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”
Tag: MCS
Difficult Relatives of Spoonies, Part Two
Happy Thanksgiving to my fellow spoonies who have MCS, MCAS, ME/CFS, Lyme, or just fragrance sensitivity! Continue reading “Difficult Relatives of Spoonies, Part Two”
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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”
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Festivus: A Holiday for Spoonies?
Christmas is great, Hanukkah is great, but I really think Festivus has excellent potential as a holiday for the chronically ill. Hear me out. Continue reading “Festivus: A Holiday for Spoonies?”
Miss Diagnoses 