Personal Independence Payments

Debate between Jo Platt and Laura Pidcock

Wednesday 31st January 2018 Westminster Hall

[Laura Pidcock]

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.

[Jo Platt (Leigh) (Lab/Co-op)]

I thank my hon. Friend for securing this debate. I have lost several members of my family to motor neurone disease, a progressive disease for which there is no cure—people do not get better. Does she agree that people with terminal illnesses such as MND should not be up for reassessment?

[Laura Pidcock]

There are hundreds of stories of people with conditions that will not change being reassessed. That is terrible.

There are extensive concerns about the suitability of PIP assessors—that was a clear theme throughout the correspondence—who often do not have the medical expertise to assess claimants with particular medical conditions. A midwife, for example, may assess a claimant with mental health problems, but they will not know every sign and symptom of every mental health condition, as they are not qualified. That calls into question the accuracy of the assessment.

Constituents have told me how brutal and gruelling the medical assessments are, as they lay bare the claimant’s disability and how they cope with it, but they are based on a medical model of disability rather than a social one. One person put it brilliantly: they said the assessment was like a functionality test, and that it did not capture or consider how someone can live their life each day. The fact that assessors do not take notice of professional medical assessments from doctors or psychiatrists, and that that information is considered only at tribunal stage, is not even questioned. Assembling that information at assessment stage is such a waste of energy for people, especially since doctors charge for medical assessment letters. In my view, that cost should be met by the state, not by the person making the claim.

State Pension Age for Women

Debate between Jo Platt and Laura Pidcock

Wednesday 5th July 2017 Westminster Hall

[Laura Pidcock (North West Durham) (Lab)]

I have yet to meet anyone who does not agree that the WASPI women are in a terrible position, and that the failings are the Government’s, not theirs. It is hard to dispute the idea that not enough energy or resources were put into informing the women of the changes early enough for them to prepare psychologically and comprehend what the rest of their working life and their retirement plans would be.

Approximately 5,000 of the affected women live in North West Durham, and I have not met many who have been able to save. They now live in hardship. What an indignity that is, after they have served their communities through their labour for so many years—to end their lives in poverty. I do not think that it is disputed that adequate notification was not given. The DWP’s own research said that six out of 10 women expected to reach state pension age earlier than they will do.

[Jo Platt (Leigh) (Lab/Co-op)]

My hon. Friend is right on that point. There are 4,000 WASPI women in Leigh and they have had to set up their own group to support other women who are affected by the changes. From the time they found out what they had not initially been made aware of, the issues have been ongoing.

[Laura Pidcock]

My hon. Friend is right to point out that when the state fails people will organise.

I have witnessed what is happening at first hand. My mam only found out about her pension changes because of the WASPI campaign and I saw her disappointment, worry and anger that after working from the age of 13 she had to work more and more, and was robbed of nearly £40,000. For those women, who have not had enough time to prepare, who have had inadequate correspondence from the DWP and who through no fault of their own have ended up in poverty, the right thing to do is to compensate those who have already reached state pension age and provide a bridging pension for those who have not, in humble recognition that, as other hon. Members have said, it is not a benefit—it is rightfully theirs.

As other hon. Members have recognised, in the past couple of weeks we have seen that, when the political will is there, money can be found quickly to remedy a problem. I urge the Government to apply the same urgency to the present situation. There are many lessons to be learned from what is happening, but there is no justification for not putting it right. I want pension justice for those women now.