Register now for the world’s first CCSVI EXPO ~ 36 hours of live broadcast featuring YOU, CCSVI researchers and doctors, and the entire CCSVI online community!
Drop in and chat with others online, watch a doctor chat casually or share a favourite recipe, demonstrate your rehab moves or simply tell your own story.
Register now (it’s FREE!) and we’ll send you more details soon!
National CCSVI Society
The National Chronic Cerebrospinal Venous Insufficiency Society (NCS) is a registered volunteer driven, non-profit society dedicated to improving the lives of Canadians affected by CCSVI primarily through advocacy, research and education. Our mandate is to serve as a resource for individuals with and at risk for CCSVI, their families and caregivers, government, the public at large, and medical and research communities.
We provide services through three primary methods: Advocacy - to advance the awareness and acceptance of CCSVI to government and health care professionals and to champion CCSVI treatment; Research – to gather knowledge of CCSVI and related venous neurovascular conditions; and Education – sponsoring and/or leading educational forums.
For further information, please visit us at www.nationalccsvisociety.org.
http://www.eventbrite.com/event/2009551623/efblike