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: ME/CFS
Things Not to Say to People With Invisible Illnesses, Part Two
“Can’t you just have a little bite of [thing I can’t have a little bite of]?”
“Gluten-free is the trendy thing nowadays, I guess.”
“Will just one piece kill you?” (I don’t know — do you want to come to the emergency room with me after I eat it?)
Continue reading “Things Not to Say to People With Invisible Illnesses, Part Two”Share this:
Valentines for Spoonies, Part Three
When I was young, I hated Valentine’s Day. I was never a hearts-and-flowers person. I was a Depressed-Cynical-Black-Leather-Jacket person. Then I had a boyfriend who hated Valentine’s Day even more than I did, and suddenly I wanted the cheesiest cards and the tackiest flowers. It’s weird how that works.
Share this:
Things Not to Say To People With Invisible Illnesses, Part One
The infamous ”but you don’t look sick” is usually at the top of the list of things not to say to people with invisible chronic illnesses.
Continue reading “Things Not to Say To People With Invisible Illnesses, Part One”Share this:
The Mold Wretchedness, Part One
In October 2020, my housemate and I discovered we had stachybotrys (toxic black mold) and other evil molds in our apartment. We realized we had to move—we knew the Extremely Cheap and Annoying Landlord would not do a good job remediating, and I already had Lyme disease and mast cell activation syndrome (MCAS).
Continue reading “The Mold Wretchedness, Part One”Share this:
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.
Share this:
Spoonified in the Time of Corona, Part One
Hello Spoonies,
I’m sure many of you have experienced things like this. 🙂 Continue reading “Spoonified in the Time of Corona, Part One”
Share this:
The Spoonie Awards, Part Three
Hello my dear fellow spoonies,
Wow, suddenly everything is much more terrifying! I hope everyone is doing relatively okay without any Corona with Lyme or other new problems. Continue reading “The Spoonie Awards, Part Three”
Share this:
Some Say That Chronic Illness Is a Gift: A Cartoon with Two Endings
In my vague and fuzzy brain-fogged memory, I remember reading an interview in which someone said her chronic illness was a gift. Continue reading “Some Say That Chronic Illness Is a Gift: A Cartoon with Two Endings”
Share this:
Difficult Relatives of Spoonies, Part Three
This is for my fellow food allergy sufferers who have Difficult Relatives: Continue reading “Difficult Relatives of Spoonies, Part Three”
Share this:
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”
Share this:
Spoonie Guest Artist:Yulia Greyman (@FunWithCFS on YouTube)
I first learned about Yulia through her hilarious ME advocacy videos on her channel, @FunWithCFS. Yulia was a Ph.D student when she got sick and she is one brilliant, multitalented spoonie! This is a tiny bit longer than my other guest posts, but every word is worth the time. Please read her painfully relatable, funny, beautifully written memoir excerpt and be sure to check out her videos in the middle of the post.
Continue reading “Spoonie Guest Artist:Yulia Greyman (@FunWithCFS on YouTube)”
Miss Diagnoses 