From illness to activism, Olivia just keeps going
I first became aware of Olivia Goodreau about six years ago. I was at my…
This blog has several goals. First, to explore the personal side of Lyme disease and how it affects individuals and families. Second, to highlight useful information for people seeking answers about this complicated illness. Third, to help foster a sense of unity and shared purpose among the many diverse members of the Lyme community. Dorothy, who serves as President of LymeDisease.org, has a family member with Lyme disease. She is co-author of a book called When Your Child Has Lyme Disease: A Parent’s Survival Guide.
I first became aware of Olivia Goodreau about six years ago. I was at my…
Hacking Lyme Disease: An Action Guide to Wellness is a compilation of articles from Dr….
From the beginning of the coronavirus pandemic, questions started swirling through the Lyme community. Two…
Popular San Francisco radio host Jeffrey “JV” Vandergrift often spoke on the air about his…
Zoe Lu, a fine art photographer based in New York, was diagnosed with neurological Lyme disease and…
The third and final report of the Tick-Borne Disease Working Group has been submitted to…
Josh and Ethan are two young men from Utah who share a special bond. Not…
This week, about 350 Lyme advocates from 45 states donned their special green neck scarves…
The National Academies of Sciences, Engineering, and Medicine (known collectively as NASEM) are private, nonprofit…
A piece of music representing what it feels like to experience Lyme disease and co-infections…
End of content
End of content