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I am so sorry to hear that you have been to numerous doctors, and have not found relief yet. I am not familiar with pudendal neuralgia, but I skimmed some professional journals (the ones your doctors should be reading), and provided the summaries below. I am not a doctor, so please know these are only the articles I found; there may be others that say surgery is not an option. (Can you get your hands on these journals through a university library, in order to do some further research?)

1) "Pudendal neuralgia is poorly recognized and poorly treated. Improvement is gained with conservative therapy. Injections and decompression benefit one half and one third of patients, respectively. Neuromodulation needs further evaluation."

This article mentions three types of therapy: conservative, injection/decompression and neuromodulation. I could not gain access to the full article, so am not sure what "conservative therapy" is.

2) I could not even gain access to this articles' abstract, but the title was intriguing: "new diagnostic and treatment algorithm". It also mentions something called "infiltrative therapy". Again, if you can get this article from a library, or at least there is another specific therapy term you can ask your doctor about

3) This article provided results for the LION technique (laparoscopic implantation), which was successfully performed...but he sample group was only three patients. They did find "significant diminution of pain without need for further medical treatment". "Conclusions: Laparoscopy allows optimal implantation of electrodes on all pelvic nerves through a minimally invasive approach. In addition, it permits new applications of neuromodulation for pelvic polyneuropathies or mononeuropathy, not covered by classical spinal cord or transcutaneous techniques."

Lostindiapers, I hope this didn't make you more confused, but I wanted to give you some information and technical terms ("doctor speak") for you to ask your doctors about! Please let me know if you can not access these articles through a university library, and I can try to help further!

Lastly, have you thought about seeing a naturopath or other health professional who helps people with chronic pain? The longer I've been on this site, the more posts I see from people in chronic pain (regardless of the source or condition) who have sought the alternative/complementary medicine professionals and have found this very beneficial. Here's a great website to get started: http://nccam.nih.gov/

Sources:
1) American Journal of Obstetrics and Gynecology
Volume 192, Issue 5, May 2005, Pages 1663-1668
Pudendal neuralgia, a severe pain syndrome
by Jesse Thomas Benson MD and Kenneth Griffis MD

2) Clinical Neurophysiology
Volume 117, Supplement 1, September 2006, Page 204
Abstracts of the 28th International Congress of Clinical Neurophysiology
P17.2 Neurophysiology in infiltrative therapy for pudendal neuralgia: New diagnostic and therapeutic algorithm
by S. Malagutia, M. Spinellia, M. Citeria, L. Zanolloa, J. Tarantolaa and T. Redaellia

3) Neuromodulation
Volume 10 Issue 1, Pages 18 - 23
Published Online: 10 Jan 2007
The Laparoscopic Implantation of Neuroprothesis (LION) Procedure to Control Intractable Abdomino-Pelvic Neuralgia
Marc Possover, MD, PhD Jan Baekelandt, MD Vito Chiantera, MD

October 5, 2008 - 6:07am

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