LYMEPOLICYWONK: MyLymeData, powered by patients, helps drive Lyme research
I want to thank Mimi MacLean for featuring me on Lyme 360’s Heal podcast. Mimi…

Author | LymeDisease.org
Dorothy Kupcha Leland is President of LymeDisease.org. A writer and longtime advocate, she focuses on Lyme disease education, policy awareness, and patient support. She is co-author of Finding Resilience: A Teen’s Journey Through Lyme Disease and When Your Child Has Lyme Disease: A Parent’s Survival Guide.
I want to thank Mimi MacLean for featuring me on Lyme 360’s Heal podcast. Mimi…
The Tick-Borne Disease Working Group is supposed to bring together 14 people—scientists, doctors, health officials,…
I delivered the following public comments by phone to the federal Tick-Borne Disease Working Group…
Carl Hamrin was born in Sweden, emigrated to the United States, and became a US…
The Center for Lyme Action (CLA), a nonprofit organization dedicated to increasing federal funding for…
Alicia White suffered from bizarre, often painful physical symptoms for years. Consulting numerous doctors, the…
Bonnie Crater, co-founder of the Center for Lyme Action–a lobbying group seeking more federal funding…
Chronic pain–defined as ongoing pain that continues for longer than six months–is a common complaint…
LymeDisease.org is one of the foremost Lyme patient advocacy organizations in the United States. We…
The federal Tick-Borne Disease Working Group held another online meeting Tuesday. Its upcoming Report to…
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