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: myalgic encephomyelitis
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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Spoonie Rent-A-Family (TM) for the Holidays
For those of you who have to see your more insensitive/clueless family members during the holidays, I created this new-and-improved family unit consisting of only people who say the right things… Continue reading “Spoonie Rent-A-Family (TM) for the Holidays”
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Spoonie Guest Artist: Alexandra Baker (@yourachingart_m.e)
Hi Spoonies,
For a long time, I’ve been noticing that there are many outlets for writers with chronic illness but comparatively few for artists with chronic illness. I decided to create these “Spoonie Guest Artist” posts, featuring some of the super-talented visual and multimedia artists I’ve met since I started blogging. I found Alexandra on Instagram (she’s @yourachingart_m.e). I immediately started following her because her work is creative, relatable, funny, lovely, and comforting. She’s also an excellent writer; I admit I teared up reading parts of this. Check out her story and artwork. Continue reading “Spoonie Guest Artist: Alexandra Baker (@yourachingart_m.e)”
Miss Diagnoses 