It's awful isn't it @Auriel my body actually jerks when I'm in a flare and cold. This has been my 2 winter with Fibro. The first winter I didn't know it was fibro, this winter I had been diagnosed so wasn't quite as freaked out at how it was making me feel and how difficult the cold made everything. Already I'm dreading the next winter although that said I have managed to find ways to cope and survive the really cold spells. Every day is about educating yourself when you have this awful and quite often debilitating condition. Happy FridayYour the same as me @Looby69 cold gets me every time! ️ 🌨
Wow - Hi sismith, and welcome! I spose you need a climate with only occasional weather changes to be able to discern this at all. No chance here, it changes quite a bit every few days, and since climate change even more so... So I'm grateful that the weather doesn't seem to influence me that much, or at least I am schooled in reacting fast. But who knows, praps in a stable climate I wouldn't be in a continual full flare.I definitely suffer for about a week before a weather change and nothing alleviates the pain and fatigue. It takes a couple of days of complete rest after the weather change to get back to “normal” again where I can function. I can forecast the weather better than the meteorologists!
for most people, a warm and dry climate in the winter will help.I, too, live in the Midwest and my flare-ups are very closely aligned with changes in barometric pressure. I have some pain, but mostly extreme fatigue which makes it difficult to do anything. I found visiting Arizona during the winter months really helps the fibro!!
Oh no, as opposed to @Tiny horses in my case it doesn't have to be high winds, 5' of any wind'll do!I thought I was the only one that was affected by windy days! Sounds crazy, but it's true.