It's great that they're all talking about it:
But will it lead to clinical trials in the near future... I'm worried that the current research that "will produce results in the next few months" has all been funded by the MSSC and seems not to have gone to anybody that really knows anything about CCSVI. Am I being paranoid?
And why can't Canadians be tested and, if appropriate, treated in Canada (even on their own dime) for a blood flow problem just because they have MS? At least a few of the Health Ministers are using some common sense (finally): start following up on the people who have already been overseas.