Has anyone been treated for Myocardial Bridging at Mayo?

Posted by raweber @raweber, Apr 5, 2018

Has anyone been treated for myocardial bridging at Mayo in Rochester?

Interested in more discussions like this? Go to the Heart & Blood Health Support Group.

@bernicew51

I have a myocardial bridge in the LAD. I only found out 4 years ago that I have one. I am now 71. I have had issues my entire life with mine. Whenever I was around age 1, my parents had to rush me to a hospital and the doctors thought I was having a seizure. Until my general practitioner in Mobile, AL noticed a problem with my EKG and ordered a heart cath and found mine. I made so many trips to the ER, because I thought I was having a heart attack. They could never find anything. I am very interested in communicating with anyone that has a myocardial bridge. I would like your advice on where to go to see a doctor that knows about it. I can't find a doctor in Mobile that has any other patients with Myocardial Bridge.

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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.

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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 Although my cardiologist identified it his information was out of date.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.

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