Personal Independence Payments Debate
Full Debate: Read Full DebateDepartment: Department for Work and Pensions
Emma Hardy
Main Page: Emma Hardy (Labour - Kingston upon Hull West and Hessle)Department Debates - View all Emma Hardy's debates with the Department for Work and Pensions
Personal Independence Payments
Emma Hardy Excerpts(6 years, 3 months ago)
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Emma Hardy (Kingston upon Hull West and Hessle) (Lab)
I will focus my contribution on how the PIP system treats those with less visible disabilities by talking about epilepsy. Epilepsy Action has said that nine out of 10 people with epilepsy felt that the Government’s decision maker did not understand their condition—and no wonder! The assessment forms, the descriptors and the face-to-face assessments are not set up in a way that accurately reflects the nature of epilepsy.
It comes as no surprise that three out of five people with epilepsy who were already on benefits had their award decreased when they applied for PIP. In raw numbers, that is 18,000 people, 20% higher than for any other condition. I am concerned that the Department’s previous announcement on supervision and safety—the change that could have the most impact for people with epilepsy—is in danger of being neglected.
People with epilepsy have contacted the Epilepsy Action helpline with their key concerns. First, what is the review’s timeframe? People are waiting to find out whether their award has been changed, but as they will only be notified if there is a change, how will they know when to stop waiting? Secondly, why are claims disallowed before 9 March 2017 not being reviewed, when it is clear that the guidance was wrong before that date? Thirdly, if the DWP has reviewed a case and decided there should be no change, does the claimant have a right to appeal?
There have already been two significant reviews, and many problems with the PIP assessments remain. There are three changes the Government should urgently introduce. First, they should make sure that only those assessors who have received training for a particular condition, such as epilepsy, are allowed to make decisions on that condition. Secondly, they should increase the timeframe for providing evidence from one month to two months, to make it easier for an applicant’s doctor to provide the supporting evidence that they need. Thirdly, they should commit to a full review of the “repeatedly and safely” requirements and issue guidance to ensure that it is being applied correctly for people with less visible conditions.
Taking those measures will not ease the stress of the undoubtedly stressful application process, but it may go some way to helping achieve a fairer system and to granting applicants what was promised in the name of the benefit: independence.