LymeDisease.org will soon launch a patient-powered research project called MyLymeData.
It promises to be the largest study of chronic Lyme patients ever.
Our latest issue of The Lyme Times explains all about it. You can read this issue online (for free) by clicking here.
(Note: Usually, you need to be a member of LymeDisease.org in order to have free online access. However, we’re making this one available to all, because we want everyone to have an opportunity to learn about the MyLymeData project.)
Dorothy Leland
Dorothy Leland is a longtime advocate and researcher focused on Lyme disease education, policy awareness, and patient support. She has contributed to numerous publications and works closely with medical professionals and organizations to improve understanding and treatment of tick-borne diseases.
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