Housing Benefit and Disabled People

John McDonnell Excerpts

Wednesday 23rd January 2013 Westminster Hall

[Jeremy Lefroy]

I thank the hon. Gentleman for that intervention and I agree with him. Certainty is vital, which is why I am asking for clarification, and hopefully clarification in the terms used by the then Minister for disabled people in the House of Commons last year.

[John McDonnell (Hayes and Harlington) (Lab)]

I thank the hon. Gentleman on behalf of the whole House for pursuing this matter so consistently, and I congratulate him on having the benefit of having as a constituent John Turner, who I know is an assiduous campaigner on this matter.

Consistency across the country is also necessary. There needs to be monitoring by central Government of how the policy is being applied, because I think we will discover, as we are already discovering in some areas, inconsistency of approach by individual councils.

[Jeremy Lefroy]

I thank the hon. Gentleman for his intervention. He is right: in the two cases that I have outlined of Stafford borough council and South Staffordshire district council, we can already see some differences. Those differences have arisen not for ideological reasons, but because each council takes a slightly different approach. I am all in favour of local councils making their own decisions, but if we end up with a situation wherein some councils’ conditions for DHPs are drastically different from those of other councils, there will be serious problems. Of course, there is also the question of the different profile of housing stocks in different parts of the country, which has an impact on what the hon. Gentleman has said.

To continue discussing space, the size of the rooms also needs to be considered, but the rules specifically rule that out. A typical tenancy agreement may describe the bedrooms as “two plus one plus one”—in other words, one double bedroom and two single bedrooms. The single bedrooms are described as single for a reason—they are often very, very small, as I have seen for myself. Yet a family comprising, for example, a couple and two boys under 16 would be considered as under-occupying that type of property. The rules encourage that family to move to a two-bedroom property, which may itself be described as “two plus one” and where they would effectively be in breach of the tenancy. Surely, size of rooms needs to be taken into account when determining whether there is under-occupancy. I ask the Minister to reconsider the rules.

Of course, the family that I have just spoken about might not be able to find a such a property. In many areas, there is a shortage of suitable housing into which tenants can downsize, which is a serious problem, and it is probably the most significant reason why disabled people are by far the most likely to be affected by the changes to the housing benefit rules, given that, as the impact assessment stated, disabled people will tend to be in smaller households. There is nothing that disabled people, or indeed anyone else who is affected, can do about that situation. They cannot move into properties that do not exist.

--- Later in debate ---

[Esther McVey]

That is precisely why we are monitoring and evaluating the scheme, and we will continue to do so for two years to see what extra support might be needed. Of course we are watching and observing what is going on. [Interruption.] I will complete my comments here. However, we are committed to undertaking the independent evaluation of all housing reforms. The first report on the private sector is due to be published later this year, and work on evaluating the social sector changes will be implemented in April, with initial findings being available next year.

I trust that I have answered many of the questions that have been raised today. On other specific matters, I will get back to my hon. Friend. As I have already said, this is an important debate, and it is crucial that we closely monitor the situation. We are considering the most vulnerable people in society, and we have a commitment to them.

[John McDonnell]

I do not want the Minister to sit down thinking that there is no housing crisis out there. She referred to the predictions on housing benefit not coming true, but they have in my constituency. I have the worst housing crisis since the second world war. Nevertheless, she has mentioned monitoring, which is critical. Will she give an assurance that that monitoring will be published regularly, so that the House can receive and debate it? The points raised by the hon. Member for Stafford (Jeremy Lefroy) are critical. We must see what is happening on the ground, because a number of local authorities might want to work with Government to plan a transition over time. There will be a number of families for whom alternative private accommodation or social housing is not available and might not be available for years. An assurance that the monitoring will be published and that we will be able to debate it in the House would be helpful.

[Esther McVey]

The hon. Gentleman makes a good point. Of course, we have to monitor the situation, and I have confirmation from colleagues that the monitoring and evaluation will be made public. At the moment, there is much speculation about what might happen, but that is hypothetical. We do not know about that, but by monitoring closely, by introducing a discretionary fund and by working in a common-sense way with people on the ground who know best about local needs, we can get this right.

