UN Convention on the Rights of Persons with Disabilities

Dan Carden Excerpts

Wednesday 20th June 2018 Westminster Hall

[Dan Carden (Liverpool, Walton) (Lab)]

In Liverpool, when a constituent tries to appeal one of the rulings of an assessment centre, there is a nine-month wait at Liverpool tribunal services. The case that I raised with the Prime Minister of my constituent Anthony has been resolved individually, but thousands of constituents are affected.

[Rosie Duffield]

I have heard of similar waiting times, too. It is really distressing and adds to all the trauma that has been going on. I will give an example: Julius Holgate, who is a double leg amputee, won an appeal. The Department for Work and Pensions told him that he was fit to work because he could

“climb stairs with his arms.”

Because he lost his benefits, Julius resorted to selling his belongings in order to survive. The DWP claims that this was a clerical error, but in reality, it was an error caused by a lack of humanity.

Article 28 of the UN recommendations calls on the UK Government to ensure that all eligibility criteria and assessments for PIP, employment and support allowance and universal credit are in line with the social model of disability. When is that being done? Despite the repeated, serious and notorious assessment failures by Atos and Capita—the outsourced companies that conduct the assessment—the Government have renewed their contracts to run the assessment process for two more years. These organisations have repeatedly failed to meet their target of 97% acceptable tests, and 100,000 people have won appeals against their assessments. How much is this flawed system costing the Government? If we ignore the human element just for a second and question how much each reassessment and court challenge costs, surely we can agree that this money would be better spent on rolling out decent provisions for the disabled and on remedying those affronts to human rights by introducing a holistic, bespoke assessment service that includes a home visit.

The PIP assessment system is highly traumatic and often misassesses; in January of this year, it was ruled by our own courts to be severely in need of remedy and review. In January this year, the High Court ruled that the PIP system is “blatantly discriminatory” against people with mental health conditions. That criticism is echoed by many mental health and disability organisations. I am sure we all appreciate that not all wounds and maladies are necessarily physical and observable. A single-day assessment is therefore a ludicrous way of properly gauging whether a person is in need of financial assistance because of mental health conditions.

It is high time that this Government turned their focus away from tax breaks for bankers towards a system of disability welfare that is, at the very least, in line with basic human rights outlined by the UN. The convention needs to become part of UK law. The UN committee noted last year that there had not been a full review of the UK’s laws and policies in the light of the convention. There is not enough information on what the UK is doing to stop disabled people being negatively affected as the UK leaves the EU. A statement by Inclusion London explains:

“Disabled People’s organisations are seriously disappointed by the Government response and its failure to adequately take on board any of the UN inquiry recommendations. This response brings into question the Government’s commitment to the progressive realisation of Disabled people’s rights.”

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[Dan Carden (Liverpool, Walton) (Lab)]

It is a pleasure to serve under your chairmanship, Dame Cheryl. I congratulate my hon. Friend the Member for Canterbury (Rosie Duffield) on securing such an important debate.

My hon. Friend the Member for Oldham East and Saddleworth (Debbie Abrahams) hit the nail on the head in her speech: the report is a condemnation of the Government. It cannot be emphasised enough just how damning the 2016 UN report is. Conservative Members can talk all they want, with weasel words, about the system getting better, but we know that that is not the case—certainly not in constituencies such as mine in north Liverpool, which is one of the most deprived in the country. I want to tell the hon. Member for Henley (John Howell) that we have had our two jobcentres closed. The council has worked so hard—tirelessly—to develop co-location plans and put any proposal in front of the Government to save those jobcentres, to absolutely no avail. I wish him better in Henley, but it certainly has not worked in north Liverpool.

The chairwoman of the UN’s Committee on the Rights of Persons with Disabilities described the Government’s treatment of sick and disabled people as a “human catastrophe”. That is not poetry or a rhetorical flourish; that language is used deliberately and precisely, based on the weight of evidence behind the report. That report came to the conclusion that the Government’s welfare cuts have resulted in “grave and systematic violations” of the human rights of disabled people. It is a national scandal, and one that I see in my surgeries every single week. I am going to talk about a few cases that I have had to deal with in recent months. The situation should be a wake-up call to the Government, but they learn no lessons. My constituency casework is loaded with complaints relating to personal independence payments. Instead of supporting people, the process is dehumanising and inaccurate, and it exacerbates the health conditions that my constituents suffer from.

