Has anyone had neuromuscular testing and did it show anything? Yves Jammes is doing evoked potential testing of muscles in ME/CFS patients and finding interesting things, e.g. http://www.ncbi.nlm.nih.gov/pubmed/19457057 and I'm pretty sure I'd found another group finding same thing. All small studies, though. I have a chance to go to a neuromuscular specialist and I don't know whether it would be worth it. Super tired of having a disease that is "well, not any disease we know about"... despite noteable pathology which the doctor commented on, "probably that particular problem is caused by deconditioning, or stress"