I was diagnosed finally on july 27 2002 after yrs of misdiagnosed. My older sister who Im estranged from first told me about fibromylagia. Wondering does anyone else feel that certain temps affects them? I live in the Okangan Valley of Canada where the winters are mild and I love it but the summers can be HOT. I can handle, not be in so much pain and actually feel better when its cooler weather. The heat is the worse. I have to sleep with my air conditioner on 24/7 and have frozen water bottles in my bed to try to get some sleep.