🚨 Your voice is needed: Timms Review on PIP reform

Community_Scope
Community_Scope Posts: 2,179 Scope Online Community Coordinator
A white paper background with text: 'Your voice is needed. The Timms Review has opened a public call for evidence on PIP reform.' There is a yellow icon with a purple megaphone at the bottom.

https://www.gov.uk/government/news/call-for-public-views-to-improve-disability-benefit-for-millions

🚨 Right now, the government is working on future Personal Independence Payment (PIP) reform. This work is known as the Timms Review.

And now it wants to know what disabled people think.

It is collecting evidence on how effective PIP is and whether the assessment provides fair access to the right support. As well as our experiences of claiming PIP, and whether the experience changes between different groups of people.

📢 This is a crucial opportunity to make our voices heard loud and clear. Because disabled people deserve a welfare system that is not confrontational. And is built with them.

It’s vital that the government understands the impact that PIP has for the disabled people that claim it. And where it isn't working.

PIP exists because life costs more if you are disabled. And this needs to be at the heart of any decision making.

But we must be clear: the government must not use this review to fit in predetermined decisions or spending plans.

✍ Respond to the call for evidence by 28 May

Comments

  • Catherine21
    Catherine21 Online Community Member Posts: 9,625 Championing

    A member of scope has highlighted questions on timms call for evidence i feel this is amazing they are working hard in the back ground so more will follow

  • Catherine21
    Catherine21 Online Community Member Posts: 9,625 Championing

    Most of us work better with colour highlights

  • nimnim
    nimnim Online Community Member Posts: 1 Listener

    All they want to do is save themselves money. Pity it never applies to MPs expenses.

    Obviously they don't really care about disabled people, otherwise it would be a room full of disabled people creating a fair system.

  • MarkH75
    MarkH75 Online Community Member Posts: 45 Contributor
    edited March 26

    I took would like to have clearer forms. Having PTSD is very hard at the best of times but filling in forms is as hard as anything I have to deal with daily more so with pip/government forms. Making them more user friendly would certainly help me.

    Having made the initial claim and 1 renewal I was extremely anxious and having to wait for so long and not being able to chase up the claim add to the stress. So maybe a better system to keep claimants better informed through the claim and renewals would certainly benefit me.

  • MarkE19
    MarkE19 Online Community Member Posts: 4 Connected

    The form is a joke. The first time I oompleted it I scored 0 points - even though I am registered as blind and have severe mobility issues. I ended up going to a tribunal and was quickly granted my claim.

    Instead of looking for key words to score applicants they should actiually read the answers.

  • Dordymychavvy12
    Dordymychavvy12 Online Community Member Posts: 7 Listener

    It's about time the government took notice and listen to disabled people and how hard it is to get PIP, it's like a miracle if you can get the form filled out because it's completely different to any other form I have seen in my life. Forms need to be simplified so every disabled person can get what they need. Life is hard as it is and having cost of living to try to get just the necessary things and bills, the government needs to support us properly instead of voting to get a pay rise for themselves, what about us, care workers who are unpaid and work tirelessly all of this is disgusting this country is a laughing stock around the world, other countries don't send money abroad for other countries before helping their own, it's about time your countrymen are seen first and not last. Our elders fought and died so we were free and it's disgraceful to them and us now.

  • Toppy64
    Toppy64 Online Community Member Posts: 10 Listener

    I actually had nightmares about those forms , they are frightening… they make me feel bad having to justify my illness. Then weeks later after all the night terrors of waiting for a reply you get told that a health professional is examining your forms … why ! if you have evidence and GP has signed you off why ! Awful z

  • Catherine21
    Catherine21 Online Community Member Posts: 9,625 Championing

    It is very triggering and inpacting on our mental health anyone who hasnt gone through this would never understand the fear and anxiety but remember this shall pass you done your part its the waiting hopefully you hear soon

  • Shellb18
    Shellb18 Online Community Member Posts: 1 Listener

    I have let them know that I am responding by email as it's difficult to go back and read these forms and make sure you've written something legible and not gobledegook! I dont want them dismissing my evidence as on my phone I can't go back and correct. Let's hope it's all taken into account.

  • Wibbles
    Wibbles Online Community Member Posts: 3,372 Championing

    "I am responding to the review of Personal Independence Payment (PIP) to share my experience as someone whose condition has worsened over time.

    I have lived with mobility problems since around 1990, and in recent years my movement has deteriorated further. I also have arthritis and bicep tendonitis, which affect my ability to carry out everyday tasks and move around safely and reliably.

    PIP is essential for me because living with these conditions brings extra costs that non-disabled people do not face. These include increased difficulty with mobility, pain management, and the need for support with daily activities. The financial support is not a luxury—it helps me maintain a basic quality of life.

    However, the assessment process does not always reflect the reality of living with long-term and worsening conditions. My experience is that it can feel stressful and does not always fully capture how my condition affects me day to day, especially as symptoms can vary and worsen over time.

    A key issue is that conditions like mine are long-term and degenerative, yet the system often treats them as if they might improve. Reassessments can create unnecessary anxiety and uncertainty, even when there is clear evidence that the condition is not going to get better.

    I believe the system should:

    • Better recognise long-term and worsening conditions without repeated reassessments
    • Take more account of how pain, fatigue, and limited mobility affect daily life over time
    • Be less confrontational and more based on trust and medical evidence
    • Ensure that assessors have a proper understanding of fluctuating and degenerative conditions

    PIP exists because disability increases the cost of living. This principle must remain at the heart of any reforms. Without this support, people like me would struggle to manage basic day-to-day life.

    I hope this review leads to a system that is fairer, more understanding, and built around the real experiences of disabled people."

    is what I sent……

  • Trufflecake
    Trufflecake Online Community Member Posts: 30 Connected

    Applying for PiP is quite a lengthy process.

    I think that things could be difficult for most people with long-term health conditions and other disabilities. I think that they should change the way you have to report a change of circumstances. Why should someone have to fill out another form, then either have a written and phone based assessment? If you send in evidence, then this is what it is. If you have long-term conditions that are progressive, they should taking this into account from your very first form you gilled in. It is just common sense. I have asthma, degenerative disc changes, arthritis in my lower and middle back, toe and trochanteric bursitis. Most of these condition are progressive and if you have medical evidence from the hospital, why then do I need to have another assessment. It does not make any sense for them to put you this.

    PIP also help people financially to help with bills, good, travelling in order to survive as some people with disabilities can only work part-time or just a few hours. The form should be more simple to fill out and the assessors need believe medical evidence from the hospital etc., in stead of trying to alter what you have said during your assessment. PIP is very much needed and people rely on it for all different reasons. Having a disability definitely cost more in terms of money due to just having long-term health conditions etc.,

    I think the points system should be based on each individuals health condition as no two people cope in the same way.

    You should not have to get a certain amount of points in order to qualify for PIP because you would still have the disability regardless of how many points you had compared to someone with no health conditions at all.