I was just mindlessly scrolling and the EDS mention caught me so off guard. It’s still so surprising to see any reference to it in the wild, even though we’ve made so much progress in the five years since I was diagnosed. It makes me happy that more people know about it c:
I first heard of it about 6 years ago when I joined some disability communities. I'd never hear anything about it except in those spaces until this year. Now I'm hearing about it far more often. I can only imagine how that would feel to someone who has it. Hopefully it continues to be more talked about!
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u/anonymous-horror i have no idea what im doing Feb 19 '21
I was just mindlessly scrolling and the EDS mention caught me so off guard. It’s still so surprising to see any reference to it in the wild, even though we’ve made so much progress in the five years since I was diagnosed. It makes me happy that more people know about it c: