Hey everyone, hope your all well. I was diagnosed with relapsing remitting ms about 4 years ago and when my doctors told me about the dmd’s i picked Avonex as it was only once a week so i thought it would be less hassle, but unfortunately the side effects are the biggest and worst kind of hassle. So after 3 years I’ve decided to switch to Copaxone as it doesn’t have the flu like symptoms, but after reading some peoples posts about Copaxone it sounds a little scary. How bad are the site reactions and the lumps/dents in the skin? And is there any major effect when switching between injections?
Thanks guys 🙂
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