Episode 593: MyLymeData: 10 Years of Patient-Powered Lyme Research – Dorothy Leland | LIVE from ILADS
LIVE from ILADS: What happens when nearly 20,000 Lyme disease patients pool their experiences to help researchers understand what patients are actually living through?
Tick Boot Camp sits down in person with Dorothy Kupcha Leland, President of LymeDisease.org to explore the power of MyLymeData, patient-driven Lyme disease research, sex-based differences in persistent Lyme disease, evidence-based patient education, and the importance of giving people reliable information without telling them which treatment they should choose.
This conversation was also personally meaningful for Tick Boot…
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