(9 years, 9 months ago)
Lords ChamberMy Lords, I welcome the Government’s manifesto commitment to halve the disability employment gap. I sincerely hope that the Bill will help to achieve that, but there are challenges along the way.
Scope’s analysis of the labour force survey indicates that between July and September 2011, 18.5% of the total number of unemployed people were disabled. The statistics from April to June 2015 indicate that disabled people now make up 26% of the total number of unemployed people. It is also estimated that a 10 percentage point increase in disability employment would increase GDP by £45 billion by 2030.
I believe that disabled people should be in work, but it is a complex issue. The Government have consistently said that they support the most vulnerable but it is no surprise that I have concerns about how we might achieve that. The importance of the annual report has been highlighted by the noble Baroness, Lady Doocey, and she is absolutely right, but it is more likely that a disabled person will be asked at interview how they go to the bathroom than whether they have the skills to do the job. In other contexts, I have frequently been asked that question. A non-disabled person would be utterly appalled if they were asked that in an interview, but disabled people wrongly expect this as the norm.
I hope that in Committee we will be able to explore what good reporting will look like and how value can be added. That is important because, once out of work, disabled people face considerable barriers to returning. Some 10% of unemployed disabled people have been out of work for five years or more, compared with just 3% of the non-disabled population. I live in the north-east of England, where in the past eight weeks 5,000 jobs have been lost. The chances of a disabled person finding work in this environment will be few and far between. In recommissioning for the work programme and Work Choice in 2017, the Government must develop detailed plans for specialist employment support programmes for disabled people, as recommended by the Commons Work and Pensions Select Committee last month.
The current back-to-work support for disabled people is ineffective. The work programme may have been successful in helping to address cyclical unemployment but it has struggled to address the historically low employment rates among disabled people. Job outcomes for disabled people on the work programme are only 7.7% for new ESA customers and 3.9% for other ESA incapacity benefit customers. This is compared to a job outcome rate of 21.5% for JSA 25-plus customers. People referred to Work Choice between July and December 2014 had a job-start rate of 57.3% by June 2015, but Work Choice is small in scale and poorly targeted at disabled people on ESA.
I hope that the Minister will consult experts on what support into employment should look like, because the work capability assessment does not assess employment support needs. The level of financial support that a disabled person receives determines the employment support that they receive, but that is unhelpful because those two things are just not related.
I must apologise to the Minister that I am unable to attend the weekly Cross-Bench meeting tomorrow, where he will be speaking to my noble friends about this Bill, because I am launching a Citizens Advice report called Waiting for Credit, which looks at the universal credit rollout. It is vital that we get the correct implementation of this because it affects how disabled and non-disabled people are able to move in and out of work.
The noble Lord, Lord Low, has already mentioned that he, my noble friend Lady Meacher and I will be looking at ESA. I do not wish to pre-empt the findings but I imagine that there may be quite a number of amendments in this area. There is a great deal of concern. I do not want disabled people to be disincentivised from getting into work, and we need to explore further whether it creates a greater incentive for claimants to want to be placed in the support group. Given the limited support available to disabled people in the support group, it could have the negative impact of moving people further away from the workplace.
I would welcome a further discussion with the Minister about the impact assessment. I struggle to see how cutting support could incentivise disabled people into work, and I am looking forward to the DWP’s convincing arguments in this area.
There are also a number of issues to do with carers, who could be penalised by the lower benefit cap in the Bill. They make a huge contribution to society, but there is great complexity about whether they live in the same property and whether they are counted as a separate household, even if they do. We must consider how protection can be offered to carers who do not live in the same household. There are also many considerations for people with a life-limiting and potentially rapidly declining condition.
The noble Lord, Lord Borwick, raised the issue of Motability. I had a Motability car when I started learning to drive at 17, because insurance for a disabled person was ludicrous, twice the price of that for a new driver, which was blatant discrimination. It is better now, but under the changes that are coming, if a person loses their benefits they will lose their car. There was a recent case of Olivia Cork, a leg amputee, who was told she was not disabled enough. She went through the process and asked for reconsideration but was turned down. She now has to find £4,900 to be able to keep her car. In a Britain where there are many issues of accessibility to public transport, this is far more disabling than it is helping a disabled person get into work. Whizz-Kidz launched a campaign today looking at accessible travel. In London it is fine, but if you live in the north-east like I do it is really difficult for a disabled person to get around.
There is so much that can be done to help disabled people, but so much is outside the Minister’s remit. I dream that one day we will actually have a joined-up Government. I am chair of ukactive, and last week we released Blueprint for an Active Britain; it contains a whole host of recommendations, such as having activity experts in GPs’ surgeries to help everybody become more active. The Minister said that work is beneficial—activity is beneficial too. We need to be looking at physical literacy for all. Many disabled children are excluded from physical activity and PE in school and there are clear links between educational attainment and activity, but that is outside the remit of the Bill.
