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tatertot731

668d

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?

    • Tomato

      662d

      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

☝ This content is generated by our users and it is not a substitute for professional medical advice. Please consult with your physician before making any medical decision

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