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Thursday, November 18, 2010 8:23 PM
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Roanne Hanel
It will be an interesting year for the MS walk. My husband and I are (were) huge supporters, bringing in around 6-10 thousand every year. Again I will be there, but this time with a table giving out information about CCSVI and the reluctance of our Government and MS Society to acknowledge it. Thank you to Bev for mentioning that she did this in Richmond BC, I think the idea is brilliant! We should grab as many friends and family to join us. I will also call City News in Toronto to let them know of our quiet (protest) information booth. Hugs to all going through this garbage of discrimination. I was thinking, I should not be taking my asthma meds as I'm sure they were tested on "real" people not MS people - shameful, there are so many loopholes that the idiots don't even know they are idiots.
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