I am also chair of the national Wheelchair Leadership Alliance; it is looking at provision of day chairs, which in England is a complete postcode lottery. I am grateful that we have had a lot of support from MPs and CCGs but the wrong wheelchair causes harm. It excludes children from school and people from work. To highlight the issue, I had a picture of myself taken in a wheelbarrow. It has a seat, wheels and handles but is absolutely no use to me. That is the problem of providing a wrong wheelchair. Access to Work has been through reforms. I am currently dealing with a case—it provided a woman with a chair but only gave her five-sevenths of the money towards it. It then suggested that she leave it in work over the weekend so she would not wear it out. These changes are simply bonkers. Instead of encouraging people to work, they are making it really difficult.
Finally, I was today considering why we are here and what we are trying to achieve. I saw a story in the Bristol Post this morning about a young lady called Lily Grace Hooper, who is at primary school. She had a stroke as a baby and is now blind. After a health and safety assessment, she was told that she cannot use her white cane in school in case she tripped people up, but she should have a full-time adult helper instead. What a waste of resources. I am sure there are decent intentions behind it, but it is patronising, it does not promote socialisation, it does not aid her education and it takes away any aspiration. This case sends out a really poor message to disabled people about their independence. The message is, “Why bother?”. I know that this decision was not made by the DWP or the Minister, but the message it sends out about the value of disabled people in society is very worrying. If the Government want disabled people in work, we need to look at the wider issues, not just treat them in isolation. If children are important—if we genuinely want to look at their life chances—children like Lily Grace Hooper deserve a much brighter future.
(11 years, 5 months ago)
Grand CommitteeMy Lords, I thank my noble friend Lady Campbell of Surbiton for tabling this debate.
In my time in your Lordships’ House, I have had the pleasure of participating in, among others, the passage of the Welfare Reform Act and the legal aid Act, and the Care Bill. Through the legislation that has been passed we will see some of the biggest changes to the lives of disabled people in many, many years. While there have been varying amounts of media coverage over the welfare and legal changes, the effect of disbanding the Independent Living Fund has happened rather under the radar—perhaps because the role and funding available has been gradually eroded over time.
Inclusion London has argued that the ILF provided both value for money and value for disabled people. The ILF has only about 2% overhead costs, compared to 16% on average, for local authorities. The £350 million the ILF costs in government funding each year supports around 20,000 disabled people. This equates to, on average, £17,500 per person, equivalent to approximately £337 per week, or £48 per day. This compares—I was going to say “very well”—extraordinarily well to the notorious Winterbourne View private hospital, where the average cost was £3,500 a week.
The user base of ILF is mostly young disabled people; only a small percentage, around 6.4%, is over 65 years old. The ILF has had consistently high user outcome satisfaction, ranging from 94% in 2009-10 to 97% in 2012-13. Perhaps that was because it was centred on the person. I, like many, was extremely disappointed that the journey of the ILF appears to have been so tortuous recently and that disabled people, having been through the High Court case, were thrown a lifeline only to have it removed again. That was very ably explained by my noble friend Lord Low.
My Lords, it is important to remember that the Independent Living Fund was designed to give disabled people the same rights as anyone else: to work, to socialise, to have a family, to participate in society and—I know it sounds a bit dramatic—just to live. That was brought home to me when a number of people got in touch with me because of this debate. Fran said that it enabled her,
“to live, not just exist”.
Right now, I feel very lucky that, at least for the time being, I do not have care or support needs.
We are debating this issue at a time when the media coverage surrounding disabled people is inherently negative. You only have to scan the coverage to see that they—or rather, “we”—are being portrayed as scroungers and skivers who are a drain on society. The size of the welfare budget is endlessly debated, but what it widely encompasses is usually not. Scope’s report, which was launched this morning, highlighted how little attitudes have changed in many areas over the past 20 years.
My real worry is that it will become “too expensive” for disabled people to live independent lives. If the funding is not ring-fenced, a disabled person’s independence is balanced against a contribution to, say, upgrading street lighting. There is a real danger that it becomes a decision about the benevolence that we choose to bestow on disabled people rather than something that should be clearly defined.
I mentioned that a number of people got in touch with me, and this is a snapshot of what I was told. Sue told me that they would move from being able to fit care plans to people’s needs to having to plan around care visits. Jackie said that once the ILF goes, so does the safety net around disabled people. Rachel said that disabled people are frightened for their future, and that they may be made to live in care homes. Fran, who I quoted earlier, gave a very balanced response:
“By employing and managing my own support, I create full time permanent jobs for personal assistants on a living wage at zero profit (I manage, including paying Tax and NI and recruit my staff for free) rather than carers on zero hour contracts on min wage with private companies profiting. Also it has been strongly evidenced that this central fund costs less than equivalent social services support per hour, due to low central administration and overhead costs, so care packages will need to be cut to create any saving. I am deeply scared this is putting thousands of Disabled people back to the pre-1980s era—unseen, institutionalised or trapped at home with inadequate support”.
I believe that the time to save the ILF in this format has passed. However, I like the idea put forward by the noble Lord, Lord Kirkwood, that we need to reconfigure what we are doing. It is essential that what happens from here, and the protection of the budget, get the urgent consideration they require.
(11 years, 5 months ago)
Lords ChamberMy Lords, I very much welcome the debate tonight and commend the work of the committee. It has produced a very detailed report covering many areas, but I hope that the detail of the report and some of the challenges that the committee highlighted mean that this matter will not be ignored in the future. I have said repeatedly, both before and since the London 2012 Games, that we cannot just expect legacy to happen, but there are many different ways in which we can encourage it.
