(14 years, 3 months ago)
Grand CommitteeMy Lords, I have a few words to add to those of the noble Baroness, Lady Thomas, about people in manual wheelchairs. I have been contacted by a number of disabled people recently who are very keen to get into work, but they have told me some heartbreaking stories of the hidden discrimination that they have faced. One young lady had very good skills and qualifications and she applied for more than 40 jobs but was turned away from each of them for some quite interesting reasons. It all boiled down to the fact that it would be too difficult to employ her. I think it was a case of providing a little extra support. We want to get that group of people into work and they want to be in work. It is important for them to be in work so that the rest of society can see their range of impairments and disabilities. That will encourage people to be much more open-minded. I am really concerned that we are not doing everything we can to ensure that that group of people get a fair crack of the whip.
My Lords, we support this group of amendments, which seeks to ensure that a person’s long-term health condition or impairment is taken into account, both when drawing up a claimant commitment and when considering compliance and, therefore, possible sanctions. Amendment 51CE requires that evidence from a claimant's own health professionals is part of any health assessment required in drawing up the work preparation requirements, along the lines set out by the noble Baroness, Lady Hollins, and emphasised by the noble Baroness, Lady Meacher.
The amendments affect both those claiming ESA and those who fail the assessment process and are asked to claim JSA instead. They apply to people with long-term physical or mental health conditions and impairments. I particularly bring to the attention of the Committee the fact that many of these long-term conditions also fluctuate, as has been mentioned, particularly things like multiple sclerosis. As the Committee will know, MS is twice as prevalent in women as it is in men, so it will excuse us taking a moment on it. Some long-term conditions, such as relapse-remitting MS, also happen to have what can appear to be very non-specific symptoms, such as fatigue, generalised pain and cognitive difficulties. It is vital that the assessors understand those, along the lines mentioned by the noble Baroness, Lady Meacher, and that the advisers take full account of the claimant’s own physician.
The DWP note states:
“Claimants with a health condition, or who are undergoing regular treatment to manage their health condition (but do not have limited capability for work) will be required to provide evidence of any limitations on what work (hours, nature of work, and location) they are capable of doing. This will be taken into account when setting … requirements”.
However, as has already been touched on, if a claimant raises reasonable objections to their work availability and work-search requirements, although those will be considered by the adviser, where there is no agreement, the claimant can only get them reviewed by another officer. That was mentioned earlier by my noble friend Lord McKenzie. That falls short of a proper right of appeal.
As we know, the process for assessing whether someone has limited capability for work is not perfect. It is not easy. Will the Minister update us on the implementation of the year 2 recommendations from the Harrington review following last month’s closing date for evidence? This continued process and the very real concerns that it is causing disabled people mean that it is important that long-term health conditions are considered when the claimant is asked to sign up to that claimant commitment or when good cause is being considered as to whether a sanction should be imposed for failure to comply.
Even if the review process is perfect, there will still be some people with long-term health conditions who are able to undertake work search but who need their conditions to be taken into account. They may, for example, be able to work very competently and fully but for only part of the day or a few days a week from time to time. In other words, they can work well but not necessarily on a sustainable basis. The resulting absences or the requirement for additional time to travel to work or extra support at work need to be taken fully into account when assessing both their search for jobs or subsequent work record. The descriptors relating to fluctuating conditions will be crucial in assisting the assessors.
Because the claimant commitment is new, we do not know the extent to which DWP advisers will take long-term or fluctuating conditions into account. There is a precedent for health conditions to be taken into account when good cause for turning down a job is considered. Those are already set out and include,
“any condition … that suggests that a particular job or carrying out a jobseeker’s direction, would be likely to cause you excessive physical or mental stress or significant harm to your health”.
The draft regulations do not list how this issue will be dealt with under universal credit. Will the Minister outline what is intended in this regard?
I want to finish by bringing to the attention of the Committee the concerns of Scope, which is very worried about the proposals as they stand. It fears that,
“there will not be adequate safeguards to ensure that sanctions are not applied to disabled people who are unable to meet the conditions due to factors relating to their impairment or condition”.
Scope is,
“not convinced that applying long-term sanctions … will incentivise those to comply after the sanction has been introduced”.
Moreover, Scope is,
“deeply concerned that the use of stricter sanctions will impact upon disabled people receiving JSA”.
After all, sanctions are most likely to affect those who did not fully understand that penalties could be imposed. This frequently involves claimants who already face multiple barriers to work, including various disabilities.
Scope also believes that there is little to suggest that sanctioning such claimants in this way will actually do much to change behaviour when a claimant, perhaps with a learning disability, has not understood why they were sanctioned in the first place. Scope is concerned that conditionality requirements and sanctions, as has been mentioned by other noble Lords this afternoon, will not be applied to disabled people until there has been proper consideration of need. A thorough assessment of need and barriers to finding work must be carried out before any decision is taken to apply a sanction. I look forward to hearing from the Minister how he responds to the concerns raised by the noble Baronesses, Lady Hollins and Lady Meacher, and other noble Lords who have spoken.
