Health Organization for Pudendal Education

http://www.justicenewsflash.com/2013/06 ... 11438.html

This article begins

Historically the management of pudendal neuralgia was only available at a select few centers throughout the country. The reasons for this is that pudendal neuralgia was quite rare, often overlooked, and under diagnosed by the medical community. There are only a few doctors in this country who have received the advanced training in the management of this disorder. Even fewer have the advanced surgical training. A great number of physicians do not have a base understanding of the pudendal nerve and are unaware of pudendal neuralgia. In addition, because of the complexity of care in taking care of these patients is has been recognized that there may be a need to employ several specialties to manage an individual patient using a team approach. The team might include a urologist, gynecologist, neurosurgeons, neurologist, physiatrist, and physical therapist. Coordinating such a team is often logistically difficult and not economically possible. Current treatment consists of medication management, physical therapy, CT guided diagnostic and therapeutic injections, and surgical decompression with or without intraoperative monitoring of the main trunk or branches of the nerve.

Which I'm sure we all can relate to.
It goes on to say that POP surgery with mesh can cause severe complications and "In essence the FDA has determined that pelvic pain is an unacceptable postoperative outcome caused by the vaginal mesh."

Oh yes.

In particular, I think it is interesting to note that this article states: It appears that full removal of the mesh is necessary to flush out the problems regarding ongoing pain in patients who have received mesh.

And yet so often it is impossible to remove the mesh, not completely... I still have a fair amount of mesh left which is not accessible, it is literally embedded in the pelvic floor.

Hopefully, more attention to the complications from mesh will safe many others from growing through what those of us with mesh have. The author should have also pointed out that individual can have both obturator and pudendal neuropathy, such as myself. I am glad more attention is being paid to these post-op complications.