I have a number of interests to declare. Everything is listed on the register but the most pertinent ones for tonight are that I sit as a board member of LLDC and Transport for London. I did work with LOCOG and am a trustee of SportsAid.
Tonight, I shall cover several areas of the report. The Paralympic Games were amazing. They exceeded every expectation that I could possibly have had. On day 1 of the athletics, at 9.50 am, with the session starting at 10 am, the stadium was packed with 80,000 people. Going back to the days when I competed in Atlanta where we could literally name the crowd, I never thought that we would get to a Games where the public would engage in such an amazing way.
Looking back, it perhaps seems that some of those things were easy to achieve. But there were many challenges along the way and a number of people deserve praise, not least the noble Lord, Lord Holmes, for his work in integrating the Paralympic Games into the organising committee. I also worked closely with the diversity and inclusion team, which should be congratulated on the incredible work that it did in employment, procurement and volunteering, which will have a long-term effect, although some of the challenges are difficult to measure.
I am convinced that the Paralympic Games changed the attitude towards Paralympians, but I am not sure that it did much to change the attitude towards disabled people in general. We only have to look at the disability hate crime figures, which when last reported were the worst they have been in 10 years, to see that there is a mismatch between how the public view Paralympians and disabled people.
I strongly welcome the new Sport England targets on disability participation. This is the first time that any governing body will be seriously measured on what it does for disabled athletes, although it has been included previously in various plans. We need to be careful about how we measure participation and that we do not have double or triple accounting, and that we genuinely measure the number of disabled people who have opportunities.
In terms of how we measure equality within sport, I would be interested to find out how many of our Olympic and Paralympic national governing bodies employ disabled people. These data are probably not available now but, in terms of disability rights, we spend a great deal of time talking about co-production, and the idea of working with disabled people and them being part of the decisions that affect them. From what I see of our national governing bodies, we do not have enough disabled people working in the bodies, coaching or volunteering. With a little effort, that easily could be achieved. Through my work with the Women’s Sport and Fitness Foundation, we know that there are not enough women on sports governing bodies. It is my guess that the representation of disabled people is even less.
Wearing my LLDC hat, I am really pleased that there are no white elephants, although I have to say that all that work was done before I joined the board. However, London set the most amazing standard for inclusion for spectators. For the first time ever I went to a sporting event and was able to sit with the people with whom I had bought tickets. My family were not sent 10 rows in front of me and my daughter was not sent to sit in another stand completely. The sightlines were amazing and you could see everything that was going on. The platforms were built in such a way that when everyone jumped up at the start of the 100 metres, we were still able to see. There were some very simple things: for example, the toilets were in appropriate places and the access to food was amazing. In addition, the Games makers were trained to be positively helpful.
Where we are now was raised by the noble Lord, Lord Faulkner of Worcester, as regards spectator seating in football clubs, which is not good enough. To have three clubs that provide decent access is poor. We are missing out on a massive opportunity. I strongly support Joyce Cook from Level Playing Field when she said that the clubs need to react to the DDA and Equality Act legislation. It is not as if they have not had a decent amount of support. Information that the clubs have been given goes back as far as 1995 and they still have not done enough to rectify this. The Government provided a detailed, self-explanatory response, so I do not expect the Minister to respond on this matter. But I would strongly support any work that the Government were going to do in that area.
I also do not think that it is acceptable for fans who are wheelchair users to have to sit with the opposing team. That is completely unacceptable. But I also strongly disagree with clubs that offer either a specialist pricing programme or a different way of accessing tickets. What that usually means is that disabled people cannot just buy a ticket the same way as anyone else: they are reliant on a smaller body within the club to allocate them tickets. That is not always a terribly fair way of allocating them. It also means that a disabled person cannot complain. If they complain about the sightlines or lack of access to toilets or food, they will not get tickets next time and they will be even further excluded from watching the sport they love. I was therefore delighted when the noble Lord, Lord Holmes, mentioned that the EHRC will be helping those sports that require to be pushed in a slightly more positive direction.
Transport at Games time was amazing. Last week, I helped to launch “turn up and go” for London Overground, which is about disabled people not having to book 24 hours in advance to travel on the overground in London. The booking system that exists whereby wheelchair users have to book 24 hours in advance makes some sense to me, but disabled people need flexibility in their lives and should be able just to turn up on public transport and travel whenever they wish. I really hope that this will expand out across the whole of the rail network.
Just last week, I was invited to take part in a radio interview with a disabled businesswoman called Sarah Rennie. She was on a train but found out that the only accessible space was in the quiet coach, so she was not able to work. Just a couple of days later, I found myself in exactly the same position when I was travelling from London to Cardiff. I also found out that on a two-hour journey there were no accessible toilets. That particular train company, First Great Western, has since said that on those services it does not have accessible toilets in that particular carriage. It is hard to see that disabled people in the areas of transport are not experiencing some level of discrimination, and I plan to write to the Department for Transport on that particular matter.
