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/r/ehlersdanlos/

r/ehlersdanlos

87k members
r/ehlersdanlos is a subreddit with 87k members. Its distinguishing qualities are that the community is large in size, and has high activity.
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! _._._._._ Feedback Forms: https://www.reddit.com/r/ehlersdanlos/s/fwQN2A4c2n

Popular Topics in r/ehlersdanlos

#1

Eds

101 posts
#2

Pain

57 posts
#3

Frustrating

50 posts
#4

Hate

49 posts
#5

Made

46 posts
#6

Expensive

26 posts
#7

Worst

17 posts
#8

Diagnosis

14 posts
#9

Splints

9 posts
#10

Video

6 posts

Member Growth in r/ehlersdanlos

Yearly
+24k members(38.4%)

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