How many times have you been asked whether you have tried celery juice? What about kale/coconut oil/turmeric/yoga/colonics/algae/walking barefoot?
Continue reading “Things Not to Say to People With Invisible Illnesses, Part Three”
Category: brain fog
Spoonified in the Time of Corona, Part Two
Hello Spoonies and Non-Spoonies,
Long time no see! I haven’t been posting because I was attacked by toxic mold and had to move to a new apartment, but now I’m back. I will have tons of posts about mold, but I wanted to start with some coronavirusy cartoons.
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Spoonie Artist Guest Post: Bethany@lymelifecomics
I followed Bethany on Instagram because of her beautifully drawn, professional-looking comics that reminded me of my favorite graphic novels, only they were about Lyme disease! I love Bethany’s style, humor, and the painfully accurate way she reflects the patient experience. Continue reading “Spoonie Artist Guest Post: Bethany@lymelifecomics”
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The Spoonie Awards (Because We All Deserve a Medal): Part One
Do you ever feel that everyone who has a chronic invisible illness like Lyme, ME, fibromyalgia, or MCS deserves an award for everything we deal with? Me too! Continue reading “The Spoonie Awards (Because We All Deserve a Medal): Part One”
Miss Diagnoses 