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#9 | |||
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This has always been a fear of mine. I mean, Im injecting this chemical into my body, and not really knowing exactly whats happening in there. Just hopes. Im taking dmd's for the wrong reason I believe. I had 2 really bad flares one in October and then another in December and they left me disabled. Doc said it was time for a dmd and my dh agreed and said I had to give it a chance for at least a year. So, Im doing it, for them. Im doing a dmd, taking baclofen and amitriptyline, doc wanted me on something for the tremors and really pushing tysabri and yada yada... NO MORE DRUGS!!!
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Dx RRMS April 1992 Yearly flares from 92 to 11 MS induced seizures 2002 Flare Oct 2011 Flare Dec 2011 Left disabled after 2 previous flares Betaseron '02, Copaxone '12, Tecfidera '13 (allergic reaction to all) No longer taking any MS therapy meds |
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