In terms of participation, there are some really good things happening, but it does not always feel like that work is joined up. In terms of a living legacy, associations such as SportsAid, which has been around for a very long time and will continue to be around, is doing great work in terms of helping talented athletes, but also working with them to find the next generation of practitioners, strength and conditioning coaches, physios, and sports psychologists, and finding different ways to develop young athletes’ skills. But I firmly believe that we need to have other schemes that do not have such a huge profile, such as the talented athlete scholarship scheme, which helps athletes stay in education while they are training to make sure that when they leave sport they have other things to go on to.
That leads me to my view on elite sport. I sat on UK Sport for two terms and I also sat for one term of “Mission 2012”. I completely understand and accept that the “No Compromise” situation for London was okay, but we need to think differently about how we support our sports teams and how we enable them to get up to a decent international level. Over the years, I have seen many national governing bodies have several attempts to get it right. The sports that are now successful were not immediately so when lottery funding first came in. Gymnastics was one sport that was funded, then not funded and then funded again. It was a maelstrom for athletes and coaches who did not know where they stood. I wonder whether there is anything we can learn from history. By now, we must know quite a lot about performance planning and about how to be efficient with money. I do not think we are talking about huge sums in terms of helping athletes to be the best that they can.
I was really disappointed to learn that water polo, basketball, goalball, synchronised swimming, visually impaired football and wheelchair fencing today lost their appeal. Particularly on water polo I received a huge number of e-mails—possibly the largest number that I have ever received in the time that I have sat in your Lordships’ House—from young girls who want to play water polo saying that they do not know where to go. That is the sport that they want to play and they do not want to be talent transferred to another sport, but they do not feel that they have any options.
At the moment, we are in danger of telling people who have an aspiration to be an Olympian or Paralympian that they cannot do the sport they love. I understand that lots of sports such as lacrosse do not have much funding, but they are not Olympic or Paralympic sports. At the moment, we are consigning these sports to little chance of international success. David Owen, the journalist mentioned by the noble Lord, Lord Moynihan, has been vocal about this—he tweeted this evening that we should,
“think about medallists, not just medals”.
Team sports can create many role models but bring in only one medal. I think that the current view is short-sighted. I do not want to be where Australia was in London 2012. I enjoy the friendly rivalry with the Australians and I love beating them, but I like to beat them when they are good, not when they are bad.
Finally, I would like to talk about physical activity. I thank the Select Committee for mentioning my work chairing the schools and physical activity task and finish group on the role of PE in Welsh schools, and I pay tribute to the members of that group who were all experts working on the ground. I worked hard on the project and it led to quite a radical report that made one single recommendation, which was to make PE a core subject. The idea behind it is about physical literacy and balancing that between literacy and numeracy. It is also about influencing teacher training and measuring equality of experience. It is not about measuring how high children can jump or how quickly they can run but about measuring the core skills they acquire. So I was delighted to learn yesterday that the Welsh Assembly Government have announced £1.78 million for a new physical literacy programme and a further £2.35 million has been agreed in principle to continue this work, subject to review.
In England, the money that has been confirmed for English schools is welcome, but I wonder whether the Minister can explain what plans Her Majesty’s Government have to help teachers make cost-effective use of that money. I have seen amazing teachers working in primary schools, but most of the time it feels like it is down to luck—it is because of the sporty teacher, the person who wants to do it. Some teachers find it a struggle and some head teachers may not understand the benefits of sport. They will not make the best use of this money. The situation in schools is this: if our children were being taught maths by someone who stopped engaging with maths at the age of eight, had a really bad experience of it, and then went to teacher training college where the tuition on how to teach the subject lasted four to six hours, there would be universal outrage, but that is happening in PE. I accept that that is a gross generalisation of the worst of the worst, but how can we expect our children to acquire the correct skills if we do not equip teachers to help them in the best way they can? I firmly believe that our children deserve better.
The Games alone cannot change the world. They did a huge amount to move things forward, but we still have an opportunity to do better. I am sure that we will return to this debate and I look forward to the Minister’s response.
(11 years, 9 months ago)
Lords ChamberMy Lords, I declare an interest in that I am in receipt of DLA but not of a Motability car. Regardless of whether the Government know the figures of who will be affected, this will affect a significant number of people. I travelled on a train this morning from Darlington to London. There were two spaces for wheelchairs and no accessible toilet on board. Can the Minister explain what consultation there has been with other government departments to ensure that when this huge number of people is affected, the public transport system will be able to cope?
My Lords, we have had a very thorough consultation on this. I cannot bring to mind right now the exact level of consultation with the transport department. I will need to write to the noble Baroness with that information.
(12 years, 6 months ago)
Lords ChamberMy Lords, the amendments would remove the benefits paid on behalf of children from the scope of the Bill because that disproportionately hits children and families. That is why I have added my name to them. Where 30% of all households are affected by the Bill, nearly nine out of 10 families with children are affected, including 19 out of 20 lone-parent families.
In total, the Children’s Society has estimated that about 11.5 million children are affected by the Bill. As the right reverend Prelate explained, Amendments 14 and 19 would together remove child benefit and child tax credit from the scope of the Bill. That is made particularly necessary by the fact that child benefit has already been frozen for three years before the measures contained in the Bill take effect. That means that child benefit will increase by only 2% over the course of half a decade. Over the same period, prices as measured by CPI will have risen by more than 16%. I say that that justifies the removal of child benefit from the scope of the Bill but, in truth, it would be unjustifiable not to remove it.
