Health Organization for Pudendal Education

I know i dropped off the forum a while ago, I was trying to return to work and healing from the second surgery. I just did not want to think about PNE more than i had to.

But now i am traveling down the permanent disability road and find my self fighting the battles that so many of you have faced, and thought it was time to reconnect.

Sorry you have had to return. After moderating the forum for 10 years I can't really remember very many people who have been permanently cured. I think often the goal is to achieve low levels of pain, to be functional, and to be able to enjoy life again. I do hope you can get back the ability to do all of those again.

Take care,

Violet

Hi Violet,
Hope you are better. I have a long history of PN and many, many treatments and several surgeries- to no avail. I just posted (my first post) under pudendal stimulator and was wondering if you know of any successes after the implant. I am having it done by Dr. P , MI. in June. My surgeries or treatments have not worked- I work as a nurse in the Chicago area and will retire or try for disability as well- however I can't afford it, currently.
Your past articles have enlightened me.
Cyndi in Chicago

Cyndi, you will probably be interested to read Gwen's story in the neurostimulation section of the forum. Actually, I see you already saw her post but I'll post it again in case anyone else is reading this thread. http://www.pudendalhope.info/forum/view ... =74&t=5739

Violet