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Tecfidera/new Copaxone
I've been on tecfidera for over a year now, and I'm just concerned with the lowering of white blood cells. Has that happened to anyone? If so how did it physically make you feel?
Also is anyone on the newer copaxone? The 3x a week one? Thoughts?
I'm on 3x a week Copaxone. It's great. Doesn't give me flu symptoms at all!!
@A MyMSTeam Member yeahhh you're supposed to get tested twice a year!
I was on Techfidera for a about10 months..changed doctors and he has put me on Copaxone, he says because it has 0 side effects and the Techfidera kills our liver.
I been on all the different needles pills and nothing helped me so I am now in the secondary progressive of Ms I hate it because when my Nerologist ask me to remember words and numbers I forget them right away and he told me today I got a memory loss and abad case of dementia makes me so sad 😌😭
I have been on Copaxone since 2013. When I first went on.it,it was 20 mg and had to take 7 days a week. Then went on 40 mg 3 times a week. I am doing good on it.
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