(6 years, 10 months ago)
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Those stories are so, so common. The changes have hit those most in need of a social security system while reducing the overall welfare budget, and have taken away the safety net for a massive number of people. When cost-cutting is the motivating factor behind changes, we hit trouble, just as we have with universal credit. Let me take Members through some of the difficulties that my constituents and many other people—
I am making progress. There are 20-odd people down to speak; it would be disrespectful to them not to do so.
The initial claimant form is often daunting and time-consuming. People have to rely on stretched services and support agencies to complete the form. At the same time, the questions are very restrictive and do not fit the description of everyone’s illness. Following that, claimants are invited to a medical assessment by an outsourcing company—Atos Healthcare or Capita Business Services, depending on their location in the United Kingdom. The accessibility of venues is often cited as a problem: claimants are invited to assessments miles away from their homes and in inaccessible rooms. Some say that that is a test from the outset. There have also been reports of assessments taking place in expensive gyms and spas in my area, which makes claimants feel on edge. Some people are sure that they were filmed upon entering the assessment, and I believe them.
That is right. I will come on to mandatory reconsiderations in a second.
The outsourcing of the assessment process is very much part of the problem. Some 60% of assessment reports completed by Capita healthcare professionals and sent to the DWP were judged to be of an “unacceptable” standard. Neither Capita nor Atos has ever met the DWP contractual target that no more than 3% of reports should be found unacceptable. I wonder what it would take for those companies to lose a contract with the Government. No action is taken, because the Government are ideologically wedded to the outsourcing model, despite such poor results. Incredibly, I have read that those companies pay people bonuses for completing extra assessment reports, which in my view incentivises rushing and contributes to inaccuracies. Many feel as if they have been lied about in their reports—that is all part of the same inadequacies. I have even had reports of healthcare professionals who conduct the assessments asking claimants if they have thought about killing themselves. While I understand that it is a difficult subject to broach, sensitive language needs to used when dealing with such topics; otherwise, it can be damaging and triggering for that person.
If a claimant is not awarded the points they think they are entitled to, or they are told that they are not entitled to PIP, they must challenge the DWP’s decision through a mandatory reconsideration. Constituents of mine, and many people who have been in touch, have said that the process is completely pointless due to the DWP not reviewing medical evidence or investigating whether the decision maker’s report was accurate. Actually, DWP workers feel unable to challenge the assessor’s report. Advice and support agencies also state that hardly anyone has their decision overturned at that stage. I cannot help but think that is just another stage in the process to grind people into submission.
If the mandatory reconsideration process is unsuccessful, the decision must go to tribunal, putting tribunals as well as claimants under enormous pressure. Advice and support agencies say that they are under a great deal of strain, trying to deal with the demand from people seeking representation. Latest figures show that 68% of PIP decisions are overturned on appeal, so the DWP’s systems are clearly not working. That is completely indefensible: all that trial and trauma for claimants to be proved right, if—it is a big if—they manage to go that distance. People have reported that they have to wait over a year for a tribunal date.
What is very clear is that the assessment process is working against claimants entitled to the benefit. Many campaigners believe that the companies who provide medical assessments are heavily encouraged to hit targets by the Government in order to cut the welfare budget, and I believe them. Perhaps it is because there is an ambivalence to these people, or—more likely—because the Government do not see it as the state’s role to provide that support.
I will give way once more to the Conservative side, and that is it.
I thank the hon. Lady. I would not necessarily disagree with some of the criticisms she is making of the assessment process. Some of my constituents face those challenges, and we would be happy to work across the House to try to fix them. Does she recognise that under PIP, 66% of claimants with mental issues now get the higher rate of benefit, versus 22% under DLA? Can I ask her for a little balance when she comes to look at the system rather than just criticism?
The balance is that thousands of people are locked out of the system and never even get an award because they are so ground down by the process. The Government need to realise what a cruel and callous system they are putting people through and the knock-on effect that has on our constituents. I am a bit shocked by the disbelief on the Conservative side—they look stunned that this is taking place. That is the reality for disabled people in this country. People are falling further into depression and self-harm, having suicidal thoughts and becoming reliant on food banks. All of those things are harmful for our society. Losing Motability cars was a consistent theme, along with falling into debt. The NHS is also being put under much strain.