I was just wondering if anyone had any first hand experience with any POTS or dysautonomia specialists at Mayo Clinic in Rochester, Minnesota. I was recently diagnosed with POTS by a local Electrophysiologist who only sees handful of POTS patients each year. He offered to make a referral to Mayo on my first visit, which leads me to believe he really isn't up to the task of treating another patient, so I was just curious if anyone had any suggestions about any specialists at Mayo in Rochester.
Thanks