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#7 | |||
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I'm on 20mg 4x a day. Most of the time it helps but there are times when severe pain pays me a visit without notice and I have to up it to 40mg for that particular time combined with other meds and the spasticity calms down. I don't know what stage you are or what level your pain is but its always a good idea to discuss this with your neuro. That's how I can take my meds the way I do.
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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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