Health Organization for Pudendal Education

Violet, I’m in Delaware. So far Dr. Conway who accepts insurance seems to be my best option at this point along with a listed PT an hour from me. I am not really in that much “pain”, unless burning counts?

I see many posts in the past with no recent updates on how they are doing or what is going on. I see people have persevered for years. I don’t think I will be able to afford or get the surgery. Do people stop coming because of despair? I hope suicide is not the final solution. My faith says suicide ...

Which doctors in the USA allow insurance to cover treatment and surgery?

Does numbness indicate pudendal nerve entrapment?

Hi, I have been immersing myself in the HOPE site and other pudendal nerve sites for information. I have some clarification questions. I have read that if you are experiencing symptoms to “not delay diagnosis and treatment”. My symptoms starting about a month ago have been some periodic quick stings...

Pain is increasing in pelvis, some numbness and stinging. Violet, April, are there home exercises that I should employ, no PN and/or PNE diagnosis. Off the bike, what about speed walking. Don’t see the neurologist until December 15. I think I hurt myself biking and bicep curls.

I am a 67 year old male who has been diagnosed with pre-diabetes for several years now. In trying to evade diabetes in the last couple of months,I have incorporated a no sugar low carb diet and have been strenuously biking and lifting weight on a daily basis. Several weeks back I noticed a periodic ...