability has not visited a health professional for many years, why go through the expense of getting evidence? It would be unnecessary; it would slow the process down; and there may be someone else whom we would not have thought of including in the Bill who is much better placed to provide information and evidence for the assessor. We need to pull out the cumbersome implications of the mandatory process—the point made so precisely by my noble friend Lord Kirkwood.

We have made it clear that face-to-face consultation should form part of the claim process for most—but absolutely not for all—claimants. Ultimately, consultation will play a key role in creating a fairer and more objective assessment. It needs to be done sensitively and proportionately, but where sufficient evidence is available, we are in absolute agreement that there does not have to be face-to-face consultation. There will be many examples where that is unnecessary.

We are talking about something very close to, if not exactly, the tiered process recommended by the National Autistic Society. That is what we are planning to adopt. We have flexibility in the Bill to do that.

18:30

[The Countess of Mar]

My Lords, I should have said this when I was making my initial speech. About 60,000 people with ME are either bedbound or housebound. To go to a face-to-face interview would cause enormous stress and probably exacerbate their symptoms. Will that be taken into account? They cannot provide medical evidence because there is no treatment; yet they cannot come out of their homes. How will the Minister deal with that?

[Lord Freud]

My Lords, one thing I was trying to get over about trying not to have a two-tier process so that the rich can get their evidence and the poor cannot, is that we turn the burden on to the assessors, so that when someone cannot come out, that requires a house visit if we cannot use paper evidence. There will be examples where paper evidence will do the job; where it cannot, the onus is on the assessor to do the checking, rather than the other way round. That is how we will provide that protection.

I hope I have gone through all the specific issues and given assurances on all those important matters. We are planning to meet the concerns expressed around the House. All I am asking for is that we have the flexibility to go on running the system as things change, as they inevitably do, and that we do not lock it up in primary legislation so that if we need to make changes it takes years. That is really what we are talking about.

[Baroness Meacher]

I apologise for interrupting the Minister. I just wanted to make a point about ME patients, who have the most awful time. I have direct personal experience of that—not myself but through people close to me. Does the Minister accept that Amendment 50ZR would enable someone bedridden with ME who has not seen a doctor for years to call their GP and have a proper assessment? They are bedridden; they cannot go to assessments. That would avoid getting into a benefit assessment straight off. That is the whole point of the amendment. There has been support around the House because of the many situations where tremendous distress can be avoided by an appropriate person—perhaps a nurse, perhaps a doctor—doing a full and careful assessment, rather than getting into the benefits system.

[Lord Freud]

My Lords, I hope that I have made it absolutely clear that if we write into the Bill that it must be the GP, who may not be the right person, we are stuck. If you give us the flexibility, we are not stuck and in those circumstances we will go to the person’s home to do the assessment, or take someone else's piece of paper on the tiered approach.

What we are planning will be better for people suffering from ME and other illnesses because we will be able to respond. I think that the market will change. My noble friend Lord Kirkwood said that there is not an adequate market in this area. Occupational health and support for people of working age is a Cinderella service. We will be building that. As things change, we can move the assessment. If you tie it up, we will be locked in to 1948 as the years go by. The only difference between us on this, I think, is how mandatory and prescriptive we want to be, and it would be most unusual to put it in the Bill.

Let me cover the technicalities. The Government consider that Amendment 50D is directly consequential on Amendment 50C; the others are separate, so I ask noble Lords not to press them to a vote and the noble Baroness to withdraw the amendment.

[Baroness Grey-Thompson]

My Lords, I thank the Minister and everyone else who has taken part in the debate this afternoon. On a point of clarification to the noble Countess, Lady Mar, although the wording of the amendment was “relevant healthcare professionals”, in her speech she mentioned doctors; it is much wider than that.

The amendment is a fundamental cornerstone of what is necessary in the move to PIP. I recognise that the Minister has moved a long way. I am still not comfortable with some part of his statement on the broad training for professionals. You do not know what you do not know. It is very difficult to instil that knowledge in people. I would like to know an awful lot more about the detail of how that training and education will take place.

There has been broad support around the House for my amendment, and I am grateful to noble Lords for that, but considering that the Minister has moved further than perhaps I expected, there is an awful lot to think about in what he has said. I beg leave to withdraw the amendment.

Amendment 50ZR withdrawn.

Amendment 50AB

Moved by

[Baroness Thomas of Winchester]

50AB: Clause 79, page 58, line 6, at end insert—
“(d) shall not take into account aids, appliances or adaptations used by the person.”

[Baroness Thomas of Winchester]

My Lords, we had quite a debate about the use of aids, appliances and adaptations in Grand Committee, at the end of which I found myself more confused than ever about how the PIP assessment was going to take them into account. I have already declared one interest; I feel that I should declare another in having most of the aids and appliances known to mankind in my house.

My purpose in tabling the amendment is not so that we can have another debate about the detailed use of all kinds of aids—

[The Deputy Chairman of Committees (Lord Brougham and Vaux)]

Order. I ask Members of the House to leave quietly, because otherwise the Chairman cannot hear the speech.

[Baroness Thomas of Winchester]

My Lords, I am not going to have another debate here and now about the detail of all kinds of aids and appliances, but I want to signal my concern about the question and to ask the Minister whether he would consider hosting a meeting for interested Peers on this topic, together with the relevant officials from his department.

I quite appreciate that those who have been working on the second draft criteria for PIP have tried to do their best to incorporate the views of many organisations and people, including disabled people, but we must not forget that the Government want to cut the bill for DLA by bringing in PIP, which may mean that some of those who currently receive DLA will not receive PIP. If so, it is very important to make sure that some people do not fall through the net because their particular needs have not been met.

We have to keep in our minds at all times the purpose of PIP, which is to help a person to carry out daily living activities and mobility activities if that person is limited or severely limited by their physical or mental condition. The Minister has repeatedly made it clear—we heard it just now—that the Government are looking not just at the medical model of disability but at the biopsychosocial model, which tries to include part of the social model. The responses of disabled people and organisations to the first draft criteria were instructive. Many were keen to point out that taking the use of aids and appliances into account does not necessarily remove a barrier to participation. Those of us who have mobility problems can all testify that there are still a lot of buildings such as restaurants, shops and even hotels which are not accessible, as well as dropped kerbs which are positively dangerous and public transport which is not suitable. The mobility descriptors are, in my view, worryingly minimal, and here again the responses to the “Moving Around” section were useful. While moving outside, for example, no account is to be taken of the gradient or texture of the ground, or the weather, and there was no box for whether the physical support of another person was needed for those with poor balance.

I turn now to a very basic issue—managing toilet needs or incontinence. One response was that toilet needs outside the home should be considered. Most disabled people can manage in their own homes, many with aids, but going out is a different matter, as we heard from the noble Countess, Lady Mar, who is not in her place at the moment. This has not been included but it may make all the difference to whether someone can participate in society. If that is the criterion for receiving PIP, why is there no suitable box for it? Or perhaps there is and I have not been able to find it.

Before ending, I should like to raise one matter that has concerned me for some time but about which I may not have to worry—that is, the difference between using an aid or appliance for work capability and using the same aid or appliance for ordinary living purposes. For example, we know that a person in a manual wheelchair is no longer classified as having limited capability for work simply because of their use of a manual wheelchair, so they will not automatically get ESA rather than JSA. Although I am not happy with that state of affairs, that is the situation at the moment. However, if that person applies for PIP under the new regime, knowing that PIP will be an in-work as well as an out-of-work benefit, and because they might need extra help with daily living activities, then I can see no good reason why they should not receive it. Therefore, I hope that whether a person has “passed” or “failed” the work capability assessment will not be taken into account when they are being assessed for PIP. I think that this is why the noble Baroness, Lady Grey-Thompson, thought that she might be ineligible for PIP.

I understand that the aim for PIP is to take account of aids and appliances which are actively used by individuals and those which could reasonably be expected to be used to reduce barriers to participation. If the Government expect a person to buy and maintain aids, the least they can do is to help to pay for them.

The case studies that the Minister promised us I found extremely valuable, but they also beg a few questions. For example, the phrase “Needs to use an aid or appliance to bathe” means using a shower seat to take a shower, but what about those who can use a shower only if there are suitably placed grab-handles and the shower has the lowest step possible, or if the person has a wet room but has to use, say, a walker while using the shower?

In view of the very late appearance of the PIP thresholds and the case studies, I hope that the Minister will agree to an early meeting between concerned Peers and the relevant officials at the DWP to talk in more detail about how aids, appliances and adaptations are going to be used in the assessment. I beg to move.

18:45

[Lord Low of Dalston]

My Lords, I have added my name to the amendment and I have here an eloquent speech in its support. However, I do not propose to deliver it because I am aware of even larger fish to fry a little way down the track, and I think it is important that we should reach those as soon as possible. However, I want to make it clear that that in no way reflects any lack of support for the amendment of the noble Baroness, Lady Thomas. I support and agree with every word that she has said, and I entirely agree with the approach that she has suggested of getting together with the Minister and his officials to see whether we can find a way through before Third Reading.

[Baroness Gardner of Parkes]

My Lords, I support the amendment. I have raised this issue with the Minister in private in the past. Many people on the existing benefit have used the money to increase their possibility of living normally by putting it towards aids or adaptations, and it would be very wrong if they were disadvantaged because of that.

[Lord Freud]

My Lords, a fundamental principle of PIP is that support should be targeted at those who are most affected. I reassure my noble friend Lady Thomas that we will not be penalising people who use aids and appliances.

We know that many disabled people have a greater level of participation because of the help provided by aids, appliances and adaptations. If we were to disregard entirely the use of such aids, we would penalise individuals whose health condition or impairment could not be helped through their use. In those circumstances, the needs of those individuals would seem less of a priority, even though their levels of participation might be lower. Therefore, there is a balance to be struck here. I would be the first to admit that the use of aids, appliances and adaptations do not of themselves eliminate needs, barriers or costs. We accept and understand that, and that is why we are applying points in the assessment when such aids are in use. The number of points will vary depending on the aids in question and the levels of need.

With regard to the daily living component, the entitlement thresholds have been set at such a level that an individual who requires aids to carry out a number of activities may receive the component at the standard rate. I am pleased to reconfirm to the noble Baroness, Lady Grey-Thompson, that with the mobility component, individuals who use aids and appliances to move short distances can receive the standard rate, while someone who needs to use a wheelchair to do so—whether it is a manual or an electric one—will receive the enhanced rate. In that sense, it is a different assessment and it does things differently from the WCA for ESA. The valuable point has been made tonight that people do not understand that, so clearly we need to put across information about it.

As I informed noble Lords in Committee, the approach that we wish to adopt for PIP is the same in this area as that currently used within DLA. We take into account aids that are currently used by individuals as well as those which might reasonably be expected to be used. Let me be precise—I mean those that are easily and cheaply available. We will not, for example, say that an individual’s needs would not be present if they simply bought themselves a wheelchair, a stairlift, or a walk-in shower. That would not be reasonable, and we will have guidance available to make sure that claimants are treated consistently.

I will, however, be delighted to host a meeting with my noble friend, and any group she wishes to bring. Clearly, there is a big consultation exercise going on in precisely this area. I know this is an area in which she has great interest, and I will be very pleased to host that meeting. I urge her to withdraw her amendment.

[Baroness Thomas of Winchester]

My Lords, I am very grateful to the Minister for agreeing to such a meeting, and for clarifying that there is a great difference between the assessment for the work capability assessment and PIP. With that, I beg leave to withdraw the amendment.

Amendment 50AB withdrawn.

Amendments 50ABA to 50D not moved.

Clause 80 : Required period condition: further provision

Amendment 50E

Moved by

[Baroness Grey-Thompson]

50E: Clause 80, page 58, line 26, at end insert—
“( ) The Secretary of State must lay before Parliament an independent review of the plans for implementation of the assessments under section 79 before the provisions are brought into effect, and such plans must in particular provide for—
(a) a trial period before any assessment process is implemented fully for new applicants and those transferring from DLA;(b) disabled persons organisations to be involved in formulating the assessment process.”

[Baroness Grey-Thompson]

My Lords, the purpose of the amendment is to ensure that there is an independent report on the plans for both the PIP assessment and its implementation before implementation starts, and a trial period before it is implemented in full.

We have spent much time today debating why disability benefits matter so much, but perhaps I may briefly point out that nearly one-quarter of individuals in families with at least one disabled member live in relative income poverty, and over 50 per cent of working-age disabled adults are not in paid employment. One-third of working age disabled people are estimated to live in poverty.

There is huge concern about the effect of DLA reform. The thresholds for the new benefit were announced only yesterday. The modelling suggests that the second draft will produce a 2015-16 caseload of 1.7 million people receiving PIP. Without introducing the new benefit, we would expect the number of 16 to 64 year-olds claiming DLA in 2015-16 to be 2.2 million. That is a reduction of half a million people who will not receive any help with the cost of disability, who would have been receiving DLA.

Just last week an analysis of organisations’ responses to the original government consultation on DLA reform highlighted the amount of concern about the proposed changes. The extent of this concern was not clear from the DWP response to the consultation. Scope, in its report, The Future of PIP: A Social Model Based Approach, says:

“We remain very concerned that this decision is based purely on budgetary targets, rather than on robust evidence as to how the benefit is used and by whom”.

I just do not believe that there has been time to analyse who will lose out. The Disability Benefits Consortium stated:

“We are very concerned that there has not been due consideration of the impact this reform will have both on those who lose all their entitlement and those who are left with a reduced award following reassessment”.

The thresholds were published only yesterday, but without those thresholds it is impossible to look in detail at who will lose out. Without them, it is almost impossible to have an informed debate about this part of the Bill. The few examples in the consultation document, while helpful, cannot possible address this properly.

Why do we need an independent review and trial period? Some early analysis has suggested that one of the groups who might lose out are those with mental health conditions, who currently receive the lower rate of mobility. Many people with a mental health condition find it impossible to use public transport. They frequently use their DLA to pay for taxis. If they are unable to get out, it is likely to make them more socially excluded, and push them further from the job market. This is just one possible unintended consequence.

There needs to be careful scrutiny of who will be affected by these changes. Many more groups will emerge in the months and years ahead, together with some unintended consequences. I have a real concern that it could lead to a deterioration of people’s health. Will it impact on the social care budgets? There are so many more things to consider in this. For such a major change as this, it is important to be much clearer on what the changes will be.

There is concern not just about the test or the thresholds but about the way that the benefit is assessed, and this is a much greater change than the move from IB to ESA. An independent report on the plans for both the PIP assessment and its implementation, before the implementation starts, would provide an appropriate level of scrutiny, given the huge impact this reform will have on disabled people.

The trial of the IB reassessment process in Burnley and Aberdeen threw up a number of important lessons which the DWP learnt from and implemented in the full rollout. It is so important that there is a trial of PIP in a similar way before the full rollout to either new or existing claimants. I beg to move.

[Lord Low of Dalston]

My Lords, I declare my interest in these debates as a recipient of DLA. This amendment is every bit as important as those we passed last week. Noble Lords will know from their postbag that people are looking to us to ameliorate the worst excesses of this Welfare Reform Bill. Although the Bill has some very sensible and progressive things at its core, in the shape of universal credit, nevertheless it goes too far for most people’s consciences in the way that it takes vital support away from some of the most needy in our society, in ways that have been movingly illustrated—far more eloquently than I could—in earlier debates.

Let me be clear about what the amendment does and does not do. It does not entail the Bill being paused, as happened with the Health and Social Care Bill, and as it has been portrayed outside. It merely states that the new assessment regime should not be commenced until Parliament can be given the benefit of an independent review—a common enough procedure regarding the introduction of particular statutory provisions.

