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r/ehlersdanlos

71,383 subscribers

Notice: This subreddit is not actively monitored, so the posts here are only a small subset of what exists on reddit.

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Questions Discussion Vent Success! hEDS Trigger Warning: Body Image/Weight Discussion Rant/Vent Article/News/Research Seeking Support TW: Body Image/Weight Discussion hEDS Removed: Polls, surveys or research #9 JHS Resources TW: Eating Disorder/Disordered Eating Rant Does Anyone Else Connective Tissue Disorder Not Otherwise Specified Career/School TW: Death/Dying No Advice, Please No Advice, Please. HSD Product Recs
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to r/ehlersdanlos by Helen_Cheddar
4 months ago
Preview thumbnail for I have no words… image
I have no words…
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to r/ehlersdanlos by Mira_Maven
1 year ago
Struggles With Surgeon - Seeking Empathy
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to r/ehlersdanlos by whiskkerss
1 year ago
EDS is messing with my chances. (Advice welcomed)
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to r/ehlersdanlos by Bake-Me-Away
1 year ago
Sex Injuries
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to r/ehlersdanlos by Secret779
1 year ago
I'm a hEDS wheelchair user and am always asked whether I'm diagnosed or if I "feel" it's something I have.
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to r/ehlersdanlos by Helen_Cheddar
4 months ago
Ah, Supportive Dads…
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to r/ehlersdanlos by Helen_Cheddar
4 months ago
Raise your hand if your doctors often just diagnose you with “fat”. ✋
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to r/ehlersdanlos by llamallamabarryobama
7 months ago
Preview thumbnail for Faking my way through the pain: image
Faking my way through the pain:
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