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I'm new to this app. I just got diagnosed with ehlers danlos syndrome late last month and am going to a cardiologist to see what type of dysautonomia I have soon. I just feel kind of alone in this new diagnosis and being chronically ill in general. I'm wanting to meet more people I can relate to with my diagnosis. I hope other people on this app will reach out to me, so I have more people to relate to.
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hi! welcome to the app! i have suspected EDS and dysautomnia, among lots of other things. you aren’t alone although i know it’s hard not to feel like that. 💗
@stxrberrym00n I hadn't considered eds as a possibility til mid last year, so this is all a new thing for me. I'm glad there's other people like me out there.
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