It may be said that it is pointless to pass such an amendment, and that the Commons will only reverse it. However, there are two reasons for passing it, notwithstanding that. First, it sends a strong signal to the Government that they cannot be too cavalier in the way that they drive the juggernaut of reform over those who are weakest and most defenceless in our community. Secondly, as we have seen in the last week, it ensures that they cannot do this below the radar of public attention.

I support the amendment from my noble friend Lady Grey-Thompson because I think that this is all being rushed through far too quickly to meet Treasury targets, before it is ready. The latest consultation draft of the assessment criteria reached us only yesterday, as we have heard, which has left little time to carry out the necessary analysis, but enough to see that it is still very much work in progress. For instance, just one day before we were due to discuss the Government’s plans for the future of DLA, the number of disabled people likely to lose help through the new assessment process was revised upwards to 500,000, as we have heard.

When the proposals were first announced in the June 2010 Budget we were told that a 20 per cent reduction in case load was likely. At that time this represented 360,000 disabled people, so the figure for the total of losers from the Government’s proposal has risen by 140,000, to which we should probably add the 80,000 care home residents who will no longer lose their mobility payments.

The Treasury’s target saving of 20 per cent was always arbitrary, being cost-driven rather than evidence-based. The Government themselves admit that the level of fraud is very low with DLA, at only 0.5 per cent. There are even suggestions that the increased figure for losers which we heard of yesterday will not achieve the Treasury’s target, either. At all events, the DWP is giving the impression of making it up as it goes along, all in an effort to satisfy its Treasury masters.

Disabled people do not have confidence in this process, which all serves to underline the fundamental unfairness of taking needed support away from the most vulnerable simply to meet Treasury targets. Confidence is not enhanced by the experience disabled people have had of the work capability assessment for out-of-work benefits. This was trialled on new claimants and regionally piloted for 18 months before national implementation, and has been the subject of two independent reviews, yet still gives rise to considerable difficulty, with 40 per cent of appeals upheld. This is a massive waste of money. We need to be sure that we have got the system right for the personal independence payment before it is introduced. So far, the DWP has tested the proposed assessment for PIP on fewer than 1,000 people. A sample of fewer than 1,000 is simply not enough to get a proper handle on the complexity of the issues that will arise when the full DLA caseload of 2.2 million people is put through the reassessment process; it is not like saying whether you vote Labour or Conservative.

19:00

DWP research suggests that more than half of those receiving DLA have four or more health conditions or impairments. The process of reassessing everyone is set to cost £675 million, to say nothing of the cost to the NHS of providing 2 million medical reports. Is it really worth such a massive outlay in public expenditure —all of half the anticipated saving—when, with a much more modest overhaul of the system, the money could be used to maintain support for vulnerable disabled people, which the Prime Minister made a great play of pledging to do, rather than taking it away from them?

Particular issues have arisen with the work capability assessment for people with fluctuating conditions such as MS and ME, and also for people with mental health problems. I do not believe that the Government can yet demonstrate that these issues have been resolved for the new PIP assessment, which adopts a similar points-based approach. We all want an efficient, effective welfare system that delivers support only to those who need it, but I do not believe that the current assessment proposals will achieve this, and they could cost as much in long-term NHS social care and tribunal costs as they save, to say nothing of the distress and hardship that certainly will be caused to individuals. For these reasons, I urge the Government to pause the full implementation of this provision until a proper study has been undertaken of the testing system, of those affected and of the costs to individuals, families and the Government.

From the Government's point of view, this makes good sense if they want to avoid the kind of debacle we witnessed with Atos Healthcare’s conduct of the work capability assessment. I simply do not believe that the new system will be ready to go by April 2013, when it is due to come into force. From where we are now, there must be a 15-week consultation period on the latest draft of the criteria, followed by a modicum of time for the Government to respond if the consultation is to be genuine. Regulations will have to be prepared and consulted on. The DWP states that the regulations will not be ready until the end of this year. After that, the details of the assessment will have to be finalised before contracts can be tendered and set for carrying it out. This cannot be rushed if the sort of problems that bedevilled Atos Healthcare, the company that carried out the work capability assessment, are to be avoided. Therefore, it is as much in the Government's interests as those of disabled people that we take the time needed to get this right.

[Lord Newton of Braintree]

My Lords, for the second time today I feel that I need to say something, however brief, because of my history. Just as I engaged in badinage earlier with the noble Baroness, Lady Lister, about the Social Fund, I now have to declare to the House—possibly as a proud boast—that as a Minister I was responsible for introducing the disability living allowance in the early 1990s. I was given huge help by someone who deserves a great deal of credit, namely my former and unhappily now late colleague, Nick Scott, whom some noble Lords in the House today will remember with respect and affection.

On that occasion, we cobbled together a slightly curious construction based on the existing benefits of mobility allowance and attendance allowance, using the maximum amount of money I could extract from the Treasury at the time, to extend help to various groups who had previously been excluded, including the mentally ill. Perhaps we did a better job than I thought at the time because it has not only stood the test of 20 years but has survived with people now seeking to defend it against all comers, in much the same way as they defend the Social Fund.

What I say to the House may be uncomfortable for the noble Baroness, Lady Grey-Thompson, and the noble Lord, Lord Low, for whom I genuinely have huge respect. This is not flannel; they are immensely valuable Members of this House. However, I have been taken down a different path. If somebody had told me 20 years ago that that structure was to be seen as anything near a settled state for 20 years, I would have been surprised, because there were obvious ways in which it could have been developed and carried forward to build on what we had achieved at the time. That is what the Government now seek to do. I say to the noble Baroness that I am not sure that it is right now to try to slow down the process by yet another review after the many that we have had.

Only yesterday the Government published a revised review of the assessment process. I accept that neither I nor anybody else has had a chance to digest it. However, it makes it crystal clear—this picks up on the second half of the noble Baroness's amendment—that this will be worked through steadily and carefully, in conjunction with organisations representing disabled people. I assume that account will be taken of the results of that consultation. Of course I accept that it would be nicer in a perfect world if we had all the details now, and that there will need to be a good deal of tweaking—or perhaps more than tweaking—as the consultation proceeds. However, I also accept that we have a Minister who knows his stuff, who cares about the subject and who has shown himself to be willing to listen to those representations. We should let him get on with it.

I do not accept the tenor of the e-mails that jammed my system from yesterday through the early hours of the morning into today, which suggested that the Government had a dastardly plot to do down disabled people. It is not the case, and I would not say this if I believed that for a moment. It is clear to me, having glanced at some of the e-mails—I have not been able to read them—that a number of them came from people who will not only not lose but may well gain from the proposals that the Government made. I hope that the senders will reflect on that.

This is not the moment for the House to agree this amendment. If we want to agree amendments, I suggest that between now and Report both the Minister and the House might reflect on the desirability of some extra-affirmative procedure of the kind used in the Public Bodies Bill for affirmative resolutions—I hope that they will be affirmative—that will come forward as a result of all the consultation. That would be far more productive than trying to slow the whole thing down with another review.

I have other points to make but the hour is late and the House wants to get on, so I will conclude by saying that at the end of the day I speak only for myself when I say that this would certainly cause delay, and would almost certainly add to the cost of an already expensive government programme. There may be smaller issues later, including those espoused by my noble and learned friend Lord Mackay, on which I may take a different view; but this amendment is strategic, damaging and mistaken, and I hope that noble Lords in all quarters of the House will join me in opposing it if it is pressed to a Division.

[Baroness Browning]

In the context of this amendment and the ability of health and social services to carry out their statutory responsibilities under the Autism Act, will my noble friend agree to take a look the number of people who currently have DLA but are predicted to lose it? There is a read-across here, because small levels of support have been identified as having prevented people taking their place in society and gaining independent living.

As I mentioned previously, I am concerned that as regards those who will lose the allowance—some will and others who apply in the future will not get it—the measure is going to have an impact on the way in which we have required health and social services to implement the Autism Act. Does my noble friend agree that there will be some hardship for those who lose it and that we have to face up to that reality, and that the Government should have a clear and examined view of how they are going to square that with the new statutory responsibility?

[Lord McKenzie of Luton]

My Lords, we support this amendment, moved so comprehensively by the noble Baroness, Lady Grey-Thompson, and spoken to so effectively by the noble Lord, Lord Low. I would say to the noble Lord, Lord Newton, that in doing so we are not motivated by a belief that this is all some dastardly plot, but a belief that we need to be assured that the system does not just need to be tweaked but that it is fit for purpose before this major change is introduced.

This amendment is aimed at helping the Government get right the process of transfer from DLA to the personal independence payment. It calls for an added layer of safeguards within the process of reform, with an independent review of the plans for operation of the assessments before they start and a trial period when the assessment process first comes into effect. Crucially, it calls for the full involvement of disabled people and their organisations in this process, ensuring that they have confidence that the assessment process for the new benefit will be fair. The need for safeguards in this area has been all too fully revealed with the experience of the employment and support allowance. The noble Lord, Lord Newton, told us that he was responsible for introducing DLA—which in Committee the noble Lord, Lord Low, called an “iconic” benefit—and he should be proud of that achievement. I have some responsibility for having introduced the employment and support allowance so I cannot claim any such accolade.

It is clear that the assessment process has not been working and has caused not only distress to too many disabled people but considerable headaches for the Government. We all know that 39 per cent of appeals have led to a decision about ESA being overturned in favour of the claimant, and the unreliability of the assessment procedure has also made it difficult for the Government accurately to budget for the cost of these reforms. The Office for Budget Responsibility’s November economic and fiscal outlook states:

“ESA changes have resulted in an increase in expenditure of £1 billion by 2015-16”,

and the latest administrative data suggest that fewer people than previously assumed will be judged fit for work as a result of the initial ESA work capability assessment and the reassessment of incapacity benefit cases, and more will be placed in the support group. This accounts for around four-fifths of the increase. Other changes arise from a change in assumptions about the composition of the ESA caseload, which results in higher average benefit payments per person and higher inflows. The costs of getting this process wrong can therefore be high, and we know that the Government have benefited from the independent review of the ESA assessment process undertaken by Professor Harrington.

As other noble Lords have said, we received just yesterday the document providing further information about the second draft of the PIP assessment criteria, together with proposals on entitlement thresholds, impact modelling and case studies. While this technically fulfils the Minister’s commitment that we should get it before the Report day, as we have previously noted, there has hardly been time for detailed study and analysis—although it is hard to miss the startling figure that some half a million disabled people will be excluded from the new benefit in comparison to existing DLA arrangements. Before causing this to happen, the Government should be called to account for the impact that this may have on the disabled people who are missing out.

19:15

The January document launches a 15-week formal consultation on the assessment criteria and this is welcomed as another opportunity for disabled people to input their views. However, this is no substitute for what this amendment calls for: that before these provisions are implemented, there is an independent review focused on implementation, with trial periods before the full rollout. There can be little doubt that proposals to abolish DLA for working-age claimants and substitute the personal independence payment have caused genuine consternation among disabled people. The representations we have received reflect that. What we have heard from our own colleagues, noble Lords in particular, who are powerful advocates for disabled people, in Committee and again today reinforces this.

We accept, as do many people, that DLA in its current form needs updating but the huge difference the benefit has made to the lives of millions requires the absolute maximum assurance to be provided before any replacement is implemented. That reassurance is made more difficult by the 20 per cent cut in the budget provision and in the context of some £18 billion of cuts from the coalition Government, which the IFS and others confirm are careless of the circumstances of the poor and disadvantaged. Whatever the Government’s protestations, there is a strong belief that the changes are about securing cuts.

The Minister will argue that the proposed assessment process will be assessing different things in a different manner, but the parallels with the work capability assessment are clear. Most would accept the concept of the WCA, but implementation has been chaotic and the assessment process flawed. Improvements are under way but these were driven by the independent report of Professor Harrington. Indeed, it was the independent report of the noble Lord, Lord Low, which brought about the Government’s change of heart, which we appreciate, on the mobility component and care homes.

The changes from DLA to PIP could cause a major upheaval in the lives of millions of people, many of them extremely vulnerable. We do not argue against change, but for a precautionary approach in introducing that change. This should include an independent report before the start of change, focused particularly on the assessment process, trials before general rollout and, above all, meaningful engagement with disabled people, because they deserve no less.

[Lord Kirkwood of Kirkhope]

The noble Lord is an experienced hand and has made a very interesting speech, but it would help the House enormously if he could be tempted to give an assessment—if he was the Minister facing Amendment 50—of how long he thinks it would take to discharge the responsibilities contained in the amendment.

[Lord McKenzie of Luton]

It is clear that the Government are going to have to do some of this anyway, but in terms of an overall time period it is clearly a matter of some months rather than weeks, but not a matter of years. It depends on the determination and effort that the Government bring to bear. They have the levers and the resources to cause this to happen quite quickly, I would suggest, but there has to be full engagement with disabled people for it to be meaningful. This does not mean endless delay in the introduction but it does mean a real level of reassurance before we embark upon this very significant change.

[Lord Freud]

I will come to my conclusion first. Basically, we are doing a lot of trialling in this process and the way that this particular amendment is drawn would delay us very significantly. At the end of my speech, I will give the noble Lord the actual cost that we estimate the delays will represent.

I will spend a bit of time highlighting our approach to developing, testing and refining the assessment criteria that we already have. We have been developing those in collaboration with a group of independent experts, including disabled people and disability organisations. We had initial proposals on which we then carried out 16 weeks of consultation. We met 60 disability organisations; had 170 written responses; and carried out testing involving sample assessments of around 900 volunteers selected from current or recent DLA claimants. Both the testing and the consultation were very effective and allowed us to review, revise and improve the draft assessment criteria from that published in May. We provided a second draft in November in advance of discussing the PIP clauses in Grand Committee. Since publication, we sought the initial views of disabled people and the organisations that represent them in an informal way to listen to their thoughts. Yesterday, as promised, we published a further document detailing our initial thinking on entitlement thresholds for the rates and components of PIP. We have now commenced a formal consultation on the entire assessment criteria, including the weightings and entitlement thresholds which will last for 15 weeks.

That gives disabled people and disability representative groups the opportunity to tell us what they think the criteria will mean to them and their members and what amendments might be needed before we finalise the regulations. I can assure my noble friend Lord Newton that those regulations, which we will lay later this year, will be subject to the full affirmative procedure of both Houses. We are confident that we will be able to test the impact of these using the data we gathered during our earlier exercise. If for any reason this is insufficient, we will carry out additional testing to support our analysis. In response to a specific request from my noble friend Lady Browning, I will personally look at the impact of this on our autism obligations and I will make sure that that is done as a key part of this process.

There have been, and there remain, significant opportunities for involvement from disabled people and their organisations, and significant opportunities to influence our proposals to ensure we get them right. That, however, is not all. In terms of the delivery and operation of PIP, we intend to continue to develop a number of our operational processes in conjunction with disabled people and their representative groups through our implementation development group, which I talked about a little earlier this evening. This group has already played such an important role that it is our intention to retain its services after April 2013 in order to work with it to help evaluate the new delivery arrangements.

We have also created a number of customer research panels, made up of groups of disabled people who share similar characteristics, in order to understand, and gain an insight on, how the process impacts upon them. We will also test our operational processes in a model office environment, allowing us to see how they work without affecting individuals’ benefit entitlement. The trouble with a formal trial, of course, is that it would change what people actually get even though we are trialling. Here, by doing it in a model office, we can do it in a way that does not actually affect what they receive, but we know exactly how it will work.

