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r/ehlersdanlos

This is a support sub for those with Ehlers-Danlos syndrome (all types) and HSD—diagnosed or waiting to be diagnosed. This is a welcoming place for those affected (or those simply wanting to learn more) to ask questions, share successes and failures, feel less alone, and discuss everyday life. Before participating, please read our rules. This subreddit does not allow medical advice. Thank you!

Subscribers
1.7K
1,662 total

Subscriber history

Overview

Subreddit
r/ehlersdanlos
Subscribers
1,662
Tracked posts
2 shown (top 10)
Data points
1

Most popular posts

Title Upvotes Comments
New name for cEDS? 88 32
Different tests, same results, big doubt. 5 2