Welfare Benefits Up-rating Bill

John McDonnell Excerpts

Monday 21st January 2013 Commons Chamber

[Dr Whiteford]

I start by paying tribute to the work of the Scottish Campaign on Welfare Reform, which has done so much to draw attention to the impact of the measures in the Bill. It speaks volumes that more than 60 charities, Churches, other faith groups and trade unions have come together to speak with one voice to express their concerns about this heartless Bill and to support amendments that might mitigate some of its most adverse impacts.

The problem with what we are debating tonight is that an uprating cap of 1% is entirely arbitrary. It will inevitably cause hardship not just to those on low incomes but to those on middle incomes. I want to try to focus on amendment 7, which was supported so eloquently by my hon. Friend the Member for Brighton, Pavilion (Caroline Lucas). It is important that we try to restore a link to prices this evening. The problem with a below-inflation flat-rate uprating of benefits is that it represents a real-terms cut in the incomes and living standards of those who already live in the most straitened circumstances and will continue to do so for the next three years. Some 70% of those who are adversely affected are families with children and an estimated two thirds of the savings derived will be taken from the pockets of people in low-paid or part-time work.

Tonight, we have repeatedly heard, not least from the hon. Member for Gloucester (Richard Graham), that it is unfair, when people in work may be receiving below-inflation rises, not to impose a real-terms freeze in the uprating of benefits. That is a particularly facile argument, which we rehearsed on Second Reading. It goes without saying that whereas someone with a job with average pay would receive £200 or £300 for a 1% increase, depending on whether they were a man or a woman, a person on benefits of £70 a week would see an annual increase of £36. That probably would not even take me beyond the boundaries of my own constituency. It is wrong to pretend that 1% of not very much is equivalent to 1% of an average salary—or, indeed, of the very generous salary that so many people in this place enjoy.

As others have highlighted, there is a great deal of uncertainty in the Bill. If inflation stays in line with OBR predictions, the Government’s approach will result in a 4% real-terms cut in tax credits and benefits by 2015. That is a very big “if”, though: the OBR’s crystal ball has not been very effective to date and it has certainly not been good at predicting inflation—or, pretty much anything else. If inflation is higher than the guesstimates from the OBR, the impact on low and average-income households will be greater than we predict today. That is why we must preserve the link between social protection payments and the cost of living.

The Government’s distributional analysis of the impact of the autumn statement shows that next year the people in the five lowest income deciles will be worse off as a consequence of the cumulative impact of the Government’s changes to the tax and benefits system, and the least affluent will be the most affected. In contrast, three out of five people on average incomes and above will be better off. That exposes the truth of the matter: the Government have set themselves priorities and made choices that make those on low and average incomes pay for the tax breaks for the very wealthy. The poorer half of our society is being asked to carry the can for a financial crisis and a failure of political leadership that is not of its making, rather than seeing that burden shared across society.

The other key point that I want to make this evening—again, one that I made on Second Reading—echoes points made by the hon. Member for Gateshead (Ian Mearns) earlier today. It is that the measures of inflation that we use are not especially good at measuring the impact of inflation on lower income households. We know that low income households spend a far greater proportion of their resources on essentials such as food and domestic fuel. In the past five years, food prices have risen by around 30%, and the prices of some staple foods, such as potatoes, have risen by 40%. Projections for next year are for rising prices for a number of staple commodities because of poor harvests in north America and many parts of Europe, not least in our own country. Thrifty shoppers, as we know, are adept at switching to cheaper brands when money is tight, but when global prices are on an upward trajectory there is often nowhere to hide.

The other disproportionate expense for low income families is domestic energy, which is another area where prices have soared and fluctuated in recent years. The 20% increases in gas prices announced before Christmas are just the latest in a series of cumulative hikes in the price of fuel in recent years. There is snow on the ground outside today; that may be unusual here in London, but it is just normal winter weather in my constituency. In such conditions, families, especially families with young children, need to heat their homes adequately.

Although neither the consumer prices index nor the retail prices index captures the full impact of inflation on the lowest income households, the retail prices index includes some housing costs and is more likely to reflect the actual inflation that poor people experience. The Bill will cause tangible hardship, quantifiable in real money terms and in practical ways for people on low incomes. Hundreds of thousands of people who are disabled, who are carers, who are lone parents, will be particularly hard hit. It will hit families, whether they are in or out of work, dealing with the added expense of bringing up children. It will not cut the deficit—indeed, it will take money out of local economies and inhibit recovery at a time when we should be trying to get local economies going. On the basis of the Government’s own assessment, 200,000 more children will be pushed into poverty by this part of the Bill alone. We know that the long-term cost of child poverty cannot be measured only in financial terms. The long-term implications for children who grow up in deprivation are well quantified. The results are devastating and store up problems for the future, some of which we are still dealing with from the last period of austerity and the last poverty measures back in the 1980s and 1990s.

