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Board index » Treatments » Chronic Cerebrospinal Venous Insufficiency (CCSVI)

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jackiejay
PostPosted: Fri Jun 11, 2010 7:37 pm 
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just wondering if the study at St.Joe's in Hamilton/McMaster University with Dr. Haacke, applied for funding from the MS society?
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garyak
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PostPosted: Fri Jun 11, 2010 8:24 pm 
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http://www.cbc.ca/health/story/2010/06/ ... earch.html
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oreo
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PostPosted: Sat Jun 12, 2010 6:35 am 
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They applied.
They didn't get.
According to article in this morning's Hamilton Spectator they will be going ahead anyway, funded by patient contributions.

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blossom
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PostPosted: Sat Jun 12, 2010 3:17 pm 
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remember this is a big piece of the puzzle dr. haacke is working on. gotta dig deep and help his research too. whoops!! sorry ms society i'm only giveing to those really involved with ccsvi research and testing and treatment. if they don't watch what they are doing with our money someday they may be experienceing a real PLACEBO EFFECT which will be we thought we had all this money coming in but now we are imagineing it. is it real?
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annie66
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PostPosted: Mon Jun 14, 2010 4:49 pm 
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blossom....oh my gosh.....you made me laugh out loud!!! that was a good one about the placebo affect... :0)
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Board index » Treatments » Chronic Cerebrospinal Venous Insufficiency (CCSVI)

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