i want to break down some disability stats because i see a lot of people balking at the idea that there are 16 million disabled people in the UK (only 3.6 million of those on PIP, and only 37% of those claimants on the highest amount of £737 a month)
let’s have a 🧵 shall we?
at any one time, it’s estimated that there are:
-3.5 million cancer patients in treatment in the UK
-7.6 million people have some form of circulatory or heart disease
-982,000 have dementia
-150,000 have MS
-153,000 have Parkinson’s
-1.2 million have COPD
and these are just the diseases everyone has heard of
it’s estimated that:
-4,400 people per year are diagnosed with a new spinal injury
-3 million people have some form of osteoporosis
and we aren’t even onto lesser-known genetic or acquired conditions
-my genetic ataxia, for instance, unique in presentation as it is, accounts for 10,500 patients across the UK and that’s inclusive of a number of different disorders that huddle under the ataxia umbrella
but these numbers, across a population level, soon add up
the fact only 1.3 million people of a 68.3 million population are entitled to the ‘riches’ (lol) of £737 a month, many of whom are still in work because *PIP is NOT an out of work benefit* is testament to the fact many disabled people go without help, not that it’s over-awarded
a couple of people have asked me this in the comments so: the lowest amount of PIP someone can be awarded (above £0) is £28.70 a week, which is £114.80 a month,
so remember that when the media tries to whip everyone into hysteria over this benefit. it is often a pittance
ok friends i’m going to bed and don’t want to wake up to hundreds of notifications so i’m going to mute this now! 🙏
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one day we’re all going to have to have a serious conversation about the differences between someone who’s disabled but whose body is otherwise healthy (amputation etc) and people who are disabled systemically through chronic illness & degenerative conditions
this is what i mean when i say disability isn’t a monolith: & why i both respect paralympians & know the paralympics can do a lot of harm to disabled people who have systemic conditions in terms of public perceptions of disability and the concept of the Super Crip
disabled people are the most diverse minority group in the world, but disabilities themselves are diverse and the people you see at the Paralympics in wheelchairs etc are by and large *healthy*, alongside being disabled
honestly one of the prime tells of whether a leftist knows anything about disability imo is whether they’re aware of the decades of institutional abuse that’s led to them believing CFS (really ME, a neuro-immune illness that kills people) is nothing to be bothered about
like, arguably the treatment of this patient group is one of the biggest medical human rights scandals since the AIDS crisis - patients have fought and died for recognition & treatment since well before AIDS happened, yet too many supposed revolutionaries know sweet FA about it
you’re in the middle of a viral pandemic, people are dropping like flies with post-viral illness. there are political reasons there’s no treatment & apparently while we’ve been staging worldwide Millions Missing protests every year you’ve just been going ‘la la la can’t hear you’
CFS is the rebranded name of ME - a devastating neurological condition that was first described by Infectious Diseases Consultant Melvin Ramsay following a viral outbreak at the Royal Free Hospital in 1955 (🧵)
Melvin’s tests at the time of the nearly 300 people who became violently unwell revealed major immune dysfunction, and damage to the nervous system. he would spend the rest of his life working on post-viral disease until his death in 1990
it was widely accepted as a neurological illness - the WHO classified it as one in 1969 - until 2 psychiatrists by the name of McEvedy and Beard wrote a report in 1970 in which they claimed the Royal Free outbreak was mass hysteria, in direct contradiction of test results