I had self-diagnosed pudendal nerve entrapment a few years ago when I tweaked something exercising, and it was brutal. The symptoms were so bizarre, but unmistakable once I saw the symptoms of PNE. I managed to get rid of the problem by doing a lot of stretching, but I know I was lucky.
I certainly hope your bout with pudendal neuropathy is short-lived. It can't be pleasant.
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Originally Posted by heb1212
Hi, all... I've been reaching out to fellow NeuroTalkers for support and knowledge since the onset of my neuropathy, now several years ago. The history in a nutshell... bad, bad virus followed in a couple months by severe body-wide nerve pain, including my face and mouth, nose, throat. Everywhere... so I thought, until the last couple months. Now, Oh, my God, it's everywhere in my most private areas. I burn, ache, stab and twist in places I didn't even know existed. I've researched my symptoms and come up with Pundendal Neuropathy. I'm wondering if anyone has ever experienced this type of small fiber nerve damage from an autoimmunue response?
As Always... thank you for responses.
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