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Anyone with POTS/MCAS been treated at Mayo MN for both syndromes?


redpeach

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  • 2 weeks later...

Hey redpeach, to answer your topic question I did go to Mayo in MN for POTS though I do not have MCAS. They did do some thorough testing, though I was a neurology patient at Mayo since 2009 before my POTS got worse so I've had lots of tests done there over the years. I did think that their autonomic specialists were the best ones I've been to but it was more for diagnosis only, not for continued care. And for me since I seem to almost be suffering more from a complication of orthostatic hypotension than just POTS itself, they weren't able to help me get any better.

I've never been to a place with better medical treatment with Mayo. 

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