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Canadian Politicians Seek CCSVI debate
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Canadian Politicians Seek CCSVI debate
by FlashHack » Mon May 10, 2010 10:32 am
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FlashHack - Family Elder
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- Location: Portland, OR
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by Shueywho » Mon May 10, 2010 10:50 am
This is fantastic! I keep reminding my very pessimistic partner that the more agitation there is, the closer we are getting. The movement is trudging along. And I am proud that Canada is at least having the conversation....soon *fingers crossed*...soon.
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Shueywho - Family Member
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house of commons
by scotland » Mon May 10, 2010 11:05 am
Every canadian in TIMS should send a letter or email to their mp to keep this
in their faces. It represents relatively very little cost for a huge possible return financially and for quality of life going forward for MS patients.
I know we have to do more research, but lets get the testing going Canada, even on a user pay basis.
Scotland
in their faces. It represents relatively very little cost for a huge possible return financially and for quality of life going forward for MS patients.
I know we have to do more research, but lets get the testing going Canada, even on a user pay basis.
Scotland
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scotland - Family Member
- Posts: 36
- Joined: Wed Feb 23, 2005 4:00 pm
- Location: ontario
by PCakes » Mon May 10, 2010 11:26 am
..send evidence!! research.. testimonials.. letters such as the Gwen Valentic-Morrison/ lilsis 'open' letter..Dr. Haacke's letter in support of the Victoria I.R. , Ginger's blogs.. videos.. evidence!!
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PCakes - Family Elder
- Posts: 849
- Joined: Sun Dec 13, 2009 4:00 pm
- Location: Canada
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