Health Organization for Pudendal Education

Update. I don't know if my case was actually PN or whatever else. Doctors can't tell. Surely there has been a neural damage by fluoroquinolones confirmed by an orthopedician. As a fact, following a further course of cypro I had to take forcibly last Winter in few days I developed chronic pain in my ...

Sorry I can't quite follow this thread and interact properly, given email notifications seem not working for me. Anyway, my little update. I was close to see a pelvic floor therapist but I was not convinced yet. After all the last urologist who visited me suspected that PN could be chronically infla...

Hey, I ended up in this thread googling. I have an experience which *could* be compatible with your theory about antibiotics triggering pudendal neuralgia ! Please read and forgive my poor English, I am not natively speaking. I am 40 and otherwise healthy. This is the third time in my life I develop...

Your story is quite different than mine though.I have not any concurrent health issues and no suergeries done. Anyway, for an update. Three doctors were convinced it was pudendal neuropathy. But I was not responding to Lyrica or to Amitriptyline either. The other day I saw a proctologist expert with...

Hi I am new, I found this forum and I decided to post my story because I am now hopeless. Sorry for my poor English, I am not natively English speaking. A due premise on my clinical condition: for a genetic defect I was born without an uterus and with malformed genitalia and I had a corrective surge...