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Dealing with the Summer Heat When You Have SMA
I’ve posted before about how summer weather is more conducive to me getting out and spending time with friends than the winter. I try to get out as much as I can during the summer and hang out, walk my dog, go on trips, etc. It makes up for the amount of time I’m cooped up inside during the wintertime.
Nevertheless, there are still problems I have to deal with – the biggest is the heat. As I’ve mentioned in previous posts and articles, I wear an external catheter and sweatpants almost everyday. The catheter makes it easy for me to pee when I’m on the go, and wearing it means I don’t have to transfer in and out of my chair during the day.
The problem is that when it’s hot outside, I much prefer to wear shorts. Wearing shorts means that I can’t wear my catheter, and as such I have to rely on my parents or someone to help me use my urinal. It’s just one of those things I have to do, and sometimes it’s unavoidable. If it’s a hot Saturday and I know I’m going to be out, wearing shorts and packing a urinal in my backpack is sometimes the best option.
I have a few close friends who are comfortable helping me use my urinal if I do run into this situation, and I think it’s good to have a close social circle that is willing to help with personal matters like that. It makes having some independence a lot easier.
What about you all? Do any of you experience similar issues when it comes to dealing with the summer heat? Share your experiences and feel free to ask questions.
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