Author | LymeDisease.org
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.
This morning, I (and a whole lot of others on social media) took offense at…
The National Education Association is the largest labor union in the United States, representing public…
Along with new and continuing challenges for the Lyme community, there is also much…
LymeDisease.org today announced the launch of MyLymeData, a first-of-its-kind national patient-powered research project aimed at…
In May 2014, I reviewed lyme light: a memoir, by Natalie London. It’s now available…
LymeDisease.org will soon launch a patient-powered research project called MyLymeData. It promises to be the largest…
Last month, at the IDSA Lyme protest in San Diego, I met Michelle Trostler, who…
A valiant group of Lyme activists braved a record-breaking heat wave in San Diego Oct….
When the Infectious Diseases Society of America opened its annual conference in San Diego yesterday,…
LymeDisease.org CEO Lorraine Johnson has been selected to participate in a White House forum hosted by the…
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