Further update: it's recently been suggested to me that I should get checked out for Sjogren's Syndrome. I had a chat with the SS helpline, and it does indeed match me suspiciously well, but I'm having so much trouble getting the dysautonomia diagnosed right now that I think I'll have to shelve investigating it for the time being. Meanwhile, it's food for thought. I'm considering raising the dose of my Omega 3 oils, and wondering if the vulvodynia is indeed connected to my dry eyes (and mouth. And nose. And my skin's none too happy either). If it were SS, would that lead me anywhere in terms of treatment for the vulvodynia?