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How do you use humor to cope with ALS issues?
Sometimes, humor can be a powerful coping mechanism. Whether it’s ALS-related or just something else entirely, for me, it helps to identify the things that ultimately don’t matter as much. I call this my “I don’t care” list.
We are all affected differently by ALS, so some things may not resonate with every pALS, but, for example… “I don’t care what dinner tastes like because I’m using a feeding tube anyway!”
Or “I don’t care if they want to draw more blood, I get a spinal tap every 28 days!”
The list shouldn’t be insulting or hurtful, just a way for us to poke fun at our situation if we choose. ALS definitely isn’t funny, nor is it easy, but perhaps we can use our humor as a coping skill.
How do you use humor to cope with ALS issues?
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