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Real members of MyMSTeam have posted questions and answers that support our community guidelines, and should not be taken as medical advice. Looking for the latest medically reviewed content by doctors and experts? Visit our resource section.

Tecfidera/new Copaxone

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?

edited, originally posted almost 8 years ago
A MyMSTeam Member said:

I'm on 3x a week Copaxone. It's great. Doesn't give me flu symptoms at all!!

posted almost 8 years ago
A MyMSTeam Member said:

@A MyMSTeam Member yeahhh you're supposed to get tested twice a year!

posted almost 8 years ago
A MyMSTeam Member said:

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.

posted almost 8 years ago
A MyMSTeam Member said:

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 😌😭

posted 3 months ago
A MyMSTeam Member said:

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.

posted 3 months ago
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