r/eds
Ehlers Danlos Syndrome (EDS) is a underdiagnosed connective tissue disorder characterized by a genetic fault in collagen. It manifests as hypermobile joints and affects every organ system because we’re all made of connective tissue! We welcome all EDS subtypes, hypermobility spectrum disorder, Loeys Dietz, unnamed genetic disorders that present like EDS, self-diagnosed & suspected zebras. || || || Crowdsourced medical care saves lives. We welcome medical advice!
r/eds Subreddit Stats & Analytics
r/eds is a Medical Advice subreddit in the World category with 29,495 members. Use this page to track r/eds stats, subscriber growth trends, daily and weekly analytics, and similar subreddits with related audiences.
Recent r/eds growth: +83 members today (+28.22%) and +389 members this week (+133.65%).
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Similar subreddits to r/eds include r/ehlersdanlos.
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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!