I have not been diagnosed with MS, and hope I won't be. I just had the MRI of the brain and C-spine a couple days ago, so it will be a few days before I hear anything from the doctor. I HAVE BEEN diagnosed with Lupus, Sjogren's, Rheumatoid Arthritis, and Autoimmune Hepatitis, and now they SUSPECT MS. I started taking low dose naltrexone on November 13th, and was able to drop SIX other medications for it, and am feeling MUCH BETTER! It's been 3 weeks and I have minor swelling in my hands, but no pain, no heat in my joints, I'm stronger where I was weak, I no longer have urinary dribbles and can urinate when I need to instead of sitting in there waiting for my brain to decide it's time to go.... and I have much more energy. My liver no longer hurts! I am still having trouble with my ability to type a word that I want to type; I keep mixing the letters up. That started when all the other symptoms started in 2001. But for the most part, I am 99% better and loving it. I wish they would put this medication out there for the world to choose, like a vitamin, over the counter! It's awesome. There are issues for some people that take it, and it doesn't work for all..... but it DOES work for MOST! I truly wish everyone could have it.