Our Generation Lyme co-founders recently sat down with Fred Diamond, host of the “Love, Hope, Lyme” podcast, for an emotional conversation about the power of community.
My name is Presley Taylor. As a passionate advocate for Lyme Disease, I’ll be contributing to Generation Lyme to share insights with patients, families, researchers, and anyone affected by this difficult disease.
Generation Lyme and Center for Lyme Action are pleased to announce a new Community Partnership to leverage each nonprofit organization’s distinct resources to support current and future Lyme disease advocates.
Scroll through the gallery for our activity and progress in 2023! Even if all you did this year was get through it, that’s huge, and we’re proud of you.
We are thrilled to announce a milestone in our mission to empower Lyme disease patients and supporters everywhere: Generation Lyme has achieved 501(c)3 nonprofit status.
For years, the CDC has been the backbone of a medical establishment that has denied the chronic symptoms of Lyme disease. This week, the CDC changed its stance on Lyme.
