Lyme Disease: Our Story

The Brunke Family: Mark, Christy, Michaela, and Angelina

Family picture from November 2014, just months before we moved to Maryland. Photo by Stephanie Kuecker.

What are your greatest fears?

Since we moved to Maryland in May 2015, one of mine has been that my husband, daughters, or I would get Lyme disease. We had traded the cold, crime, and bad traffic of Chicago for an adversary the size of a sesame seed. How could we fight a foe we could barely see?

Lyme Disease Risk in the United States

Photo courtesy of myblindspotjourney.wordpress.com.

As you may know, Lyme disease is spread through the bite of infected blacklegged ticks. Also known as “deer ticks,” these bugs are much smaller than other ticks. Depending on the stage of their development, they range in size from a pinhead to an apple seed.

But the damage they cause can be life-changing. Our neighbor had to retire early and still suffers from pain in his back and knees. A sweet friend from church struggles with brain fog, debilitating fatigue, and physical limitations. Combined, these problems led to her having to go on disability.

In both their cases, they had Lyme disease for years before it was diagnosed. And untreated Lyme disease can cause arthritis, meningitis, nerve paralysis, and even heart problems.

Later signs and symptoms of Lyme diseaseIn contrast, the CDC says, “People treated with appropriate antibiotics in the early stages of Lyme disease usually recover rapidly and completely.” Hence, the incredible importance of discovering the disease quickly.

Five years ago, my father also contracted Lyme disease, but his story gives us hope. Because he realized what it was within a week, he was able to recover from it without any permanent damage.

His story and ours are why I’m writing this blog: to help you recognize the disease early before it wreaks havoc on your health. Even more important perhaps, for parents, is to recognize it in your little ones.

Seven-year-old girl with her baby bearded dragon.

Michaela on her seventh birthday–Tuesday, August 28, 2018–with her baby bearded dragon.

Our seven-year-old, Michaela, is strong, energetic, and independent. She delights us with her inventiveness, her creativity, and her surprising and perceptive observations.

But winter mornings with her can prove challenging. Even if it’s literally freezing outside, she almost never wants to wear a coat. To prove she doesn’t need one, she’ll stand on our deck for .2 seconds and say, “See? It’s not cold!”

But on the way home from her late August birthday party, she started complaining she was cold. The next day, on the way home from the zoo, she said the same. That evening—the Friday before Labor Day—she was hot to the touch. I took her temperature, and it was 103.4 degrees.

Seven-year-old girl at the Maryland Zoo in Baltimore.

Michaela at the Maryland Zoo the day we discovered she was sick.

My husband, Mark, checked her from head to toe and found nothing unusual. Since her doctor’s office had closed by that time, he took her to a clinic, and they concluded she had a virus.

On Labor Day, after days of no symptoms except chills, fatigue, and fevers, I discovered a rash. At first, I thought it might just be a pressure mark from her long nap on Mark’s recliner. The middle of the night proved that theory wrong.

Just after midnight, Michaela came into our bedroom crying. Her head hurt, and her fever had spiked to 103.9. I checked the oval red mark on the back of her upper thigh, and it was still there.

I gave her medicine and a lukewarm bath and left a voice mail for the on-call pediatrician. When he called back, he advised me to bring her in first thing in the morning.

Seven-year-old girl 24 hours after starting antibiotics.

Michaela eating lunch 24 hours after starting antibiotics. You can still see the red circles around her eyes, but her bright smile is back and her hair is messy, because she was playing superheroes.

I did, and another doctor examined her and ruled out common causes of fever. Then she called in a third doctor to check out the rash, which was clearing in the center. They agreed she probably had early Lyme disease and started her on antibiotics.

(Diagnostic blood tests aren’t usually accurate until four to six weeks after infection, so they start treatment for early Lyme disease based on your symptoms.)

Most importantly, since the doctors think we caught it very early, they don’t predict any long-term problems. And because I want you to catch it early too, here are my main tips:

First, don’t just check for the rash once. The circular red area usually takes 3 to 14 days to appear after the tick bite and can appear as late as 30 days later. Some people never get the rash.

Second, don’t forget to check your scalp and areas where your skin creases when you stand.

Third, don’t assume it has to look like a bull’s-eye. The erythema migrans can take many forms (see the chart below).

Erythema migrans can present itself in many forms.In my dad’s case, his rash looked like a normal rash but then spread to other parts of his body. In Michaela’s case, the rash didn’t appear until several days after her symptoms started. If your fever or a loved one’s persists, check for the rash again and see your primary care physician.

So now we know a little more about how to catch Lyme disease early. But how do we prevent ourselves and our loves ones from getting it in the first place? Check out 12 Ways to Lower Your Risk for Lyme.

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9 thoughts on “Lyme Disease: Our Story

  1. Thank you so much for this information. My prayers and my heart go up for Michaela and you as you go through this with her. God bless!!

  2. Hi Christy, Curtis contracted Lyme disease in 7th grade after spending a night with Wade and then the next night with Tim. We had just moved to Hagerstown. I thought it was a chigger, it was such a tiny dot. I sealed it with fingernail polish :(. He was not caught early because , when he was taken to the ER, they thought it was spinal meningitis. I asked them to do a Lyme yeast and they didn’t. The pediatrician said it was the flu and refused a Lyme test, too. Fortunately, I was able to look it up online and compare the secondary rash, erythema migrants. We had to demand our pediatrician give him erythromycin, although he gave him too small a dose. I then took home to a specialist and he received the proper dosage.
    Since then, I have learned that COLLIDAL Silver kills spirochetes and would recommend this to be added to an antibiotic regimen. Amazon sells it. Betsy

  3. Thanks for sharing! My daughters pediatrician called it an exotic disease and didn’t wish to do an invasive test (blood test) to determine if she indeed had Lyme . She ultimately was tested (mom can be a very strong and determined advocate) this happened 2x! We then changed pediatricians. Lunes is not an exotic disease And it is necessary to be caught early so treatment to cure is possible. So glad Micheala is being treated early! God bless!

  4. My daughter was diagnosed with Lymes. She was diagnosed one day before we went to a 4-H conference at the University of Maryland where one of the workshop leaders was working closely with the CDC on Lymes. She said you MUST be put on a 30-day antibiotic. Our daughter had only been given a 14-day supply. Our pediatrician refused to change the dosage. Luckily we had some on hand from something else that we used to make up the 30 days. According to the workshop researcher, the CDC changed their parameters on the treatment of Lymes, but most doctors do not keep up with all the changes. She actually was willing to talk to my doctor (he still didn’t change his mind regarding my daughter, but luckily we had current info). So very glad you caught it when you did. You were a great advocate!

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