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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theatre and I are there already. I'm having a very berry tea with crackers, cheese and cherry tomatoes and she's having a joint with some beer and we're both on really comfy recliners on thick pile carpet. we need some help with the decor if anyone is around??
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I'm trying to exercise daily. I was doing fairly well until I sprained my ankle 2 weeks ago but now I'm getting back on the horse. Today I walked over a mile with my arm weights that are about 22lbs total. I was out of shape and it was hard on my arms. I also did my 30 situps. I'm also going to drink a lot of water and try to eat healthy. I do tend to have a sweet tooth but I'm cutting...
