Health Organization for Pudendal Education

Hi, I've given up trying to find a Swedish doctor to diagnose my Pudendal nerve pain and PGAD (I'm pretty sure myself..., but I can't find a doctor who has had any experience with this or takes my problems seriously). I'm going to London in June and thought I should attempt to get find a sympathetic...

Thanks Violet! No, I haven't tried any of these neuropathic pain drugs. I haven't found a doctor taking this seriously yet, so they are not prepared to give me strong pain killers. (I live in rural Sweden with no choices and long referral times to the hospital.) But I'm a bit scared of these pain ki...

Hi Catherine and Voilet, Thank you ever so much for getting back to me. I realize as I read that I'm desperate for support and a shoulder to lean on. I'm stuck in a state of panic right now and it is not making things any better. Pain increases and my search for help is getting desperate to where I ...

Arrived to this board after about two months of sharp pain - like from a tripple bee sting - following certain moves and increasing as the day goes. Finding all the talk about Pudendal nerve pain is like finding the "home" of my pain. I'm in a state of panic. My doctor has no idea and does...