Having different Lyme reporting rules for some states makes no sense
I delivered these comments at the Tick-Borne Diseases & Associated Illnesses: National Community Engagement Initiative…
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 these comments at the Tick-Borne Diseases & Associated Illnesses: National Community Engagement Initiative…
The following book review first appeared on the CanLyme website. By Catherine Kinsella Finding Resilience:…
My name is Talan Yorn, also known as “The Lyme Ninja.” In a previous blog…
by Ann Maher I am from Kilkenny, Ireland and I never thought that I would…
by Fred Diamond When I was researching information for my book “Love, Hope, Lyme: What…
by Pamela Andrews In 1991, my daughter, Leya Schiller, graduated from high school. She had…
The Wyss Institute at Harvard University seeks Lyme patients to donate blood cells to support…
In a recent interview about burgeoning tick populations in the US, the CDC’s Sue Visser…
By Jessica Harris My mother was diagnosed with ALS by several neurologists and even had…
By Jill Wussow It’s May again – Lyme Disease Awareness Month. I want to focus…
End of content
End of content