Hi, my name is Jerry. I was diagnosed with ppms for the third time August 3, 2009 by a University of Pennsylvania Hospital 'big shot' MD, Neurologist.  His diagnosis was a confirmation of 2 previous findings if 2 different local neurologists.  I have been given the same stories as all of the others on this site and I am going out on my own.  I was told that Copaxone may do something, then again, maybe its just going to make me fell better that I am trying something, Pharmaceutical.  I am not taking anything that has not been proven to releive my symptoms, period.  I have been following some natural guidelines that I found in Dr. Andrew Weil's book, pontaneous Healing.  If you don't know Dr. Weil or believe in his stuff, I feel sorry for you. I started on a regimen of many different vitamins, which I found in his book, as soon as I came home from one of my many neirologist visits,  You know, the type of visit where the credentialed guy in the white coat tells you that there isn't anything for you.   Bull !! there is something but these guys are not going to tell you anything that isn't pumped out of a pharmaceutical machine.  | did not know about the doses of B-12 and the vitamin D.  Thank you all for your info. II hope you all can stand and fight this, I will.  Best of Luck to All,  there will be a cure , or we will find one for ourselves.Jerry