Results from a prospective, randomized, sham-controlled, double-blind clinical trial of venous angioplasty in individuals with MS who display signs of CCSVI
August 7, 2014
MS Society funded study assesses diagnostic criteria for CCSVI
June 6, 2014
New data on CCSVI from Canadian study using ‘gold standard’ technique
October 8, 2013
Results from MS Society of Canada funded study exploring CCSVI and MS in children
August 21, 2013
New results from MS Society of Canada funded study exploring CCSVI and MS
July 30, 2013
CCSVI Case-Control Neurosonography Results Announced
February 27, 2013
CCSVI in the media
New study challenges controversial multiple sclerosis treatment - Globe and Mail
What is CCSVI?
Do these reports of a possible association between insufficient vein drainage and MS mean that MS is caused by venous insufficiency?
Why can't Canadians get treatment in Canada, when it is available in countries like the US, Scotland, Australia and others?
The science surrounding CCSVI seems to be evolving rapidly. Are the seven studies funded by the MS Society of Canada and National Multiple Sclerosis Society (USA) still relevant?
Many people with MS can't afford to wait until these theories are proven or disproven, there is nothing else working for them. How can the MS Society not support treatment for CCSVI, at the very least on a compassionate basis?