u/Ok_Acanthisitta_8627

Fat loss in hands

hi all. Been a long time since I’ve posted here, I’m doing much better these days which I can give an update on soon. I was severely floxed in May 2025

Has anyone who suffered severe collagen loss ever recovered over time? My hands lost significant collagen/fat and continue to look deflated and skeleton like. It’s been 15 months and very little change so I’m not too hopeful, but if anyone has found something helpful please let me know

Hang in there yall 💓 I am just now starting to live life again, things can get better

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u/Ok_Acanthisitta_8627 — 19 days ago
▲ 8 r/eds

hi all, newly diagnosed as of last year. I wanted to ask if there truly is a spectrum with this condition? Last year I took a Fluoroquinolone not knowing I had EDS and it took all my “weird” chronic health problems sky high

I’m hypermobile, but prior to the Fluoroquinolone I think my main issues with EDS were slipping ribs, collapsed foot arches, everything cracking/popping, and easy scarring. I feel like I could have gone my whole life not having a diagnosis until the antibiotic caused severe instability in all my joints

Is it possible to go from mild to moderate/severe with a trigger? thank you!

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u/Ok_Acanthisitta_8627 — 4 months ago