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I have been in so much pain lately, my neuro says its nerve pain. He has now added to my already long ( to me) list of meds Topomax. Hes increasing me from 25mg to 200mg a day over the course of 4 weeks. I know nobody likes a pity party, but Ive been on 3 new meds and none of them seem to be working. I hope topomax will work, but this waiting to see stuff is still leaving me in so much pain. The other nite I seriously told my dh I just wanted to end it all if this is what my life is going to be like. But thank God and all the saints dh was there to say, "but I love you, and think of the grand babies, they love you too!" What a way to snap me back into reality and continue fighting!
QUESTION??? Does anyone else take topomax for nerve pain and does it do anything for you?
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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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