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Board index » Treatments » Chronic Cerebrospinal Venous Insufficiency (CCSVI)

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dizzyintx
 Post subject: CCSVI and the NMSS
PostPosted: Fri Feb 12, 2010 9:48 pm 
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Joined: Sat Aug 29, 2009 3:00 pm
Posts: 5
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!

Kim
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Board index » Treatments » Chronic Cerebrospinal Venous Insufficiency (CCSVI)

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