Ever wonder how someone with so many arm injuries managed to do a post with a ton of drawings? The answer is, it really came back to bite me in the ass. Continue reading “A Very Unfortunate Blogging Hiatus”
If Santa Claus had brain fog, he might have problems with dates. Continue reading “If Santa Claus Had Brain Fog”
Note: This post has a TMI Warning. Continue reading “As The Stomach Turns: My Lyme Treatment Update”
Because of the above situation, I recently joined the Chronic Disease Book Group on goodreads.com. Continue reading “The Hypothyroid Lymie Book Club”
Doctors can say the most awful things to chronic pain patients. Continue reading “Shit Doctors Say”
I was very honored to be asked to do a guest post for the Hypothyroid Mom. Continue reading “Guest post for the Hypothyroid Mom: ADD or Hashimoto’s Brain Fog?”
I have combination skin, so I always liked the squeaky-clean-face feeling you get from using toner. But after being diagnosed with allergic contact dermatitis, rosacea, Lyme disease, and a genetic defect that weakens my ability to remove toxins, I figured I couldn’t use toner anymore. Continue reading “Miss Diagnoses’s Favorite DIY Skincare Products, Part Two: Green Tea and Apple Cider Vinegar Toner”
Well, I’ve been taking Armour for a few months now, and it’s been a mixed bag.
Ah yes, sandal season is definitely here.
Since Lyme awareness month is about to end, I thought I would tell a story about what can happen when there’s no Lyme awareness. Continue reading “Misdiagnosed Despite a CDC-Positive Test: My Lyme Disease Story”
Hello! It’s not only Lyme Awareness Month but also Fibromyalgia Awareness Month, Food Allergy Awareness Month, Multiple Chemical Sensitivities (MCS) Awareness Month, Myalgic Encephalomyelitis (ME) Awareness Month, and Asthma Awareness Month. Continue reading “Lyme Awareness Month: Lyme Myths”