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Cold Extremities with IPF.
For the Canadians on this site, it looks like winter has officially descended upon us. Earlier this week the weather was raining and 15 degrees Celsius and last night the temperatures dropped significantly to -14 with the wind chill. Naturally, I felt very chilled as my body adjusted to this drastic temperature change. However, there were certain parts of my body that felt much colder than others, even as I lay buried under my blankets, and I can’t help but wonder if this is related to my idiopathic pulmonary fibrosis (IPF).
No matter how hard I tried last night I couldn’t warm up my toes, my fingers and my nose! I put warming socks on, tried to keep my hands under my duvet and pull the blankets up to my face as much as I could tolerate and I was still cold.
I remember last winter I struggled with feeling excessively cold compared to the years before my IPF. Since the diagnosis of this life-threatening lung disease, I have become intolerant of the cold. The snow this morning is really pretty while glistening in the sun, but I have no desire to go outside in it.
Since your diagnosis of IPF/PF, have you become more intolerant of the cold?
Do you struggle with keeping your extremities warm in the chilly temperatures?
Share your experience with us, and any tips you might have for helping with this.
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