We're looking forward to joining the experts and advocates working to improve the lives of people affected by Lyme and other tick-borne diseases at the 2026 ILADS Annual Scientific Conference.

Signed into law on September 30, 2026, this legislation builds on the original 2019 law named after the late Senator Kay Hagan of North Carolina.

Generation Lyme joins the LivLyme Foundation at the 6th annual LivLyme Summit for a talk about the importance of community.

Generation Lyme Co-Founders Jennifer, Brooke and Jesse recently sat down with Fred Diamond, host of the “Love, Hope, Lyme” podcast, for an emotional conversation about the power of community.

Presley Taylor is a passionate advocate for Lyme disease and Generation Lyme contributor sharing insights with patients, families, researchers, and anyone affected by this difficult condition.

Generation Lyme and Center for Lyme Action announce a new Community Partnership to leverage each nonprofit organization’s distinct resources to support current and future Lyme and tick-borne disease advocates.

We are thrilled to announce a milestone in our mission to empower Lyme disease patients and supporters everywhere: Generation Lyme has officially earned 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 publicly changed that stance.

There was no holiday to celebrate the people of the Lyme disease community. So we created one.

Progress moves slowly—but during Lyme Disease Awareness Month 2021, we took a leap forward.

Project Lyme and Generation Lyme are spreading the word about Lyme disease to express the urgency patients experience in their pursuit of help.