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Re: Have you switched to Tecfidera? Are you glad you did?
Posted: Fri Nov 08, 2013 1:51 pm
by xpsychiatricmd
Went to Tecfidere after a bad relapse which put me in a wheel chair. Done well with the GI symptoms but the niacin effect has been bothersome. Worse of all has been the sleepiness/tiredness. Diagnosed as SPMS by Neurologist. Looking at Rituxan.
Re: Have you switched to Tecfidera? Are you glad you did?
Posted: Sun Jan 04, 2015 11:53 pm
by Jimpsull
I was on Tecfidera for 17 months. I did well on it ms wise and had no perceptible side effects, however total lymphocytes were low and continuing to fall. As of dec 28 I am on no meds. Will go back on copaxone once lymphocytes rebound.