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I get electric shocks all the time. The L'hermittes (sp??) I believe is when you bend your neck down and get the shocks up and down your spine. I dont have that either. I get the shocks in my hands ALOT!! I also get shocks in my legs from the knees down alot too. Can barely shave my legs anymore because of the "shocking experience". Ive told my neuro, and he just replies, "MS gives a person tons of sensory problems and thats just one of them". I guess if he's not too concerned, I wont be either. I just learn to live with them.
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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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"Thanks for this!" says: | daisy.girl (07-14-2012), dmplaura (07-14-2012), new2net98 (08-04-2012), SallyC (07-14-2012), Twinkletoes (07-17-2012) |
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