Dickens has been mentioned several times today. Whereas some speakers have talked of “A Christmas Carol” and the days of Scrooge, I was set thinking of “A Tale of Two Cities”, and indeed a tale of two countries. Today the Scottish Government announced an extra £5.7 million for advice services to support people who have to face the problems associated with these welfare cuts. It is a sad state of affairs when people are using food banks; it is a sad state of affairs when disabled people who, through no fault of their own, cannot persuade an employer to give them a job, are being pushed further into poverty and are being blamed and vilified for the state of the wider economy. People in Scotland have a choice and I look forward to the day they will get to make that choice in a referendum on their future governance, because never again will they have to take the Tory policies that they did not vote for.

Amendment 7 would make this deeply flawed Bill slightly less iniquitous and slightly less unfair, and would ensure that the very poorest families do not carry a disproportionate share of the burden in tough economic times. I urge Members across the Chamber to support us this evening when we push it to a vote.

[John McDonnell (Hayes and Harlington) (Lab)]

I apologise, Mr Amess, for persisting in seeking to speak at this late hour. I sat through the five hours of Second Reading and time did not permit me to be called then, and I have tabled an amendment tonight which we will not reach. One could become paranoid at times. I wanted the opportunity to set out my views briefly on this core element of the Bill for my own constituents.

I will vote for every amendment that seeks to ameliorate the Bill. That includes the amendments that have been tabled from both sides, including by my own party. I feel there is a moral imperative to do so. There was a consensus for a time in our country about how we dealt with welfare benefit upratings: they would increase on the basis of either earnings or inflation, whichever was the higher. That consensus was achieved because there was a moral commitment to protect the poorest in our society—in a civilised society. It went alongside a steady rise in wages at the time. What we have seen recently—it has impacted on my constituents particularly—is wage cuts and wage freezes across the public sector and in some parts of the private sector. I opposed the wage freeze in the public sector that was supported by my own party.

In the past 12 or 15 months we have seen a succession of measures—more than a dozen key measures—that have cut the income of my constituents. The Bill is the last straw. People in my constituency are suffering and will suffer more as a result of this measure. As I mentioned in a recent debate in Westminster Hall, there is a gulf between the views and experiences of some Members of the House and the experiences of many of our constituents and the way that they suffer. I thought that might be particular to my community—a working-class multicultural community that is taking a battering at present—but I looked at some of the statistics in the briefings that were prepared for this debate.

The Government’s own household survey of those living below the average wage identified 11% of families in that category who cannot keep their homes warm. I looked at the Save the Children survey, which found that 14% of children do not have a warm coat this winter. I looked at the survey undertaken by Contact a Family, the charity that works with families who care for disabled children. It was an extensive survey which found one in six families going without food, one in five without heating, one in four without the specialist adaptations that they need, and a third taking out a loan to pay for food and heating.

I looked at the Zacchaeus 2000 Trust work that has been undertaken by the Centre for Research in Social Policy, which demonstrated how the basic income from benefits has decreased in relation to the inflationary impact on basics such as food, heating and rents. I also looked at the work it had done on nutrition for expectant mothers and the concern, which was echoed some time ago by the Minister himself, about the incidence of poor maternal nutrition resulting in low birth weight.

The right hon. Member for Ross, Skye and Lochaber (Mr Kennedy) expressed his fear that this was, effectively, dog-whistle politics, that the poor were being used as a political football between the parties. I share those fears. I wish I did not. That was the tenor of the debate that was opened up in the budgetary statement by the Chancellor of the Exchequer—the reference to curtains, and the debate that has gone on in the media about skivers and strivers. I have more faith in the British people. I do not believe that they accept the terms of that debate. I think the British people have a sense of fairness and a sense of moral commitment to people less fortunate than themselves. That is why I do not think there is majority support for the measure. I think that, as a result of this debate, understanding is overcoming prejudice. Prejudice will be defeated by humanity; there will be an upsurge of popular support for those of us across the House who will oppose this legislation tonight and are calling for the Government to think again about the whole trajectory of their welfare cuts.