These benefits are paid to working families from all walks of life, as well as non-working families. The Children’s Society’s benefits uprating cap impact calculator shows that a couple with two children with one earner working as a primary school teacher and earning £600 a week would lose £424 a year by 2015. A couple with three children and one earner, a corporal in the Army, say, earning £619 a week, would lose £552 a year by 2015, so we can see the impact of having extra children.
As we have heard, Amendment 17 would remove the 1% uprating cap from the lower child disability addition under universal credit. That is particularly justified by the fact that rates of support for children in that group are already intended to be halved under universal credit. At present, families with a disabled child for whom they are in receipt of some level of disability living allowance, may be entitled to receive support through the disability element of child tax credit, currently worth £57 a week. Under universal credit, that support is to be provided through disability additions within household benefit entitlements, but it is proposed to cut that support in half to just £28 a week. That change will affect all families with a disabled child unless the child is receiving the higher rate of care component of disability living allowance or is registered blind.
The review of the noble Baroness, Lady Grey-Thompson, Holes in the Safety Net, of the impact of universal credit on disabled people and their families surveyed 1,400 families with disabled children about changes to support under universal credit. The evidence received suggested that, for those likely to be affected by the cut, the impact could be disastrous. Two-thirds of those likely to be affected said that if they received £30 a week less in benefits for their disabled child, they would have to cut back on food. At this point, I cannot resist asking: if the Minister shares other noble Lords’ disappointment at the greater resort to food banks, what does that say about her view of the government policy that she is supposed to be defending, as it is government policy that is leading to people’s greater resort to food banks?
Returning to the review of the noble Baroness, Lady Grey-Thompson, more than half of those surveyed said that the changes would lead to them getting into debt, more than one in 10 that they might even need to move home. One parent told the inquiry:
“My child would have little quality of life and would lose much of the social interaction he needs. It would be like a prison sentence”.
Another simply expressed their desperation, saying:
“This would have such a huge impact on us I really don’t know what we would do”.
The Bill will further compound that cut. For a family with one disabled child, the impact of the change in uprating would be about £42 a year. It should be noted that that impact is on top of changes to the uprating of other benefits received by the family.
The Children’s Society estimates that the cost of uprating the lower child disability addition would be only £2.4 million in 2014-15 and £4.2 million in 2015-16. All this hardship for such a paltry saving. The disproportionate impact of the Bill on children cannot be overstated or justified. It is not the first time that austerity measures have had a disproportionate impact on children and families. In fact, as the noble Baroness, Lady Sherlock, told us, the Institute for Fiscal Studies found last year that, even with universal credit fully in place, taking together all the tax and benefit measures introduced or to be introduced between the beginning of 2011 and April 2014, families with children will lose a higher proportion of their income than either pensioner households or working-age households without children across the whole income distribution.
We have heard a lot this afternoon about the measurement of child poverty, but the IFS estimate of a growth in the number of children living in poverty of 400,000 between 2011 and 2015 and 800,000 by 2020, has been referred to more than once. The noble Lord, Lord Newby, said that we cannot set too much store by such predictions because we do not know what direction government policy may take. All I know is that the last time I heard, the Government intended to take a further £10 billion out of welfare. The Bill can only serve to increase the level of child poverty. Indeed, as the noble Lord, Lord Newby, acknowledged, it will add 200,000 to the number of children in poverty; 100,000 of them will be in working households.
Children do not have a vote. If they did, it is impossible to believe that they would be voting for the Bill as it stands.
My Lords, my name is also attached to all three amendments in this group. I thank the right reverend Prelate the Bishop of Ripon and Leeds for explaining the amendments.
First, I will cover Amendments 14 and 19 together. Households with children are much more likely to be affected by the Bill than households without children. Many families with children will be affected even when someone is working full time. A single person or couple with children obviously have much greater costs than those without dependent children. For this period of their life, the income they need to meet the basic living costs of their household is clearly greater. That means that the amount someone can be earning and still need extra financial support from benefits and tax credits stretches much higher up the income scale than for those without children.
The level of childcare costs and of rents—especially in the private rented sector— combined with the lack of a living wage means that people who can only find work at or near the minimum wage cannot escape from needing that extra financial support, for however much time they work. If they work more hours, they need more help with childcare. Many are already struggling to manage.
For example in a local paper in the north-east of England, where I live, Pauline Chambers, chief executive of Sedgefield and District citizens advice bureau in County Durham, said that the team had encountered levels of hardship not seen for 21 years. Telephone inquiries have increased by 100 per cent in the last two months, with many people struggling to pay for basic food and utilities. That view is repeated up and down the country. Julia Cornelius, manager of Luton CAB was quoted in a different paper. She said:
“Every day we see people who are struggling to keep a roof over their heads or put food on the table as wage squeezes, price rises and benefit cuts wreak havoc on household budgets”.
Those in work and on benefits gain little from their earnings increasing. A single person earning £250 a week who receives a £2.50 rise in their earnings will keep about £1.70 of the increase after deductions for tax and national insurance. If they have children, and so need to rely on benefits and tax credits, they will reduce as their income rises, so they will be left with a net gain of 10p from a rise in earnings of £2.50.
