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i have it in my toes, but it is because of herniated disk. I believe the involvement with MS is that my core is weak and more pressure is on the spine leading to the herniation. I will get a fusion before too long.

In December, Accentia Bio changed the name of their Multiple Sclerosis therapy Revimmune (HiCy or High Dose Cytoxan) to Cyrevia. As the company is working toward starting PH III trials this year, it is also registered the domain name www.cyrevia.com to reserve the name for Cyrevia. In step with thes...

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While everyone else was looking and hoping for CCSVI, Revimmune has been slowly getting their ducks in order and is poised to get on the market shortly. If a drug is working good for you, and you don't want to get rid of this disease, then that means I dont have to wait as long to get revimmune. We ...

we shall see - the FDA is set to approve Revimmune for treating MS (it has been approved for years and years for other things) before year end. They issued orphan status to protect Accentia's stake in development of the drug about a month or so ago - maybe six weeks now. By doing such, the FDA is ba...

^^The neuros feel that BG-12 will be available early 2012 (ph III results due within two weeks or so) and revimmune should have FDA approval for MS by year end.

I need a little clarification from the group about the upcoming changes of the MS drugs scene. BG-12 and Revimmune are set to go to market within the next 6 months or so, but TIMS isnt really tracking it. 1) There are hundreds of folks out there that have been in trials for BG-12 and I havent really...

Would someone please tell me why this is getting almost no attention from these boards?

Ive been waiting on this for years and its almost here!

i thought this was dead on arriveal - but i still want to try it

Most folks with MS have this issue - i discussed this with my ccsvi doctor and he blieves that there is a strong correlation to pressure and venous outflows due to the unequal pressure of the head and the rest of the body.

wow - its hard to believe that this many people are living with MS without insurance

knowing what i now know, i wouldnt do it.

Even skilled technicians have a 50/50 positive result.

CONGRATS!!

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I will be there too!