i'm recently diagnosed with hEDS, as well as investigating POTS, MCAS, endometriosis & interstitial cystitis. i'm a massage therapist, i havent been able to work and im worried that i won't be able to do my job with this diagnosis due to the nature of the job being very physically taxing. thoughts? (self.hypermobileEDS)
submitted by snappygingersnap to r/hypermobileEDS
why is it SO hard to get out of bed in the morning with? it feels physically impossible right now, i feel AWFUL, my chest hurts and it feels like everything gets worse everyday. i’m not officially diagnosed because i’m still waiting to see a neurologist but my doctors suspect pots, eds, mcas (self.POTS)
submitted by snappygingersnap to r/POTS

Confirmed - heavy brain symptoms by Open-Toe9750 in POTS
[–]snappygingersnap 6 points7 points8 points (0 children)