Disabled People

Debate between Ian Mearns and Yvonne Fovargue

Wednesday 10th July 2013 Commons Chamber

[Ian Mearns (Gateshead) (Lab)]

I am grateful to my Front-Bench colleagues for choosing to debate this cause, which I brought to the House’s attention in a Westminster Hall debate at the end of last year, on 18 December, when I urged the Minister for disabled people, the hon. Member for Wirral West (Esther McVey), to conduct a cumulative impact assessment on the real-term effects of welfare reform on the most vulnerable people in our society. I am sure she will remember that very well-attended debate.

The Chancellor and the Prime Minister have repeatedly lectured us about the need for fairness and said that we are all in this together. However, it is clear that it is not the richest, most powerful and most able in our society who will pay the costs of this Government’s cold calculation and uncaring disregard. Instead, it will be the least able, the most vulnerable and the least powerful—the disabled—who will pay the price.

We call for a cumulative impact assessment because a range of cuts and changes is taking place at the same time, and we need to assess their cumulative effect. I am sure Members have read, or at least heard of, the report “The Tipping Point” by the Hardest Hit campaign, which concluded:

“Many disabled people feel that they are living on the edge, and that the loss of even a small amount of income could tip their already complex lives into greater dependence and insecurity.”

That has been brought into stark relief by campaigns outside this House by organisations such as the National Association of Citizens Advice Bureaux, Mind and Carers UK, and the WOW petition and Pat’s petition. They have brought this to our attention, although I think Members already knew about it because in our surgeries we and our caseworkers are dealing with it in person, on the telephones and via e-mail on a daily basis.

“The Tipping Point” study discovered that disabled people and their families are struggling to make ends meet and feel increasingly nervous about the future, and because of that the Government need to act urgently to arrest disabled people’s slide into entrenched isolation and poverty. Members have heard of Pat’s petition, which had been signed by 62,500 people at the last count that I saw. It called on the Government to:

“Stop and review the cuts to benefits and services which are falling disproportionately on disabled people, their carers and families”.

I ask the Government not only to listen, but to act.

Let us look at the elements of welfare reform that are having an impact on disabled people, and their carers and families. The introduction of the universal credit will result in 2 million households seeing a drop in their income, with disabled people being among those worst affected. The DWP’s own equality impact assessment from November 2011 predicted that disabled households would lose £37 a week, compared with a figure for non-disabled households of only £26 a week.

Another major change is the introduction of the personal independence payment. Last year, in a Westminster Hall debate, the Minister with responsibility for disability matters said that 160,000 claimants would get a reduced award and 170,000 would get no award—that was before a single individual assessment had taken place, so it was a very mean prediction. That announcement concerned me greatly, given that the Minister already had figures on those who would get a reduced award and those who would receive no support before any assessments had taken place. Surely that suggests that the Minister is capping the number of those on PIP, rather than basing that benefit on individual need.

The issue of contribution-based employment and support allowance is affecting many of my constituents. The time limit of 365 days—one year—on those in the work-related activity group, and its retrospective implantation, is forcing many disabled people on to jobseeker’s allowance, given that there is no magic tree spouting jobs these days in places such as north-east England. As I am sure the Minister is aware, unemployment there is going up, not down, yet we seem to be expecting more people with disabilities, or profound disabilities, to get into the world of work, where jobs are already scarce.

Let me give an example from my constituency. It concerns a lady suffering from bronchial pulmonary dysplasia, who was too ill for a heart and lung transplant and who had been on steroids for 37 years. She had brittle bones—osteoporosis—kidney failure and was unable to walk. She regularly had fractures, she had osteoarthritis and she was diabetic. She was initially placed in the work-related activity group and told she would need to find work. As I am sure hon. Members have already fathomed out, she was housebound and bedridden. Thankfully, intervention from my office and other support groups showed that the DWP had clearly made a mistake and it was forced to retract that initial assessment.

I do not wish to talk extensively about the bedroom tax, but so many people who face it do not have spare rooms. These rooms are used to store specialist equipment or are for a family carer, often a spouse or a partner, to sleep in; if those rooms were not available, they would not get that much-needed sleep. We need to remember that those carers save the Government about £100 billion a year, because they take on the role of caring for those disabled people almost exclusively.

Before I move on, I need to talk briefly about Atos, its shocking assessments and the assessment process. I would need all day to discuss that, but I shall just say that the citizens advice bureau in Gateshead has undertaken 1,400 appeals on behalf of people, 1,200 of which have been successful.

[Yvonne Fovargue (Makerfield) (Lab)]

Does my hon. Friend agree that it is not just the welfare reform assessments that are affecting the people with disabilities, but the legal aid changes, which meant that people can no longer appeal against these welfare benefit decisions with help from the CAB?

[Ian Mearns]

I very much welcome my hon. Friend’s intervention, as she describes exactly why we need this cumulative impact assessment. So many different strands to this debate are having an impact on disabled people, and their carers and families.

Before I finish my contribution, I want to refer to a website, calumslist.org, which shows how many suicidal deaths have been directly attributed to welfare reform by a coroner’s court. The total so far is 33. When we had the debate in Westminster Hall in December the figure was 24, so that cost is going up by the month. We need to ensure that the assessment criteria take proper account of the full range of barriers faced by people with disabilities and health conditions, making the assessment and reassessment processes as simple, transparent and proportionate as possible and ensuring that robust evaluation and monitoring processes are in place. We need to bring all the strands together—the bedroom tax, housing, the welfare reform and the changes to legal aid. All those things will have an impact on people’s capacity to deal with the real changes occurring in their lives day by day. I ask all Members to support the motion.