r/rareEhlersDanlos

This subreddit is designed for users who have a confirmed diagnosis of a rare Ehlers Danlos subtype. (mEDS, clEDS, spEDS, kEDS, BCS, cvEDS, pEDS, mcEDS, dEDS, aEDS, cEDS, vEDS). People with other rare CTDs are welcome. Doctors, physical therapists, occupational therapists, or any medical professional with a heavy interest in the Ehlers Danlos Syndromes are encouraged to join!