I was wondering if anyone had any experience with vaginoplasty despite having ehlers danlos. I have mild EDS classic type and had vaginoplasty about a year ago with Dr Burke at ECMC. I had massive swelling, apparently the most they'd seen, and a fair amount of dehissence (sutures popping). Because of this I have a fair amount of scar tissue around my vaginal opening which I'm trying to break up through dilating, it's been slow going. They tried to remove some scar tissue/open up the vaginal opening when I had a revision, but it mostly dehissed and scarred in again. I'm just getting to the point where I can almost get the full diameter of the p2 (petite orange) dilator inserted but it takes a lot of warm up each time and that's only about 1 inch in diameter which is less than I was hoping for. My surgeon was fine but not great so I'm debating whether getting another revision with a better surgeon would be worth it or if I'll just keep getting more scar tissue. Debating seeing a pelvic floor Physical therapist to help break up scar tissue adhesions. Anyone with similar experience would be great. Thank you.
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