I did research on Google this physician and the treatment. It does seem plausible. For the MS society to get involved is certainly encouraging. This group can't get any more cautious and conservative. I'll be going to my neuro this next month and I'm going to ask his opinion. I'd be willing to pay to see if I have it. When I get a massage, I seem to do better, so I get one every week .My massage therapist works heavily in the neck and head area which just might stimulate blood flow. I cannot say enough for one to cease aspartamine consumption. It really impacted my symptoms. Now, a neurologist will nearly always say 'coincidental' and I'm not going back on it to see.