We want similar arrangements to be in place with regard to the processes of the eventual supplier of the assessments of the benefit. We will be making it clear to bidding organisations that we expect them to work with disability organisations on the design of their processes, to improve the customer experience. This will be before, during and post-implementation. This will be a clear requirement in the contracts.

As well as getting the whole development process right, I recognise the value in moving away from a big-bang approach to implementation which would see both new claims and reassessments beginning in April 2013. Since the Committee stage, a significant amount of work has been undertaken to investigate the options for ensuring a sensible implementation which allows us to learn from early experience. Therefore, I can inform the House that, in addition to the pre-implementation testing work that I have already mentioned, we will limit the number of new claims for personal independence payment to a few thousand per month for the first few months of implementation. This will allow us fully to trial all the processes in a truly live environment. We are still developing the details on how we can meet our claimant target over the first few months.

Once we are satisfied that the new processes are working as intended with this reduced number, we will allow all new claims for personal independence payment to enter into the process. We will continue monitoring and reviewing the processes to ensure they are working effectively and appropriately and to see how claimants are finding the experience. We will begin to reassess existing DLA claimants in a co-ordinated way six months after the initial implementation. Again, we will stagger this process. We expect the first stage of reassessment to start in the autumn of 2013, beginning with individuals on a DLA fixed award who will need to renew their claim and those claimants who report a change of circumstances on their existing DLA claims.

At the same time, we intend to conduct a pathfinder trial reassessing individuals who would not, in the ordinary course of events, come up for reassessment. We expect the pathfinder to run for around three months to ensure the processes for identifying and contacting people and taking them through the claim processes are working satisfactorily. Allowing a small number of existing DLA claimants to advance through the reassessment process ahead of full national implementation will enable us to be sure that our approach to engaging these customers into the claims process is working effectively ahead of widening the selection. Also very relevant here is the independent review and report on the assessment that we are legislating for in Clause 87.

During Committee, the noble Lord, Lord Rix, laid an amendment seeking to increase the number of independent reviews carried out. Noble Lords will remember that I promised to take this matter away and consider it further, and I have done that. Our revised proposal is that we legislate for two biennial independent reviews within the first four years of the implementation of PIP. The first would report within two years, beginning with the date on which the first assessment regulations come into force, and the second within four years of that date. Although it is only two reviews formally in legislation, we commit to undertake a third if the second review demonstrates ongoing issues with the operation of the assessment which need to be addressed in this manner. That is a firm commitment from me and my ministerial colleagues.

In reality, in the way that we are structuring this, we are trialling it in any real sense; we are doing it on a gradual basis. If we do it in this way, we will get the assessment and wider benefit processes right; we will involve disabled people and we will learn from the earlier delivery of the benefit. We do not think, therefore, that the formal trial proposal in this amendment is necessary. However, if we do it that way, the House should know that it would push back the implementation of the benefit. Our estimate is that the loss will be £1.4 billion of savings over the reassessment window. Clearly, that has to be found somewhere else. I know that noble Lords opposite think that is funny.

[Lord McKenzie of Luton]

Could the noble Lord give us a bit more detail of that estimate? The figure of £1.4 billion seems to trip off the tongue as the cost of any amendment that we pursue.

[Lord Freud]

That is an assessment based on the delays that we anticipate from this amendment, which is actually similar to the previous amendment where I used the same figure. It would have the same effect of delaying the whole process. That is the Government’s position, having worked through the implications of the amendment.

I remind the House of where the Opposition have got to with their amendments. We estimate that as a result of the votes on amendments so far, over five years they have imposed £3.8 billion-worth of extra costs, and this amendment will take that figure to £5.2 billion.

[Baroness Hollis of Heigham]

I am sorry to see a Minister, whose integrity and respect for evidence has been apparent to the whole House, going back to the box-ticking, false assumption that there are no political choices available to this House. There are plenty of political choices if the Minister wishes to use them—for example, freezing council tax, increasing council tax bands, looking at some of the things that go on in pensions tax relief and so on. It is not clear to me that the economic growth of this country depends on taking away DLA from some of the most disabled people in the country.

[Lord Freud]

My Lords, I do not want to debate where alternative cuts would be found by the Opposition if they were in government and needing to balance the budget. All I can tell you is that the effect of the amendments that the Opposition have supported comes to that figure. It is amazing how, given an amendment here and an amendment there, pretty soon you are talking serious billions. I am afraid that this is another amendment which involves a serious amount of money and, for that reason, it is not acceptable to the Government. I urge the noble Baroness to withdraw her amendment.

[Baroness Grey-Thompson]

I thank the Minister for some of the reassurances that he has offered tonight. He has, once again, moved further than I expected, although it would have been wonderful to have heard some of it a little earlier. I thank the noble Lord, Lord Newton of Braintree, for his consistent honesty and for what he has done for DLA. Unfortunately, I am genuinely sorry that I do not agree with him tonight because we have to get this right.

The noble Lord, Lord Low, talked about confidence and, even with what the Minister has said today, there is such a lack of confidence among disabled people about where we are going with this that I am really concerned.

The Minister referred to costs, which are important, and huge financial sums are involved here. I would like to talk about cost—the social cost of what we are doing to the lives of disabled people. A number of disability organisations—I shall not go into how many—have contacted me and are telling me that we are not in the right place; disabled people are telling me that we are not in the right place; and my personal belief and conscience tell me that we are not in the right place. I wish to test the opinion of the House.

19:33

Division 1

Ayes: 213

---

Labour: 158
Crossbench: 37
Democratic Unionist Party: 4
Ulster Unionist Party: 3
Independent: 3
Liberal Democrat: 2
Plaid Cymru: 1

Noes: 229

---

Conservative: 148
Liberal Democrat: 63
Crossbench: 13
Ulster Unionist Party: 1

Consideration on Report adjourned until not before 8.48 pm.

Freedom of Information Act 2000

Tuesday 17th January 2012 Lords Chamber

Question for Short Debate

19:48

Tabled by

[Lord Hennessy of Nympsfield]

To ask Her Majesty’s Government how extensions in the scope of the Freedom of Information Act 2000 and their transparency agenda will affect the availability of government records to the public.

[Lord Hennessy of Nympsfield]

My Lords, I very much welcome this evening’s debate on access to official information and I am grateful to so many noble Lords for wishing to speak. It is, I think, the first time that your Lordships’ House has had a chance to discuss the plans for additional openness announced by the noble Lord, Lord McNally, on 7 January 2011. He outlined four changes that the coalition proposed to make: increasing the number of organisations to which freedom of information requests can be made by bringing in such bodies as the Association of Chief Police Officers and the Financial Services Ombudsman; consulting on drawing in a range of further bodies, such as examination boards; undertaking post-legislative scrutiny to see how the Freedom of Information Act 2000 has worked in practice—a task which the Justice Committee in the other place will take up next month; and—especially dear to my historian’s heart—making most public records available at the National Archives after 20 years instead of the current 30 years.

I know that the noble Lord, Lord McNally, is keen on this. He has been a good friend to historians. He has always been willing to talk to my students about the 1976 IMF crisis when he became a prime historical exhibit while working in No. 10 for the greatly missed Lord Callaghan of Cardiff.

Perhaps I may this evening mirror the Government’s approach by taking a wider-lens view of freedom of information and look at it as a question of access to official information as a whole. To do so, our field of vision needs to encompass not just the workings of the Freedom of Information Act, for access is a matter of linkages embracing with FOI the output of the public records system and the often neglected, although related, matter of government-commissioned official histories—a subject on which the noble Lord, Lord Rodgers of Quarry Bank, led a debate in your Lordships’ House four years ago.

Before turning to public records policy, I must first declare an interest as president of the Friends of the National Archives and as Attlee Professor of Contemporary British History at Queen Mary, University of London. Given my trade, I especially welcome the coalition’s pledge to implement the provisions of Part 6 of the Constitutional Reform and Governance Act 2010, which was passed in the last days of the Labour Government and created a new 20-year norm to replace the 30-year rules that have been operational since 1972. The plan is that from January 2013 an extra year’s worth of declassifications will be added to the 30-year process until the 10-year gap has been closed.

I understand that the statutory instrument for triggering the new archival flow has yet to be signed. I am neither a pessimist nor a sniffer of conspiracies but I would welcome reassurance from the Minister on this point. In the same spirit, I would welcome publication of the 20-year rule guidelines for record reviewers in government departments—who are fondly known as “the weeders” —so that Parliament can check that they will be no more restrictive than the current ones for 30-year releases.

I am confident that the new 20-year rule will stimulate a cataract of fine theses and excellent books, for a fresh run of documents is like giving the historical profession a new currency with which to trade. This is precisely what happened in the 1990s after the noble Lord, Lord Waldegrave of North Hill, who I am delighted to see in his place, as Sir John Major’s Minister for Open Government, put in place what we historians called, and still do, the “Waldegrave initiative” whereby departments were encouraged to re-examine particularly sensitive files that had been retained for longer than 30 years.

By 1998, when Whitehall stopped measuring its yield, 96,000 files had been declassified as a result, which filled gaps in the defence, intelligence and nuclear elements of the post-1945 secret state. I am full of admiration for the departmental records teams in Whitehall and the staff of the National Archives. I am equally aware of the pressure on budgets and manpower, but I urge the Government to consider commissioning a “Waldegrave 2” to run alongside preparations for the 20-year rule to ensure that as little possible remains in departmental strong rooms, including files that were still too sensitive to release in the 1990s but that might safely be declassified now. If the Minister agrees, we might even call the initiative “McNally 1”.

Those 30-year releases are a form of delayed freedom of information. FOI disclosures are welcome and often highly revealing, but they are fragmentary and it is runs of documents that historians need. FOI, to be candid, is not an unmixed blessing for scholars because it has led to greater caution in what is written down.

I turn now to official histories. I have not written one myself, but I am very grateful to those who have, not least for providing a window into Whitehall short of 30 years, and, in Christopher Andrew’s authorised history of MI5 and Keith Jeffery’s history of MI6 up to 1949, opening up windows into the necessarily most opaque parts of the secret state. The Cabinet Office, under the energetic guidance of Mrs Tessa Stirling, is the engine room of official histories. Thirteen have been commissioned since 2000, eight of which have already been published. The Pilling report of 2009 urged still more and suggested enhancements in the commissioning process, while the Hamilton report of the same year laid out improvements in the marketing of the books produced. The Government have not yet pronounced on Pilling-Hamilton. I hope the noble Lord, Lord McNally, will this evening be able to accept the recommendations and undertake to implement them when funds allow.

For the general public the most visible manifestation of the public records system is the annual festival of 30-year revelations in the media between Christmas and the new year. This time, understandably, it was the riots of 1981 that attracted most attention. Few noticed a security file in the No. 10 papers of the noble Baroness, Lady Thatcher, dealing with a leak inquiry instigated by the noble Lord, Lord Armstrong of Ilminster, then Cabinet Secretary, into a story on civil contingencies planning that I had written in the Times as that paper’s Whitehall correspondent. I am glad to say that the investigation got absolutely nowhere, but its declassification, as I think my noble friend Lord Armstrong would agree, has brought a frisson of amusement to both of us—a kind of bond between us after all these years.

There is, however, a truly hidden treasure in the latest releases for those with a taste for personal and political drama, after, perhaps, seeing that remarkable film “The Iron Lady”. It is a Cabinet Office file containing the records of the third world war that never was of March 1981: a transition-to-war drill exercised in great secrecy in Whitehall every two years in which officials role-played Ministers. It ends with the United Kingdom under conventional and chemical weapons attacks from the Soviet Union and its allies, and the British War Cabinet reaching and crossing the nuclear threshold, with the role-played—I emphasise that—Mrs Thatcher declaring that never before had a Cabinet been faced with such a grim choice between capitulating to a powerful and malevolent aggressor and embarking on a course of action that could end with the destruction of civilisation. It is gripping, desperate and—mercifully—fictional stuff, which cries out, I think, to be converted into a film script.

To finish by returning to reality, I stress that well organised and sustained access to official information, current and past, is crucial to the accountability of our system of government and the richness of the historical residue that clings to the Velcro of our collective memory. Such practices enhance the depth and quality of the rolling national conversation about government policy and politics without which no open society can flourish.

19:57

[Baroness Shephard of Northwold]

My Lords, I have two rather narrow points to make in this valuable debate so brilliantly introduced by the noble Lord, Lord Hennessy.

First, it is obviously in the interests not only of historical accuracy but, I would add, of transparency in the democratic process that there should be access to Cabinet and other government papers.

Secondly, if such access is not well structured and organised, and accompanied by well observed conventions, the public will inevitably be more interested in the political disclosures involved than in greater historical understanding of the events concerned. I believe the increasing use of FOI requests illustrates this point.

The conventions are all-important. Without them, the noble Lord’s objectives of a clearer and more accurate understanding of the past could be at risk. The convention that a Government cannot examine the files of their predecessor was breached by Ruth Kelly as Education Secretary in 2006, when she sought to make public her predecessors’ decisions on teachers debarred from working with children—the famous List 99—with no prior consultation. This was regrettable. It was an enormously sensitive issue, which was, inevitably, hyped up by the media. This resulted in inaccurate press coverage, problems for children, for schools and for individuals and, in the end, a negligible increase in public understanding of the issues concerned.

There may not have been time to develop conventions with the Scottish Parliament. Something tells me that the Scottish Government might not be too interested in discussing these things, but their decision unilaterally to reduce the no-disclosure period to 15 years—again with no consultation with their Westminster counterparts, who, by definition, are the ones who will be affected—raises a number of questions, not least about political motivation.

It is obvious that the public interest is served by the orderly and properly structured publication of government decisions, but without observed conventions the more accurate and informed public understanding of past events that we all want could be threatened by short-term sensationalism and even political manipulation. The conventions and their observance are key in achieving the noble aims so eloquently described by the noble Lord, Lord Hennessy.

20:00

[Lord Thomas of Gresford]

My Lords, “Transparency”, said Sir Humphrey Appleby cynically,

“afflicts all incoming administrations. It used to be called ‘open government’, and reflects the frustrations they felt when they were in opposition and could not find out what was going on, combined with an eagerness to discover and publicise the deception, distortions and disasters of their predecessors … But it does not last beyond the first few months. As time passes they realise they have more to lose than to gain from public knowledge of what they are up to. Each month increases their tally of catastrophic misjudgments, pathetic deceptions, humiliating retreats and squalid compromises. They very soon come to understand that sound and effective government is only possible if people do not know what you are doing”.

I am grateful to the noble Lord, Lord Hennessy, for introducing this debate. It is to the credit of this Government that they have maintained the commitment in the coalition agreement to build on the Freedom of Information Act and to,

“extend transparency to every area of public life”.

The Act has been in full operation for upwards of seven years. When it was introduced, local authorities recorded information in a more traditional way. The right to data now being introduced will ensure that public authorities make electronically stored data readily available in a reusable form. I spent 10 minutes this afternoon looking at complaints about the potholes in the road outside my home in Gresford, which are published on the local open website and was happy to realise that, in the past six months, my very good local Lib Dem councillor had managed to resurface the whole of that area.

The Act has been extended, as the noble Lord, Lord Hennessy, said, and proposals in the Protection of Freedoms Bill will extend it to companies owned by a number of authorities. There are real social and economic benefits, apart from for the writing of history, to be gained by enabling businesses, non-profit organisations, volunteers and others to use freely the datasets held by public authorities for social and commercial purposes.

