how have any of you with dysautonomia gone about getting checked for EDS? i think i may have it but i’m terrified to go back to having a million dr appointments and medical gaslighting. what kind of symptoms or signs do u have that made u think that you have EDS?
Ehlers-Danlos Syndrome (EDS)
Disorder of Autonomic Nervous System
I have always suffered from bruises even when the hit wasn’t too strong. And for the years before my diagnosis I suffered from persistent dislocations of my shoulder. My pcp knew right away that I suffer from EDS
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