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.
Has anyone gotten a headache with copaxone? I would like to know!
deleted_user
not me and not my cousin.i have gotten nerve pain headaches from the m.s. they are intence
deleted_user
Copaxone was the first medicine I tried, but, I don't think I experienced headaches with it. I mean, I would get huge ones before my diagnosis, and I probably did continue to get them while taking this medicine, but, I don't think it's from Copaxone. But, you should ask your doctor, or even call shared solutions for help. Good luck to you!
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I have been here before, a long long time ago and now I am back.Forgive me for not just saying what I want to say,even under a triple dose of antidepressants it is still raw and seeping and I am hesitant at revealing it as at least under the bandages around my heart I don,t have to look at how raw and wounded.My child was cleaved from my heart by his own actions. my child of ten,turning eleven...
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