I have had Lupus and Fibro since 1997. I am some muscle relaxers, and pain blockers at night. I have trouble sleeping, and the fibro fog is sometimes really bad ( like today :-) ) and the heat absolutely kills me. I try to look at the bright side, it could be worse. At least I am not dying, though some days you would think that. Keep telling yourself:
I control the disease, the disease does not control me........