My wife has MS she was diagnosed 13 going on 14 years ago. We lived in Edmonton when she was diagnosed I worked for Telus we had to move because she needed shots and they were not covered there. Moved to Winnipeg where they are covered I liked it there but she did not and wanted to move. so here we are in BC her MS is getting worse and there really is nothing that can be done for it the shots slow it down a bit and she hates the shots and MS. I was lay-ed off last fall and feel that it is very necessary to work close to home as things do down hill for my wife. We have three daughters ages 9,7, 4 they are my first concern.

Thanks all for helping to find a cure but no money realy gets to the one that have the disease it basicly gose to the R&D and some get respite days out of the money.
Bill