Joining a #LongCovid online support group is definitely something...a 🧵[thread]

Listening to people who were able bodied experiencing disability for the first time definitely brings up so serious feelings for me, anger, frustration, annoyance 1/8
I just want to sit in the middle of it all and shout and the want to shout "some of us live like this all the time and no one cares!? Now you can finally see what that feels like."

But I don't want to dismiss anyone's very valid feelings about having their mental and 2/8
Physical health stripped away from them.

They are now part of the Disabled community, *my* community. But they bring with them so much shame and unhappiness. Feelings I totally understand and are valid but are very difficult to listen to as a long term Disabled person. 3/8
It's like having our space invaded by people, who for the most part ignored us and now want help, support and love now that *they* are chronically ill.

It doesn't really work like that tots. 4/8
But I sit and I listen and I see myself and my other chronically ill friends reflected in what they say, how they say it, the emotion that comes with it.

The grieving of your previous ability, body and self.

Its painful to read and there's no answer to people's 5/8
Questions of "why me?" "Was it that one time I forgot to wear a mask at the shop?" "When will I go back to the way I was?".

None of these answers are clear or easy. And for most of these people we won't go back to how we were, ever. 6/8
This is us now, in all our extraordinary struggles with the most mundane of tasks. Strugglijg, drowning in a world which doesn't have the resources to help even if they wanted to. 7/8
Covid has created another group of Disabled and chronically ill people with no support, no answers and with such poor mental health.

I am angry. I am beyond angry that Disabled people are just so dispensible in our world.

/end
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More from @social_parasite

Jul 1
So, my plan for #PrideMonth was to write something every day.

It's my plan every Pride Month but Attention Hyperactivity, brain fog and life gets in the way!

It is so vital that we share our stories, resources, information love and acceptance all year round but...
...especially in a month where big corporations make rainbow dollars with no regard for LGBTQIA+ support. Or a passing performative we'll-bung-some-money-at-the-most-obvious-Queer-charity.

It's a month where some Queer charities are uplifted but come July 1st, are dropped...
...like a stone and left fumbling for help the other 11 months of the year.

Today the flags get taken down - the pink pound has been squeezed enough from us folk who tend to have less money anyways...
Read 4 tweets
Oct 8, 2021
At group yesterday a physically disabled person referred to themselves as a crip and crippled.

A lot of people recoiled in horror at those words and the MH 'specialist' said that would need unpacking another time.

Their reaction is so problematic. 1/
Us disabled folk are continuously abused, ignored and patronised by those around us.

And when we finally own who we are as crips, disabled whatever words *we* choose we are policed. /2
I have this in research, I have to go to a lot of effort to explain why I, an autistic person, want and need to use identity first language.

This person had it at a MH group, it was implied that she was somehow wrong referring to her bodymind in that way.
Read 17 tweets

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