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Anyone out there diagnosed with Pudendal Neuralgia?

Chronic Pain | Last Active: Oct 14 2:50pm | Replies (200)

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@johnbishop

Hello @dhc684, Welcome to Mayo Clinic Connect. Darrell @dmburns54 may not have seen your message since he was not specifically tagged using his member name. Hopefully he will see this message. You may also be interested in another discussion - Pudendal Nerve Entrapment/Neuropathy/Damage: https://connect.mayoclinic.org/discussion/pudendal-nerve-entrapmentneuropathydamage/ to see if other members can recommend a surgeon.

Have you thought about getting a second opinion from a major teaching hospital or Mayo Clinic?

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Replies to "Hello @dhc684, Welcome to Mayo Clinic Connect. Darrell @dmburns54 may not have seen your message since..."

John, Thanks for your reply. So far I have seen doctors at Stanford and a doctor in private practice who was formerly at the Cleveland Clinic. None of these have been surgeons as I don't think anyone does this surgery in northern california. What's left for me seems to be either implants or surgery. I located a surgeon who says I'm a good candidate for his surgery, but it's hard to get independent verification or to know if he is the best doctor. I'm hoping to find someone who has experience with a surgery.