(14 years, 4 months ago)
Grand CommitteeI hope that the Committee will forgive me; I omitted to declare my interest when I spoke about the work of National Grid Transco. I have received hospitality from them on a number of occasions and I have declared that.
I was asked yesterday morning to come into this room and check for accessibility. I came in at 2.15 pm to check that there was enough room and we are fortunate that a huge amount of work had gone on to make sure that there was enough space for wheelchair users who might come to speak or to deal with various colleagues’ needs. On the point about voting, my personal view is that it is incredibly important that if I take part in a vote, I actually walk, or push, through the Lobby. As much as being able to see my name in a list, it is important to me that Members of your Lordships’ House see which way I push. If there is a Division—I hope not today—I will be going to vote and that is something important that we should all have the opportunity to do.
I know that not all my fellow Peers feel as strongly about walking down one of the Lobbies as I do, but it is very important in terms of democracy.
I have a brief point in support of the noble Baroness, Lady Campbell. As we later consider the disability living allowance and the PIP which will replace it, we need to bear in mind that our understanding of the consequences of living with disability is limited. We demonstrate that by the way in which we conduct our business. People will judge the extent of our understanding in the discussion we have about social security arrangements for them. It is a hugely important issue.
(14 years, 4 months ago)
Lords ChamberMy Lords, I understand the need for reform of the welfare system, and I support a system that is more simplistic and better able to deliver what is required to those who need it. I am pleased to hear that the most vulnerable and those in greatest need will get the support they deserve, but it must not be at the expense of others who need it to live equally.
My concerns cover a number of areas. Like many in your Lordships’ House, I have been contacted by many disabled people who are terrified that this is the first step towards an insurance-based, perhaps Americanised system which will further discriminate against those in need. I am concerned that the Bill will leave a significant number of disabled people in a precarious position where they do not get the help and support that they require. Under the new system, those people may not be considered disabled enough to be supported, but may be considered by society to be too disabled to play a full part in it.
As many disabled people as possible should be in work, but many will still experience discrimination in the workplace, will be in the lowest paid jobs, and will struggle to reach their potential without support. The new system may provide those in low-paid work with a higher earnings disregard, but it looks likely that a narrower group will be able to access this than those currently receiving the disability element of working tax credit. We need to ensure that this group is able to make the transition into real work and to have the right support until this is possible. I believe that the ethos of support needs to change. Perhaps now is a good time. Until now, to get support has been about proving what you cannot do. We need to look at what people, whoever they are, can achieve if the correct mechanisms are in place.
Disability is not homogenous. Even two people with the same impairment—for example, with my level of spina bifida—will have very different needs, depending on their upbringing, on where they live, on their education and on what support they have around them. The Joseph Rowntree Trust has estimated that it costs 25 per cent more to be a disabled person in the UK due to housing costs, aids, transport, et cetera. Being disabled puts a great burden on the individual and their families.
The media coverage of disabled people is already varied. Disabled people are either portrayed as athletes or as work-shy benefit scroungers. There is not much in the middle. The reality is that we know that the rate of abuse of the current system is 0.5 per cent. From my own personal experience, I know that if I am recognised as “the one who used to be the athlete” or as someone in your Lordships’ House, I am generally treated extremely well. However, if I am seen as “that woman in a wheelchair”, or more usually, “that wheelchair”, then my treatment can often be somewhat less favourable. Recently, on returning to the UK by air, I had a difficult experience, when I was left sitting on the plane for a time. I was removed, left at the gate, then left sitting in an airport without any mobility and very nearly crawled through passport control because I wanted to get home. As it was, I missed my connection and an hour and a half later I managed to get to where my bags were and finally to my wheelchair.
I am very concerned that the 20 per cent cut to working-age DLA expenditure, although estimated at £1.3 billion, will affect the care and mobility support that disabled people can access, and increase reliance on council services. I have great concerns that this could radically change people’s ability to work and push the problem into other areas, such as health.
Those who will fall outside the system could be pushed into a ghetto from which it will be hard to escape. I wonder how far away we are from a point where we have the “deserving disabled”, who require support, and the “undeserving disabled”, who are left in limbo. Growing up, I did not see many disabled people. They existed but they were locked away in schools and care homes—and I never want to return to that. We have to ensure that disabled people are still allowed to be independent.
Take me, for example. I am relatively healthy—perhaps not as fit as I used to be. Without the support of DLA I might have been able to learn to drive at 17, but I would not have been able to afford a car or insurance. I would not have been independent. I would not have moved away from home. I would have found it nearly impossible to go to university and I would have struggled to become an athlete. Because of the support that I had then, I am now able to give back. I am fortunate that I am now in a position to buy the equipment and support that I need, but 99 per cent of disabled people are not.
