Paper on informing doctors about PN
Paper on informing doctors about PN
I don't remember where I saw it or under what topic, but it was a page on explaining PN to doctors. I made a copy to give to my doctor but I want to have my husband read it. I can't find it anywhere and I did read it on this website. Can anyone tell me where I read it. Judy
Symptoms came on so slowly they were hard to explain to anyone much less myself. Discomfort sitting one day and not the next. Foreign object feeling in various private parts. Doctor to doctor. Mis- diagnosed many times. Un-needed surgery, depression pills and finally a diagnosis of PN. EMG testing in NH. Unsuccessful nerve blocks. Will start PT in a few weeks. Finally I don't think I'm crazy!!!
Re: Paper on informing doctors about PN
Judy, there are two.
http://www.pudendalhope.info/forum/view ... ?f=3&t=953
http://www.pudendalhope.info/forum/view ... ?f=3&t=247
http://www.pudendalhope.info/forum/view ... ?f=3&t=953
http://www.pudendalhope.info/forum/view ... ?f=3&t=247
PNE since 2002. Started from weightlifting. PNE surgery from Dr. Bautrant, Oct 2004. Pain now is usually a 0 and I can sit for hours on certain chairs. No longer take medication for PNE. Can work full time and do "The Firm" exercise program. 99% cured from PGAD. PNE surgery was right for me but it might not be for you. Do your research.