Pudendal Neuromodulation for PGAD

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Violet M
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Pudendal Neuromodulation for PGAD

Post by Violet M »

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.
sadie
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Joined: Sat Apr 23, 2011 7:50 pm

Re: Pudendal Neuromodulation for PGAD

Post by sadie »

https://doi.org/10.1093/sexmed/qfaf073 (or via PMC12459093. Came to post the same thing violet posted but a different link it looks like ...( hers looks more legit) I will try this n get back if my dr will perscribe it and if medicare will D part will help pay. Dont c dr till June. Keep looking every one there has to be a cure .. leave no stone unturned....n think outside the box .love sadie
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Violet M
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Re: Pudendal Neuromodulation for PGAD

Post by Violet M »

Thanks,Sadie. I think you meant to post the article in a different thread about that medication - not this thread about neuromodulation. Here's the thread about that medication:
viewtopic.php?t=12155
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.
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