Personal Independence Payments

Debate between Laura Smith and Rosie Cooper

Wednesday 31st January 2018 Westminster Hall

[Laura Smith (Crewe and Nantwich) (Lab)]

It is a pleasure to serve under your chairmanship, Mr Hosie.

Let us imagine how anxious someone must feel, knowing that they have to sit through an interrogation process that will deem whether they are quite disabled enough to be eligible for a helping hand. Not only does that person have the already huge day-to-day disadvantage of being disabled or suffering from mental illness, but now, thanks to the Government, they are forced to sit through a point-scoring process to judge whether they are fit to work. PIP is not fit for purpose when it comes to many physical conditions, and it certainly has not been fit for purpose for those suffering from invisible illnesses. How disgraceful that in 21st-century Britain a Government are implementing public policies that clearly disadvantage those with mental health problems.

My constituent, George, suffers from a range of debilitating conditions, and he is prescribed a huge amount of medication just to enable him to get through the day. He is also almost completely reliant on the use of a wheelchair. After working for his entire life, George, at 63, thought that when his health deteriorated, there would be support to help him to survive and pay his bills. At first, that support was there, and George received higher rate mobility and the highest rate care components of disability living allowance. However, when he was called for his PIP assessment, things took a dramatic turn for the worse.

George will not mind my saying that he is reaching an age at which he would be likely to retire soon if he was fit and well, but he has been put through a process whereby he was tested to see whether he was disabled enough. One observation that was made during his assessment was that he could walk unaided for 20 metres, but not 50. That is not considered a restriction on his ability to walk. Leonard Cheshire Disability, the charity for disabled people, makes the point that the change to the criteria obviously means that far fewer individuals qualify for the enhanced mobility component of the benefit. That is penny-pinching at the expense of someone’s dignity.

The charity has also gathered the information that 74% of disabled people surveyed did not feel as though the assessor understood their disability. That was and remains one of George’s biggest frustrations: he did not feel that the assessor listened to him, understood his needs or treated him with any compassion. How can someone hold so much weight in determining the future of an individual’s life without being held accountable? Also, why cannot assessors consult experts in any condition or disability to help to fill their knowledge gaps? That would surely ensure that they asked the right questions in the assessment and accurately determined the individual’s ability to carry out an activity reliably, repeatedly, safely and in a timely manner.

[Rosie Cooper (West Lancashire) (Lab)]

Will my hon. Friend give way?

[Laura Smith]

I am sorry, but I must get through my speech; I am conscious of the time.

George was assessed by Atos on 1 June 2017. He is now going through the process of appeal, but the timescale is being put further and further back and he still does not have a date for his case to be heard. He is struggling to survive financially, and he has said that he is feeling more depressed every day and having sleepless nights. He has stated—this is the important bit, to me—that if it were not for his wife, he would feel as though he could not go on any more, and he has contemplated not taking the medication that he needs. The way in which he and many, many others in my constituency have been treated is absolutely diabolical. I urge the Government seriously to stop burying their head in the sand and face up to the reality that has been created by their own policies.