CCSVI and the NMSS

A forum to discuss Chronic Cerebrospinal Venous Insufficiency and its relationship to Multiple Sclerosis.

CCSVI and the NMSS

Postby dizzyintx » Fri Feb 12, 2010 9:48 pm

I LOVE the NMSS! They have done a lot for my family and I during the 26 years since my dx. It was due to the NMSS advocacy program, that I found out that I do have a voice and one person can start a movement!

I believe that due to the fact that research from Buffalo supports Dr. Zamboni claims on CCSVI THE NMMS NEEDS TO GET MOVING, it should not take 4 months to decide who gets to do the research. WE HAVE WAITED LONG ENOUGH! I really believe that we should DEMAND they speed up their funding process or we should ALL quit walking, riding, or fundraising until the CCSVI is funded. A internet sit in!

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