It is no surprise that there is widespread distrust of the assessment, when 68% of PIP decisions that are taken to tribunals are overturned. As I said earlier, that means a nine-month wait to get the right decision and, often, to get the original decision overturned. In that time people lose their mobility vehicles—at what cost to Government, when they must return them? Something that I have seen happen in the system—and I wonder whether it is systematic—is people going from a low rate of care with high mobility to a high rate of care with low mobility. That seems to happen in case after case, because if someone’s care rate goes up they get a couple of quid extra a week, but if they lose their high-rate mobility they lose their car and their ability to leave the house—they lose their ability to exist.

At Prime Minister’s questions on 25 April, at column 879, I challenged the Prime Minister on a specific case—that of Anthony, who has a chronic, debilitating illness. After his PIP assessment he had a nine-month wait. Once that was raised in Parliament, the DWP intervened to overturn the decision. However, I see that every week—the Prime Minister is asked about this issue, and it is always an individual case. Well, it is not an individual case—it is built into the system. I should like to know what work the Minister is doing with the Ministry of Justice about tribunal waits. Is she working on that? There must be investment in the court system if the problem is to be resolved. I do not see any work being done on it at all.

The Government’s contractors, Atos, Capita and Maximus, have consistently failed to meet basic performance standards. One of my constituents was asked by an assessor about her cerebral palsy—a lifelong condition from birth. She was asked how long she had had it and whether it would get better. What on earth is going on, and what do the Government do when such cases are brought to light? Several other people have told me that the information in their assessment report was inaccurate and did not reflect what was said in the assessment, but for some of my constituents even getting that far is a challenge. My office has been inundated with reports of the unsuitability of assessment centres for disabled people. The range of problems includes a lack of suitable parking, no drop-kerb for wheelchairs and no disabled access button to open doors. A report released this month by Muscular Dystrophy UK found that two in five respondents had been sent to an assessment centre that was not accessible for disabled people. You could not make this stuff up. It is not a matter of individual cases, one by one. There is a systemic problem at the heart of the Government’s policy, and until they wake up to that fact nothing will improve.

[Bill Grant]

Will the hon. Gentleman give way?

[Dan Carden]

I will not.

The pointless reassessments of people with severe, long-term or progressive conditions are cruel, and an absurd waste of resources. I have a constituent with Down’s syndrome whose payments stopped after she was transferred to PIP, as did those of another constituent, who has multiple sclerosis. I welcome the announcement this week that the Government are preparing to end such unnecessary reviews of people with severe or progressive conditions, but that should not have taken the determined effort of disability campaigners. The Government need to understand that what they are doing is already debilitating for the people in question. Having to be part of national and local campaigns just to get basic human dignity in the assessment process is outrageous.

In any case, it is it is simply not enough to tinker around the edges. The truth is that all the problems are not glitches in the system. They are the system itself. Research published this month by the Joseph Rowntree Foundation found that almost 650,000 people with physical or mental health problems were destitute in the UK last year. That means being so poor that they cannot afford essentials such as heating, regular meals or basic toiletries. The systematic impoverishment and denial of basic rights highlighted in the UN report and others are part of what we now know to be a “hostile environment”, not just in one or two Departments but across the board. If a society is judged by how it treats its most vulnerable, what does that say about ours?

We must treat disabled people, and the vulnerable or dispossessed, with dignity, and it is absurd to think that we can do that when we have a programme of austerity and cuts in local authorities and across the board. That is what the report signals. Not only does the Government’s austerity agenda harm communities and society; it hits the most vulnerable and the poorest hardest.

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[Marsha De Cordova (Battersea) (Lab)]

It is a pleasure to serve under your chairmanship, Dame Cheryl. I begin by congratulating my hon. Friend the Member for Canterbury (Rosie Duffield), first for securing this important debate and secondly for the incredibly powerful speech she gave. She was right to highlight that no Government should introduce legislation that discriminates against disabled people. She rightly stated that the Government’s record is a national shame, and highlighted the dire inequalities in social security and access to justice, the increase in poverty, and the lack of access to information. There are huge difficulties in access to digital information, as my hon. Friend the Member for Batley and Spen (Tracy Brabin) highlighted, and alternative formats for people living with sight loss are lacking. My hon. Friend the Member for Canterbury was right to call out the fact that there is a lack of legislation covering intersectional discrimination.

I also want to pay tribute to some of my other colleagues, including my hon. Friends the Members for Hartlepool (Mike Hill) and for Liverpool, Walton (Dan Carden). My hon. Friend the Member for Oldham East and Saddleworth (Debbie Abrahams) made a powerful speech. She has led the way and has held the Government to account powerfully for many years. I thank her for all the work she has done and will continue to do. She rightly highlighted that the Government chose not to include the charter of fundamental rights in the European Union (Withdrawal) Bill, which is a shame. My hon. Friend the Member for Peterborough (Fiona Onasanya) shared the powerful testimonies of some of her constituents. I thank everybody for all their efforts. It is right to point out that this is a shame, and there is no other way of looking at it.

