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Research Teams Report on 18 Months of Progress from MS Societies' Initial Studies on CCSVI and MS
January 27, 2012
MS Society collaborates with CIHR in call for CCSVI clinical trial research proposals
November 25, 2011
Research Teams Report First Year's Progress From MS Societies' Initial Studies on CCSVI and MS
July 14, 2011
MS Society of Canada welcomes federal commitment to fund CCSVI trials
June 29, 2011
MS Society welcomes new national monitoring system
March 23, 2011
Research Teams Report Progress from First Six Months of 2-Year Projects Focusing on CCSVI and MS
January 31, 2011
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CCSVI in the media
FDA warns about multiple sclerosis vein procedure - CBC.ca
ccsvi ontario - Wire Service Canada (press release)
Clinical correlates of chronic cerebrospinal venous insufficiency in multiple ... - 7thSpace Interactive (press release)
FDA Warns of 'Liberation Therapy' Dangers for Multiple Sclerosis - Family Practice News Digital Network
News in Brief: Week of May 14-18 - AAFP News Now
Hoag doctor's reports credited with prompting FDA warning - OC Metro
FDA Warns Of Potential Dangers Of Controversial Multiple Sclerosis Treatment - RTT News
FDA Issues Warning on Dangers of Libation Therapy - CisionWire (press release)
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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?
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