I get alot of pain in my scalp. Could try looking up TN (trigeminal neuralgia- sp??) Thats another common thing with MSers. I had it for many years before I finally learned what it was. It also occurs commonly in the face.
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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
Last edited by KittyLady; 03-17-2013 at 05:28 PM.
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