How We Make a Difference in the Struggle of Lyme Patients

  1. Stop Denials of Care

    LymeDisease.org provides the advocacy muscle to challenge medical societies and protocols that deny treatment, to hold public policy makers accountable, and to promote patient-centered legislation.

  2. Train Physicians

    LymeDisease.org funds the training of healthcare providers who attend conferences at the International Lyme and Associated Diseases Society.

  1. Make Grassroots Advocacy Work

    LymeDisease.org maintains a national network of online state-based advocacy and support groups. These groups promote state and nationwide advocacy efforts.

  2. Get The Word Out

    LymeDisease.org is the go-to source for news, information, and health care policy analysis in the Lyme community. We keep you up-to-date via our website, blogs, Facebook & Twitter, as well as our quarterly journal The Lyme Times.

  1. Fund Research

    LymeDisease.org funds research critical to improving patient diagnosis and treatment outcomes. We also conduct and publish the largest patient surveys on the critical issues like access to care and burden of illness to help inform health care policy makers.

IT’S TIME FOR A CHANGE.

Only YOU
can make that difference