Wednesday, August 18, 2010

Nova Scotia Opposition backs CCSVI research funding

More pressure - finally a little in the Maritimes: http://thechronicleherald.ca/NovaScotia/1197408.html.  Thanks for the tip, Shelley.

5 comments:

  1. Funny that you only speak of the positive stories about ccsvi, how about those who had the procedure and it did not work!!!!!!!!!!!!!!!

    When you speak so highly of ccsvi & the fantastic outcomes you make those who did have it done and it did not work feel like CRAP!!!!!!!!!!!!!!!!!!!!

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  2. To the person who made the anonymous comment about feeling like crap because they feel that angioplasty for CCSVI did not work for them: Your disappointment is understandable but Ted has been nothing but fair, honest and objective. It is heartbreaking to hear the few stories we hear about the treatment seemingly not helping some people for reasons that are not yet well understood which is all the more reason we need to keep putting pressure on our government and the MS Society to be leading the CCSVI cause here in this country. Some sufferers will need more time to heal than others, some may suffer a restenosis that warrants a second procedure, in some patients a blocked vein elsewhere or a faulty valve could have been overlooked...all the more reason we need to work together so that testing, treatment and proper follow up care can be provided in our own country. I truly wish you well and hope you see health improvements soon.

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