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.
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…
By Carolyn Degnan One of the biggest problems that chronically ill patients face is “gaslighting”…
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…
by Arlene Brailey For eight years, my son has been fighting a war against Lyme…
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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