Green Paper Related Discussions
Comments
-
Morning Catherine hope you had a good weekend. I missed you on the forum yesterday. I don’t have MS, I have ME which used to be called chronic fatigue syndrome. I can’t pronounce the long scientific name for ME though 😂.
Yes you’re absolutely correct. I have several conditions as do a lot of us so I’m not special in any way but can only talk about my own conditions and effects. It’s like domino’s . Fibromyalgia causes pains in my legs plus cramps in hands that are getting worse. Migraines which then have a knock on affect in my arthritis in my neck and vice versa. Gentle exercise helps the muscle pain but that causes post exertion malaise . The constant stress has had a knock on effect on my anorexia ( not nerves) so I’m not eating much and nothing at all unless nagged 😂. Then there’s IBS which has been made worse by Covid. The fibromyalgia causes wide spread general pain and aches which in itself makes me tired. It also causes different pains in any particular area that can last for many months then it goes and reappears elsewhere. I don’t know if anyone else on here with fibromyalgia and/or ME has the same symptoms but I’d be interested to know how it affects others as I’ve never been on fibromyalgia or ME forums . I’ve just been diagnosed and then left and prescribed painkillers and muscle relaxants. But I imagine a lot of us on here suffer fatigue as pain and depression etc causes fatigue. Being in pain is just tiring but we get used to it and don’t realise how much we can’t do compared to others. This whole severe criteria I hope doesn’t turn out to be unfair and expect a particular symptom or the condition itself to be constant each day as even if you get a while of respite stress or over exertion can bring on a set back in any condition.
0 -
I have fibromyagia and c.f.s
I have lived with it for 15 years along with a multitude of other health issues.
My symptoms are very similar to yours.
I have been medically diagnosed by specialist consultants so if it comes down to us being required to have a formal diagnosis I do have that evidence.
I hope you manage to have a reasonably good day but I know you will always be in pain and fatigue like I am.
Take care. X
0 -
Morning luvpink
Yes I’ve been diagnosed about that length of time too after a second infection of glandular fever. So I’ve most likely had ME 35 years. I really think if there was going to be an improvement in out health it would of happened by now .
Yes three years , well actually less than 3 . Originally assessor said two but dwp increased to three but on my letter the review date is less than three years. My first pip took two years of fighting to higher tribunal after being awarded zero points . I really hope I don’t go back to that again.
Take care and enjoy the nice weather x
0 -
Hi Catherine,
I know but it’s the assessors, all down to luck .
Try and find time to relax Catherine, this isn’t good for our MH. Watch a good horror to take your mind off things . I get to the stage where I can’t think about it for a while so I can recharge x0 -
Sadly our condition will not improve and there is no cure for us.
I only ever got 3 year awards despite this being life long and me providing evidence how much it impacts my daily life.
0 -
If these reforms go through I hope at least the severe criteria applies to us and everyone will conditions that won’t improve . They could save money by stopping these reassessments. I was discussing this Friday and yesterday with Chiaried who explained what they think about it . If you’re up to it check out the conversation to see what you think .
0 -
Yeah I agree our conditions are severe and life long with no effective treatment or cure and I have often said that money could be saved by stopping these ridiculous degrading assessments.
2 -
I’m looking forward to that one
0 -
I wonder how she is now . First time I got it I didn’t know what it was GP was useless. I had flare ups of bad throat every month for about 6 months. So sore couldn’t even drink water .
0 -
Honestly I don’t understand all this nonsense the governments , Tory and Labour , sprout out about making it so we need a diagnosis. Considering the amount of medical evidence we all have and how hard we fight for pip I can’t see how anyone could possibly get pip without a diagnosis. Just another media and government lie
1 -
Starmer panicking I think though . He’s apparently told all MPs they have to vote when before he said they can abstain. He must think he doesn’t have enough support as he’s threatening them now
0 -
Labour rebels could jump ship to form Left-wing 'real socialist' party amid anger over proposed welfare cuts?Sir Keir Starmer faces the threat of a new left-wing 'real socialist' party amid mounting anger from Labour backbenchers over controversial welfare cuts.
The Mail on Sunday has learnt that disaffected Labour backbenchers are already being approached to consider joining a new 'radical Left' political movement.
Sources said that to inflict maximum damage on Sir Keir, the proposed new party – master-minded by supporters of ex-Labour leader Jeremy Corbyn - could be launched during Labour's national conference this Autumn.
The plans emerged amid forecasts that so angry are Labour backbenchers at their Government's plan to slash disability benefits, that scores of MPs could refuse to back it at next month's crucial Commons vote.
