The disability benefits system is broken. It has not adapted to a world where disability and ill health are more prevalent, and more complex in terms of the variation of impact on people's lives or the support that could help.

Disability often results from medical conditions, and is worsened by challenges accessing health services and social care. It is also exacerbated by the barriers to participation in society and the economy – such as limited access to education, poor quality transport infrastructure, employment discrimination, and inflexible workplaces – that disabled people face.

Over the last 20 years the main policy response, in the face of rising costs, has been to make claiming disability benefits more difficult.

Additional Links/Reading: CWs in spoilerCWs: ableism, discussions of trauma, medical ableism, neglect and abuse, eugenic and capitalist undertones/viewpoints

Disability Benefits in Different Countries

Half of disabled people ‘humiliated’ during benefits assessments, new research finds

Center For American Progress - How Dehumanizing Administrative Burdens Harm Disabled People

Disability News Service - UN committee asks government: ‘Why are you demonising disabled people?’

Cryptpad for copied report from Australian Federation of Disability Organisations (AFDO) on harm caused to individuals with disability by their interaction with Centrelink’s Disability Support Pension (DSP) application and review processes from 2021


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[–] 7 points 2 days ago (4 children)

Spent all day at the hospital today. Just horrible. First I had my stroke clinic check up, which I hate because they are so pushy about trying to make me have extra meds and blood tests. They were over an hour late for my appointment and then sent me down to the phlebotomist where I had to wait for nearly another hour to be seen, dreading it the whole time as I am very squeamish and sometimes faint. Then I had my eye clinic appointment in the afternoon and they are always so late and do so many tests and you have to wait to be seen in between each test, in the end I was sitting around in the hospital from about 10am-6pm and now I am just exhausted. I wouldn't keep going through this if I didn't need to do it for my benefit claim, it doesn't even bring me any health benefits. It means disabled people don't have the same rights as everyone else - if other people want to quit medical treatment they can just do that, but if I want to quit they'll use it as an excuse to impoverish me to death.

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  • [–] 5 points 2 days ago (3 children)

    This is degrading beyond words, having you go through all of this over and over again for the benefit thing is absolutely not okay. Like you said, they do this on purpose, but it's always horrible to read what they put you through. I'm sorry your day was like this, I really wish it could have been nicer cuddle

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  • [–] 5 points 2 days ago (2 children)

    Thanks. meow-hug On the plus side it looks like I'll be getting discharged from physiotherapy soon, as it is not working and the physio basically said it's a waste of NHS appointments. It's tiring going to physio and doing all the exercises all the time for no reward. I've only kept up with it this long for my benefit claim, and I'm long since resigned to being permanently disabled. My only worry is that at my next assessment the DWP will use this against me, saying "You're not having physio? Then there is nothing wrong with you!" But if I've spent years having physio and it hasn't worked, how is that my fault? I will ask the physio to write me a letter saying I've had all the treatment and it hasn't worked and they won't treat me any more, but the DWP will only accept letters that are less than 6 months old and by the time of my next assessment it will be older than that.

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  • [–] 5 points 1 day ago (1 child)

    Okay, first I'm glad you don't have to attend physiotherapy any longer if it doesn't work for you. second, I really hope you don't get into trouble for not having to go there anymore when the next benefit claim comes around the corner.

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  • It's the only thing I'm worried about. At previous reassessments they have used the most spurious excuses to deny my benefit claims. Straight after my stroke, I was on the waiting list waiting for physio to start, and they used that as an excuse to stop my benefits: "You are not having rehabilitation for the stroke, therefore it is my judgment that you are capable of the physical activities you say you cannot do," or words to that effect. The fact that I was on the waiting list for treatment was ignored. Also I had spoken during the assessment about how the stroke had caused me to lose a quarter of my vision which was giving me trouble crossing the street safely etc, and the assessor suggested I could just walk around constantly rotating my head 360 degrees to achieve a full range of vision, and so it was decreed that my visual issues would not be taken into account and I was given zero points and my money stopped. They will use literally any excuse and make me go through appeal.

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