Thank you Sally.

Chris...it's great that you are so gung ho about this and you are doing well...but you have to understand that not every treatment works for everyone.

The number of people on this treatment is not enough to call this a cure. Even the scientists who are administering Reimmune who are "just playing by the government rules" as you call it, are not saying it is a cure for MS. (if they are, I've missed it. I believe they are calling it a potential cure.) It's a treatment in the trial stage.

This is sounding like the arguments that took place when Tysabri first hit the market, then was pulled, and came back on the market! It's a cure, it's the best treatment on the market, it's efficacy is better than all the other DMD's out there. Well, yes and no. It depends on who is taking it. It works for some but not for others.

Chris, you know that about Tovaxin. If you don't produce MRTCs, it won't work for you. You can't get the vaccine made. And not everyone with MS produces MRTCs. And even if they do, not everyone produces them in the quantity to make the vaccine. So they move on to something else.

The facts can speak for themselves about Revimmune...we don't have to debate the facts.

We can discuss the facts like rational adults. We all know from experience that what works for one person may or may not work for another.

We are all in this together. Let's work on it together. We don't have to agree, but let's not beat each other up about it. It's just not productive.