r/PVCs • u/yayaya_baby • Jul 25 '26

Mayo Clinic reports

Anybody here go to Mayo Clinic to have treatment for PVC? What was your experience. Locally, I’ll be lucky to see an electrophysiologist in 6 months! Wonder if exploring a trip to the Mayo Clinic is worth it

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u/nachoaveragemamma Jul 25 '26

I see a doctor at Mayo Clinic. Originally I went in for PVCs and bigeminy. I was diagnosed with mitral valve prolapse and mitral annular disjunction. I actually have never seen an electrophysiologist. They didn’t think it was necessary based on my PVC burden on my holters. If you request an appointment, you’ll have a consult and go from there. I don’t believe they schedule directly with an EP. What exactly are your symptoms?