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Lyme Science Blog

Why Patients With Lyme Disease Feel Exhausted Despite Sleeping

Why Patients With Lyme Disease Feel Exhausted Despite Sleeping

Exhausted despite sleeping in Lyme disease Many patients with Lyme disease describe the same experience: they sleep through the night yet wake feeling depleted. This article focuses on biologic fatigue and impaired recovery, not sleep duration alone. Feeling exhausted despite sleeping reflects non-restorative sleep, a state in which sleep occurs but the body does not […]

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Brain Fog and Cognitive Dysfunction in Lyme Disease

Brain Fog and Cognitive Dysfunction in Lyme Disease

Many patients with Lyme disease describe a frustrating and often frightening experience: they can no longer think the way they used to. Concentration is harder. Words feel just out of reach. Tasks that once felt automatic now require intense effort. This constellation of symptoms is commonly referred to as brain fog in Lyme disease. While

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Why Pediatric Lyme Screening Can’t Wait

Why Pediatric Lyme Screening Can’t Wait

Pediatric Lyme screening is rarely part of routine medical care, even in regions where tick exposure is common. When early Lyme disease is not recognized, diagnosis and treatment are often delayed until symptoms become more complex and disruptive. In children, missed or delayed pediatric Lyme screening can have lasting consequences, affecting learning, behavior, and long-term

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Why Constipation Is Common in Lyme Disease

Why Constipation Is Common in Lyme Disease

If your digestion has slowed and nothing seems to help, you’re not alone Constipation is a common and often frustrating symptom in people with Lyme disease. Some patients notice fewer bowel movements. Others experience hard stools, straining, bloating, or a constant sense of incomplete emptying despite adequate hydration and fiber. This symptom is common in

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Chronic Lyme vs PTLDS: The Debate

Chronic Lyme vs PTLDS: The Debate

The debate over chronic Lyme vs PTLDS isn’t just about words—it’s about whether patients feel validated or dismissed. Many patients use chronic Lyme disease to describe ongoing fatigue, pain, and brain fog. Some clinicians prefer post-treatment Lyme disease syndrome (PTLDS), a term that sounds more neutral but often feels minimizing. Did You Know? Most patients

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post-treatment Lyme disease syndrome (PTLDS)

What Is Post-Treatment Lyme Disease Syndrome (PTLDS)?

Many patients expect Lyme disease to resolve once antibiotic treatment is completed. For some, however, symptoms persist or evolve long after therapy ends. Post-treatment Lyme disease syndrome (PTLDS) is the term used to describe ongoing fatigue, pain, cognitive dysfunction, and neurologic symptoms that continue for months or years following standard treatment for Lyme disease. For

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Immune Dysregulation and Neuroinflammation in Lyme Disease

Immune Dysregulation in Lyme Disease

Many patients with Lyme disease experience persistent symptoms due to immune dysregulation in Lyme disease, even long after the initial infection has been treated. These symptoms are often misunderstood or minimized. Increasingly, they are recognized as reflecting immune dysregulation and neuroinflammation—a state in which immune signaling fails to return fully to baseline and continues to

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When Vision Lingers: Understanding Palinopsia and Repeating Images

When Vision Lingers: Understanding Palinopsia and Repeating Images

When Vision Doesn’t Let Go Some patients notice that an image disappears, but their vision does not fully reset. Lights may trail, words linger on the page, or objects seem to echo briefly in space. These experiences can be confusing and unsettling, particularly when they occur without warning. This phenomenon is known as palinopsia. Although

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When Medicine Says There’s Nothing More to Do

When Medicine Says There’s Nothing More to Do

When symptoms persist beyond what medicine can easily explain Author’s note: I wrote this because I often meet patients who have been told there is nothing more to do, even though their symptoms persist. This post explains why that phrase usually reflects the limits of a medical framework—not the limits of a patient’s illness or

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