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I find this is some good information. I have not had CCSVI done yet either even though I have had MS for 38 years. I can walk with a cane but need an arm and or wheel chair most of the time. I will post all of this info on my website after I have Intererstim surgery for my bladder tomorrow so it wil...

When I used it for those 13 months it was really expensive hopefully it is a little cheaper. I wish I could afford it because I can tell I am just starting to get vertigo, I had it twice when I last used SF1019 and it very quickly got rid of that vertigo..I miss that stuff. Prednisone will have to d...

I don't know a lot but I believe it has not yet been FDA approved, possibly Alan Osmond has some info ??? I wish I knew more. I have really noticed a big difference over this past year since I stopped eating the foods my blood showed I have an intolerance to. I am only using food as my treatment, I ...

I used SF1019 for 13 months, it gave me tons of energy, something I do not have now. My worst symptom is chronic insomnia, it did not help with that but I had so much energy and no exacerbation's of weakness in my arms & legs. I cannot afford it anymore but if I won the lottery I would order it ...

I agree with you! This disease is extremely limited in medications that actually help. The SF1019 vaccine is #1 as far as I'm concerned, but I too cannot afford to keep using it. So until the FDA approves it I decided to have my blood tested for foods that I may truly have an intolerance to. I had ...

The information directly below was from my website, when I was using the vaccine I was asked to remove the information on ICPF because it was old information and ICPF is not used anymore. I was fortunate enough to use the SF1019 vaccine for 13 months, I wasn't walking great for a few months but over...