Could anyone share their experience with the mayo clinic in Rochester mm?
I saw dr pollock there and he was a total asshole. I had my MRI/MRA done there. They couldn’t see any compressions apparently. I went back and saw dr Myers and he said more than likely I did have TN and he would do an exploratory mvd but only gave me 30-40% chance it would work. What you have to remember about Mayo is that if you are the “perfect candidate” they won’t really want to do any procedures in you. They have to keep their success rates high so they turn away those people like me, who don’t have obvious compressions. I’m sorry to break the news. I loved dr Myers. He was kind and took a lot of time talking to me. Dr pollock took 10 minutes and was a jerk with no empathy. I was crying by the time I got to the elevators. Best of luck to you and please keep in touch with me. Find me in Facebook!