Do people who have no winter or very light winter where the barometer does not change much a and humidity is on the dry side like Arizona ? You have Fibromyalgia do you have less flare-ups and pain from change
of wearher?
Yes. I live in South Africa, and moved here from Tasmania (Australia). We have wet summers and dry winters. My pain is usually bearable, and flare-ups are minor. Cold damp was always the worst.
I have found that taking a hot bath, using a heating pad or an electric blanket on low works good.
@TO ALL FIBRO SUFFERERS:
i HAVE TRIED ON TWO OCCASIONS TO PRINT THE EXTENSIVE BLOOD WORK DONE:
ANA Titre, Vitamin B-12, CRP, Sm.Antibodies, Magnesium,
All but the ANA Titre were normal. The ANA Titre showed positive for Lupus.
Sure hope this will help others in the future.
THOUGHT FOR THE DAY:
I live in sunny California and my flares are worse due to the extreme heat we have here. The weather affects us wherever we live. I do think having winters is not good for our pain level.
The heat makes me sweat bad because of meds but yes less rain and cold really helps me a LOT