Can I get more specific? Does the MS Society know how many MS patients have gone to the U.S.? I have the perception that there has been a huge number of people, at some considerable cost, I would imagine, going to the U.S. because this new treatment is available when it hasn't been in Canada. It does leave us with the feeling that we are behind. Do you have any idea on how that's looking?
On May 1st, 2012. See this statement in context.