Cold intolerance is a major issue for many people who have Fibromyalgia. Sleep deprivation and being constantly in the flight/fight mode due to stress does not allow the body to operate efficiently. And because of this our ability to regulate our body temperature simply goes awry.
According to the NHS when listing the symptoms of Fibromyalgia it states that “feeling too cold is because you're not able to regulate your body temperature properly.”
Raynaud’s disease seems to go hand in hand (pardon the pun) with Fibromyalgia. With Raynaud's disease as a response to cold temperatures, anxiety or stress the small arteries that normally allow blood to flow to the skin narrow. This narrowing affects the blood circulation.
The extremities of fingers and toes are usually affected and can feel very cold, stiff, and painful and turn white or blue due to cold or stress. And as previously mentioned people with Fibromyalgia are under constant stress, so it is no surprise that many also suffer Raynaud's disease.
At my worst, my hands and feet were like ice blocks. No matter the temperature outside or indoors my hands and feet would be freezing. I even got very painful chilblains on my feet. I knew this was a sign of poor circulation and I knew I had to do something about it. I bought numerous items of clothing to keep me warm – long johns, thermal gloves and socks, hats, padded jackets etc.
I wore socks to bed. I also made myself some wheat bags to warm up in the microwave. I used big ones for my feet and pocket sized ones for my hands. I needed a blanket in the car and another one for lounging on the sofa. I used a heated blanket at night.
I found that I could not tolerate shopping in the freezer section of a supermarket – even in summer- it was just too cold to be near.
At the same time as the cold intolerance I would also have hot sweats – mainly when I drank tea, had sugar or alcohol – but sometimes for no good reason. I would have night sweats too which would disturb my sleep. I would strip off my clothing until I became cool. Then I would need to wrap up warmly again as I was freezing cold. Heat intolerance is just as bad as cold intolerance to people with Fibromyalgia and is just further proof that our ability to control our body temperature is out of whack.
I found that even in the summer months I could not retrieve food from my freezer, nor prepare cold vegetables for a meal. Even touching cold cutlery or glassware whist eating or drinking would chill me to the bone.
When there was a drop in temperature I would
feel it immediately. It seemed to make all my Fibromyalgia symptoms
worse – pain, fatigue, depression, anxiety etc.