For my own part, I would extend the provisions of the Act to private companies carrying out public work paid for by the taxpayer. I agree with the Public Accounts Committee which said recently in its 44th report published last July:

“Transparency on the full costs and benefits of PFI projects to both the public and private sectors has been obscured … commercial confidentiality should not restrict the ability of the public, Parliament and decision makers to access information”.

I hope that the Minister will be able to comment upon that view; I am sure that Sir Humphrey would not agree.

20:03

[Viscount Colville of Culross]

I thank my noble friend Lord Hennessy for having secured this debate on such an important issue. I declare an interest, having been a journalist, both on newspapers and in television, for most of my career. Since the introduction of the Freedom of Information Act, I have seen at first hand the beneficial effect of its principal aim, that of improving the openness of public bodies to wider scrutiny.

The Ministry of Justice will consult 200 bodies carrying out public functions and receiving public funds which are not covered by the Act. I should like to focus your Lordships’ attention on several of these bodies.

There will be consultation with two examination boards, AQA and Edexcel. Edexcel is a private company which is the UK’s largest award-giving body; AQA is an education charity providing GCSE and A-levels to English and Welsh schools. I remind the Minister of the concern felt across the educational establishment about the aggressive manner in which these examination bodies compete for GSCE and A-level business. An investigation last year by the Daily Telegraph exposed how privileged information was being given by these bodies to teachers at feedback seminars. Ofqual is now looking into the matter. There is concern also about the uneven quality of marking by these boards. A survey last year by the National Association for the Teaching of English expressed great anxiety about the qualityof the marking of English at A-level. These processes and these boards need to be made open and public.

The Local Government Association and the NHS Confederation are also being consulted on the extension of the Act. The LGA has campaigned against the vexatious and expensive effect of FOI requests on its local authority members, citing a fourfold increase during the past six years. I would argue that this figure is evidence of the success of the Act. Certainly, it has revealed stories such as the 6,000 council houses lying empty in London last year and the £31 million in fines paid by utility companies for overrunning roadworks. In fact, the Constitution Unit found that 95 per cent of local authority FOI officers felt that the Act had brought increased openness to local government. If the LGA's members have so benefited, I suggest that their representative body would garner similar advantages.

The NHS Confederation is also up for consideration. In autumn last year, its trustees agreed a new transparency and accountability policy which would ensure that it was open and transparent to the public. However, the voluntary nature of this agreement means that there is no right of appeal to the Information Commissioner. An extension of the Act would rectify this omission.

I urge the Minister to bring the Justice Ministry’s consultation on these bodies to a speedy conclusion. The last exercise to extend the FOI Act was launched on 25 October 2007, but was not implemented until four years later. I hope that this new consultation will be carried out in a fraction of the time.

20:06

[Lord Armstrong of Ilminster]

My Lords, I am glad to be contributing to this short debate initiated by my noble friend and former adversary Lord Hennessy of Nympsfield. I say “former adversary”, because when he was the Whitehall correspondent of the Times and I was the Principal Private Secretary at 10 Downing Street, I was required by my political masters to see that Whitehall did all it could to frustrate his knavish tricks, designed to extract information about the working of government which government would have preferred not to disclose. He collected nuggets of information with indefatigable diligence, like Squirrel Nutkin collected nuts, but, unlike Squirrel Nutkin, he always knew where he had stored his nuggets and where to find them when he needed them.

Now that the noble Lord is no longer a mischievous journalist but a learned professor, and I am a mandarin long since put out to grass, we are firm friends. I can acknowledge that, though he did not win them all, he did win more than we could have wished, and that much of what he succeeded in extracting was relatively harmless if occasionally a little embarrassing.

I am much in favour, and always have been, of the greatest degree of transparency in government as is reasonably possible. That is owed by government, central and local, to Parliament and to the councils to which they are accountable, and to the people they represent. But freedom of information is not, at least in its current legislative form, an unmitigated boon and blessing to men. Tony Blair expressed the point in his memoirs in his own characteristically vivid style:

“You idiot”—

he says, addressing himself—

“You naive, foolish, irresponsible nincompoop”—

his words, not mine—

“I quake at the imbecility of it”.

“It” is the Freedom of Information Act. He goes on:

“Where was Sir Humphrey when I needed him? We had legislated in the first throes of power. How could you—

“you” is now Sir Humphrey, I think—

“knowing what you know, have allowed us to do such a thing so utterly undermining of sensible government?”

It is a well attested fact that, if I was the model for anyone, it was for Sir Arnold Robinson, not for Sir Humphrey Appleby. None the less, I am sorry that I was not around to be consulted in Mr Blair’s hour of need. I was already, unfortunately, well into my retirement.

I am afraid that there is no doubt that the risk of unwarrantable disclosure created by the Freedom of Information Act is liable to be damaging to the quality of governance. My successor, the noble Lord, Lord O'Donnell, has gone on record with his anxieties about the threat that the Freedom of Information Act presents to the usefulness of the minutes of the meetings of the Cabinet. Those minutes are not a verbatim record; they are none the less a comprehensive and accurate account of what the Cabinet decides and why. They are a valuable tool of administration. Their value depends upon their comprehensiveness and their accuracy. Their value would be diminished—they could even be misleading—if they had to be edited or bowdlerised to minimise risks of unacceptable disclosure under the Freedom of Information Act.

More generally, Ministers and officials, and indeed other people, now hesitate to put in writing things which are important, and which ought to be conveyed to their readers, but which they would not want to see having to be disclosed in response to Freedom of Information Act requests. The result is not only that discussion among colleagues is less candid than it should be but also that policy decisions may be taken on inadequate information.

The perverse effect of freedom of information legislation is thus to make important information less freely available where it is most needed and to impair the quality of governance. This is a problem that may well need to be addressed by amending legislation if its effects are not to become cumulatively more damaging.

I just add my support for the programme of official histories and my hope that the Minister will be able to assure the House that, despite the need for austerity in public spending, the programme will be maintained.

20:10

[Lord Black of Brentwood]

My Lords, I declare an interest in this subject as the executive director of the Telegraph Media Group. It is worth remembering the opening words of the 1997 White Paper on freedom of information, which began thus:

“Unnecessary secrecy in government leads to arrogance in governance and defective decision-making. The perception of excessive secrecy has become a corrosive influence in the decline of public confidence in government”.

Fifteen years on, such sentiments remain as forceful as ever. That FOI has perhaps not lived up to all the expectation is perhaps because, in my view, the 2000 Act did not go far enough. The Government’s transparency agenda, including the increase in scope of that Act, is a welcome step to remedying some of its initial deficiencies. I wish it went further now, to include all contractors performing public functions on behalf of public authorities—an extension all the more vital because of the contracting-out provisions of the Localism Act and the health service reforms currently before this House. Will the Minister look at that?

There are concerns—eloquently expressed by the noble Lord, Lord Armstrong—that FOI has had a negative impact on government decision-making by increasing the practice of what is termed sofa government, with damaging consequences for government record-keeping. As a historian, I am only too well aware that a comprehensive and accessible archive of government decision-making is a precious legacy to future generations. However, I believe that those concerns are misplaced. The last inquiry that looked into them—the review of the 30-year rule led by Mr Paul Dacre, working with the distinguished historian Sir David Cannadine—concluded that:

“We accept that ‘sofa government’ may have occurred at certain times in twentieth-century British history– indeed, long before FOI and the introduction of the 30 year rule; but we believe that it is more likely to be a reflection of leadership style and political circumstances than to be motivated by any concern regarding the timing of the future disclosure of official documents”.

For those interested in maintaining a comprehensive record of the deeds and doings of government, which is available to the public under FOI or the 30-year rule, there are far greater concerns than FOI, of which the most vital is the vulnerability of digital records. Most business is now recorded digitally. These records are subject to rapid obsolescence, with often a natural life of only five years. Already the oldest digital government records from the early 1990s are lost for ever, because appropriate software is no longer available or storage media is corrupted.

There is also the problem of digital information overload, with, in the words of the 30-year review,

“vast amounts of ephemeral information paralysing the system”.

Although digital technology may assist in making government more open, it has the paradoxical effect of making a permanent archival record far more difficult to establish, because documents disappear into digital landfill. Those two problems present a huge issue for the long-term maintenance of government records. That is a deeply worrying problem to tackle. It would help to hear from the Minister about what the Government are doing to ensure that electronic record capture is an integral part of government IT infrastructure—the key point for all of us who are concerned about the maintenance of government records.

20:14

[Lord Wilson of Tillyorn]

My Lords, in this very short debate, for which we are all grateful to my noble friend Lord Hennessy, I want to touch briefly on two issues. One is the effect on the Foreign and Commonwealth Office in particular of the Freedom of Information Act and the other is the consequences, again essentially for the Foreign and Commonwealth Office, of reducing the period of restriction on government records down to 20 years. I fear that on both I have a more suspicious and restrictive view than my noble friend Lord Hennessy.

Maximum openness of government is something that everybody wants, historians particularly, although my noble friend Lord Hennessy has managed to produce fantastic accounts of British policy and the way the government machinery operates without any changes in the way in which the records are dealt with. However, there are dangers, particularly for departments of state such as the Foreign Office. We always say we want officials to speak truth to power. However, will those officials be speaking as much truth if they think they are not talking just to power but to the whole population as well? Will they not, as my noble friend Lord Armstrong suggested, avoid written communications and get into huddles in corridors? Is that really for the benefit of the nation as a whole? Perhaps the Minister could comment on how this sort of danger might be avoided.

Then there is the problem of reducing the restriction of access to public records from 30 years to 20 years. Legislation is already in place to do that. Some years ago, I did a PhD on British policy in the 1920s towards the rise of nationalism in China. Most records were open, but there was one fascinating file that was closed for 70 years. It was the response by a senior Foreign Office official to a paper from the number two in the British mission in Peking, Owen O’Malley, around 30 pages long, about what British policy to China should be. I puzzled about what this reply from the Foreign Office said—clearly it revealed key things about British policy. I went to see Sir Owen O’Malley later. He said, “You must see the reply I got to my paper. It was so abusive that the Foreign Office has closed it for 70 years”.

That did not need closing, but I suggest that other things do. Imagine a conversation a young person in a British embassy has with a friend in a country. The friend is frank about the failings of his country and the people who are responsible. Later, he becomes a senior official. Does he want those sorts of things to be in the hands of his enemies, only 20 years later, when he has risen to a high position? I think there is a serious issue there. Perhaps again the Minister could suggest how “McNally 1”—which I think it is going to be—could somehow deal with this issue; lest, as I fear we might, with the best possible intentions, we finish by shooting ourselves in the foot.

20:17

[Lord Bew]

My Lords, I thank my noble friend Lord Hennessy for initiating this debate. My remarks will follow broadly in the spirit of his remarks and, like him, I have to declare an interest as a practising university historian, at Queen’s University Belfast, and as secretary of the All-Party Group on Archives and History.

There is an important Irish dimension to this question, relating to the decades of commemorations that are about to come upon us in Ireland: of the signing of the Ulster covenant, the Easter Rising and the war of independence. There are still important documents in Kew that have not been released in this context. I am interested because historians need to be armed. Quite rightly, there is a certain nervousness in both Governments about the emotional consequences of some of these commemorations. For some, they are a rather bad model—the argument is that the commemoration in 1966 of the Easter Rising played a role in triggering the subsequent Troubles. Historians need help, and we have formed an ad-hoc group of historians on a north-south basis, under the chairmanship of Professor Eunan O’Halpin of Trinity College, Dublin. We all feel that the more help that we get from Governments to release documents, the more valuable we can actually be.

I am not talking about spasmodic release. For example, when Tony Blair was Prime Minister, Bertie Ahern, the Irish Taoiseach, wrote to him and said, “Could we please have Roger Casement’s SIS files released?” and they were released. I am talking about something somewhat more systematic. There is one thing in particular that Her Majesty’s Government could do: they could get in touch with Commonwealth states—Canada, Australia, New Zealand—and say to them that they could safely declassify Irish material from the period 1913-23. We strongly suspect that it remains locked away because it contains security-related exchanges with London that no longer have any particularly poisonous dimension to them. I very much hope that the Minister, who has been a friend to historians, will help us in this matter.

However, I would like to add something slightly more cautious in the spirit of my noble friend Lord Wilson’s remarks about the move to a 20-year rule. I am certain that before long our political class will agree to this, and there is a reason for that. Even the great figures of our current political class, a Thatcher or a Blair, are at the top for only 10 or 11 years, so a 20-year rule is something that they can feel quite comfortable with. For good or for ill, there are no longer any Mr Gladstones, who sat in Peel’s Cabinet in the 1840s and was putting through the third Home Rule Bill in 1893. If we had politicians who spent 50 years at the top, I am certain that we would not be talking about a 20-year rule.

It is not politicians or their reputations that worry me; it is the young officials. I have talked to members of the committee that made this recommendation, I believe that it is the spirit of the times and I support it broadly. However, even under the 30-year rule young civil servants have been embarrassed by material that has been released. We need to be a little cautious about this matter.

20:20

[Lord Turnbull]

My Lords, the FOI Act has, as intended, brought important benefits to citizens by giving them information on decisions affecting their lives. However, one area of the Act is not working as intended—the so-called safe space. In all the discussions leading to the Act, the code of practice, the White Paper, the Bill itself and reports by committees, the need for a safe space was repeatedly acknowledged. The noble and learned Lord, Lord Falconer, speaking on the Bill in 2000, said:

“I should … make clear that many people on both sides of the debate consider that it is appropriate that policy making should not take place in a goldfish bowl: that there should be a process which allows Ministers, public authorities and civil servants to exchange views in a way that they feel will be private to give them that space to think and make decisions”.—[Official Report, 24/10/00; col. 282.]

When taken with the principle of Pepper v Hart that the courts should be able to look at the parliamentary record as well as at the specific wording of the Act, it is crystal clear what Parliament intended. Why, then, has the safe space been under repeated attack? It is because Section 35 does not confer an absolute exemption but requires a balancing public interest test. In applying that test, however, the commissioners and the tribunal have tended to focus narrowly on the information sought in the request, not the wider signal that the disclosure produces. Any release contains two forms of information: that inherent in the document, and that which provides signals how about the commissioner/tribunal are expected to respond in future cases. There will be cases where the information itself may cause little harm but where releases of similar documents could have a big effect on the behaviour of Ministers and officials. The commissioners and the tribunal appear to place little weight on this wider impact despite the advice of many distinguished people.

There is a further dimension. The Civil Service is required to give its best advice to Governments of different complexions. This will inevitably become more difficult if the advice given by named officials is revealed to successor Governments, a danger referred to in the papers by none other than the noble Lords, Lord Heseltine, Lord Mandelson and Lord Butler. There are two ways out of this: either the commissioner and the tribunal pay more heed to the original intention of Parliament or the use of the ministerial veto, always intended as a backstop, will, sadly, become more frequent.

20:22

[Lord Cormack]

My Lords, I can think of nowhere else where such a brief debate could contain so much. We are all enormously grateful to the noble Lord, Lord Hennessy, for the manner in which he introduced the debate, just as many of us are grateful to him for all that he has done for contemporary history.

I speak as one who for some 24 years was on the Royal Commission on Historical Manuscripts and sat on the council of archives, and who occasionally had to chair a panel to adjudicate on whether a certain document should indeed be released. I therefore have a great deal of sympathy with the general case that the noble Lord so brilliantly and wittily made when he opened the debate.

There are other things that we have to consider, though, and some of them have been touched upon in this debate. The importance of archives is such that we must not endanger them or their preservation. My noble friend Lord Black talked about the digital and electronic archive, which is something to which we have not yet devoted sufficient attention.

