#eds

3 posts · Last used 18d

Back to Timeline
Morgan ⚧️ @raphaelmorgan@disabled.social · Jul 25, 2026

DuckDuckGo is being unsurprisingly unhelpful with this because all results are influencers or brace brands (most of whom don't even specialize in hypermobility or EDS):

  • Can anyone with hEDS or similar show me a shoulder brace that lets them use their arms but protects their shoulders from subluxation? *

I only need pictures, can't afford to buy one myself so I'm gonna try to DIY 😅 additional information also appreciated, I'll be researching anatomy for it too

#hEDS #EDS #hypermobile

6
1
23
Broadwaybabyto @broadwaybabyto@zeroes.ca · Jul 24, 2026
Boosted by Furbland's Very Family-Friendly Account™ @GroupNebula563@mastodon.social
My disability impacts my proprioception… meaning I’m constantly bumping & banging into things. A few weeks ago I developed a nasty foot infection, and two days ago I sliced open my hand cutting the gauze FOR the foot infection. Chronic illness is no joke. If I owe you a reply or an email, this is why I’m late. My gauze paw is slowing me down! PS… when dealing with chronic illness it’s important to have a well stocked first aid kit! Mine is a first aid bin… it’s one of those large underbed storage containers. Having instant access to emergency supplies is a necessary accommodation to improve quality of life. #chronicillness #disability #eds #ehlersdanlossyndrome
28
0
11
Z @6@plasmatrap.com · Jul 06, 2026
Please share, if you can. I'm so deeply sorry & embarrassed. I'm desperate and not doing well without my medications. 😖 #NEISvoid #hEDS #chronicpain #marfansyndrome #EDS #MECFS #POTS #MCAS #AuDHD #actuallyautistic #ADHD #disabled #longcovid #mutualaid #spooniechat #chronicillness #crowdfund #emergencycrowdfund RE: https://plasmatrap.com/notes/aoctlai1vp
0
0
0

You've seen all posts