HOW YOU CAN BE INVOLVED
LymeDisease.org is the largest communications network in Lyme disease. Our website draws millions of unique visitors a year providing up-to-date and timely news and Lyme disease education.
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.
MAKING A DIFFERENCE
Laurie’s Lyme Disease Journey
It is daunting to write about having chronic Lyme disease, as most of my life I have spent hiding it like a deep, dark family secret. Putting on a good face, acting as if I...
Awareness + Compassion + You + Me = A Cure For Lyme Disease
Seven Simple Facts: Lyme Disease is the fastest growing vector-borne disease in America (Center for Disease Control - 2014) Tick-borne diseases can be spread by deer, ...
Make Time for Tea
Have you ever wanted to donate to a fundraiser but you didn’t want to attend the event? Well here is your perfect opportunity to participate and not leave home. The Make Tim...
why we ADVOCATE for people with Lyme disease
