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r/ehlersdanlos is a subreddit with 83k 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!
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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
+22k members(35.4%)
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