My right hon. Friend the Member for Birkenhead (Mr Field) has done immensely important work about interventions to tackle deprivation. There is a whole range of them, and they are not just about income. However, his work has found that those interventions are impeded from the outset if people are struggling simply to put food on the table, heat their homes and have some kind of decent standard of living.

Clause 1 is a major setback for large numbers of people right the way across our country. It undermines their standard of living and diminishes the whole of our society. It will have repercussions for a long time to come, unless we defeat it tonight.

Atos Work Capability Assessments

John McDonnell Excerpts

Thursday 17th January 2013 Commons Chamber

[John McDonnell (Hayes and Harlington) (Lab)]

Someone said that what we are debating is a party political issue. Let me be clear: I opposed the system when it was introduced by the last Government and I oppose it now—for the same reason. I see it as a brutal attack on the weakest and most vulnerable individuals in our society and an exercise by private companies to profiteer at those individuals’ expense.

I started raising the issue in Parliament early on. My first constituency involvement was like that of many other hon. Members: it involved someone who was mentally ill, went for the assessment and had a nervous breakdown. That had an impact on the whole family—the mother, in particular.

I was then contacted by a range of organisations, which came together and produced the Spartacus report. I urge Members to read it. In the last debate on this issue, in Westminster Hall, we read some of its case studies into the record. They are horrendous examples of human suffering and what can only be described as abuse by the system itself.

I also refer Members to Calum’s List, which has a website. It is a list of people who have died, including by suicide, as a result of, or where there has been a contribution from, the loss of benefits. The first example on the list was that of Paul Reekie. Some Members may have known Paul, an award-winning writer and poet in Leith, Scotland. He did not leave a suicide note, just two letters on the table beside him. One was about his loss of housing benefit and the other was about his loss of incapacity benefit. He died.

The other example is that of Mark and Helen Mullins from Bedworth. They could not access their benefits. They were walking 10 miles a day to a Salvation Army soup kitchen. They committed suicide together because they could not access their benefits. Read Calum’s List, which has example after example of the brutal effect of the system.

This is at least the sixth debate that we have had on the issue. The concern expressed by Members about an issue of public administration in all those is unprecedented in recent decades. There is example after example of human suffering on a scale unacceptable in a civilised society. That is why 117 Members of Parliament have so far signed our early-day motion calling for the scrapping of the system.

I have read Mind’s briefing for today’s debate and I urge other Members to do the same. It has put forward what is wrong with the system. Yes, it has recommended improvements, but one of the key factors coming out of its survey of people facing the work capability assessment process was that 51% of them said it made them have suicidal thoughts. Any system involving that level of risk is irretrievable and unreformable. That is why I believe it should be scrapped and why the British Medical Association has said it should be scrapped.

I say the following, and I do not say it lightly: we now know that the system does not work. We know the human suffering that is occurring. The responsibility is now on us to do something about it. We will be to blame for every injury, harm, suicide and other death as a result of the system if we do not scrap it now and bring in something that is fair and based on proper medical knowledge—assessment by a person’s own GP, reinforced by expertise. We need something that gives advice and emotional support for people when they go through the system, not something that leaves them at risk.

[Ian Lavery]

rose—

[John McDonnell]

If my hon. Friend does not mind, I shall not give way as other hon. Members want to speak.

I conclude by saying that we all have a responsibility to say, “Let’s end the system now, start again and make something fair.” We will be to blame for all the injury and harm if we do not.

Welfare Reform (Disabled People and Carers)

John McDonnell Excerpts

Tuesday 18th December 2012 Westminster Hall

[John McDonnell (Hayes and Harlington) (Lab)]

Sometimes our role as MPs is to bear witness, so it is important that the words spoken by people with disabilities and their carers are put on the record. Professor Peter Beresford of Brunel university, working as the chair of Shaping Our Lives, the national disabled people’s and service users’ organisation network, undertook a massive survey of people with disabilities and their carers. The Spartacus report was published earlier this year, and has now been revamped. I just want to quote a few brief statements from people with disabilities. This is one person’s family member:

“John is so severely disabled he has to wear nappies and is fed through a tube. He is blind and deaf, cannot speak, suffers frequent seizures and requires 24-hour care. But he has now been told by a Government decision maker that he is ‘capable of work’ — and that he is no longer entitled to benefits. Family members have contacted officials who say that an appeal against the decision will have to be lodged.”