If we are to support changes, much more needs to be done to ensure that discrimination in the workplace disappears and that there is an improvement in public transport, which outside London is not generally that accessible. If I want to travel by train, I am meant to book the exact train time 24 hours in advance. Can anyone imagine a non-disabled commuter having to do that every single day? This is the unseen reality that disabled people face.
Like many in your Lordships’ House, I am concerned about the DLA removal from residents of council-funded care homes. Many disabled people living in residential homes use this component to pay for either a mobility aid, such as a wheelchair, or travel costs to see family and friends. If this is removed, we remove people’s freedom. I listened to the Minister’s opening remarks and look forward to future discussions in this area.
We must also have faith in the PIP assessment process and, as was clear from listening to the remarks of the noble Baroness, Lady Campbell of Surbiton, disabled people do not. Many of these assessments are complicated, but they must take into account all the medical evidence that is available and use the best documentation. They must ensure it is done properly the first time, and that the use of appeals is not a delaying tactic in providing the support required.
I also have concerns about time-limiting ESA to one year. I will refrain from commenting now, with the constraints on time that we have, but I acknowledge the speeches of the noble Baronesses, Lady Hollins and Lady Morgan of Drefelin, and the noble Lord, Lord Rix. Will the Minister assure us that all disabled people will continue to get the support that they need to live equal lives? Can I have his assurance that we are not dooming a generation of disabled people to a life of hardship? Does he consider that I have disability-related costs? People like me are afraid that we will lose vital allowances. Will we?
Yes, we are in tough economic times and there is a need for change, but we need to ensure that these changes help disabled people fulfil their potential and not hold them on the first rung of the ladder.
(14 years, 10 months ago)
Lords Chamber
Baroness Howe of Idlicote
My Lords, I congratulate the noble Lord, Lord McKenzie, on his amendment and I thank everyone for the very warm support that it got. Obviously, I would rather that amendment had won, but the vote was indeed very narrow. With that in mind, I would certainly want to support the proposal of my noble friend Lady Greengross, which would certainly do something along the lines that the noble Lord, Lord McKenzie, was trying to achieve with his amendment.
If the Minister can find a way to accept that, it will give some comfort at least to those who feel strongly—and have shown how strongly they feel—about this issue. I hope he will bear that in mind when he comes to reply.
My Lords, I rise to speak to this amendment as someone who is certainly not an expert in pension provision; I admit to finding a lot of it rather confusing. The amendment tabled by the noble Baroness, Lady Greengross, is a very positive and useful way forward.
What concerns me is not the arguments that we heard earlier about the 2.6 million women having to wait longer than expected, the 330,000 who will have to wait 18 months or even the 33,000 who will have to wait two years to receive their pension, but the fact that, of the current pensioners who live in poverty, two-thirds are women. The Joseph Rowntree Foundation has made estimates about the poverty level, which it set at around £14,000 a year, and recognises that one in four women retiring today has less than £10,000 a year to live on. We know that women earn less pay on average, while taking time out to raise children means that they earn less over their lifetime. For me, though, the inequality in savings that women have access to is a stark reminder of where many women live today. The average savings in pension schemes of women between 51 and 59 are £37,000, compared to the £54,000 that men hold.
We have heard many case studies. I am very fortunate. I employ someone who is 56 and has a sister who is four years older. Maureen will have to wait 10 years beyond the age of her sister to receive her pension. This is someone who worked for a number of years, took time out to bring up a disabled child, went back into part-time work and, with nothing impelling her to contribute to a pension scheme, made decisions to try to save money but also had to recognise that there was a huge potential loss of salary in contributing to a personal pension scheme. I fear that we are going to alienate a large group of women and penalise them for making sound family choices to stay at home and bring up children and look after them.
It may be true that we need change and need to move on. It might be true that women have relied too heavily on their husbands’ careers and earnings in setting their pension limits, but I strongly believe that women deserve to have more time to adjust to this change in thinking.
We are very sympathetic to the noble Baroness’s amendment. I congratulate her on an important contribution to this debate on an issue that the Government must address. A number of reasons have been explained, in this debate and in the preceding debate, on why that is important. Men are not being disadvantaged by more than one year, but over half a million women are. The period of notice is inadequate. Women in this age group are some of the most disadvantaged in terms of their pension provision. We have to accept that there is a contradiction with the coalition agreement. We are expecting some assurances from the Government in this debate, but we also accept that this is largely a negotiating matter with the Treasury. We welcome the announcement in the Budget of the new basic pension.
The noble Baroness, Lady Hollis, complained at Second Reading that the Pensions Bill ignored the £140 new basic pension, and said that it was like Hamlet without the prince. Now we have Hamlet with the prince but without a script. We want to see some details of the government proposals before committing ourselves to new transitional arrangements. We know that in present value terms the amendment will cost £7 billion, but the Government need to address the problem and come back with a considered amendment during the passage of this Bill in the other House with regard to how women affected by these transitional arrangements will benefit from the new higher basic pension.