Been (33y)having widespread fascic for 2.5 months.Seen 3 neuro's;1 private practice,1 UNC,and the last one in the Duke MDA/ALS Clinic (Director).The PP Neuro gave me an NCV/EMG on the right leg, arms (it was an old machine not like the one at UNC/Duke).Anyway, he said it was normal.UNC had neuro exam,blood work including HIV, Lyme,thyroid,etc. all neg except my B12 was 238-UNC neruo said that a level below 400 is low to a neurologist so am taking b12 pills-UNC Neuro ordered EMG/NCV b/c of fascic but the Neuromusclar Spec at UNC completed the NCV which was normal then said that he felt like there wasn't a need to do the EMG since if I had ALS I would have shown signs clinically +on NCV he called the UNC Neuro & he agreeded no need for EMG.Went back to UNC for f/u & Neuro had never heard of BFS until he consulted w/another UNC older neuro who had never seen me but knew of my symptoms and he told the resident that he has pts all the time with fascis who think they have ALS but actually have BFS. Still not satisfied and got an appt.Duke in the MDA/ALS clinc for eval.neuro exam normal, had a comprehensive NCV/EMG done 2 days later on 11-26-02 at Duke (all 4 limbs, tongue, back, throat) NORMAL-going back for f/u with neuro in Feb. His initial diagnosis before the EMG was BFS(said that he has seen more ALS than I could ever imagine and this didn't look like ALS-even said that Neurophysiology docs would probably think he was crazy but better safe than sorry-gave me valium.Still having widespread fascis, intense cramping esp. calves, arms,now fingers cramp.Does this sound like ALS?