My noble friend Lady Shephard of Northwold talked very eloquently about the need for conventions. It is truly important that we have those. What we do not want is an incentive to destroy or an incentive for people to go into the back garden of an embassy, which I was once told about when I visited an iron curtain country. That was the only place where people dared talk. We need to have the conversations between Ministers and civil servants recorded and released at the appropriate time.

However, the appropriate time is not always necessarily after 15 or 20 years. Sometimes it has to be longer. Although the noble Lord, Lord Bew, said that we no longer live in the age of Gladstone, in which a statesman could be active for 50 years, maybe he is being a bit premature. We live in an age of longevity. At the moment we have three party leaders who could well still be active in politics in 20 years’ time. I should not like to think that they were being driven to make difficult decisions on the sofa or somewhere that are not adequately recorded so that the Hennessys of the future and those who look back, not as contemporary historians but as historians viewing a whole sweep of history, are deprived of essential evidence.

In this, as in all things, we have to get the balance right. If we take the judicious approach of the noble Lord, Lord Hennessy, tempered by the cautious words of the noble Lords, Lord Wilson and Lord Armstrong, we will have the ideal solution. I know that my noble friend Lord McNally has a reputation for being something of a Solomon. We will have to hear what he says to us tonight. However, I hope he will be able to assure us that he has a passionate care for archives, but complete archives, and that he will do nothing to damage in any way the material that future historians will need.

20:26

[Lord Wright of Richmond]

My Lords, I, too, congratulate my noble friend on initiating this debate. However, I should like to draw attention, as others have, to rather a different problem—namely, the extent to which the Freedom of Information Act in its present form and application, and the Government’s existing transparency agenda, may affect the readiness of public servants at home and diplomats abroad to record their frank advice to Ministers, even though there are exemptions in the Freedom of Information Act designed to cover confidential advice to Ministers and damage to international relations.

Does the Minister agree that there is a real potential constraint on officials if they believe that their confidential advice is liable to be open to early public access in spite of these exemptions, as illustrated by the recent decision to stop valedictory dispatches by departing heads of mission? I personally deplore this, having benefited three times from the experience and assessments of my ambassadorial predecessors. I regard the problem as being not so much the availability of government records, but whether important advice to Ministers is failing to be recorded for eventual inclusion in the National Archives. There is also a potential problem for future historians, unrelated to the Freedom of Information Act, in the failure to register many of the constant official exchanges by e-mail.

It is, I hope, an exaggeration—although I have heard it said—that the application of the Freedom of Information Act has led to a climate of fear in Whitehall, and to a marked reluctance by officials to put their frank and confidential advice in writing, whether by minute, letter, dispatch or valedictories. The Minister knows well, from our service together in 10 Downing Street many years ago, the importance that we both attach to a relationship of mutual trust between Ministers and their advisers. Does he accept that there is a real danger of that mutual trust being eroded by the excessive application of the Freedom of Information Act?

20:28

[Lord Thomas of Swynnerton]

My Lords, like other noble Lords I am grateful to the noble Lord, Lord Hennessy, for introducing this debate. I am also grateful to him for his work over many years in elucidating problems of great interest in English politics, particularly his discussion of how the nuclear weapons of this country were developed. He also developed well the idea of how we would manage to survive a nuclear attack in his book The Secret State, to which he alluded.

I have on one or two occasions come up against restrictions on the freedom of information. I remember writing a book and needing the text of the Non-Intervention Committee in Spain in the 1930s. I was told it was an official secret. I argued but I did not get very far until I found out that the Dutch version of these minutes and documents could be available to me if I went to Amsterdam. I discussed this with the Public Record Office, which eventually relaxed its control.

I had another experience once when, already a Member of this House, I tried to get the late Lord Dainton, then chairman of the British Library, to tell me how many people had visited the British Library— the old, noble British Library, which I still regret—the previous year. He told me—this is difficult to believe—that it was an official secret and I could not be informed. Recently, I have come across a different problem—if it is a problem. Letters that I wrote to the noble Baroness, Lady Thatcher, in the 1980s are now available for scrutiny in Churchill College, Cambridge. I do not mind that: I know that on one occasion I wrote a very important paper about the Ming dynasty in China because she was just about to go to China.

In this debate, we are trying to discuss where the line lies between the need for confidentiality: the need for Ministers, for civil servants and for private persons to have private conversations which are not leaked immediately; and the need which public persons, private persons, historians, journalists and others have for information. The difficulty of deciding this line has been touched upon very well by many noble Lords. I was particularly interested by the speeches of the noble Lords, Lord Wilson and Lord Armstrong, who pointed out the difficulty of immediate indiscretion, so to speak.

I feel have to sit down in a minute—I can feel a glare upon me. In conclusion, it is essential for public servants and politicians to be able to write down statements of policy and not just commit them to the telephone or to conversation. Dr Kissinger makes that point very strongly in an introduction to one of his volumes of memoirs and I very much agree with him. It is the written document which we need.

[Baroness Royall of Blaisdon]

My Lords, I, too, thank the noble Lord, Lord Hennessy of Nympsfield, both for securing this debate and for his own role, not just as an historian, but as a constitutional activist who has done a great deal more than most in pushing at the boundaries of official information.

First, I would like to endorse the proposal from the noble Lord, Lord Hennessy, for a “Waldegrave 2”. Just as the initiative of the noble Lord, Lord Waldegrave, helped historians understand our recent past, so, too, would a reconsideration of the issues now. Secondly, I would also endorse his call for the Pilling and Hamilton reviews on the official history programme to be implemented.

However, my main concern is the Government’s proposal to review the operation of the FOI Act 2000. Although the FOI Act was passed by a Labour Government, this does not of course mean that everything about it is perfect. The wriggling of this Government in relation to the Department of Health’s risk register is clear evidence of that. So we on these Benches—well, my colleague and I—welcome the establishment of a review of the 2000 Act, in the form of a post-legislative scrutiny of the legislation.

There is a continuing need for consideration about whether the Act has got right the balances it seeks to strike: for instance, between disclosure and operation in government; between transparency and the need to reduce regulatory burdens; between, in effect, good government and open government. In that respect, I welcome the intervention by the noble Lord, Lord O’Donnell of Clapham—whom I am delighted to see in his place—in his final remarks as Cabinet Secretary. My own experience in government suggests that there is indeed a need for proper policy-making space in government and also suggests that FOI, as a piece of legislation, has had some negative as well as positive effects. Discussion in government can be less open as a result of FOI. Fewer things are now written down in government as a result of FOI. These are not good outcomes either for good governance or for future historians.

Set against that are the clear and real successes of FOI, as detailed in the Government’s helpful memorandum on the Act, published last month, which will form an important part of the review of that Act. At present, the review is to be carried out by the House of Commons Justice Select Committee, chaired by Sir Alan Beith, the Member for Berwick-upon-Tweed. The Select Committee is a very fine body and its chairman a very fine chairman, but there is a case—a strong case—for the form of that inquiry to be expanded.

Today’s debate gives me the opportunity to propose that even at this late stage the vehicle for the review of the operation of the FOl Act 2000, first suggested by the Government in January last year, should be extended to a review carried out by a committee of both Houses. That would also be in line with the spirit of the Goodlad report, and the Leader of this House has always said that he is in favour of this House undertaking post-legislative scrutiny. The expertise of your Lordships’ House across a whole range of activities is clear.

A Joint Committee of both Houses might well be the best means of carrying out a review. Or perhaps, given that the work of the Common’s Justice Committee on the matter is already under way, there might be scope for that Committee to co-opt or include in some way as part of its process Members of your Lordships’ House, and this House should explore and pursue this matter further with the House of Commons.

20:36

[The Minister of State, Ministry of Justice (Lord McNally)]

My Lords, in the spirit in which the Leader of the Opposition intervened, perhaps I may say that it is an interesting idea to broaden the post-legislative scrutiny. The rules are that it is within the scope of the relevant committee to do that, but I will draw her remarks to the attention of Sir Alan. It would be useful if that committee made use of the experience and expertise available. One of my memories of the original Act was the ludicrous situation at that time whereby there was pre-legislative scrutiny by two committees—one from this House and one from the Commons—sitting at either end of the Corridor, with witnesses moving from one to the other.

First, I apologise to all noble Lords who have taken part. This should have been a three-hour debate that gave the eminent people who have contributed a proper opportunity. I will not do my usual practice of trying to refer to the individual points raised. Instead, I should like to provide a considered omnibus reply that I will send to each Member who has participated and put it in the Library of the House, because the issues raised are too important. If I tried to reply to each in turn, I would look up and all my time would have gone. With the permission of the House, I will do it that way.

I must say in passing that I have never seen so many mandarins in one place since my school production of “Chu Chin Chow”, and it was great to see them all out. I am of course immensely grateful to my old friend and colleague, the noble Lord, Lord Hennessy. He is quite right—it is about time that I got a PhD from Queen Mary college because of the number of times I see a letter beginning with, “Professor Hennessy has suggested you might be able to help with my research”. I am grateful in one way because I am in several footnotes to history around the various work that is done. My time goes back even further than his clash with the noble Lord, Lord Armstrong, because I was working for Harold Wilson when the Times, with great fanfare, announced this new creature that was going to pace the corridors of power: a Whitehall correspondent, one P Hennessy—to which Harold announced that any civil servant found talking to this new creature would be fired on the spot. Such was the spirit of the age.

The Leader of the Opposition pointed out that the Freedom of Information Act was the work of the previous Government. Let me put on record my admiration for the noble Lord, Lord Clark of Windermere, who produced the first White Paper on freedom of information and on which the Act was built.

I am grateful to the noble Lord, Lord Thomas of Gresford, for the quotation from “Yes, Prime Minister”. I do not think that any of us who have watched “Yes, Prime Minister” and “Yes Minister” and have actually worked in Whitehall and Westminster have ever considered it as comedy; we watched it more as documentary. In passing, I should say that I still have not worked out how in those days Sir John Hunt could manage to get from his office way down in 70 Whitehall to the foyer of No. 10 to greet the Prime Minister without any of the electronic devices that we have today to know that the Prime Minister was about to return, but now as I watch it on the cable channels I find the show still very pertinent.

As many Members are aware, I am a long-standing enthusiast for transparency and freedom of information. I therefore continue to be proud to have an opportunity to help shape the next phase of freedom of information in this country. I note what the noble Lord, Lord Armstrong, said with his vivid quotation from Tony Blair’s memoirs and indeed the valedictory from the noble Lord, Lord Macdonald, who I am very pleased to see in his place. They are matters and opinions certainly to be taken in evidence, although it leaves me, as a proponent of the Act, also to argue that when Prime Ministers and mandarins object, this Act might actually be doing something that it was intended to do.

The noble Lord, Lord Hennessy, has placed considerable emphasis on the Government’s pledge to replace the current 30-year rule with a 20-year rule. I hope the noble Lord will appreciate the enormity of the task. Central government departments alone hold more than 3 million files that will need to be reviewed during this process.

However, just before I depart from the points that were made by a number of noble Lords about the battle—and this has been the battle throughout—between the safe space and the culture of secrecy, all I would say is: let the Parliament system work. The Act has the process of post-legislative scrutiny built into it. Let this process tease out some of the weaknesses that have been named today, and let the Government look at them, and let those who believe that those weaknesses exist give evidence of them. That can be nothing but healthy.

The detailed work has now been done to develop an implementation plan that will balance our intention to reduce the 30-year rule with the burdens that this will impose. I reassure noble Lords, and in particular the noble Lord, Lord Hennessy—who asked for my guarantees on this—that the Government remain committed to this course of action and that further details will be announced in due course. Let me also give him a guarantee that that is not Whitehallese for some time, never. Not on my watch it won’t; we will press ahead with this.

I know that the noble Lord, Lord Hennessy, is also keen for there to be a new Waldegrave initiative and an expansion of the current programme of official histories. I fully recognise the benefits to historians that such initiatives bring and I am sympathetic to his view. However, the subsequent introduction of FOI since that time means that the public—including historians—are free to request any records. Moreover, the reduction in the 30-year rule will result in more and more government records being made available earlier year by year.

I hope noble Lords will recognise that such a significant undertaking as the reduction in the 30-year rule would make additional simultaneous initiatives very difficult at this time of financial restraint. I also hope that noble Lords will recognise the unprecedented level of transparency that was not available at the time of the Waldegrave initiative. However, I will continue to keep the suggestion under review and I pledge here and now that it will be called Waldegrave 2. I have no ambitions for it to be called anything else.

As for the official history programme, a good deal of work is already in progress, and I hope that we can review future work in happier economic circumstances. I emphasise again my enthusiasm for the programme of official histories. It would be a tragedy if we were to allow them to wither on the vine after 2013.

Hand in hand with FOI is the transparency agenda being pushed through government by my right honourable friend Francis Maude. The transparency agenda is about much more than historical information; it is about much more than government records in the traditional meaning of the phrase. It is about the information and data that we deal with day to day to inform our decisions and provide our public services. Making that information available is what makes the transparency agenda truly revolutionary. More information than ever is being published proactively by this Government. In excess of 7,500 data sets have been made available to increase accountability, empower the public and foster innovation and economic growth.

As noble Lords will be aware, the Protection of Freedoms Bill includes provisions that introduce a new right to data to ensure that public authorities, including government departments, make data sets available in a reusable format where they can and make them available for reuse when releasing them in response to requests or through publication schemes.

The Government will also be developing a transparency and open data strategy and plan to publish their response to consultation on the form that it might take early this year. There is a strong public interest in increased transparency by all bodies in receipt of public funds, including those in the private sector. The Cabinet Office is considering the type of bodies to which an open data policy will apply.

Many noble Lords will also be aware of the significant steps that we are taking to extend the Freedom of Information Act to more bodies through the Protection of Freedoms Bill and secondary legislation under Section 5 of the Act.

As I said in my opening remarks, I am a long-standing supporter of freedom of information and transparency. I am proud that, on my watch, the Act has been extended and the independence of the Information Commissioner strengthened. I am well aware that the FOI still has its critics among both Ministers and officials. It was never meant to make those groups comfortable, but as the Minister responsible I have played this matter by the book. My department has consulted widely on how the act works in practice. We have produced a report that, I believe—I am grateful for the noble Baroness’s comment—is a model of objectivity in the post-legislative scrutiny process.

That is how matters should work. It is now in the hands of the Justice Select Committee, which has in turn asked for written comment by 3 February and urged interested parties to give the committee their views. As I said, I will pass on the noble Baroness’s comments about widening the basis of the group considering that.

I am confident that FOI is robust enough to survive rigorous post-legislative scrutiny. It is that process that will expose any flaws, if there are any. In the mean time, I thank the noble Lord, Lord Hennessy, for initiating the debate and all noble Lords who have spoken. As I said at the beginning, the tragedy is that a speakers list of this quality and a topic such as this should be crammed in to the dinner hour, but I will write to noble Lords on the points raised. In the mean time, I am most grateful for all contributions.

Welfare Reform Bill

Tuesday 17th January 2012 Lords Chamber

Report (4th Day) (Continued)

20:49

Amendment 51

Moved by

[Baroness Thomas of Winchester]

51: Clause 80, page 58, line 30, leave out “6” and insert “3”

[Baroness Thomas of Winchester]

My Lords, never have I minded less about changing my original speech so extensively, because the Government have conceded on the qualifying period for PIP being brought back to three months from six months. I am grateful to the Minister for listening to the concerns expressed by many disabled people and the organisations that support them about the hardship that such a long qualifying period could cause. The reasons for changing the time back to three months are compelling, particularly in relation to those who have sudden onset conditions or a serious accident, and there is now no need to rehearse the arguments yet again. I beg to move.

