Ten years strong: How MyLymeData works to transform Lyme research
A decade ago, LymeDisease.org introduced MyLymeData, now recognized as the largest patient-driven registry for Lyme disease in the United States. What is a patient registry? It’s a system that collects information about patients with the same medical condition, in order to figure out the best ways to improve their care. Why is this significant? Because […]
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Touched by Lyme