Sorry. I've gotten much of my information about the Canadian Health system and what is available for MS from Dayle and Patricia2. Haven't spoken with Mark Freedman in a little over a year. He, at that time, said that Canadians had access to most of what US citizens did for MS care but Canada Health was watching some of the newer trials longer and more closely before adopting them. IVIg...not sure why.

And I think dayle has a firm MS diagnosis but with the degree of illness this year, they have not yet decided where she has settled in the spectrum. I will let her give details of the broad range of therapies that have been tried.