[The Parliamentary Under-Secretary of State, Department for Work and Pensions (Lord Freud)]

My Lords—

[Lord McKenzie of Luton]

My Lords, I, too, shall be brief because, as the noble Baroness, Lady Thomas, has said, the Minister has flagged his acceptance of the amendments in this group.

The debate in Committee led by the noble Baroness, Lady Thomas, centred in particular on the importance of keeping a qualifying period for PIP at three months, but obviously the concept of increasing the prospective period from six to nine months to align PIP with the definition of “long-term disability” in the Equality Act has been helpful to the process. However, the arguments for a three-month qualifying period are strong, and it is commendable that the Government have accepted the case. We have not heard them today but those arguments concerned conditions of a long-term nature having a sudden onset, conditions which are not diagnosable immediately after the onset of symptoms, and conditions which have an immediate devastating impact.

I have just one question for the Minister on the required period condition. This has been touched on before but is not the subject of an amendment today. On the basis of what is before us as an amendment, to be eligible for PIP it has to be determined whether, as respects every time in the previous three months,

“it is likely that if the relevant ability had been assessed at that time that ability would have been determined to be limited or … severely limited by the person’s physical or mental condition”.

The issue is how this requirement is to be interpreted for those with fluctuating conditions. At a recent meeting to consider how things should work for those on the autistic spectrum, we were assured that, although the wording was a bit clumsy, it covered the situation. It would be helpful if the Minister could confirm that or, as we are at one on this issue, commit to tidying it up at Third Reading.

However, all in all, the Government are to be commended for doing the right thing on this, as indeed is the noble Baroness, Lady Thomas, for having led the charge and continued to press the matter.

[Lord Freud]

My Lords, I tried to rise to speak earlier because my name is added to this group of amendments tabled by my noble friend Lady Thomas, and I am very pleased that I have been able to support them. We have had a lot of responses from people whom we respect and whose advice we find very useful, including Macmillan and CLIC Sargent, and I thank them for the time that they have given.

When we looked at this issue in Committee, I think it was generally agreed that an overall 12-month required period condition was right, but there was a lot of concern that the six-month period in question here was too long. Bluntly, we were trying to balance two factors: payments being made sooner against the potential for more assessments to ensure that ongoing payments were correct. That is why we ended up with periods of six months plus six months. However, we have been listening to the arguments and have been persuaded that the balance should shift. There was a clear consensus that a three-month qualifying period and a nine-month prospective test offered the fairest solution, and that is why we are able to support the amendments.

On the point raise by the noble Lord, Lord McKenzie, I think it is easier if I write to him, as this is a fairly technical matter. On that basis I am very happy to support the amendment tabled by my noble friend.

Amendment 51 agreed.

Amendment 51A not moved.

Amendment 52

Moved by

[Baroness Thomas of Winchester]

52: Clause 80, page 58, line 34, leave out “6” and insert “9”

Amendment 52 agreed.

Amendment 52A not moved.

Amendments 53 and 54

Moved by

[Baroness Thomas of Winchester]

53: Clause 80, page 58, line 46, leave out “6 months” means the 6” and insert “3 months” means the 3”

54: Clause 80, page 59, line 1, leave out “6 months” means the 6” and insert “9 months” means the 9”

Amendments 53 and 54 agreed.

Clause 81 : Terminal illness

Amendments 54A and 54B not moved.

Clause 82 : Persons of pensionable age

Amendment 54C

Moved by

[Lord Low of Dalston]

54C: Clause 82, page 59, line 34, at end insert “other than by virtue of an award made before the person reaches the relevant age”

[Lord Low of Dalston]

My Lords, this amendment would ensure that those who are awarded either the daily living component and/or the mobility component before pensionable age can continue to receive it after they reach pensionable age. Currently the Bill states that persons of pensionable age are entitled to neither award.

The matter was fully debated in Committee, when the argument was fully rehearsed, so I do not intend to speak to it at great length this evening. The noble Baroness, Lady Grey-Thompson, said in moving the same amendment in Committee—on 16 November at column 303 of Hansard—how the Disability Alliance and other charities were being approached regularly by disabled people worried about what the current proposals would mean when they reach pension age. She maintained that the amendment would clarify the position and put many minds at rest. She also drew the committee’s attention to the fact that the Dilnot commission highlighted the pivotal role that DLA plays in preventing high-level needs from escalating. Receiving DLA helps disabled people manage their health and prevents avoidable NHS costs or people entering residential care prematurely, or at all, with potential savings in the long run.

The noble Baroness understood that the Government intended to provide in regulations for those who received DLA before pension age to retain it after they reached pension age, but she said her concern was not allayed by the Minister for Disabled People stating in the Commons that the Government wanted the matter to be addressed in regulations to allow for flexibility. Such flexibility, she said, could easily include altering the entitlement in the future and denying support to disabled people reaching pensionable age. It would offer a significant boost in confidence for many disabled people, she said, to receive the reassurance in the Bill that their support will not be withdrawn when they reach pension age.

The Minister made it clear that the Government intended to make regulations for PIP that will allow people who have reached the upper age limit to continue to receive PIP. He said:

“Our priority is to support those individuals with established, long-term health conditions or impairments that would put them at a financial disadvantage over a long period … The intention behind this amendment is to ensure ongoing support throughout later life for individuals whose abilities are limited earlier in life, recognising that they may have had less opportunity to earn and save for later life. I can assure noble Lords that this is also our intention and that it can be achieved without amendment to the Bill, but instead through regulations. As it currently stands, the amendment would potentially widen the scope of personal independence payment and undermine our intention of creating a more affordable and sustainable benefit”.—[Official Report, 16/11/2011; cols. GC 304-05.]

He also made clear the Government’s intention of replicating, under PIP, the one-year linking rule which operates under the DLA regime, which allows individuals over 65 to renew an award within one year of their previous award, without losing DLA entitlement.

The matter seems quite straightforward. The assurance that those who have DLA when they reach pension age can keep it is provided in current legislation. The Government propose to remove this insurance in the Bill before us. They say that they will maintain the guarantee in regulations, but we all know that regulations can be changed much more easily than primary legislation. What possible motive can the Government have for removing from the Bill the guarantee to pensioners? One cannot blame people for asking the question or for being suspicious of the answer.

If the Government intend to give the assurance in regulations, what skin would it be off the Minister's nose to give it in the Bill? In circumstances where he needs all the confidence-building measures he can devise to take disabled people with him through the legislation, this would be an obvious and cost-free concession. The Minister referred to an earlier amendment as being the priciest yet. Surely this is the cheapest. If the wording needs to be fine-tuned in order to avoid widening the scope of PIP, I would be entirely amenable to working with him to find the appropriate wording before Third Reading. I beg to move.

21:00

[Baroness Wilkins]

My Lords, I, too, put my name to the amendment. I declare an interest as someone who was awarded mobility allowance for life and was then moved to DLA at its inception. I have continued to receive this past pension age. I strongly support the amendment, which would put in the Bill the assurance that awards of PIP will be retained after retirement age, as is the case with DLA. When the amendment was discussed in Grand Committee the Minister tried to sound reassuring, but unfortunately the Government are not trusted.

We know that all Governments prefer to use regulations, which give them more scope and power. However, to quote Sir Bert Massie, the chair of the much lamented Disability Rights Commission, the difference between now and 1992, when the DLA was introduced, is that this Government are playing with false cards. If the Government are sincere in their assurance that PIP will be retained after retirement age, why will they not behave transparently and place the commitment in the Bill? Clause 82 only grants a power. The amendment of the noble Lord, Lord Low, imposes a duty. There is a massive difference.

Sir Bert fears, as I do, that the Government are planning to use the payment of post-retirement PIP awards as part of the Dilnot package for social care. On the argument about cutting the DLA mobility component for people in residential care, they will discover what they regard as double provision, and PIP will be lost to pensioners. In his response in Grand Committee, the Minister almost said as much when he stated:

“By setting out these provisions in regulations we can ensure that the legislation can be adapted in response to any future changes in the social care system which might affect pensioners”.—[Official Report, 16/11/11; col. GC 305.]

Given the demands of responding to the Dilnot commission report, would your Lordships trust the Government not to use the flexibility of regulations to devote the entire PIP budget for over-retirement age to social care?

DLA is an essential contribution to so much more than our social needs. Throughout the passage of the Bill I have tried to convey the enormous complexity of disability and the very wide range of extra costs with which we are faced. DLA gives the lie to the false dichotomy that the Minister always draws between benefit recipients and taxpayers. My DLA has enabled me to be mobile and be employed. It has enabled me to be a taxpayer all my life. As I have aged, my mobility needs have become considerably more expensive. I could not have contemplated buying that “nice bit of kit”, as the policemen outside the Peers’ entrance term the considerably adapted car that I can drive from my electric chair, without the assurance that my DLA is for life. Future PIP recipients should have the same reassurance and I ask noble Lords to support the amendment.

[Lord McKenzie of Luton]

My Lords, I will speak briefly in support of the amendment. The case has been very clearly made. The amendment is seeking the assurance of something written in primary legislation rather than the comfort that was given that this could be dealt with in regulations.

Perhaps I may take the opportunity to clarify a part of the debate we had in Committee. The Minister said:

“Turning to the current rules, broadly speaking, current DLA provisions have a one-year linking rule. This allows individuals over 65 to renew an award within one year of their previous award without losing DLA entitlement. Similarly, we intend to allow a linking period for PIP. This will support those individuals who reach the upper age limit and have a break in their claim through temporary improvement, provided the individual makes a claim within a defined period and continues to fulfil the eligibility criteria for PIP”.

I understand all of that. The next sentence says:

“As with DLA, there will be restrictions on new and existing claims for those over the age of 65”.—[Official Report, 16/11/11; col. GC 305.]

Can the Minister expand on what particular restrictions on existing claims for those over the age of 65 he is intending to implement?

[Lord Freud]

My Lords, I should like to take the opportunity to set out our position in relation to people who are approaching 65 and over the age of 65 and, I hope, give a degree of reassurance as to what we are aiming to do and, if people could accept our firm stated intention, explain why that would be a better and more flexible way of proceeding. I hope that some of the things I said in Grand Committee and what was in our policy briefing document in May will have reassured the noble Baroness, Lady Wilkins, at least to some extent, although I am not absolutely confident of that, given the slightly questioning tenor of her remarks.

People in receipt of DLA who are aged 65 or over when PIP is introduced will not be reassessed for the new benefit from 2013. These reforms will initially be focused on people of working age. This will enable us to ensure that learning from the reassessment of working-age recipients is properly considered before any further changes are developed and implemented.

I understand that the purpose of this amendment is to ensure that financial support continues into pension age for individuals who may have had less opportunity to work and save during their working life due to their condition. I can reassure noble Lords that this is also our objective and can be achieved without amendment to the Bill, but instead through regulations, much as the detail for DLA pensioners is provided for in regulations. We intend to make regulations for the personal independence payment that will allow people who have reached the upper age limit to continue to receive it for as long as they continue to meet the entitlement conditions. Our priority is to support those individuals with established, long-term health conditions or impairments that would put them at a financial disadvantage over a long period. As we indicated in our entitlement thresholds and consultation document, we expect to consult formally on a range of issues to help inform the regulations. This is such an area and we expect to begin consultation in the spring.

It is also our intention that the rules for people over the age of 65 should be broadly similar to those that currently apply to DLA. For example, DLA provisions allow a one-year linking rule which lets those aged 65 or over renew an award within one year of their previous award expiring without losing DLA entitlement or having to satisfy a qualifying period. This provision is intended to allow for those on a fixed-term award to renew their award on a new claim or to reclaim where their condition previously improved and subsequently deteriorated.

I turn to the link question raised by the noble Lord, Lord McKenzie. Under DLA, claimants over the age of 65 cannot move up or down the mobility component rates or move to the lowest rate care component. In the main, these rules match up with attendance allowance and that is an example of the kind of restrictions currently in DLA, which we will look to and consult on maintaining in PIP. Our commitment is to maintain support for those individuals who have relied on DLA or PIP for their working lives into retirement. People who develop care needs during retirement as part of the natural ageing process, for example, and who are not receiving PIP, will be able to claim attendance allowance.

The effects of this amendment are important. It could allow an individual aged over 65 who had previously, at any point in the past, received PIP to make a new claim for the benefit. This could have the effect of allowing people over 65 to receive PIP if they have previously been awarded it, even if there was a very long break in the claim—a break of decades. We would not want that to be the case.

Under the powers we have in Clause 82, we can ensure that the regulations can be flexible to respond to future changes. The changes in the social care system were raised as an example by the noble Baroness, Lady Wilkins. Clearly, if there is a rebuild of the entire support system, that is one thing that we might want to take account of. It could, of course, go both ways: it might affect pensioners.

In terms of developing the rules and how we implement them, I would like to assure the House that we will continue to work closely with the PIP implementation development group to ensure that policy design and delivery in respect of people aged 65 and over are informed by disabled people and their representatives. We intend to consult fully on our proposals during the spring as part of that commitment to involve disabled people. Given these assurances on our approach, I urge the noble Lord to withdraw the amendment.

[Lord Low of Dalston]

My Lords, I declared my interest as a DLA recipient when I first entered the debate on PIP before dinner. However, in view of the particular relevance of this amendment to my own situation, I ought to have made it clear, like the noble Baroness, Lady Wilkins, that I have received DLA from its inception and continue to receive it now that I am past pension age.

Obviously, at this time of night, I am not going to press the amendment and will seek leave to withdraw it. However, I have to confess that I am not entirely convinced by the Minister’s answer. The strongest point he made was that, in the way it is drafted, the amendment could override linking rules and enable somebody who had received DLA a considerable length of time before he reached pension age successfully to resuscitate a claim to PIP after he reached pension age. That would not be our intention and, as I said in moving the amendment, if we could resolve that and any other matters of mis-wording to which the Minister could draw my attention by Third Reading, I would be very happy to have discussions with him and his officials.

[Lord Freud]

Perhaps I may make the position clear. The difference between us is that we would not want this in the Bill but the substance of what we are trying to do matches what the noble Lord is looking for. I am not in a position to offer anything further for Third Reading. I am, however, very willing to see him personally—and any groups he wants as well—to discuss this matter when we move into the spring period to make sure that we get it absolutely right. We are anyway having full consultation, but I am absolutely prepared to commit to looking at this so that the detailed regulations are acceptable.

21:15

[Lord Low of Dalston]

The trouble is that by the spring consultation the Bill will be done and dusted and we will have missed the opportunity. However, on the basis that the Minister is happy to meet us to discuss this matter further and perhaps bottom it more than we are able to do at this time of night, I beg leave to withdraw the amendment.

Amendment 54C withdrawn.

Amendment 54D

Moved by

[Baroness Hollins]

54D: After Clause 83, insert the following new Clause—
“Carer’s allowance
In section 70 of the Social Security Contributions and Benefits Act 1992 (invalid care allowance), for subsection (2) substitute—“(2) In this section, “severely disabled person” means a person in respect of whom there is payable either—
(a) an attendance allowance;(b) a disability living allowance by virtue of entitlement to the care component at the middle or higher rate; or(c) a personal independence payment by virtue of entitlement to a rate of the daily living component which will be prescribed in regulations, or such other payment out of public funds on account of his need for attendance as may be prescribed.””

