The Green Paper Discussion (the document link is here too!)
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Morning Catherine hope you’re ok . Yes I need to find a link to that consultation today . Will definitely fill it out .
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I'm really scared my highest in daily living was 3 now I'm far worse due to Myelopathy and Radiculopathy Stenosis and the list goes on! I can no longer dress and wash myself. I can't cook at all and need help to eat as I can't grip properly. My review is due from October this year as my award ends October 2026. I get standard mobility but as I can't be operated on and my Lumbar Stenosis is causing saddle anesthesia I'll end up in a wheelchair.
Without PIP I will not be able to afford any of the vital things I need!
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hi yes I heard that said on Noam nyles channel but it just says they’re looking into it . It doesn’t mention the 4 point problem. That’s the thing that needs changing and obviously they’ll fight tooth and nail for that .
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Hi, I am on Old style ESA (Cont) supoort group and PIP for many years due to cerebral palsay (Wheelchair user) . Does anyone know what will happen with that? Thanks
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From what I understand about 1 million disabled people will loose Daily Living PIP (even some on the higher rate) due to the new 4 point rule at their assessments from Nov 2026. I can't believe they can get away with this for existing claimants who genuinely rely on this money and work is not an option. I think our efforts should focus on ensuring that the 4 point rule should at least be flexible for existing claimants !! 😡
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I agree this the worst part of it all . I get highest care but not 4 points due to assessors ignoring the 4 point questions. This is what needs challenging. Plus the fact that esa lcwra wca is completely different from what I remember to a pip form / assessment. They haven’t incorporated anything into the pip form for lcwra . How can that be legal ?
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I received enhanced on both aspects and just read my assessment notes for the first time in a long while. I did score a 4 on care; yet was shocked to see some zeroes where it was obvious it should have been a 3-5+; which I will be arguing at my next assessment.
I wouldn't be too concerned with previous assessments as I believe the government have surely seen the high level of tribunals at present and in the past, mainly due to the assessors either being dishonest, inept or a combo of both! -(imo)
When it comes to my renewal/review, I'm going to raise all of the errors in my past assessment and mention all my provable-increasing-disabilities, since that application
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Its not just existing claimants but new claimants will also be affected.
None of it is fair.
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Same here, I sympathise. I offered to send photos to my consultant/gp, basically anyone with any interest, 🤣 strangely they all said no thanks (117 visits in 20 hrs my worse). It did cross my mind would any government people want them but that might be considered a hate crime 🤣😭. I've not heard of closmat loo I'll Google that. I can't even go on water meter which was told would ordinarily be cheaper but it won't be for me.
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That's one visit per 10 mins🤔😟
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I am caught in the abyss of being on Contributory ESA but living in Portugal. So if they merge it with JSA and make it a temporary benefit I cannot claim UC from here when that ends. I have chronic and degenerative diseases so I would likely pass the threshold to not have to have a reassessment, but if ESA is axed there is no exportable benefit I can claim. So much for the Brexit Withdrawal Agreement protecting our rights to remain in our countries and have our benefits exported! I am looking at losing over €8000 a year. ESA is my only income except PIP but that is supposed to be for my (many!) extra costs of being disabled, not my only source of income! I have obviously raised this gaping chasm in support in the Green Paper and also written to Ministers@dwp.gov.uk. I also emailed Diane Abbott hoping she may raise the issue. With no EU MP any more I don't know how else to get this raised in the 'discussions' when they change this benefit?!
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@MiddletonSadly, without going into the ins and outs of my 'plumbing' visits were frequently less than 1 minute apart, the 'luxury' of a 10 min break would have been welcome. Only took photos after c 25 visits as thought my consultant will probably not believe one could go so often as it at least records the time. If I ever lost my phone..... if it gets stolen it will serve them right.
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yes I too read that . Go to war a hero but come back injured or disabled and will be hated and destitute. Especially if you dare to get PTSD .
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@Middleton my first bowel consultant told me there's evidence Covid can remain in the bowel and my inflammation levels are always very high. Never had one issue with this prior to Covid; hoping to go on anti-viral trial next year and praying I don't have perforation prior to that.
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I've justed emailed John mcdonnell to say how it will impact us and to challenge the 4 point system
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I'm really sorry, from the sound of things you should be a 4 in one area. I'm in same boat where I'm 2s and 3s but no 4. I think they've deiberately chosen this number precisely because they know a lot of people don't have 4s.
I'm not sure when they plan to bring in the 4 points but it's not law yet, so I'm not sure if they could legally force this on people.
One suggestion I've seen is trying to document/record your struggles if you or a friend/loved one is able to. Another suggestion on the forum that looks good is if you can access them online print off all your GP notes and include them in your reassessment. If you can't access them online I think you have the legal right to request a copy of them - odds are it will be long and they will have to read them. Also get as many health care professionals (inc GP, counsellor, pyshiotherapists etc), any carers, family/friends who see you struggle it down in a letter, include that.
On your reassessment be extremely explicit and blunt about not just what you can't do and struggle to do explain the effect of it, how it impacts on you physically, emotionally and mentally. Ram it down their throats. Think about your worst day when filling out the reassessment. If you need to get someone to help you both with the form and go to any re-assessment. Also if they demand a face-to-face consider requesting a phone appointment or that they come to your home if you're OK with face-to-face, this is a reasonable adjustment you are legally entitled to under the Disabilities Act 2010.
It wouldn't surprise me if you have gotten worse since your last assessment - make sure you make that very, very clear what is worse for you, how it effects and impacts you. If there are things you can't do yourself, please make that very clear.
Also 2026 is a year away, with any luck they will be pressured to drop the 4 point thing and if they don't, I think they will be taken to court because to say someone is no longer eligiable for PIP when their health, or their condition or circumstances have either not changed since their last PIP or has gotten worse is discrimination and makes no sense legally.
There's a YouTuber Charlie Anderson who gives a lot of advice about PIP assessment/re-assesment. She is on PIP herself and helps other claiments and doesn't pull any punches about things but her advice I think it really good and she has a very high success rate.
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So, this 4 point system!
If someone has scored 4 points in a single Q for care in the past; and PIP askes "Are you still experiencing the same" -and we answer- 'Yes'! Wouldnt it make sense for PIP to search out those who did score 4's in the past and then fast track the reassessments?
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They want to get people off benefits. So unlikely they will do that.
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