What happens when those appeals take place? Let me quote a person with a disability:

“It’s like doing a crime. I am a human being who needs additional support but here I am facing a panel who are making a decision on my life. I am tired of fighting officials who seem to think they know more about my disabilities and needs than I do. It now makes me feel ashamed of who I am. I am being punished for being disabled and feel powerless.”

What happens in the assessment itself? Here is a quote from a wife:

“I can honestly say there are lies that go into that assessment. I do shorthand and I took down word for word my husband’s whole assessment. What actually came back was practically the opposite of everything he said.”

Let me quote another claimant:

“They are now ordering claimants (and their companions) to surrender any notes they have taken during the interview. Before the assessment even began, both I and my companion were warned that we had to first agree first to hand over our notes at the end of the assessment. We were told that the notes would be photocopied and stored on a database. I was told that the penalty for refusing to agree to this condition was the immediate termination of the assessment.”

The implicit warning was that they would lose benefits.

What happens in the administration of these benefits? I will give another example. The client’s husband is in hospital in a coma. He was sent an ESA50 form. The client contacted the Department for Work and Pensions to explain the situation, and was asked to obtain a letter from the hospital confirming that the client’s husband was in a coma. The client did so, and sent it to Atos rather than the local benefit disability centre. The client was then sent a letter saying that they had failed to return the appropriate form and the client’s husband was no longer entitled to the benefit.

Let me save the final words for Karen Sherlock, 44. She was put in a work-related activity group. She was required to attend interviews. She suffered from a whole range of conditions. Her husband Nigel said it was a disgrace that she was refused benefits. Last year, she lost the long process of appeal against the decision. In April 2012, as a result of the time-limiting of employment and support allowance to one year, she lost her benefits. She won her appeal a few weeks later and was finally put in the support group. She died eight days later, on 8 June.

Read the Spartacus report. It gives example after example of the inhumane treatment of people with disabilities and their families. It shames any Government to treat people in this way.

Work Capability Reassessments

John McDonnell Excerpts

Wednesday 5th December 2012 Westminster Hall

[Sheila Gilmore (Edinburgh East) (Lab)]

It is a pleasure to serve under your chairmanship, Mr Hood. Everybody here is probably familiar with some of the issues relating to the employment and support allowance and the work capability assessment. Between the introduction of the assessment in October 2008 and August 2011, 1.15 million new claimants were assessed and 687,000 were declared fit for work. Of those, 102,500 successfully appealed their decision and were awarded ESA. That means that 9% of all ESA assessments have been overturned. When we look at assessments leading to fit-for-work decisions, the figure rises to 15%. Although the proportion of decisions overturned has started to fall, the overall number still remains extremely high.

Those figures do not include all the incapacity benefit claimants currently being migrated to ESA, a process that started last year and is due to be completed in 2014. The figures published recently cover claims only after appeals have been taken into account—they have been published on a different basis—so we have no data on how many claimants in the migration are originally declared fit for work and then appeal, and how many of those appeals are successful. Although that is not precisely the subject of this debate, I hope that the Minister will see to it that we have more comprehensive and comparable data in future.

The number of incorrect assessments and successful appeals is still high. Like many of my colleagues, I have been considering a number of different aspects of the issue. Earlier this year, I secured a debate here in Westminster Hall on the work capability assessment. On that occasion, I focused on the recommendations for new mental, intellectual and cognitive descriptors drawn up by Mencap, Mind and the National Autistic Society. Although the descriptors are certainly not the only issue that needs addressing, they could have gone a long way to improving the assessment process.

Professor Harrington approved and submitted the descriptors to the Department for Work and Pensions in spring 2011. It is frustrating that officials are only now getting down to assessing properly whether the descriptors would improve the WCA, and we will not get the results of that so-called gold standard review until next summer. There will have been more than two years of delay since the proposals were published.

[John McDonnell (Hayes and Harlington) (Lab)]

I preface my remarks by thanking my hon. Friend for the work that she has done on the issue over a long period. Is her experience the same as mine? The largest number of constituents with whom I deal who have lost their benefits, and those with the most distressing cases, are those with mental health problems and those on the autistic spectrum.

[Sheila Gilmore]

I thank my hon. Friend for his intervention. That is the case. There is a flaw in how the original test was drawn up if it is not accounting properly for those types of condition. That is why it needs to be examined.

