I watched Selma Blair’s documentary the other day. It was a good documentary on her journey through her stem cell treatment. I can’t say my heart didn’t feel her fear and sadness during her MS struggles. I had a completely different path with my MS symptoms and onset. It always amazes me that this disease can be so different for each person yet we still relate completely to each other. Selma Blair and I are both the same age and…
I received an email yesterday about a new drug for progressive MS called Ocrevus. https://www.cbsnews.com/video/new-drug-provides-hope-for-those-suffering-with-ms/I don’t get it, I’ve been on Ocrevus for almost 2 years already. Is it really still new news? I wish I could rave about this drug that it has done wonders for me, but it hasn’t. I haven’t had any relapses and for that I am thankful but it certainly hasn’t halted my progression. I am worse today than I was two years ago. That…
