Oh my goodness, I'm so happy to hear that others are finding their way to the remarkable LDN that I've been taking and trying to share news about for about 5 years now. I can still remember talking about it here at the curezone back in 2002 and of course no one wanted to hear about it then but luckily the many thousands of us are shouting from the rooftops and it is being heard. I do understand why it is not happening faster because Big Pharma stands to lose billions if this comes to light. They sell therapies that harness them thousands per month per patient and we pay only about $20.00 per month so do the math. Big Pharma has the ability to put LDN into the public's hands but they certainly don't have the incentive to do something that would cost them so much. Anyway, glad to hear that you found it and that you are doing well. I've had MS for maybe about 25 years now and am doing quite well. I'm not going to say that my balance and walking is the same as it was 5 years ago but I lead a very normal life with a job where they don't even know about the MS so I'd say that is saying something. Good luck to all.