--- Later in debate ---

[Julie Hilling]

What concerns me is those people who will always have such a condition or who have a progressive condition, meaning that they will only get worse. What about them? To continue to reassess them and put them through that stress feels absolutely wrong—I cannot think of a better word—

[John McDonnell]

Cruel.

[Julie Hilling]

Cruel, yes. Why are we doing that to that group of people who will never get better?

--- Later in debate ---

[Esther McVey]

I thought I had dealt with that a little earlier when discussing the decision makers and how there is the right to look at when they feel it is appropriate to call someone back, whether three, six, 12, 18 or 24 months later. That obviously has to be right for all, whether the person assessed or the system as a whole. As the hon. Lady knows, we have reviewed the process not once, not twice, but three times under Professor Harrington. Each time recommendations have come back, and we have implemented them, so significant changes are under way.

As the hon. Lady mentioned at the start of the debate, we inherited the situation—the system was put in place before this Government—but we are trying to get it right, we have brought in changes and we will continue to do so until all parts of the House and, most importantly, those being assessed, feel we have got it right.

In conclusion, I echo Professor Harrington who has made it quite clear that the work capability assessment, designed as the “first positive step” towards work, is the “right concept” for assessing people who need our support. He also recognised, however, that there was a need to improve it, which is why we accepted and have largely implemented more than 40 recommendations made in his first two reviews.

Following our reforms, twice as many people go into the support group now as when ESA was introduced. The proportion of people with mental health conditions being awarded ESA has risen from 33% to 49%. I know the hon. Member for Edinburgh East asked specifically what was happening in that regard, and I hope that she can take some comfort from how clearly we are looking into the matter and at how the numbers have changed.

In response to the hon. Member for Ashfield (Gloria De Piero), who mentioned one of her constituents and a physiotherapist, the assessment looks at the function and not the condition. Physios are experts in this area and have comprehensive training, especially on mental health. They are only approved and allowed to be assessors if they have the necessary skills.

As for the critics, Professor Harrington made it clear in his third review:

“All they call for is a scrapping of the WCA but with no suggestion of what might replace it”,

and

“to recognise that things are beginning to change positively in the best interests of the individual would be helpful.”

Debates such as this improve the situation.

[John McDonnell]

Will the Minister meet some of those critics, such as Disabled People Against Cuts or Black Triangle, which has been occupying DWP offices and demanding meetings with Ministers?

[Esther McVey]

I am more than happy to meet them, although they might not wish to as I am not the Minister responsible. I will forward the invitation and I am sure, diaries permitting, that he will do so. I hope that today has been constructive and I thank the hon. Member for Edinburgh East for bringing forward the debate.

Question put and agreed to.

Atos Healthcare

John McDonnell Excerpts

Tuesday 4th September 2012 Westminster Hall

[John McDonnell (Hayes and Harlington) (Lab)]

Yesterday, I met constituents who have gone through the system. They call themselves victims of Atos, and I promised them that I would briefly set out the experience that they described. The assessment was exactly as others have said. Applicants are often met by an assessor with no expertise or specialist knowledge of their condition; it is a tick-box exercise—my constituents completely agree with the BMA about that. Despite the Harrington recommendations for improvements, the test bears no relationship to the real-world challenges that people with disabilities face. There is no recognition of fluctuating conditions, as has been said—particularly in connection with mental health. The procedure largely ignores the assessments and advice of applicants’ own GPs.

[Mr Philip Hollobone in the Chair]

In addition, the process even ignores previous Atos assessments. A constituent of mine was employed by Royal Mail, which used Atos to assess capability for work, and was assessed as not being capable. My constituent then retired and applied for benefits, and following another Atos assessment was found capable of being re-employed in the same type of work.

The fly-on-the-wall exposés by television programmes have exposed the pressure exerted on assessors to fail people. If people are assessed as capable of working correctly, they are then regularly harassed with challenges that they are unable to cope with, and they lose their benefit as a result. If they succeed at the assessments, they are harassed with reassessment after reassessment. We have heard the appeal statistics, but most of my constituents must wait six months or longer for an appeal. Those who have support—and I do support them; I represent people now at appeals—win. However, there is a lack of support, because of cuts in local government support for advice centres, and Government cuts so many people are not supported.

The result? To be frank, it is financial hardship. People are living in poverty because they lose their benefits. In addition, there is emotional stress, breakdowns, and, as Mind points out in its briefing, self-harm and suicide. Why do the Government defend the company? Why have they awarded it the personal independence payments process?

