CML Summertime Blues
I love summer, I love our garden,
I love floating the river, I love having our grandkids in our home and so many
other things that summer brings; what I don't love about summer however, is the
heat. I have never liked the heat of summer and have always been a bit
intolerant of the direct sun and being hot.
Hot for me is anything over 80
degrees in a dry climate, and 75 in a humid one; my intolerance doesn't bode
well for the season. Having CML has made me even more intolerant of the heat.
During the summer I must keep all of my outdoor activities to either early or
late in the day, and remain indoors during the hottest time of the day.
I have found that I sunburn more easily,
and quickly become nauseous and get headaches if I am not careful; my eyes also
ache while in the sun. In order to make the summer more tolerable, I always
wear sunglasses, light clothing, a hat and sunscreen. I also remember to stay
hydrated by drinking lots of water (sports drinks are probably a great idea,
too) and I have found that bringing a small cooler bag, filled with frozen ice
packs, is a lifesaver. I bring them everywhere I go; they are especially
helpful when getting into a really hot car. I place them on my chest and the
back of my neck until the air-conditioned cools the car. I have also strapped
them around my torso with a back brace when I am visiting the Palm Springs or
Phoenix areas.
Running cold water over my wrists,
when I am extremely hot, also helps; as does a cool shower or bath.
Remember that heat stroke is an
extremely real complication, especially for those of us with CML.
The major signs and symptoms of heat stroke include:
1. Nausea
2. Vomiting
3. Fatigue
4. Weakness
5. Headache
6. Muscle Cramps
7. Dizziness
Let’s have a great summer while
trying to remain as comfortable as possible!
Great post. I found it very helpful. It's always nice to find ways to make life with cml a little better.
ReplyDeleteThank you
Karen
You are welcome, Karen!
ReplyDeleteHope it helps.
thanks for your blog. it helps to read and get ideas from others to help with the side effects of our chemo drug.
ReplyDeleteYou are welcome, Aleta!
ReplyDelete