I have been recently diagnosed with pots and per my doctors referral am seeking treatment at the Mayo Clinic in Rochester Minnesota. I know people have posted about this in the past but was hoping for some new insight as to people's experiences with mayo. I leave on Saturday and am not looking forward to the plethora of testing they have planned for me but am really hoping for some answers and/or guidance.
Any experiences or suggestions regarding the Mayo clinic would be greatly suggested. Also, may suggestions for things to do/see/eat in Rochester would be greatly appreciated!
Rochester Mayo Clinic
in Dysautonomia Discussion
Posted
Hi all,
I have been recently diagnosed with pots and per my doctors referral am seeking treatment at the Mayo Clinic in Rochester Minnesota. I know people have posted about this in the past but was hoping for some new insight as to people's experiences with mayo. I leave on Saturday and am not looking forward to the plethora of testing they have planned for me but am really hoping for some answers and/or guidance.
Any experiences or suggestions regarding the Mayo clinic would be greatly suggested. Also, may suggestions for things to do/see/eat in Rochester would be greatly appreciated!
Thanks!