There are not enough words to express my contempt for the (relatively new?) EDS communities filled with
"Here's my 30th gifted mobility aid from a PR package and i am being paid to tell you to not go to an occupational therapist and also mobility aids only have positive effects they can do no wrong ever"
"I am the face of lifelong severe disability because i developed POTS last year"
"I was completely healthy all my life until i was 40 and i'm not really even that hypermobile but i do get stomach aches from fast food and my back aches sometimes, which all disappears when i eat a vegetable and stretch a bit"
"Watch me dislocate my joints" (proceeds to show a hyperextension, not a dislocation)
"If you buy my $500 course I can cure your EDS with products only found in the USA"
"If you go to a doctor you are a privileged arsehole who wants everyone else to die"
"Here are 10 unscientific, unsupported, scaremongering claims about EDS in a glittery font"
"hEDS is a terminal progressive incurable untreatable disease which will kill you. No I have never heard of vascular EDS what is that?"
"I would rather have cancer than EDS because at least cancer has a cure"
"Strengthening exercises can cure 100% of your symptoms and make you able bodied"
"If you make any attempt to make yourself better you're ableist"
"I wish I had a feeding tube to look ill so I'm going to deliberately make myself ill so that I feel validated in my symptoms"
"I think actually 10% of people have EDS"
"Everyone with autism/adhd has EDS"
"Everyone with EDS has autism/adhd"
"Here's my realistic aesthetic 15 step getting ready for bed program on a flare up day"