Multiple Sclerosis (MS) Support Group
This community is a place where members can discuss current events and weigh in on what's going on in the world.
This community is a place where members can discuss current events and weigh in on what's going on in the world.
1998 betaseron (had to mix the med then inject)
2000 avonex (needle seemed huge)
2001 Rebif (I liked this. Prefilled syringe & an auto injector)
2013 tecfidera (& that's where I am currently at)
I was on Rebif the longest & I liked it the best but it became unaffordable. I have no active lesions & the M.S. is not progressing & I don't have flares anymore so I guess what I'm trying to say is find the dmd that has the least amount of side effects that you can live with. I really think you'll be able to find an alternative to aubagio. I'm not familiar with anyone who has taken this & like I said in my previous post to you I had a doctor that was dead set against aubagio for women. I don't know your age but if I remember right the doctor that discussed Aubagio had other negative things to say about this since he took it off the list of contenders for me I focused more on the drugs that he said were a good fit for me. My choices were copaxon or tecfidera. I hope you find a dmd that is a good fit & you can afford or is covered by insurance, there are also patient assistance programs for many of the drugs.
Even in women who proclaim it's impossible, if you answer yes to that question, it's a no.