Faces of Loudoun: Meet Jaclyn-Undiagnosed Lyme Disease Put My Life on Hold

Ten years ago, I was proud to be following in my father’s footsteps. I had a degree from JMU and a dream job at a local winery, where I was by all measures a top performer. My hard work and studies—my determination and work ethic—were paying off as promised.

But then, I started feeling “off.”

At first, it just seemed like a bad flu. But the symptoms persisted, and they got worse—more frequent and more severe. I was walking around foggy most of the time. I lost my ability to focus; tasks that would previously take 10 minutes now took an hour. And I was in excruciating pain—even though I was taking 16 ibuprofen pills a day. I could hardly walk. Washing my hair was torture. Work was almost impossible. My mouth was so swollen, I could only eat yogurt with a knife.

Years after being diagnosed with Lyme disease, Jaclyn is now working with several organizations to help other Lyme survivors get the help they need to eradicate their symptoms.
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            Whatever this was, it was affecting my job—my whole life. And there was no end in sight. I went to a long line of doctors, who ordered a multitude of tests: EKG, EEG, MRI, CT scans. Everything came back “normal.” The consensus? There was “nothing wrong” with me. I was divorced and far from family, fearful of losing my job, feeling like I must be crazy.

No one in Loudoun should have to face a life of pain and fear alone.

The Next Chapter

            A year and a half after experiencing the first symptoms, I started to see a Lyme-literate physician who was able to finally give me a diagnosis. I had never found a tick on my body, nor had I ever seen the bull’s-eye rash. Nonetheless, I was suffering from a severe case of Lyme disease, an autoimmune disease afflicting at least 320,000 Americans each year.

My doctor put me on an 18-month journey to health. An aggressive regime of medications, a tightly controlled diet, and a commitment to reducing stress were the keys to managing and ultimately eradicating my symptoms.

During my recovery, I found a new spirituality and a personal calling—to help those who are struggling with undiagnosed autoimmune diseases. Virginia and Loudoun are at the epicenter of the Lyme epidemic. Today, I work with multiple organizations to educate the public on the prevention, symptoms, and treatment of this horrific disease.

It is my great purpose and passion in life: To help the people who must walk the path I followed. If I can just point them to the resources and information I did not have, help them advocate for their own answers, and avoid all the misinformation that warps the public understanding of this disease, I can shorten their suffering and get back to a healthy, fulfilling life.

Won’t you help me End the Need in Loudoun?

As part of the Community Foundation’s Faces of Loudoun campaign, Loudoun Now is publishing monthly articles highlighting men, women and children who have found a helping hand when they needed it most. Learn more or donate to help End the Need at FacesofLoudoun.org.

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