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My FTM friend told me his hEDS pain improved after starting testosterone, idk if this is a common experience but that’s kind of awesome.
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Anonymous 7w

Yeah it’s a common anecdote (I’m not aware of any research on it) my ftm hEDS friend has said the same thing

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Anonymous 7w

my fibromyalgia improved a bit cause of its muscle-strengthening properties

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Anonymous 7w

i would actually say it got worse for me sadly

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Anonymous 6w

idk but the men in my family have it yet i, the only woman, am also the only one disabled by it. it’s pretty commonly accepted that men’s naturally higher muscle mass significantly improves EDS symptoms. that’s my theory on why women are diagnosed so much more. the men just (on average) have less pain/fewer symptoms

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Anonymous 7w

I have PCOS/PMOS and EDS and when my PCOS/PMOS got "worse" my EDS got better, and every time I try to treat my PCOS/PMOS my EDS gets worse

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Anonymous 7w

My mysterious joint instability did too!! yay muscle mass increase

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Anonymous replying to -> #1 7w

okay so i’m not the only one who had this happen, i thought i was crazy 😭

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Anonymous replying to -> #3 7w

That’s so crazy cause mine did not😅 love seeing how things affect other people

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Anonymous replying to -> #8 6w

25% of people with EDS are really sensitive to progesterone. The men with EDS in my family have more organ issues like early hernias, organ ruptures, and AFIB as opposed to severe joint pain.

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Anonymous replying to -> #2 6w

Same

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