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r/hypermobileEDS

1,948 subscribers
A place for those diagnosed with, or seeking diagnosis of, Hypermobile Ehlers-Danlos Syndrome. This is the most common sub-type of Ehlers-Danlos, which is a rare (probably not so rare) genetic condition that affects collagen made in the body.

This is a place to speak your mind, but staying on topic would be appreciated. Nothing here is medical advice unless otherwise stated.

There are no rules past the regular reddit rules. Enjoy!

Notice: This subreddit is not actively monitored, so the posts here are only a small subset of what exists on reddit.

New Top (24hr) Top (Week) Top (Month)
to r/hypermobileEDS by raindrops_oceantops
3 months ago
Just got diagnosed with heds…
to r/hypermobileEDS by willowtreeintherain
5 months ago
Motorcyclists? 🇬🇧
to r/hypermobileEDS by willowtreeintherain
5 months ago
Hysterectomy?
to r/hypermobileEDS by ready_to_work_22
4 months ago
What are the best ways to make supplemental income? Need ideas on how to pay these medical bills
to r/hypermobileEDS by ready_to_work_22
4 months ago
what more can i do to combat my chronic tennis elbow pain?