We fight to make the patient voice stronger, to support science-based advocacy, to create legislative change, and to create a future where Lyme patients can receive the treatments they need to get well.
We are the largest communications network for Lyme disease and the most trusted source of information by patients. We put patients at the center and drive health care policy and science from the inside out. Our big data project, MyLymeData, is the largest study of Lyme disease ever conducted. There is strength in numbers.