Hello all,

I've decided to not take Gilenya, can't take take Tysabri becuaes of the auntibodies I have, failed at Copaxone and Betaseron raised my liver enzymes way too high so had to stop taking it. I'm going to start Axonex at half dose and watch my enzymes on it to see if we need to stop it. In the next month maybe? I will begin it's use. I dont know how much it costs as the insurance said, "It's too new for us so we don't even have the price on that med yet. MS is winning. No fun at all. I'm reading Minding my Mitocondria looking at diet change. I don't want to take medications anymore but I'm getting worse not being on one. Those of you that take it, how much does it cost you (out of pocket)? I wanted to hear what you all think about my situation and share the experience with you all.

Thankk you,

Eric