I completed the Wheldon Protocol for MS several years ago.
Since then, my follow-up MRIs have all been "remarkably stable". I don't hide the fact I did the Wheldon Protocol without medical supervision from my doctors - in fact I shave the documents and the MRIs under their noses any time they will let me. Still, only my primary care doctor (who is an O.D., not an M.D.) is willing to believe the treatment had any effect on the disease.
That's too bad for the other patients who could be helped by it, but great news for me.
I've decided to retire at the end of March 2018. Shortly after that, I will be moving to a region of the country were internet service, if available at all, is spotty, so I may drop off this board entirely. If that happens, I continue to urge people with MS to read my blod, learn from my experiences, follow the Wheldon Protocol to the letter and, hopefully, get the same benefits I did.