(12 years, 6 months ago)
Lords ChamberMy Lords, my noble friend Lord Alton of Liverpool has very clearly explained the amendment to which my name is also attached. I declare an interest in that I am in receipt of disability living allowance, but I do not have a Motability car. I have used the scheme in the past when I was first able to drive, because it was the only realistic and economical way that I could have become mobile.
At the briefing that was held on the PIP regulations on 22 January 2013 with the Minister, the noble Lord, Lord Freud, and the Minister in another place, Esther McVey, it was my understanding that the timescale for someone having to return their car if they were no longer eligible for PIP could be relatively short, perhaps just a matter of a few weeks. At the briefing, the noble Lord, Lord Sterling, the chairman of Motability, expressed a strong wish to do as much as possible to help people. However, I do not believe that Motability has too much room for manoeuvre.
I will not relive the debate around the 20 to 50 metres issue—I am sure your Lordships’ Chamber has heard enough from me on that matter. However, my concern is for those who have very expensive adaptations, which are what they require in order to drive—they could be left without an adequate method of getting around—and for people who live in an area where public transport is not terribly accessible. The short timescale between notifying someone of their car being removed and it being taken away could make life extremely difficult. Without some further protection, it could lead to chaos for many disabled people.
I am also concerned that there is perhaps not a lot of sympathy for some people in receipt of DLA. In the media, they are often referred to as people with a “free car”. The Daily Mail just today ran a cartoon which trivialised those who claim DLA, and compared a disabled person who was eligible for DLA to someone who had a blister on their foot. DLA helps a disabled person with the additional costs of disability—transport being significant—and the individual in many cases also has to pay a deposit to access the Motability scheme. If a disabled person was notified that their car was being removed, the amount of unused deposit would be paid back to the individual, but this could quickly be used to pay for extra costs such as taxis. As a comparison, the journey from King’s Cross to Westminster by tube is relatively easy and costs a few pounds. That is easy enough for someone who is not disabled, but if you are a wheelchair user, it costs £17 in a taxi—or that is what I paid today. It would be easy to see how quickly the money returned from a deposit could be spent.
If at a later stage, on appeal, it turns out that the person did indeed qualify for the appropriate level of support, then a new deposit would have to be found, ahead of the budgeted date, and they may not have that money available. A new car would have to be found and adapted, and the process therefore starts again. Of course, we do not know what the potential success rate at appeal is at the moment, but if people have at least the guarantee of running through to the end of their contract for a Motability car, this would give many a more adequate time to make other provision.
I have heard many people say, “Well, disabled people should just use public transport like many others”. I do not disagree with that. Public transport is okay but, in many cases, is not much better than that. London is perhaps one of the best cities in the country for disabled provision, and I declare that I am a board member of Transport for London. However, “patchy” is the best word that I can use to describe transport outside London.
My noble friend Lord Alton talks about spontaneity. He is absolutely right. Motability cars are essential for spontaneous trips as well as for getting to work or hospital, and for taking your children to school. As a wheelchair user, I have to book train travel 24 hours in advance; trains have only a couple of wheelchair spaces. I am always grateful if there is an accessible toilet on board, but the situation is not great if you are going from London to Darlington. It is not easy for disabled people spontaneously to travel by public transport. I know of at least one ongoing court case around disability access to public transport and I was informed this morning of one major bus company whose wheelchair spaces do not give priority to wheelchair users. There is so much work that needs to be done in this area.
A Motability car gives access to work and hospital, as I have said, at, I believe, a considerably lower cost than that of local authority or other services, or indeed of pushing the cost elsewhere if the car is removed. A too-hasty removal of vehicles from disabled people does not really protect those who need them.
(12 years, 7 months ago)
Lords ChamberMy Lords, it gives me great pleasure to follow the noble Baroness, Lady Browning, who makes some excellent points on independent living. When I was born in 1969 with spina bifida my parents were told that if I had been born even two or three years earlier, I would have been taken away, not fed and left to die. I know that we are now a long way from that treatment of disabled people, but many fear that we are returning to days of ghettoisation.
I declare an interest in that I am in receipt of DLA. I do not have a Motability car, but I know that it is a lifeline for many. It was interesting to hear the noble Baroness, Lady Thomas, talk about how important her car is to her. She made some excellent points and gave some excellent examples of fluctuating conditions which we must take into account. A debate on accessible —or rather inaccessible—public transport is for another time, but perhaps I may offer to take the Minister or the noble Baroness, Lady Stowell, when they have a little more time, on some bus and train journeys to show the scale of what we have to change in the United Kingdom. It is really not very good out there for disabled people.
I thank the Minister for being open to continued dialogue, for having several meetings with me and not least for his phone call this week, when he offered me some reassurances around the evaluation process. Like many, I am delighted that the words “reliably”, “repeatedly”, “safely” and “timely” will be in amended regulations. Moreover, their gradual implementation will give all of us in your Lordships’ Chamber an opportunity to play a part in the review. Some disabled people have been offered just a small beacon of hope by this.
I have to admit that I spent a great deal of time—in fact, right up to the deadline last night and beyond—considering whether this amendment should have been tabled as a fatal amendment, because fatalistic is how I and many other disabled people feel. I know that the noble Baroness, Lady Campbell, would have liked to be here tonight to support this debate, but the lateness of the hour makes it impossible.
