HOW YOU CAN BE INVOLVED
We conduct the largest research study of Lyme disease through our patient registry and research platform, MyLymeData. MyLymeData empowers patients to use their data to drive change.
Grass roots advocacy representing the patient for legislative, treatment and insurance changes. We represent hundreds of thousands of patients and provide them with the tools essential to empowerment.
The Lyme Times connects you to trustworthy information on critical research, events and treatment for Lyme disease and other tick-borne diseases.
Weekly e-newsletter and social media such as FaceBook, Twitter, Instagram, Pinterest and Instagram keep the public informed on timely topics and events facing the patient population.