[Baroness Hollins]

My Lords, the amendments would place the new arrangements announced by the Minister in Committee in the Bill to reflect existing provision for carer’s allowance passporting in primary legislation. In the discussions around the Bill, Peers, including the Minister, have demonstrated their understanding and appreciation of the huge contribution made by the 6.4 million carers in the UK, often at considerable personal sacrifice.

Despite its rather low level, carer’s allowance is a vital benefit which provides an essential independent income for families providing care. As a result, it is crucial that the prominence of carer’s allowance is maintained, as now, in primary legislation, preserving the strength and importance of these crucial rights for carers. Amendment 54D would establish this crucial link between carer’s allowance and personal independence payment in the Bill but allow the Government to prescribe the rates in regulations. However, the clear preference of Carers UK and other charities—I agree with them—is for the maintenance of the strength of existing rights by also setting out the rates in primary legislation.

Amendment 54E would establish the passporting link and that both rates of the daily living component would act as gateways, fully reflecting existing provision for disability living allowance and the details announced by the Minister in December. I remind the House that in December the Minister said:

“It has always been our intention that personal independence payment will provide a gateway through to receipt of carer’s allowance in the way that DLA currently does”.

The briefing paper went on to say:

“It is our intention that both rates of the daily living component will be used as a criterion in connection with entitlement to carer’s allowance”.

Carers UK hopes that the Minister will feel able to support the amendment, to cement in primary legislation this announcement made before Christmas and to send out the clear message that the Government do indeed value carers and that their rights and entitlements are valued correspondingly in primary legislation. Having made such a positive announcement, I can see no reason why the Government would not wish to establish these details in the Bill.

In addition to establishing the provisions announced by the Minister in the Bill, the amendment also provides the opportunity to express ongoing additional concerns about the impact of the personal independence payment reforms on carers, which were not addressed by the announcement around passporting. Carers UK and other organisations are still deeply concerned that the 20 per cent reduction in spending on these benefits as the personal independence payment is introduced will lead to the loss of carer’s allowance for a number of carers, on top of substantial numbers of disabled people losing their benefits.

Having looked at the consultation issued yesterday and other documents which I have received, I cannot see an assessment of the impact on carers of the changes. I may have missed it. We know from the statistics the impact on the relevant groups of disabled people—those in receipt of middle or higher rates of the care component of DLA, the gateways to carer’s allowance—and that these groups will be reduced by 80,000. Many, of course, will not have carers, but it is likely that some of those 80,000 will have someone currently in receipt of carer’s allowance caring for them, and when the disabled person loses his or her benefit the carer will lose eligibility for carer’s allowance.

I understand everything that has been said about the emphasis being on supporting people with greater need and that some people may receive more and that some people currently receiving the lower rate may move into the new standard rate, but concern has been expressed. So, if there has been no impact assessment, is the Minister now able to inform the House how many carers are likely to be affected by these changes? I look forward to hearing the Minister’s response to the two amendments. I beg to move.

[Baroness Howe of Idlicote]

My Lords, my name is also on this amendment and I fully support what my noble friend Lady Hollins has said. As we have heard, there are approximately 6.5 million carers. Of course, we all need to remind ourselves just how important they are and how much money they save the state in the work that they do on behalf of their families and, indeed, friends, because quite a number of carers are not necessarily directly related. Perhaps the Minister would agree that that is a very good reason for putting this proposal in the Bill. It would certainly reassure all those who, as has been said, do so much for the nation in terms of finance and for individuals with whom they have personal caring relationships.

I hope that it will be possible for the Minister to accept this amendment. Otherwise, perhaps he will give us an assurance on the questions that have been asked. That would be helpful and useful. I look forward to hearing his reply.

[Baroness Pitkeathley]

My Lords, I, too, speak in support of these amendments. We are talking about essential rights for carers. When carers give up work in order to care, it is crucial that they are able to access financial support, which provides them with an independent income. I hope that your Lordships will forgive me for a brief trip down memory lane about an independent income for carers. In the 1960s, an independent income for carers was at the very heart of what started the carers’ movement. That independent income was achieved in the 1970s and went on to be extended in the 1980s. I should like to acknowledge the very active part that the noble Lord, Lord Newton, who is not in his place, played in extending those rights under—perhaps I may remind your Lordships—a Conservative Government.

Given the importance of carers, which has been acknowledged time and again, it is disappointing that the Government have not brought forward an amendment to place these rights in the Bill. If the gateway for PIP payments is left to regulations, different groups of carers will have their rights to carer’s allowance set out in different ways. Those caring for disabled children will continue to receive DLA and will not be moved on to PIP, and carers looking after an older person in receipt of attendance allowance, which is also unaffected by these reforms, will continue to have their right to carer’s allowance clearly set out under the Social Security Contributions and Benefits Act. Yet those who are caring for disabled people of working age who are being moved on to PIP would have their rights set out only in secondary legislation, which would make for a confused picture.

I know that Carers UK, other Peers in your Lordships’ House and the Disability Benefits Consortium very much welcomed the Minister’s decision to bring forward their decision about both levels of PIP in December. But to give carers full confidence in their rights and clarity in the legislation, it is crucial for the decision to be written in the Bill.

[Baroness Hayter of Kentish Town]

My Lords, my name is also on this amendment and it is clear that we support it. The amendments are, I hope, welcomed by the Minister as an opportunity to firm up what, as the noble Baroness, Lady Hollins, has said, he said before Christmas: that carers of claimants of both rates of the daily living component will retain eligibility for the carer’s allowance, and to make that undertaking concrete by placing it in primary legislation.

The Minister and the House know well that the changes to disability benefits are causing considerable concern to disabled people and to their carers. This amendment is about providing some clarity. It cannot provide full reassurance because carers do not yet know how they will be affected by the 20 per cent proposed cuts or the exact way that the new thresholds will work. We know that half a million people will lose benefit, but we do not know how many of that half a million qualify for carer’s allowance at present. I am afraid we must assume that there will be a large number of current recipients who will no longer qualify for support.

There has not yet been any impact assessment—it is not simply that the noble Baroness, Lady Hollins, cannot find it. We hope—indeed, we expect—that there will be as part of the response to the consultation announced yesterday. However, for today, we would simply ask the noble Lord to solidify his commitment to those who qualify under the new assessment process that their carers will be able to receive carer’s allowance. At the moment, the Bill does not repeat what is there for DLA. It does not even appear to do it in regulations.

A move from warm words to an undertaking in the Bill to maintain the status of carers’ rights would be very welcome. It would be a sign that the Minister is listening to disabled people and understands their need for clarity. In Committee the Minister spoke very warmly of our 6 million carers. Along with those warm words, can we have something in legislation?

[Lord Freud]

My Lords, I welcome the opportunity to place on record the value that this Government place on carers and their work. Although times are difficult, I have managed to redesign the universal credit so that we are ameliorating the £100 cliff edge, as carers do some earning, that they dislike so much. I hope that that is a token, even in these difficult times, of how much we value carers.

The second thing I would like to mention is more than a token. I was really pleased to be able to announce before Report that both elements of PIP will be a gateway for the receipt of carer’s allowance. I am grateful for the very detailed and knowledgeable debate that we had on this matter. We have had a lot of very thoughtful and clever representations from groups such as Carers UK, which we have taken very seriously indeed. I know that our announcement has been very warmly welcomed by various groups.

There is some concern about how the decision is to be enacted. That is clearly what is driving the amendments from the noble Baroness, Lady Hollins. I want to give an absolute assurance on this. We will use the powers under Clause 90 of the Bill to make the necessary change. We will bring forward, in due course, the appropriate secondary legislation to amend Section 70 of the Social Security Contributions and Benefits Act 1992 and put the position beyond doubt by making clear that people will be able to access carer’s allowance from both rates of the daily living component of the PIP. That is how we are planning to lock that position down, and it is a commitment that I make here and now to carers in this country. We have listened to the concerns from Peers and the carers’ lobby.

The noble Baroness asked how many carers would be affected. We expect to undertake an impact analysis as we get to regulations. The noble Baroness, Lady Hayter, spoke about large numbers being affected. That is a slightly brusque assumption given that carers currently on the lowest rate would not anyway be passported. We are talking about the top two rates. The assumption of a 20 per cent cut in that budget does not marry up. It is not a cut on where we are today; it is a cut on where we would be at the end of this Parliament. We have to await the impact analysis before we can know the real figures.

On the basis of the reassurances that I have provided, I hope that the noble Baroness will not press her amendments.

[Baroness Hollins]

My Lords, I am indeed reassured to hear the Minister’s response, in particular that an impact analysis will be done as the regulations are prepared. I accept the Minister’s assurance that the passporting arrangements will be locked down. I beg leave to withdraw the amendment.

Amendment 54D withdrawn.

Amendment 54E not moved.

Clause 84 : Persons receiving certain services

Amendment 54EA

Moved by

[Lord Freud]

54EA: Clause 84, page 60, line 15, leave out from “provide” to “that” in line 17

[Lord Freud]

My Lords, I am happy finally to place in the Bill the Government’s intention to continue to enable disabled people who live in care homes to be mobile. I am equally pleased to have the noble Lord, Lord McKenzie, joining me on this amendment.

The amendments in this group put our position beyond doubt by removing from the Bill the power to make regulations to stop payment of the mobility component of PIP to people who live in residential care homes and whose costs are borne from public funds.

As noble Lords will know, we examined the evidence base, sought contributions to the debate from many disabled people and disability groups, and considered in detail the excellent report produced by the noble Lord, Lord Low, which was published in November. We established, as did the noble Lord, Lord Low, that while there was some duplication, the overall picture meant that in order to access mobility provisions within a care home environment, which we have steadfastly said we are committed to protect, the fairest outcome was to retain payability of the mobility component in those settings.

I am pleased to be able today to act upon these findings and to introduce a new, separate clause for people undergoing treatment in hospitals or similar institutions. I hope that noble Lords will feel that this reflects the fact that we do listen—sometimes, especially when people shout very loud—and that we try to get things right in this area.

I can go through each provision in turn, but I hope that noble Lords will trust my assurance that the overall effect of the amendments is that the mobility component of PIP for people in care homes will remain on the same basis as it currently is for DLA, including for those in residential schools and colleges. I commend the amendments to the House and urge noble Lords not to press theirs.

[Lord McKenzie of Luton]

My Lords, as the Minister said, we have an amendment in this group that I do not propose to move as I accept it has been superseded by the Government’s formulation—this listening Government that we have on this issue.

It is to be welcomed that the Government have accepted the arguments that have been put forward over many months and from many quarters. As the Minister indicated, we should be particularly thankful to the noble Lord, Lord Low, for his leading on the independent—I would stress the importance of independent—review of personal mobility in state-funded residential care. The report does not just focus on the narrow issue of the availability of the mobility component of DLA—soon to be PIP—but on wider issues of the mobility needs of disabled people, the role of local authorities and care home providers, and the importance of mobility to disabled people’s rights. The clear conclusion in that review found no significant evidence of overlap in the support offered by the mobility complement of DLA and that offered by local authorities and providers. If the rights of disabled people are to be preserved, it is vital that DLA mobility and its successor under PIP are retained for people living in residential care. The report offered a very clear analysis, which I would suggest the Government, frankly, had no option but to accept. Perhaps we should leave unanswered the question of what the position today might have been if the initiative by Mencap and Leonard Cheshire had not been undertaken and the noble Lord, Lord Low, had not assembled such a knowledgeable team to produce this report.

We always give voice to the proposition that disabled people are the experts in their own affairs. It is just a pity that it took so long for their voices to be heard on this occasion, but we should welcome the fact that that has now happened.

[Lord Rix]

My Lords, as Mencap has just been mentioned, I would very much like, as president of Mencap, to thank the Minister and his colleagues for accepting this situation and the Low report. I congratulate my noble friend Lord Low on his splendid research into this problem. It is wonderful to hear the Government’s change of tack. I notice that the Minister mentioned hospitals, but I was busy chatting to the noble Baroness, Lady Hollins, at that moment. Did he mention children? I was not quite sure what the position was going to be regarding children—over 16 and under 16—in regard to this mobility component. However, apart from that, we are very satisfied in Mencap. I would like to thank, both personally and on behalf of Mencap, the Minister and his colleagues for this change of heart.

[Lord Low of Dalston]

My Lords, I promised the Minister earlier on that if he just waited long enough, sweetness and light would break out. The fact that the noble Lord, Lord McKenzie, and I have our names on another amendment in this group enables me to tell him that we have now reached that point.

There is more joy in heaven over one sinner that repenteth than over 99 just persons who need no repentance. For that reason, I greatly welcome the Government’s decision to drop their proposal to withdraw the mobility component from those living in residential care. I have been given some credit for bringing this about with the review that I was asked to lead by Leonard Cheshire Disability and Mencap, but I think, in all honesty, I must disclaim this. Half of that is because I had a very good team working with me, supported by an extremely able and hard-working secretariat from both organisations; and half because I think Ministers, to their considerable credit, largely came to their decision of their own accord. Perhaps I may have provided a little cover for a U-turn—if so, I am glad to have been of service.

It would be tedious if I were to start recycling all the water that has now flowed under the bridge by rehearsing the considerations that led both the Government and my review to come to the conclusion that it would not be appropriate to withdraw the mobility component from those living in residential care. Probably the most significant of them, as has been mentioned, was that we could not detect any evidence of the double funding that was thought to exist and the Government could not either.

The Government can be proud of the fact that on this occasion, when faced with the evidence that did not support their initial conclusion, they had the grace to acknowledge the fact and reverse that initial conclusion. This is very much to be welcomed and a matter for congratulation.

[Lord Freud]

My Lords, I should take the opportunity to say thank you. It is lovely to have some sweetness and light after a few days where there has not been very much.

[Baroness Hollis of Heigham]

Has the Minister learnt from this that the best way to encourage more sweetness and light is to agree with the amendments from all around the House?

[Lord Freud]

There are some other constraints that I do not think I need to spell out. On the point made by the noble Lord, Lord Rix, we are picking up the same arrangements for DLA including those for residential schools and colleges. On that basis, I beg to move.

Amendment 54EA agreed.

Amendment 54F not moved.

Amendment 54FA

Moved by

[Lord Freud]

54FA: Clause 84, page 60, line 21, leave out paragraph (b)

Amendment 54FA agreed.

Amendments 54G and 54GA not moved.

Amendments 54GB and 54GC

Moved by

[Lord Freud]

54GB: Clause 84, page 60, line 25, leave out from second “is” to first “a” in line 26

54GC: Clause 84, page 60, line 32, leave out paragraph (a)

Amendments 54GB and 54GC agreed.

Amendment 54GD

Moved by

[Lord Freud]

54GD: After Clause 84, insert the following new Clause—
“Hospital in-patients
(1) Regulations may provide as mentioned in either or both of the following paragraphs—
(a) that no amount in respect of personal independence payment which is attributable to entitlement to the daily living component is payable in respect of a person for a period when the person meets the condition in subsection (2); and(b) that no amount in respect of personal independence payment which is attributable to entitlement to the mobility component is payable in respect of a person for a period when the person meets the condition in subsection (2).(2) The condition is that the person is undergoing medical or other treatment as an in-patient at a hospital or similar institution in circumstances in which any of the costs of the treatment, accommodation and any related services provided for the person are borne out of public funds.
(3) For the purposes of subsection (2) the question of whether any of the costs of medical or other treatment, accommodation and related services provided for a person are borne out of public funds is to be determined in accordance with the regulations.”

Amendment 54GD agreed.

Clause 85 : Prisoners and detainees

Amendment 54H moved.

Amendment 54HA not moved.

Clause 86 : Claims, awards and information

Amendments 54J and 54K not moved.