I am disappointed with these regulations because of how they are going to affect real disabled people—not the media portrayal of this homogenous group of unknowns who are living the high life on benefits but disabled people who are struggling to survive and live independent lives. The Government have listened up to a point, but not as much as I would have liked. While the Minister has said, and will keep on saying, that his Government are merely providing clarity with these regulations, he will know—not least from my Question of 24 January 2013—that I was extremely disappointed by the consultation around the change from 50 metres to 20 metres. I accept that the time is now past, but we should have had the opportunity at the very least to debate it on the Floor of your Lordships’ Chamber. Parkinson’s UK has called the 20/50 metre change a “back of an envelope” calculation.
When the regulations are combined with the outcome of the Welfare Benefits Up-rating Bill, disabled people, and many others, will be in a significantly worse position than they are now. This is not protecting the most vulnerable. Enough is enough. Once these regulations pass, we have to leave them to bed in and give disabled people a chance to deal with them. I sincerely hope that what we have here—the clarity—is not a stepping stone to something that is harsher and that the 20 metres is not going to be the upper limit for claiming the higher rate of support at some point in the undefined near future. I would like some further reassurance on this from the Minister.
The noble Lord, Lord Kirkwood of Kirkhope, talked in a wider context about the evaluation process. The right reverend Prelate the Bishop of Worcester, who is unfortunately not in his place, also made his feelings clear on this subject. Several other noble Lords, too, have raised this issue. I look forward to feeding into the review. It is vital that we have a detailed review that we can take forward and that we learn from some of the things that I still do not believe are right.
When I have talked about these changes—disabled people losing their access to transport, having to stop work and being stuck at home, it has been suggested by some that I am scaremongering. Well, I believe that it is imperative that not just the people affected by these changes but the wider public understand the implications of what we all do here today.
I am reporting back what significant numbers of disabled people are telling me about their real fears, and that fear is around disabled people’s ability to live independent lives. The most stark figure that I have seen is from the We Are Spartacus report, which suggests that around 200 Motability cars per constituency could be removed from disabled people once these changes kick in. That could be just the tip of the iceberg, as not everyone uses their DLA—or PIP in future—to pay for a Motability car.
Disabled people are going to be hit by the cuts in so many ways, not just under PIP. I do not envy the onslaught on the inboxes and postbags of Members in another place when that starts.
Perhaps the time when what these changes mean will really hit home is when our first Paralympian has their car taken away. They are not workshy scroungers; they represent our country. It is not a day that I look forward to, but I wonder what the reaction then will be—what will happen when they are no longer able to get to training or competition.
All the way through the welfare reform legislation, we heard about protecting the most vulnerable. I and many others both inside and outside your Lordships’ Chamber will be watching whether that is the case with a great deal of interest and care.
My Lords, it is a great pleasure to follow the noble Baroness, Lady Grey-Thompson. She and other Members have spoken very powerfully about PIP, and I share their concern.
I want to speak very briefly about the implications for carers, to whom the Minister referred. He prayed in aid Carers UK’s approval at an earlier stage of the process. I think he would probably accept that if it had known then what it knows now, it would have been less approving. It issued a press release saying that it finds shocking the figures in the impact assessment, which appeared only days ago—we have been trying to get it for a long time. I think that it withdrew its approval at that point.
The Minister talked about only 5,000 fewer carers being eligible. It is not “only” for each of those 5,000 people. Each of them will be worse off. That 5,000 is nearly 7%, which is a minority but still a significant number. It is based on a static analysis. The Minister is always telling us that we should do dynamic analysis. Well, Carers UK has done what I would consider to be a more dynamic analysis of the figures in the impact assessment, and it suggests that by 2015 10,000 fewer carers will be eligible for carer’s allowance. Will the Minister comment on those figures? Will he also tell your Lordships’ House whether the Government will offer any transitional protection to carers losing carer’s allowance as a result of the introduction of PIP? Also in the spirit of the dynamic analysis, by 2015 I think that we are only about one-third of the way through the introduction of PIP. Do the Government anticipate further proportionate losses to those eligible for carer’s allowance as the process continues after that?
(12 years, 7 months ago)
Lords ChamberMy Lords, autism is, as the noble Lord points out, a really difficult area for people. It is difficult to understand and see sometimes, but we have a comprehensive training set-up for ATOS and Capita, which will be conducting the assessment. Clearly, each of those people will need to be approved by the DWP. Autism is among a group of quite difficult things to assess, and I personally take his point about its importance. The Government take his point and we will make sure that, when we give the approvals for that, it is one of the issues that is dealt with absolutely properly.
My Lords, I am very disappointed that this issue did not come to the Floor of the House for proper debate. At the very least, the change to 20 metres should have been clearly stated in the consultation documents. The lack of consultation with disabled people and all supporting evidence from experts in disability access as to what distance enables practical mobility and participation mean that there is a real risk that this issue will be open to judicial review. Is the Minister willing to take that risk?
