I wanted to know if anyone here has ever had repeat pudendal nerve decompression surgery and their outcome?
I had bilateral pudendal nerve decompression surgery in Nantes in 2013 with 50% improvement up until the last 18 months when the symptoms have worsened progressively. I had a spinal cord stimulator implanted in October 2018 but it has only helped a little and its effect seems to be lessening with time.
It is possible that I have developed some surgery related scarring around the pudendal nerves and wish to consider repeat decompression surgery as my symptoms limit my quality of life significantly.
I was saddened to hear that prof Robert has retired - he was a real gentleman.
Thanking you in advance for sharing your experiences.