#eds

5 posts · Last used 22d

Almost exactly 3 months since I got these shoes and I'm still getting blisters/pain (in the same two places on each foot) any time I walk longer than 2km (which is pretty regular), no calluses or anything in sight. My feet are still soft and smooth as a baby's bottom.. Similarly with my fretting fingers, no trace of calluses at all, and I'm close to 3 months of regular practice there too. I'm chalking both of these up as more potential symptoms of #eds 🤷🏻‍♀️
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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

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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
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