Pudental nerve decompression surgery

[Milly49]

Has anybody had successful Pudental nerve decompression surgery ?

[edythe]

I suggest looking at the pelvic pain area of heath unlocked. And maybe using the search function. You should find a fair number of posts on the subject there. I hope this is helpful.

[Konagirl60]

I have. It saved my life. No medicine helped the terrible electrocuting pain. I almost died from sleep deprivation.

[Milly49 in reply to Konagirl60]

Thankyou for your reply

Can I ask if you where you had the surgery as I can see most people have gone to Nantes for the procedure?

I am struggling to get a reply from the doctors there at the moment but have received the information I require from two other Drs in France however they all do slightly different procedures and so I am unsure which way to go.

I have been advised to two successful nerve blocks before making any decision. As I have only had one so far so I am now unsure what to do

as I am unable to have another nerve block for a while yet, also the second one has in fact made my symptoms worse.

I would appreciate any help and support I can get to make a decision.

[Konagirl60 in reply to Milly49]

The doctor in France didn’t respond to me either.

My doctor in Minnesota has retired. In Europe he’d recommend you see Dr. Jacques Beco in Belgium or Dr. Bruno Roche in Geneva, Switzerland. I’m assuming you are from Britain?

Nerve blocks were useless. I needed surgery. Thank goodness I finally got it as I was on death’s door from severe sleep deprivation.