Talk of the new party also comes just days after Mr Corbyn – who now sits as an Independent MP – said he was 'determined there will be, in short time, a strong alternative democratic socialist, left-wing voice that brings people together'.
However, it is understood that Mr Corbyn himself may not himself lead the new party, with sources suggesting that role should go to a younger figure such as Coventry South MP Zarah Sultana, currently suspended from the Parliamentary part for voting to scrap the two-child benefit cap.
The spectre of a break-away left-wing movement comes with Sir Keir potentially facing the biggest rebellion of his premiership so far over plans which could mean cutting personal independence payments (PIP), the main disability payment in England and Wales, for about 800,000 people.
So worried is Sir Keir that Labour whips have reportedly threatened that anyone who simply abstained would never get a ministerial job while MPs voting against would lose the Party whip.
Last night, one senior Labour MP said those reports were 'rubbish' and cautioned that if the revolt was huge, it would not be possible to suspend '100 or so MPs'.
Even moderate backbenchers have privately vented their anger at the cuts while Left-winger Andy McDonald has branded the proposals 'a huge attack on the incomes of disabled people'.
However, the Daily Mail highlighted last week how spending on sickness benefits was on course to rocket by £18 billion a year to reach £70 billion by the next general election if nothing was done to trim the bill.
Work and Pensions Secretary Liz Kendall has warned that the country's benefits system faced collapse if costs continued to escalate.
Long-mooted plans for the new party are understood to have accelerated in the last few weeks amid mounting anger among Labour backbenchers over government policy, including the now-abandoned decision to scrap Winter Fuel payments for many pensioners and the proposed disability benefit cuts.
And last weekend, Mr Corbyn, already part of a five-strong 'Independent Alliance' group at Westminster, appeared to acknowledge that people's frustration that 'we didn't found a new political party' would soon be answered.
Sources close to the ex-Labour leader also told this newspaper that there were now 'very, very active discussions' about setting up the new movement.
However, they dismissed reports that the party would be called 'Arise' after a former Corbyn aide registered such a party with the Electoral Commission just over a week ago.
Last night, Starmer allies played down any threat from such a new party, suggesting 'a couple of ' current Labour MPs were more likely to defect to the Greens than join a Corbynsta-style group.
But one longstanding Labour MP said: 'It's all very well for Starmer's acolytes to dismiss the threat of a proper socialist party but the PM is playing with fire.
'After the winter fuel fiasco and now this attack on disability benefits, he's leaving a vacuum on the Left of British politics and someone's going to fill it.'
Mr Corbyn was originally suspended from Labour in 2020 after claiming the scale of antisemitism in the party had been overstated and later expelled for standing as an Independent against an official Labour candidate.
3 -
And he said he wanted to lead a government with transparency 😂 . Worst PM ever and they know it
1 -
I read elsewhere that the rebels said let Starmer take away the whip and we’ll just start another party . I really think if he continues he could finish Labour off for good
1 -
The user and all related content has been deleted.0
-
Labour’s cruel severe conditions criteria
Published: 22 June 2025
labour’s cruel “severe conditions criteria” (SCC) plan is not designed to protect seriously ill claimants as the government claims, it is intended to save money at their expense. Because tens of thousands of claimants too ill to ever work again will be forced to live for years on half the additional payment that current claimants receive.
The SCC are part of the Universal Credit and Personal Independence Payment Bill and are intended to be a concession to Labour MPs concerned about the effect of the cuts on disabled claimants.
From April 2026, new claimants who meet the SCC will not have to face future reassessments for health element of universal credit, though they will still be reassessed for personal independence payment (PIP).
At the same time, Labour is almost halving the limited capability for work-related activity (LCWRA) element payable to new claimants, but claimants with LCWRA who also meet the SCC will get the full amount.
The SCC qualifying conditions
The current qualifying conditions for LCWRA require one of a number of descriptors to apply to the claimant “for the majority of the time”. For example:
- Cannot pick up and move a 0.5 litre carton full of liquid.
- Cannot press a button(such as a telephone keypad) with either hand or; cannot turn the pages of a book with either hand.
- Cannot cope with any change, due to cognitive impairment or mental disorder, to the extent that day-to-day life cannot be managed.
The severe conditions criteria require claimants to meet the same criteria “constantly”.
Constantly is defined in the Bill as “at all times” or “on all occasions on which the claimant undertakes or attempts to undertake the activity”.
However, many degenerative conditions such as Parkinson’s, multiple sclerosis and muscular dystrophy follow a slow path of decreasing ability, with periods of remission. So, most days you may be unable to turn the pages of a book, but you may have occasional good days when you can do so.