My Lords, the change was made because there was great concern among disability organisations about the previous draft. The concern was that only people in wheelchairs would qualify for the higher rate—that was picked up by Parkinson’s UK, the Multiple Sclerosis Society, the Disability Benefits Consortium and the National AIDS Trust, among others. That is why the change was made. I admit that I would have preferred there to have been more consultation on the 20 metres, but there is no effective change in the number of people receiving higher-rate mobility allowance because of this change. I hope that noble Lords will accept my assurances on this. That change has made it clearer and simpler to operate this measure; it has not changed the numbers affected. Before we start reassessing people in 2015, we will have had a full independent review which will have gone through this issue, among others, by the end of 2014.
(12 years, 11 months ago)
Grand CommitteeMy Lords, I refer to the Secondary Legislation Scrutiny Committee’s comments at paragraph 13, in which it is pointed out, rightly, that the reduction will apply to,
“the total eligible rent for the dwelling, including any eligible service charges”.
Can the Minister confirm which service charge items will be eligible for universal credit? In consultation, these were different from those covered by the current housing benefit regulations, which provide a list of items that are not eligible. Will the revised regulations prescribe the range of eligible service charges and, in practice, reduce the numbers that may previously have existed? In particular, will the Minister clarify which service charges will be included in the definition of,
“services necessary to maintain the fabric of the accommodation”?
Specifically, will the maintenance of fire safety equipment, lifts, door entry schemes and other communal services be deemed necessary to maintain the fabric of the building and therefore be eligible?
Further, will the service charge currently associated with a furnished tenancy be eligible for housing benefit, as it is now? Finally, on concierge services, which include portering, security, caretaking, CCTV coverage and the cleaning of communal areas, will the service charges for these continue to be eligible? I hope they will because, if they become optional, many tenants will not be able to afford to pay and there will be reduced standards, impacting negatively on communal facilities and health and safety.
My Lords, like other noble Lords, I am concerned about the potentially disproportionate effect these regulations could have on disabled people. It is my understanding that all disabled tenants other than those who need constant overnight care will lose a percentage of their rent if they have more bedrooms than they need. The DWP equality impact assessment, which was updated last June, clearly shows the disproportionate effect that the size criterion measure will have on disabled tenants. Based on the Equality Act 2010 definitions of disability, some 420,000 of the total 660,000 households affected contain a family member with a disability, which makes the housing benefit regulations very much a disability issue, and one that is of great concern to a huge number of people. There is the discretionary housing payments fund for 35,000 tenants with homes adapted for wheelchair access, but that is a small mitigation in terms of the 420,000 tenants who are potentially affected. I feel strongly that long-established definitions of disability do not depend merely on the presence of adaptations or on the outward appearance of a functional disability. I am very concerned that disabled people will struggle with these measures.
My Lords, an enormous number of issues have been raised and I will do my best to deal with them. I know that this is an area of great concern to noble Lords. That was made clear during the process of what is now the Welfare Reform Act 2012, and I remind noble Lords that there were some government defeats on underoccupancy, which were reversed in the Commons. That is where we stand as the second Chamber when considering these regulations. However, as I say, I will do my best to answer the questions put to me as rapidly as I possibly can—in a fairly random order, if noble Lords will allow me.
I shall pick up some of the issues raised by the noble Lord, Lord McKenzie. Under the Localism Act 2011 there will be fewer tenancies for life, so both private sector and social sector tenants are less likely to have absolute security. On the assessment of the impact of the overall changes, noble Lords will be aware that we have produced impact assessments for each of them. It has been extraordinarily difficult to combine them because one is not sure on which basis assessments should be made, given all the other changes that are going on. However, people affected by more than one change have the DHP fund available to them. I should point out that when the fund is taken in its entirety, we are now looking at a very substantial amount of money. Next year, for instance, the full DHP pot will be running at £165 million, plus the localised social welfare fund will move over, which I think will be another £178 million. So a lot of money that is not ring-fenced for particular things is going to local authorities, so that they can look at the problems in their area to try to provide the appropriate support.
(12 years, 11 months ago)
Lords ChamberI agree with what the noble Lord has outlined as being part of the success of the Games this summer. I was very proud that my noble friend Lord Coe was at the Labour Party conference last week to pay tribute to Dame Tessa Jowell for everything she did as a Minister to ensure that we succeeded in getting the Games. He made the point very clearly that to build on the success of the Games—and as I said in my previous Answer this is not just about sport, although sport is hugely important and we need to build on it—we must continue that bipartisan and cross-party approach to make sure that we take all the available benefits.
My Lords, given the huge number who have been inspired by the extraordinary Olympic and Paralympic Games this summer, could the Minister explain how good access for disabled children to PE in schools and mainstream clubs can be ensured? This is not just about continuing to develop an elite pathway—in which I declare an interest—but about changing the whole culture towards healthier lifestyles.
I would like to pay particular tribute to the noble Baroness for all the vital work she did in commentating on the Paralympics—I know she also did so on the Olympics—and helping to ensure that the rest of us properly understood what was being achieved.
It is not just disabled people who are inspired by what was achieved at the Paralympics: the rest of us were, too. We need to build on the success of the Olympics by ensuring that all stages of the sporting strategy, which has been covered in great detail in a ministerial Statement which is available in the Printed Paper Office today, integrate disabled sport at all levels. I was particularly pleased to learn that when Sport England confirms its next round of investment in national governing bodies in December, it will require, for the first time, delivery of specific targets for participation of disabled people.