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MS Society Lobbies Government For 10 Million Dollars For Funding Into CCSVI And MS Research

MS Society Lobbies Government For 10 Million Dollars For Funding Into CCSVI And MS Research
Main Category: Multiple Sclerosis
Article Date: 07 May 2010 - 2:00 PDT

The Multiple Sclerosis Society of Canada is calling on the government to provide $10 million for research into chronic cerebrospinal venous insufficiency (CCSVI) and MS.

The request for funding comes as Canadians with MS continue to seek diagnostics and treatment for CCSVI elsewhere, paying out-of-pocket for tests and experimental therapies that could be provided in Canada.

"The safety and health of people living with MS is our primary concern," says Yves Savoie, president and CEO of the MS Society. "The Government of Canada can play a leadership role in addressing the needs of Canadians living with MS by funding research, including clinical trials in CCSVI and MS. Doing so will both advance research and provide safeguards to those seeking treatment."

The Government of Canada has acted quickly in the past to respond to health crises with innovative research, such as its 2009 investment of $6 million to support research to find alternative medical isotopes.

"The MS community has spoken. They want access to diagnostics and treatment for CCSVI in Canada," says Linda Lumsden, chair of the national board of directors for the MS Society. "The MS Society has already committed to funding CCSVI research and now we are calling on the Government of Canada to do its part."

Tomorrow, Lumsden will formally ask Minister of Health Leona Aglukkaq for the funding. The MS Society proposes that the $10 million be appropriated to the budget of the Canadian Institutes of Health Research and earmarked for CCSVI research.

MS Society representatives are in Ottawa for the next two days meeting with various Members of Parliament to advocate on key MS issues.

"It is obvious that the relationship between CCSVI and MS requires further investigation," says Savoie. "This funding request will give researchers the tools to examine both the prevalence of this condition and the potential benefits of treating people with it."

In late 2009 the MS Society of Canada announced a special research competition for CCSVI related studies. The results of this competition will be announced on June 14th, 2010.

"I fully support the MS Society's efforts to lobby the government for research into CCSVI and MS," says Joan Ozirny, a volunteer board member with the MS Society's Alberta Division who lives with MS. "Increased research funding is the only way we'll get closer to unraveling this complicated disease."

As part of its overall lobbying effort, the MS Society, in collaboration with other Canadian health charities, is calling on the federal government to increase overall funding to the CIHR annually to a level equivalent to 1% of total health spending in Canada. This amounts to $1.8 billion based on $183.1 billion in health care funding as of 2009.

http://www. medicalnewstoday .com/articles/188021.php
1 Responses
1137779 tn?1281542505
Thank you for posting this doublevision.

There've been no responses yet from MS community members, so I wonder what the general consensus is on CCSVI and MS?

Given that CCSVI appears to be a factor in my signs and sx, I'm rather interested in this important new research.

It makes perfect sense to me when you look at the venous (especially) and arterial mechanics involved.

Something I noted was that Canada spends more than a third more per capita on healthcare than the UK. This may go some way to explaining why UK patients have to wait so long for dxs and treatment (and possibly why our signs and sx are so often dismissed).

thanks again
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