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”
Category: Chronic Illness
Lyme Awareness Month: Lyme Myths
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”
Meditation Techniques for the Meditation-Challenged, Part Two
For those of you who did not read the exciting, I mean relaxing and contemplative, “Meditation Techniques for the Meditation-Challenged, Part One,” I described two techniques: a simplified version of the Buddhist Loving-Kindness Meditation, and an easy, one-minute mindfulness meditation you can do anywhere. Continue reading “Meditation Techniques for the Meditation-Challenged, Part Two”
My Talking Thyroid: New Medication Crisis
I’m not sure if I mentioned this, but I have a talking thyroid.
This exceptionally chatty gland tells me a lot of things. For instance, it is very upset about having Hashimoto’s thyroiditis (a disease in which the immune system attacks the thyroid). It feels very persecuted. Continue reading “My Talking Thyroid: New Medication Crisis”
Two Days in Insurance Hell: A Play in Hopefully Only One Act
Main Character, a woman with Lyme, fibromyalgia, allergies, thyroid disease, and a messed-up spine, is trying to get a doctor to authorize her brand-name Neurontin (a painkiller that works on nerve pain). She gets weird rashes and chills from using gabapentin, the generic version of the medicine. She got a threatening letter from her insurance carrier, saying that after April 1 they weren’t going to pay for the brand-name version without a doctor’s authorization. Continue reading “Two Days in Insurance Hell: A Play in Hopefully Only One Act”
This Week in Medical Limbo
What is medical limbo? It’s the time when I’m waiting for test results, waiting to find out the meaning of a new symptom; waiting to see if a new medication makes me feel better; waiting to see if that same new medication gives me double vision, an odd rash, or another strange side effect; waiting for a doctor to call me back; waiting for someone to come along and answer a question I posted in a medical forum; waiting to find out if my insurance will approve a treatment. Chronic illness involves a lot of waiting. Continue reading “This Week in Medical Limbo”
Meditation Techniques for the Meditation-Challenged, Part One
I’ve been trying to meditate for years.
I had read about the benefits of meditation for coping with Lyme disease, chronic pain, thyroid disease, allergies, anxiety, and almost every condition I have, but I just couldn’t focus on my breath and keep my mind from racing. Continue reading “Meditation Techniques for the Meditation-Challenged, Part One”
The Fibro Monster
Well, I’ve been blogging for a month, and I finally learned how to check my stats. The most popular search was an image search for “Fibro Monster,” the category I use to write about my fibromyalgia. I started to imagine the way a Fibro Monster might look. Continue reading “The Fibro Monster”
Happy Birthday to Me
“Inside every older person is a younger person, wondering what the hell happened.”
— Cora Harvey Armstrong Continue reading “Happy Birthday to Me”
Does Your Thyroid Want a Green Smoothie?
In April 2013, I had a wisdom tooth removed. It is not pleasant to do this in middle age.
My dentist thought it would be no big deal. I knew she was lying. I didn’t realize how badly she was lying. Continue reading “Does Your Thyroid Want a Green Smoothie?”
Things Not to Say to People With Chronic Illnesses
1. You LOOK so healthy.
2. Have you tried (name of very basic, obvious remedy, like ibuprofen)?
3. Are you SURE you’re sick?
4. You mean you really can’t do that tiny, tiny, little motion? Just doing that little thing causes you pain? Aren’t you being dramatic? Continue reading “Things Not to Say to People With Chronic Illnesses”
Why I Hate the Holidays
Here are some of the most annoying things about getting through the holidays with Lyme disease, ME, or fibromyalgia: Continue reading “Why I Hate the Holidays”

