Who Else Has Serious Response To Cold Temperatures? | MyFibroTeam

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Who Else Has Serious Response To Cold Temperatures?
A MyFibroTeam Member asked a question 💭

I can't live with continued poor health in a cold climate. I have seen a dangerous and precipitous drop in functioning for me each Winter. Here is a research article about cold temperatures and women with fibromyalgia. Who else can relate to this? What do you do that helps? Have you moved and if so, did it help because I intend to move and would appreciate suggestions very much.

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC38...

posted October 14, 2019 (edited)
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A MyFibroTeam Member

The cold is hard, no getting around it. During this fibromyalgia study at the Neuromodulation
Lab one of the tests is to apply heat to one arm to a perceived pain level of 6 out 10, then your other arm is in an ice bath and believe me, it is all I can do to continue and focus on the heat application. The cold is excruciating. I am not sure what they find their results to be, but I hate that part, no doubt.

For now my parents are alive and in the northeast US. They travel to warm places in the winter. I truly loathe the southeast for its humidity, as painful to me as cold. I have lived in the desert, before all this. Who knows. My partner may retire in 4 years or so. Much remains to be seen.

For now I just ordered a 2nd electric blanket, more long lasting and better settings than a throw. Good heating pads, baths...all to cope.

posted October 14, 2019
A MyFibroTeam Member

I don't do very well when the temperatures drop in mid-October. This week has been very painful (temps in low 60s). I have been having neck pain off and on from a bad fall last winter and experience pain in knees when I go into a flare. I woke up this morning exhausted and in pain from neck to knees. I have been taking tramadol with Motrin for the past 4 days. I had plans to organize some rooms and it will be going at a slower rate than I had hoped. October/November and March/April are always the worst for me.

posted October 14, 2019
A MyFibroTeam Member

Cold and wet are the worst for me. But my family my friends are all here in New York. Not leaving anytime soon. I do shake intensely when I get really cold. Bundling does help me I have to make sure my knees stay warm. I wish you all the best hugs 💙❤️💜💚🙏

posted October 14, 2019
A MyFibroTeam Member

I visited Colorado several times... It was beautiful! When it gets really cold here in January I sleep with two comforters and a heating pad on my stomach!

posted October 14, 2019
A MyFibroTeam Member

A suggestion is to put a blanket under your fitted sheet.

posted October 14, 2019

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