I share the disgust of many disability groups about Atos being allowed to sponsor the Olympics. That is a disgrace. I support Disabled People Against Cuts, and the Black Triangle campaign, which organised the protest against Atos sponsorship. I am calling for an inquiry into violence against people with disabilities who protested last week at the Department for Work and Pensions, and elsewhere. A few months ago, I tabled an early-day motion calling for Atos’s contract to be withdrawn, and for the establishment of a new system; 103 hon. Members have signed that early-day motion. Surely after that, and following debate after debate and the protests on the streets, the Government must reassess the role of Atos, and establish a new system based, as my hon. Friend the Member for Stalybridge and Hyde (Jonathan Reynolds) suggested, on reputable, fair and equitable criteria.

[Several hon. Members]

rose—

Specialist Disability Employment

John McDonnell Excerpts

Tuesday 10th July 2012 Commons Chamber

[Maria Miller]

My hon. Friend will know that 29 factories were closed under the previous Administration, and it was an error not to put more support in place for people affected. I am sure, if Labour did it again, it would do things differently, because it became apparent very early on that, of the 1,611 disabled people who left factories as a result of the modernisation redundancy programme, very few got into work. However, given the package that we have put in place today and the record of Remploy employment services over the past two years—they have helped 35,000 disabled people to get into work—we are living under a very different set of arrangements.

[John McDonnell (Hayes and Harlington) (Lab)]

The Minister referred to this as a difficult decision, but for the Remploy workers watching this debate it is a tragic decision. She has just mentioned the numbers who left work last time who have never been employed since. How many can she guarantee will be in secure employment in 12 months’ time?

[Maria Miller]

I can guarantee that by using the money differently we can help more disabled people into work. As a result of today’s measure, some 8,000 disabled people can get into work who would not have had that support otherwise.

Disability Benefits and Social Care

John McDonnell Excerpts

Wednesday 20th June 2012 Commons Chamber

[John McDonnell (Hayes and Harlington) (Lab)]

This has been a helpful discussion about policy, but the best policy is informed by our own experience of what is happening in our own constituencies. I want to put on record what my constituents are experiencing at the moment. In addition to surgeries, we now have an open-door policy four days a week, and in some ways I wish that we had not. Sometimes we want to hide, because we have been inundated with people who have problems with lost benefits.

I also help with disability living allowance appeals. This is not just about legal aid cuts; it is about the cuts overall. We have lost advisers in the area, so I represent people at DLA appeals, and we mainly win. That is not because of my articulateness, as you can tell; it is because once those presiding over the appeal see the people concerned, they can see that they have been wrongly assessed. Another problem is that people’s appeals are taking so long to arrange, once they have lost their benefits. They can wait for up to six months for their appeal, having lost their benefit, which is causing immense problems.

On the work capability test, I opposed the privatisation of the process and the bringing in of Atos, but if we are going to have a private company doing this work, we should at least be able to understand the contract involved. We should at least be given open access to what has been agreed with that company in our name, and be told what level of performance it is supposed to undertake. I am not sure what other Members have found, but when people come to see me, having gone through an Atos assessment, they tell me that they feel degraded, shamed and abused. I raised the point about suicides with the Secretary of State some weeks ago, and I was not exaggerating. Other Members will have experienced this as well. People come into my constituency office and tell me: “I can’t take any more of this. I’ve had enough.” I am really worried by the anecdotal reports of individual suicides, and it behoves the Government to monitor the situation and assess what is happening on the ground.

People have had enough of being called scroungers. We have seen the increase in hate crime towards people with disabilities because of the atmosphere that has been created by the media and by some politicians using loose language on this subject. Those people feel shamed, simply because they are claiming the benefits to which they are entitled. That is the experience in my constituency office at the moment, and it just goes on.

This is carers week. Other London MPs will also tell the House about constituents who have gone on to personal budgets, and that those budgets do not cover the wages of the carers whom we want to care for our people. It is virtually impossible to pay enough to get someone to stay overnight. Most of these arrangements have now been privatised, and people are getting a different carer coming in every day. The relationships with the carers have been broken down by this process.

Respite provision is now critical in my constituency, but what is my local Conservative council doing? It is closing the centres where people used to get respite. This is all part of the modernisation programme. It is closing three centres and modernising one. Of course, two of the centres that are being closed completely are in the most needy area of my constituency; a working-class area. It just goes on.