Or your manual dexterity may be better first thing in the morning but get rapidly worse as fatigue sets in.
At the moment, a claimant in these circumstances would get the full LCWRA amount, which from April 2026 will be £423.27 a month, because they meet the descriptor for the majority of the time.
However from April 2026, new LCWRA claimants in the same position will only get around half this amount, £217.26, because they do not meet the descriptor constantly.
But the same claimant will never improve, their condition will only get worse. So, if they are already unable to work because of a degenerative disease, they will never be able to work again in the future.
Under Labour’s new rules, however, they will have to exist on half the LCWRA element, possibly for years after there is no chance of their ever being able to work again, until they can show that they are constantly unable to carry out an activity, rather than just for the majority of the time.
So, far from guaranteeing that people who will never work again are supported, the SCC guarantees that they will live on a severely reduced income for years, until their degenerative disease enters its most debilitating stage.
For some conditions, including some severe mental illnesses, there may never be a time when the claimant is certain not to have periods of remission, so they may never get the full LCWRA award.
How long will protection last?
The SCC are claimed to protect claimants from ever being assessed again. But, as noted above, people who meet the SCC can still be reassessed for PIP.
From 2028, Labour are planning to abolish the work capability assessment (WCA) and make receipt of PIP daily living the gateway for the UC health element. But they have repeatedly failed to explain what will happen to someone who meets the SCC if they lose their PIP daily living award on review.
Will they still be able to claim UC health even though they no longer meet the basic qualifying conditions? If not, then the SCC guarantee may only last a few years, rather than a lifetime as Labour claims.
Peace of mind
In unveiling the Universal Credit and Personal Independence Payment Bill, Liz Kendall claimed that it “represents a new social contract and marks the moment we take the road of compassion, opportunity and dignity. This will give people peace of mind, while also fixing our broken social security system so it supports those who can work to do so while protecting those who cannot. . .”
In reality, the Bill simply seeks every opportunity to take more money from disabled claimants, whilst telling them it really is in their own best interests.
2 -
Hi chiarieds,
Belletango just posted this and it explains what the severe criteria means. They’re making a distinction between getting lcwra and getting the award under the new criteria which is the descriptor must be met constantly. As you say how can they show you fit the criteria constantly? I get leg pains every day , wake up with it ( fibromyalgia) and go to sleep with it . In between it fluctuates due to pain medication and if I’m able to go outside. If I do go out I won’t go out again for days or more due to worsening symptoms so how can that be proven by me ? I can’t see how anyone can fit this criteria as we can’t have the same level of symptoms 24/7 . Then of course there’s pain meds , does that mean you won’t fit the criteria? Reading it it seems to me that it will be more brutal than the current 10 Year light touch as this as Kendall says will be non negotiable so an assessor won’t be able to use their discretion and award it . I think they’ve put this out there to look good but actually they’ll just scrap the long awards while pretending they are replacing them with the severe category that no one can pass . I’ll post a couple of the screenshots that bellatango posted earlier. I hope I’m wrong on this .
0 -
40 against is nowhere near enough I think it has to be near 200. Which isn't going to happen because the mps who plan to vote against it are bring threatened and bullied. 😓
0 -
I hoe they don’t remove the mobility as although I have a lot of different symptoms and need to rest most of the time there’s no descriptor for pain or fatigue. So I couldn’t even work from home as I couldn’t concentrate anyway and I can’t sit in a chair for periods of time .
0 -
I read somewhere we need between 83 and a 100 , I guess depending on how many from other parties vote against. Tory’s have said they’ll vote against as will independents apart from reform
0
Categories
- All Categories
- 16.3K Start here and say hello!
- 7.7K Coffee lounge
- 120 Games den
- 1.8K People power
- 186 Announcements and information
- 25.6K Talk about life
- 6.2K Everyday life
- 424 Current affairs
- 2.5K Families and carers
- 888 Education and skills
- 2K Work
- 610 Money and bills
- 3.8K Housing and independent living
- 1.2K Transport and travel
- 675 Relationships
- 1.6K Mental health and wellbeing
- 2.6K Talk about your impairment
- 883 Rare, invisible, & undiagnosed conditions
- 945 Neurological impairments and pain
- 2.3K Cerebral Palsy Network
- 1.3K Autism and neurodiversity
- 41.5K Talk about your benefits
- 6.2K Employment & Support Allowance (ESA)
- 20.5K PIP, DLA, ADP & AA
- 9.4K Universal Credit (UC)
- 5.4K Benefits and income


