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Last summer, a New York Times opinion piece opened with a blunt warning: “We’re living in a tick nightmare.” It’s not hyperbole. Across the United States, people are seeing more ticks, more tick‑borne infections, and more confusion in the medical system about how to diagnose and treat them.
Now more than ever, heightened awareness, proactive prevention, and rigorous education are vital to safeguarding public health against these rapidly multiplying vectors.
Inside this issue of the Lyme Times, we dive deep into the evolving complexities of tick-borne conditions that demand our attention. We explore the rising challenge of alpha-gal syndrome—the tick-induced meat allergy that is reshaping lives. We also confront the ongoing battle surrounding persistent Lyme disease, shedding light on the patient experiences and scientific developments aimed at addressing long-term, chronic symptoms that standard treatments often fail to resolve.
Finally, we highlight the power of patient-driven research through the latest insights from MyLymeData. By pooling the real-world experiences of thousands of individuals, this vital registry continues to break new ground, offering researchers the robust data needed to drive clinical breakthroughs.
Adding to MyLymeData’s growing impact, our infographic Diagnosing Lyme in Time recently was honored with an Excellence Prize in the LymeX Visible Voices contest.
From groundbreaking research to award-winning public education, this issue reflects the power of informed, engaged communities to
drive meaningful change in the fight against tick-borne disease. We hope you’ll join us in turning awareness into action.
Click here to download a PDF of this issue of The Lyme Times.
