Wheew! It sure is hot! I have read over and over that heat is especially difficult on those of us with MS. I am not sure really how it affects me yet. I know I have been especially “overwhelmed” feeling lately. However, I honestly don’t know anyone that is enjoying the extreme heat we are currently experiencing in East Texas. If I have had a choice this summer, I have avoided being out in it. Normally I enjoy the warmer weather and being outside, but this year I have been indoors almost all summer and at this point I have a bad case of cabin fever. I am ready for some cooler weather and an opportunity to play in the great outdoors a little while!
The National MS Society has an interesting little webpage about Heat & Temperature Sensitivity that says historically physicians used “The Hot Bath Test” to help diagnose multiple sclerosis.
People were submerged in a hot bath and if they developed neurological symptoms or if symptoms they had already been having worsened it was determined that they had MS. Sounds a lot cheaper than an MRI!
I am curious how the heat affects other people with MS and how they cope. Please tell!
I know the further along my father got the heat really effected him. He had a vest that you could put ice packs in that he would wear when it got too bad.
ReplyDeleteSo far I do okay in it luckily. Considering Texas is hot most of the time (and especially this summer) I am going to have to learn strategies for the heat if it gets to be a problem! I have heard of the cooling vests but have never actually seen one.
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