Multiple sclerosis makes it tough to deal with the heat of the dog days
How I cope with summer's traditionally hottest period (a wheelchair fan helps)
I like to look up.
No, I’m not referring to my disposition, although I do consider it to be an improvement over what it once was. I’m actually pretty sunny, if you happen to think of “sunny” as burning, harsh, and damaging when you’re exposed to it.
What I actually meant was that I like looking up at the sky, the night sky in particular.
I have a telescope, which I really need to use more. It can be difficult to use from a wheelchair and with hands and eyes affected by multiple sclerosis (MS), but I know I could find a way. I also have a star finder and use Google Sky maps, but I’m not even an amateur astronomer. I’m just a guy who knows a handful of the most recognizable constellations.
One that I recognize is Canis Major, the great dog. It’s easy to find, both because of its proximity to the constellation Orion and because it contains the brightest star, Sirius. Since July 3 and until tomorrow, Aug. 11, Sirius, the Dog Star, has appeared to rise and set with the sun. That’s why these dates are known as the “dog days of summer” in the Northern Hemisphere.
Coping with the dog days
Before I learned all that, I assumed the name had something to do with actual dogs, and I don’t think I’m the only one. On what feels like the hottest days of the year, images of dogs lying around in the shade panting are easy to conjure. With the effects that heat has on those of us with multiple sclerosis, I sympathize with the dogs.
Like a dog, I too have become something of an expert on finding shade. If there’s none provided by nature or structures we humans create, I bring my own via a small umbrella clipped to my wheelchair. If there’s no breeze, I have a small fan that’s also clipped to my chair and aimed at the back of my neck. I may not be able to splay out in a cool, damp spot on the ground like a dog, but I have cooling clothing, wraps, and more that help some.
In Alabama, where I live, the high humidity turns evaporative and frozen cooling products into a warm, damp mass in short order. A hot, wet towel is nice before a shave, but unbelievably unpleasant at a ballpark. I’m interested in trying one of the phase change cooling products on the market since they’re supposed to be a dry cool and recharge quickly. When I do, I’ll be sure to share my thoughts. (If you’ve used one, please share your experience with it in the comments below.)
The reality is that I don’t venture out as much during the dog days. MS has forced me into a kind of reverse hibernation (minus the extra sleep and weight loss) during this time frame. Until autumn, I’ll spend the majority of my days indoors in the air conditioning. It’s fitting that today, the day before the dog days end, is also National Lazy Day, because I intend to honor it properly.
Note: Multiple Sclerosis News Today is strictly a news and information website about the disease. It does not provide medical advice, diagnosis, or treatment. This content is not intended to be a substitute for professional medical advice, diagnosis, or treatment. Always seek the advice of your physician or other qualified health provider with any questions you may have regarding a medical condition. Never disregard professional medical advice or delay in seeking it because of something you have read on this website. The opinions expressed in this column are not those of Multiple Sclerosis News Today or its parent company, Bionews, and are intended to spark discussion about issues pertaining to multiple sclerosis.
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