Amendment 55

Moved by

[Lord Rix]

55: Clause 86, page 61, line 14, leave out subsection (3) and insert—
“( ) Regulations will prescribe what considerations must be taken into account in deciding whether a fixed term award would be appropriate.”

[Lord Rix]

First, my Lords, I should make a correction for Hansard: it was the noble Baroness, Lady Hollis, who I was chatting to, not the noble Baroness, Lady Hollins. I inadvertently put an “n” into her name, and I apologise.

My Amendments 55 and 56 relate to opportunities for people in receipt of PIP to receive lifetime or indefinite awards of the benefits in much the same way as many people do who are currently entitled to DLA. As figures published by the Department for Work and Pensions in May 2010 revealed, of the 3,157,300 people in receipt of DLA some 2,239,500 received an indefinite award, and on closer inspection this is hardly surprising. If an individual’s disability, impairment or condition is lifelong, their needs will either remain the same or increase over time—they will not go away. Therefore, it seems perfectly logical and right for them to be entitled to the benefits indefinitely.

21:45

Individuals with a learning disability are examples of such people. At this point it is appropriate for me to declare an interest as president of the Royal Mencap Society and describe briefly what happened to my daughter, who died five years ago. She was born with Down’s syndrome, which in those days was defined as mongolism, in 1951. She had hip dysplasia, which was not operated on when she was young enough. Eventually her femur was too brittle and too thin for any hip operation to take place. She developed cataracts in her late 20s and had six eye operations at Kingston Hospital and Moorfields. She developed a certain degree of dementia at the age of 38. She gradually got worse and more blind until, at the age of 54, having developed epilepsy three years earlier, she had five seizures in a row, which rendered her unconscious. She lived for 10 days and eventually died. In that time she was incapable of movement and had to be hoisted everywhere. She was totally blind, and totally incapable of any form of communication because she had Alzheimer’s. In other words, her condition gradually progressed from bad to worse to worse still throughout her life.

Those are the kind of people that I am talking about: people who deteriorate as the years go by. It seems absurd that they cannot have a lifelong award, which would to a certain extent be covered, although I know that this is a different area of healthcare and social care. The point is that we are asking for, and being granted, annual health checks for people with a learning disability. People with severe learning disabilities will also be subject to those annual health tests, and if their condition worsens it can be reported so that the lifelong award would continue to apply.

I hope that the Minister will also see that this will save the Government a great deal of money. You are looking at tens of thousands of people who deserve a lifelong award—not only those with learning disabilities; there are other conditions as well, obviously. There are tens of thousands who would have to go for regular assessments. It is absurd. They should be allowed to have their lifetime awards, or at least lengthy awards, for which they could have a health check. I cannot remember the Minister’s exact words but he said something to the effect that people whose circumstances were exceptional could continue to have a lifetime award or something similar. I hope he is able to pronounce a little further on that. Having ad libbed this speech and moved away from my original script, which I cannot read anyway because of my eye condition at the moment, I hope the Minister will find room in his heart to accept this amendment. I beg to move.

[Baroness Hollins]

My Lords, I rise briefly to support the amendments in the name of my noble friend Lord Rix. I suspect that, after days of assessing the increased cost implications of the amendments already discussed, there will be a genuine expression of relief on the Minister’s face at proposals that will almost certainly reduce overall costs and the administrative burden on the department. I have already declared my personal family interest—I have two disabled adult children—and my professional experience of working with people with severe learning disabilities and autism over 30 years.

I should point out that an annual or short-term assessment would almost certainly be a waste of time and money. This is true not just for people with learning disabilities, but would be true for people with other conditions such as some 69,000 with multiple sclerosis who are currently in receipt of disability living allowance and, on a smaller scale, those with motor neurone disease. After an initial assessment by experts confirming the diagnosis and the degree of severity, it is surely better to leave things as they are but to respond, on the application of carers or the individual themselves, to any deterioration in their condition. That is then the time for further examination, when it may well be found that the person may need greater support.

It is also important to recognise that annual reviews may only increase the anxiety of those undergoing them and will do nothing for their morale. I think with horror of the time—currently scheduled for 2014—when my son will be due for an assessment. I hope I will have the opportunity to go with him and that I will actually know about it. It is not that there would be any intention that I would not know, but rather because he cannot read and his supporters do not always realise the importance of involving me in certain aspects of his support. I hope to be with him when that review is done, but I also know how challenging it would be for him to be reassessed. For quite a lot of people, this constant reassessment would be costly in more ways than you can imagine. I look forward to hearing the Minister’s measured reply to these very modest and cost-saving proposals.

[Baroness Hollis of Heigham]

In quite a lot of the publicity run in some newspapers preceding today’s debates, there has been—how can I put it—synthetic outrage about the number of DLA awards that have been made for life, as though they are somehow fraudulent, negligent or erroneous, thus apparently besmirching the entitlement of the holder of that lifetime award to it as of right, as though they have somehow manipulated or cheated the system and that the previous Administration has colluded with them at the taxpayer’s expense. That publicity has been extremely ugly and extremely unfair. Whether or not the Minister feels able to accept the amendments—and I hope he does—I hope he will accept that some conditions, on which the noble Baroness, Lady Browning, spoke so eloquently and movingly and of which two other Peers in your Lordships’ House have had intimate experience, do not change except for the worse and for which a lifetime award is a decent, sensible and cost-effective way of proceeding. Could he therefore ask his press hounds to lay off those people who have had them in the past and who ought, in all decency, to go on to enjoy them in the future?

[Baroness Browning]

There has been a suggestion that people with disabilities adjust to their condition. It is true, if you take the meaning of those words at face value, that people do adjust to their condition. For example, in one of the case studies shown in the paper produced by the Government yesterday, there is an account of a woman with epilepsy who did not meet the PIP qualification. It said that it was dangerous for her to use a cooker but she got round it because she used a microwave and therefore does not need to use a cooker. That may be a very practical suggestion—apparently when a cooker was needed her husband did the cooking on a proper cooker—but we have, in a way, failed to address what we mean by people with a range of disabilities coping or adjusting to their disability. Yes, there is an adjustment and yes, there are practical and psychological ways in which people cope with their disability, but it only requires something that is really unsettling to someone with a lifelong disability for those very important building blocks that have been put in place at the bottom to be disturbed or taken away and for the whole thing to disintegrate and come down like a house of cards.

Therefore, while I can understand why reassessment is necessary in some cases, a judgment has to be made about identifying those for whom reassessment, with the associated costs that have been mentioned, will add to their stress. Stability, as I said earlier, is important in these cases. If their stability is unsettled, there are consequences. The Government must make some sort of judgment about this. They will not save money and it is compassionate to recognise the types of disabilities that will present themselves when there will clearly be no improvement and degeneration is more likely. Quite frankly, if in some cases people adjust to their disability, are they not to be applauded for having made that adjustment, not penalised for it?

[Lord McKenzie of Luton]

My Lords, I simply say that some compelling and moving personal circumstances have been advanced in support of the amendment and I hope that the noble Lord will feel able to accept it, or a version of it.

[Lord Freud]

My Lords, I first want to put absolutely on the record that we are not talking about the constant assessment of everyone. That is simply not how it is going to work. To the extent that there is concern about people being dragged in to face assessors every year, that is simply not how it is going to work.

When we talk about having another assessment for some people who have deteriorating conditions, noble Lords have to remember that they might have started on the lower rate of PIP and that in practice the assessment will move them to the higher rate at that time. DLA is an understudied phenomenon. It was studied by the previous Government in 2004-05 and it was found that £630 million was overpaid. That was not as a result of fraud; it was just that people no longer fitted the rather easier criteria of DLA that were in place when they applied, although we do not know where they fitted when they did apply. Just as worrying was the finding in that year that £190 million was underpaid. We want to make sure that the money goes to people in the right way in both ways.

[Baroness Hollis of Heigham]

My Lords, I was the Minister responsible for those reports at that time, and I have to say to him that they did not apply to people with lifetime conditions. People with lifetime conditions should get lifetime awards. Clearly, if someone deteriorates, they or their carer may apply further, but the information on DLA that the Minister referred to was either about people with fluctuating conditions or about people who had become better but had not realised that they might no longer qualify as a result, and so on. We had no argument with the need to continue to review DLA for people whose conditions may change quite rapidly over a period of time, particularly if they have been recovering from an accident, and so on. We are talking here about lifetime conditions in which it is therefore decent to give lifetime awards. I can assure the noble Lord that the statistics to which he referred do not refer to that group.

[Lord Freud]

As I understand the statistics, they refer to the whole group and we clearly need a system that we can apply to everyone, within which there will be groups with lifetime conditions. Let me come back to my main point, which was my concern about the underpayments. People with lifetime conditions deteriorate, and they need to be caught at the point of deterioration in order to be paid the extra funds they need to cope with the higher level of disability or higher inability to do things.

22:00

[Lord Rix]

I apologise for interrupting yet again. The point is that if, as I said, the annual health checks are taken for these people it can be reported medically. Certainly the carers can report on this. There is no question that if your son or daughter or your friend is obviously not receiving the amount they should be, it is up to you to get hold of the necessary officials and to inform them. Equally, the annual health checks should certainly—for people with a learning disability anyway, although I do not know about other disabilities —take care of any deterioration in condition.

[Lord Freud]

My Lords, let me go through the approach we are planning to take in PIP. It will involve a personalised approach and, in some cases, awards will be fixed for a short period—maybe one or two years—but in others they will be much longer and we are looking at awards that could be five or 10 years. That will depend on the circumstances of the individual, the impact of their health condition or their impairment and the extent to which they are able to live independently and participate in society. In many circumstances, this can change for better or for worse during someone’s lifetime and that will be different for different people. Therefore flexibility in award durations is key and will allow decision-makers to tailor awards appropriately. Again, we will be working with disability organisations and disabled people to develop the necessary guidance to support these decisions over the next 12 months. There will be many chances to get this absolutely right in the months to come.

I must quote the noble Lord, Lord Touhig—who is not in his place—who quoted Lorna Wing, one of the founders of the National Autistic Society, who said, “When you have seen one person with autism, you have seen one person with autism”, which is a phrase that will remain with quite a few of us in the years to come. Our flexible approach should allow us to provide the support to meet the variable needs people have. We also recognise that the system needs to deal with fluctuating conditions and that is one of the things we need to really lock down in consultation in the next 12 months.

Even where awards of PIP are made for a fixed term and periodic reassessment is required, it will be proportionate. Some assessments may only involve scrutiny of paper evidence and will not require face-to-face consultation. That will particularly be the case where there is considerable supporting evidence on which to base decisions. Conditions or impairments that are lifelong or degenerative will have such supporting evidence. Clearly, we are going to provide guidance on the duration of an award, including when an ongoing award would be appropriate and with what frequency that award would be reviewed. That will be evidence-based and we are committed to coproducing it with the appropriate experts in the field. I assure noble Lords that we are keen to involve disabled people and their representatives in this process. We are determined to get it right.

I have to make the point that lifetime awards were abolished in 2001 and only in very rare circumstances would they be reviewed. At the moment in DLA, we have indefinite awards that can be reviewed at any time. On the other point raised by the noble Baroness, Lady Hollis, on the national benefit review, the only group excluded from that is the awards made to the terminally ill.

I hope that I have reassured noble Lords on the issue. There is still a lot of work to be done in this area. We will look to organisations that help us, including those with which the noble Lord, Lord Rix, is associated. However, before I ask him to withdraw his amendment, I must make clear the technicality that the Government do not consider that Amendment 56 is directly consequential on Amendment 55, so they are separate matters. I ask the noble Lord to withdraw his amendment.

[Lord Rix]

Yes, at this hour of the night. I would love to have further discussion, if it is humanly possible, with the Minister, but I would like to get something on paper to be able to circulate to the people concerned.

[Lord Freud]

I can certainly write to the noble Lord on this matter and see what we can do with the paperwork.

[Lord Rix]

With that, I beg leave to withdraw the amendment.

Amendment 55 withdrawn.

Amendment 56 not moved.

Clause 87: Report to Parliament

Amendment 56ZA

Moved by

[Lord Freud]

56ZA: Clause 87, page 61, line 20, at end insert “—
(a) within 2 years beginning with the date on which the first regulations under that section come into force; and(b) within 4 years beginning with that date.”

[Lord Freud]

My Lords, the government amendments are intended to support our plans for a sensible, achievable and measured approach to the introduction of PIP and to report on the effectiveness of the assessment. I went into detail on what we are planning earlier this evening, so I do not need to dwell on it too long.

The first amendment will allow us to test the processes in a truly live environment and gives us the ability to control where those early new claims will come from. We are looking at which sites to use and developing the detail.

The second is designed to support our programme of examining how PIP works against the assessment. In summary, as I said, I propose to put into the Bill a statutory duty to publish two reports to Parliament—the first within two years from the time that PIP starts, the second within four years of that date. I also made the commitment earlier this evening, which I repeat, that if there is a need for a third review and report because of ongoing issues identified in the second review, we undertake to do that. That is a commitment to ensure that the assessment and its processes are working. We have slightly adapted the idea of doing that annually, which is what happens under WCA, because that has led to a slightly piecemeal approach. We think that two-year reviews will be better and we have learnt from that.

These are sensible and practical amendments. They are of course inspired by noble Lords in Committee, whose arguments convinced me. I have already put it on record that I think that Committee Members did a fantastic job and went through the Bill in an organised, diligent manner with astonishing energy. I have tried to take all the good ideas possible—some of them are not, but I am really pleased to be able to take this one.

The Government consider Amendment 56ZB to be directly consequential on Amendment 56ZA, but do not consider Amendment 70 in this group to be directly consequential on Amendment 56ZA. Despite that, I beg to move.

[Lord Rix]

My Lords, the Minister gave the shortest reply in Committee, interrupting my amendments, and I sat down within about three seconds of standing up. The noble Baroness, Lady Hollis—I have the name right this time—said that if the rest of the amendments could be taken at that speed, we would have got through the Committee stage much faster. I am absolutely delighted that the amendments have been modified but certainly accepted by the Government. I am very grateful.

Amendment 56ZA agreed.

Amendment 56ZB

Moved by

[Lord Freud]

56ZB: Clause 87, page 61, line 21, leave out subsection (2)

Amendment 56ZB agreed.

Clause 88 : Abolition of disability living allowance

Amendment 56ZC not moved.

Schedule 9 : Personal independence payment: amendments

Amendments 56A to 56K not moved.

Amendment 56KA

Moved by

[Lord Freud]

56KA: Schedule 9, page 138, leave out lines 17 to 20

Amendment 56KA agreed.

Amendment 56L not moved.

Amendment 56LA

Moved by

[Lord Freud]

56LA: Schedule 9, page 138, line 32, leave out “, but before the “and” preceding paragraph (b),”

Amendment 56LA agreed.

Amendments 56M to 56ZD not moved.

Amendment 56ZDA

Moved by

[Lord Freud]

56ZDA: Schedule 9, page 141, line 20, after “84(1)” insert “or (Hospital in-patients)(1)”

Amendment 56ZDA agreed.

Amendments 56ZE to 56ZJ not moved.

Clause 91 : Transitional

Amendment 56ZK not moved.

Schedule 10 : Personal independence payment: transitional

Amendments 56ZL to 56ZY not moved.

Clause 92 : Regulations

Amendments 57 to 58ZA not moved.

Clause 93 : Interpretation of Part 4

Amendments 58A and 58B not moved.

Amendment 58BA had been withdrawn from the Marshalled List.

Consideration on Report adjourned.

House adjourned at 10.13 pm.