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Treatment for rrms

Not long back from the ms specialist clinic where I met the neurologist and my ms nurse (only took 3 months!) but they were talking about treatments I can take, they mentioned the biggie lemtrada, which sounds scary being in hospital plus the side effects being thyroid problems put me off, the other two drugs are Aubagio which I’m not liking the whole hair thinning side effect and tecfidera which even though side effects not great looks the best out of a bad bunch. Has anyone been on any of these treatments and how were you on it? I know everybody reacts differently but just looking for some info.