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Anyone visited Dr. Bendett at the U of Minnesota


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Hello all,

I have found this web site so helpful. I just returned from visiting my PC doc, and she loved all the info I printed off the web site. We are trying to come up with a treatment plan for this mysterious illness. I have been sick on and off for 15 years on LTD 3 times. This is the first I have been diagnosed with POTS.

I am going to the University of MN to meet with Dr. Bendett. Has anyone met with him before? If you have, what was your experience? Can I expect him to manage this strange disease?

Does anyone else have constant tremors and lots of brachycardia? I think my issue is autoimmune related, because I have lot's of other autoimmune issues. Has anyone else responded to autoimmune related treatments, and if so what were they?

Thank you all for the inspiration and support you give to one another?


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