So the reprieve was short lived, and my left arm is more numb and tingly like before. Its amazing to me the inconsistancy of symptoms.. I don’t know if it is like that for a lot of MS’ers, but sure is frustrating. It makes it hard to talk to people about what is bothering me, because it is so fickle and can change to another area in a realative short time. Makes me feel like if I actually talk about it, that I’d be viewed as crazy. Its hard for others to understand.. its hard for me to understand.