The UK was once at the forefront of disability rights: 48 years ago, we passed the groundbreaking Chronically Sick and Disabled Persons Act 1970. It was led by Lord Alf Morris, who shortly afterwards became the first Minister for Disabled People—I am honoured to be in that shadow role today. That legislation was a response to disability campaigners calling attention to the deep and pervasive injustices that disabled people face. In December 2007, we became signatories to the convention on the rights of persons with disabilities, which committed us to progressively realising the rights of disabled people—our rights to live independently, to be included in the community and to have access to education and justice. After eight years of brutal Tory cuts to disabled people’s social security, of increasingly cruel and degrading assessments and sanctions, and of being stigmatised by Government Ministers, disabled people know that the Government have not been defending our rights. The UN CRPD committee found that disabled people’s rights have been “gravely and systematically violated”. It is difficult to overstate the significance of that judgment.

The UK was not merely the first country to be found in breach of the convention’s obligations; we were the first ever to be investigated. Over the past eight years, we have seen not the progressive implementation of disabled people’s rights, but their unprecedented erosion and violation. The committee found that Departments are grossly failing disabled people.

The brutal cuts to disabled people’s social security have made a mockery of article 19, on the right to live independently and in the community, and article 28, on the right to an adequate standard of living. The Welfare Reform Act 2012 alone cut £28 billion from social security. Half of people in poverty are now either disabled or living with someone who is disabled. Almost a quarter of disabled people are now forced to miss meals because of economic hardship, and one in five cannot pay to heat their homes. Such drastic cuts to social security led the UN committee to find that disabled people were the single biggest group affected by Tory austerity policies.

The UN said that the systematic impoverishment of disabled people was an entirely predictable effect of the Government’s austerity policies. It was, of course, predicted by disability groups, but the Government ignored it and refused to carry out a full cumulative impact assessment of the cuts.

[Dan Carden]

Does my hon. Friend agree that it is disappointing and outrageous that the Government have wasted more than £100 million on pointless appeals and on putting disabled people through a nightmare as they try to access the benefits they deserve?

[Marsha De Cordova]

My hon. Friend is absolutely right.

Will the Government commit to carry out a cumulative assessment of their tax and social security reforms since 2010? In addition to the devastating cuts and suspicion, disabled people have been endlessly mistreated by the chaotic Department for Work and Pensions. High Court judgments have repeatedly found that the DWP has blatantly discriminated against disabled people. Only last week, it was found that the cutting of disability premiums from universal credit was “unlawfully discriminatory”. There has been “blatant discrimination” against PIP claimants, and employment and support allowance has been continuously underpaid.

The UN report found that disabled people are being undermined not just by the social security failings, but by the lack of social care funding. Since 2009, the number of disabled people receiving social care has fallen by nearly 30%. The UN report highlights that social care is vital, and that it allows many disabled people to live independently. Will the Minister outline whether the Government’s forthcoming Green Paper will include working-age adults? I asked the Secretary of State for Health that question on Monday but did not get a full answer.

On the right to work, the Government have not done enough to remove the barriers that disabled people face. There is a lack of high-quality impairment-specific support. The Government’s flagship Disability Confident scheme does not measure the number of disabled people it has directly helped to move into work. Access to Work must be improved, extended and better publicised. Will the Minister consider removing the discriminatory cap?

Signatories to the CRPD are obliged to promote inclusive education. Under the Government, there has been regression and an increase in the number of special school places. What is the Minister doing to encourage her colleagues to improve inclusive education? In recent months, the Government have created a cross-ministerial body that is supposed to promote disability issues across Government, but at the same time they have cut the number of staff at the Office for Disability Issues. As my hon. Friend the Member for Oldham East and Saddleworth asked, what is the group’s scope? Where are its published terms of reference?

The Government are helping to organise a global summit in July, but why should any other state take them seriously on disability rights when they are systematically violating the rights of disabled people and continue to ignore the UN’s recommendations? When will the Government publish their response to the UN’s report?

When we get into power, the Labour Government will incorporate the convention into UK law, scrap the punitive sanctions regime, and replace the assessment regime with a more holistic, supportive assessment framework. It is a shame on the Government that we have to stand here today and debate this issue once again. They must take heed and listen.