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r/ehlersdanlos is a subreddit with 90k 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
Pain
30 posts
#2
Eds
24 posts
#3
Eds
24 posts
#4
Diagnosis
14 posts
#5
Exercise
8 posts
#6
Heds
7 posts
#7
Sleep
6 posts
#8
Symptoms
6 posts
#9
Mobility
6 posts
#10
Doctor
5 posts
Member Growth in r/ehlersdanlos
Yearly
+24k members(36.8%)
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