Just to clarify, I'm not on Tysabri but I have posted comments made by other people about Tysabri. I'm actually angry that I wasn't on Tysabri two years ago, I could tell I was getting sicker and wanted the medicine Tysabri at that time but my neurologist said I was dreaming thinking Tysabri would be back on the market. I think it's safe and I think the medical profession has been indifferent, irresponsible and even immoral and arrogant ignoring the wishes of people like myself who get sicker every day with this despicable disease.

I live in Canada and the federal government only approved Tysabri 6 months after it was approved in the United States and I'm still waiting for the province of Ontario to provide funding for this medicine which I desperately need. I'm presently taking Rebif but it's doing nothing to stop the disease right now, Rebif did work initially when I was first diagnosed about five years ago.