Has anyone been treated for Myocardial Bridging at Mayo?

My history is similar to yours. Since MB's are congenital and rare, few pediatricians, GP's, let alone cardiologists have much knowledge of MBs. My mother was a doc and she never suspected an MB, thought it was neurological or metabolic in my youth. I could not compete in any sport because I tired too quickly. Abnormally fast for a child, teenager, young adult, etc. My mom had 5 children before me and all were involved with team sports in school and later for fun.
Not me.

There is an excellent myocardial bridge support group on Facebook with loads of information, files on medical studies, podcasts with world renowned surgeons, etc. I had a mild heart attack over three years ago attributed to a myocardial bridge I didn’t know I had. Although my cardiologist identified it his information was out of date. I have an appointment with tests scheduled with one of the country’s leading MB cardiologists next month to get more answers. A big NO for those of us who have MB’s are stents and to a degree open heart surgery.