Thank you,I think I'm getting the hang of it.I just finished reading someones story of their neuropathy journey.Very interesting.I'll probably be around for a while.All signs point to sfn for me because I just remembered at the beginning of last year the emg specialist said I have a touch of neuropathy on both tests and my current neuro believes with their results being slightly abnormal that I may very well have sfn.I already know I have POTS and autonomic dysfunction without a doubt,I just need the actual tests to prove it which will be on June 15 but I keep calling to hopefully get in sooner.I will have the tilt table and sweat test.Why they don't just do the biopsy and get it over with is beyond me.I'm not going to post on the actual new members forum.I'm only interested in this board for now until I figure this site out.Thanks for all the useful information and links.