After the Southern Cross debacle, the company was broken up and some of the residential homes were given back to their original owners. I give this warning now: that arrangement is beginning to break down already, because the management in those individual homes are not competent to manage the process of disaggregation and the long-term planning of care. Why? The local authority role in providing those services has been so undermined and the resources have been cut, even for the management of those individual contracts. We are facing a crisis. A number of people are trapped in this whirlpool of deprivation, and it will be almost impossible to pull them out if we continue with these policies.

I went to the GMB conference last week, spoke to the manufacturing section and met many Remploy workers. They are now absolutely desperate, and they feel completely betrayed. They might not have agreed with the Sayce report, but at least there was a process there that they saw they were working through. That has now been torn up and everything in that report has been reneged upon. They feel absolutely vulnerable, with some saying, “We will not work again.”

In the early 1980s, I sat on the first committee established to remove restrictions against people with disabilities. It was called CORAD— the Committee on Restrictions against Disabled People. I was nominated to sit on it by the TUC. It took us 25 years before we secured anti-discrimination legislation. I congratulate the last Government on achieving that. I was one who wanted to mainstream employment. In fact, I was an ardent advocate of that; over the years, experience taught me that we always need an element of supported employment. That is what Remploy does well. What does it do badly? As my hon. Friend the Member for Swansea West (Geraint Davies) argued, the management have been abysmal. All the workers are saying is, “Listen to us; we can manage these resources more effectively than the current management, but we also need the support of the Government.” As my hon. Friend said, what happened to the commitments about public procurement that we were promised over the last two years? If it had not been for the individual efforts of people such as my hon. Friend and others, as exemplified today, no procurement would have happened because the Government have done nothing.

Finally, the Government should not think that this issue or these people are going to go away because they are not: these people are mobilising. We now have a disability movement in this country of which we have not seen the equal before. Black Triangle occupied Atos offices in Scotland; members of DPAC—Disabled People Against Cuts—chained themselves in Trafalgar square. These people are not going to go away. They will be in our face—and rightly so. I will support them, including if Remploy workers opt to buy their factories.

Oral Answers to Questions

John McDonnell Excerpts

Monday 23rd April 2012 Commons Chamber

[Chris Grayling]

That is of course our approach right across ESA. We do not apply a one-size-fits-all approach. Those with the potential to return to work will receive help to do so, those who will be able to return to work in due course will get support and guidance along that journey, and those who cannot be expected to work will receive long-term unconditional support in the support group. That is absolutely how the Government should seek to work.

[John McDonnell (Hayes and Harlington) (Lab)]

T7. Members throughout the House, including Ministers, have emphasised the importance of the care that must be taken in dealing with people with mental health problems as they approach their medical and capability assessments, particularly if they lose benefits. Some anecdotal evidence is emerging of suicides taking place among people who have lost benefits. Have the Government explored any of the coroners’ reports of cases in which there has been a reference to the loss of benefits as a contributory factor, and what lessons have been learned?

[Chris Grayling]

We will always examine something like that very carefully indeed when it happens. So far, my experience is that the stories are usually much more complicated, but that does not mean we are not doing the right thing. I passionately believe that we should help such people, particularly those with mental health problems. I have met people who have been out of work for years and years with chronic depression, but whom we are now beginning to help back into work. We have to be careful, and we examine such situations carefully when they arise.

Employment Support

John McDonnell Excerpts

Wednesday 7th March 2012 Commons Chamber

[Maria Miller]

I am very happy to give my hon. Friend an undertaking that we will want to work together with individuals in factories that are in wave 2 of the process, because we want to find ways for those organisations to succeed. However, he should be aware that we are indeed able to support disabled people into employment, through the employment services programme, so although he rightly says that it can be difficult for people to make that transition, it is not impossible. With the right support, people can move from segregated factories into mainstream employment.

[John McDonnell (Hayes and Harlington) (Lab)]

The Minister referred to the £2,500 of transitional funding for the workers, and I note that that is an average figure. If it is to make up the difference between benefits and the wages that the workers would have earned, it will last about six months. If they are still unemployed after that time, will there be further transitional assistance? If not, some of those families will plummet into poverty.

[Maria Miller]

I am sure that the hon. Gentleman knows that the money I am talking about will be on top of the quite significant provision that we make for redundancy in the process.