Welfare Reform (Sick and Disabled People)

Ian Murray Excerpts

Thursday 27th February 2014 Commons Chamber

[George Hollingbery]

Indeed it did. The expert panel that sat to adjudicate on every single one of those test cases took the advice of mental health experts. A number of mental health specialists are now provided with specialist training in the testing regime. I think the figure is 30, but that is off the top of my head and it may be as many as 60.

In the fourth report, Dr Litchfield largely endorses the position I outline. He says:

“Any ‘test’ is necessarily a trade-off of many factors and the WCA appears to be a reasonable and pragmatic tool.”

There remain those who call for its abolition, but suggestions for what to replace it with are rarely forthcoming. No test is ever perfect, but the WCA has been designed with considerable rigour and is subject to a process of continuous improvement.

I hope that hon. Members will forgive this slightly tortuous journey through the WCA, but it is very important to show just how much trouble and care has been taken to design and improve it. It is not perfect and it will not always produce fair and just results, but that is what the appeals process is for and there to catch. That it is necessary to have some sort of objective test to help decision makers seems to me to be undeniable. Hence I cannot support the motion’s call for the abolition of the WCA.

[Ian Murray (Edinburgh South) (Lab)]

The hon. Gentleman is giving a very technical analysis of the WCA. My constituent, Mr McArdle, who runs the Black Triangle campaigning group, has on his website and Facebook page a whole list of human stories about how the WCA acts in practice. I wonder whether the hon. Gentleman would mind looking at that after his speech today to get some of the human side, because it is not just about a technical analysis of how these things work.

[George Hollingbery]

I hope the hon. Gentleman will acknowledge that in prefacing my remarks I made it clear that this cannot be a mechanistic process, like some sort of quality control process. It has to involve the human. I acknowledge that there are many cases where results have been, shall we say, questionable—there is no doubt about that. Nevertheless, that it is necessary to have such a test is, I think, undeniable: the Government cannot, will-nilly, go judging entitlement to benefits without any test of any sort. Yes, it is difficult to make the case that I am making without sounding dry and technocratic—I take his point absolutely.

In the time remaining, I would like to draw the House’s attention to some real outcomes produced by my local providers, which I hope the hon. Gentleman will take as a human face of what can be a reasonably successful programme. My local providers are the Shaw Trust in Portsmouth and A4e in Southampton, which is run by a team led by George Gallop. I hope that we can all celebrate some of the results of their work.

Alex, aged 20, was diagnosed with attention deficit hyperactivity disorder, and found it almost impossible to settle down to any kind of work. A4e’s relationship with Harsco, a large building services company, was crucial in enabling Alex to train for a certificate under the construction skills certification scheme, and to become a scaffolder. Alex said:

“I felt like nobody would ever employ me. I didn’t even know what 1 was doing wrong…it is the kind of job that sets you up for life and I love it. If 1 look at how my life has changed in the last year I can’t believe it”.

Daniel, aged 19, was homeless and unable to look after his young family because he suffered from depression. He was one of the first young people to enter Radian Housing’s “proving talent” programme, delivered by A4e in Southampton. He came through the scheme, and now has a permanent job in technical services with Radian. He said:

“it feels amazing to be back on track, in employment providing for my family and feeling good about myself.”

Sandra, aged 45, was a proud working mum of two, trapped in a wheelchair. Because of ill health, she was made unemployed and became dependent on employment and support allowance. At first she resented being referred to the Work programme, but her advisers and trainers helped to motivate her, and to give her the confidence and skills that she needed in order to return to work. She said:

“Now I think about what I can do, instead of what I can’t”.

David broke his back in an accident in 1997, and received incapacity benefit for more than 15 years. At an ESA work-focused interview in December 2012, he was asked when he had last had a good laugh and when he had last smiled. He replied that what had saved his life was a passion for his reptile collection. David and his wife have now signed off from ESA, and have set up their own business in a shop in Copnor road, Portsmouth, selling and boarding exotic pets.

To me, those are inspiring stories of people afflicted by disability and sickness who, with the right help from the right people at the right time, have managed to find their way back into employment, and, in so doing, have rediscovered their sense of self-confidence and self-worth. Of course there is much more to do and many improvements can be made to the system, but surely those are outcomes that we should all celebrate.

Is all rosy in the garden? Of course not. There are still many challenges, and many changes are required. There are still too many people who do not find permanent employment. There are many whose benefit applications and assessments take far too long to process, and who are left without an income in the meantime. As has already been said, the transition from disability living allowance to personal independence payments is proving to be a challenge. For all that, however, the evidence that I see on my visits suggests that many of our fellow citizens are being given a new lease of life by the Government’s approach to welfare, and the central assumption that there is nothing compassionate about—