My turn., mt turn. I'm RRMS and have been on Avonex for 2 years. Seems to be doing fine for me. Oddly (or not) I have never shared my symptoms with anyone except my neuro since diagnosis. I don't know why, anyone want to take a stab at that? It drives my family crazy.

I have had pain in my feet and hands for years that seems to be getting worse recently. I have also been getting very sharp location specific (like the tip of one finger or the arch of the foot) pain lasting for maybe a minute or less.

I did spend Saturday standing on concrete in a freezing cold warehouse for about 8 hours and am paying for it now. I hate that it takes so long to recover from a little activity.