Life with assorted ailments
Lymies of the world, we still don’t have disease recognition, accurate testing, sufficient research dollars, Lyme awareness in every state and country, and full insurance coverage for treatment. We should at least get … proper spelling. Continue reading “Lyme-not-Lyme’s Disease Awareness Month”
I usually think about what I’ve lost from being chronically ill, which is pretty much everything. But it turns out I have also acquired many odd new talents. Continue reading “Skills I’ve Gained as a Lymie”
Lots of people have heard about the dangers of parabens, but there are many other chemicals to hate in hair products. Continue reading “Formaldehyde and Other Chemical Crappage in Hair Products (Plus Bonus Easy DIY Hair Recipes!)”
Remember when our biggest problems were doctors not taking us seriously and people’s lack of understanding about our health issues? Are you nostalgic for those days? Me too! Continue reading “How to #Resist Without Using All Your Spoons”
So most days your sex drive has been replaced by a raging headache, but sometimes you have your moments. Or maybe you’re headed towards remission and feel like giving it a go with your sweetie. Either way, here at Miss Diagnoses we I have some ideas. Continue reading “Lyme Sexy Tyme: Valentine’s Day Special”
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?”
Hello bloggy world! I am back! Continue reading “My First Herx”
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”
