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Member
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Join Date: Apr 2012
Location: Indiana
Posts: 430
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Member
Join Date: Apr 2012
Location: Indiana
Posts: 430
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My neuro never took my blood count. Said it was not necessary. I said I thought it was from everything I had read and from the FDA website and all, and he said no, was not necessary. I stopped because of all the side effects. Even with the preventatives to the side effects, I was still getting some of the side effects, so I said I had enough. It was my second time trying the drug, so it was a mutual NO between me and neuro.
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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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