Regional Information
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Nancy
“Though CCSVI is not a cure, it is a treatment and it does offer hope for a future free of pain, blindness, and the unyielding “handicapped” stigma. It is freedom: Freedom from the symptoms of MS, and to me – freedom is everything.”
Sarah
“I don’t just believe in miracles…I depend on them!”
National CCSVI Society
The National CCSVI Society is dedicated to improving the lives of Canadians affected by CCSVI. We serve as a resource, advocate, and educator for individuals with and at risk for CCSVI, their families and caregivers, government, the public at large, and medical and research...
Aileen
“CCSVI has given me hope for a new life without the many potential negative effects that MS may cause in the future.”
Global CCSVI Expo – Were you part of CCSVI history?
The National CCSVI Society is proud to have hosted the Global CCSVI Expo. We brought our CCSVI family and the world together as one during a full 36 hours of live broadcast featuring YOU, CCSVI researchers and doctors, and the entire CCSVI online community. NOW SHIPPING! Click...
Leslie
“Based on family medical history, no doubt others have CCSVI also, but not with an MS diagnosis.”
Learn
Learn more about the National CCSVI Society’s mandate and our goal to provide information to those affected by CCSVI.
Participate
Participate in our events as a patient, caregiver, medical practitioner, or volunteer. Come find out more.
CCSVI Brochure now available.
See our NCS-brochure-March-2012 for more information.
The National CCSVI Society is pleased to present a series of essays written on issues of particular interest to MS and CCSVI patients, caregivers, health care practitioners by experts in the field. Click here for more information.
The National CCSVI Society Announces CCSVI Support Circles - in your city! Click here for more information.
What is CCSVI?
Chronic Cerebrospinal Venous Insufficiency (CCSVI) is a relative blockage or delay in outflow of blood from the brain and spinal cord. This delay causes insufficient oxygen flow to some parts of the brain (slow stroke) and venous hypertension.
Donate
Participate in some innovative ways to support NCS and our mission.
Global CCSVI Expo Video
We hope you enjoyed the Global CCSVI Expo held November 20 and 21, 2011 featuring Dr. Paolo Zamboni and many other CCSVI researchers and doctors. Click here to order your DVD set. For more information about the Expo, click here.
Discover
Listen, watch, and read more information about CCSVI for patients, caregivers, the medical community, and policy makers.