The mission of Global Lyme Alliance is to cure Lyme and other tick-borne diseases through innovative research, awareness, and empowering the patient voice. GLA has gained national prominence for funding some of the most urgent and promising research in the field by awarding over $16 million to our research program to date. GLA supports patients through every step in their journey, from finding a Lyme-treating physician to a peer-to-peer mentor program and a wealth of resources and information on its website. GLA also offers an ambassador program for volunteers to raise awareness through education, create fundraising events in their area, or collaborate to advance GLA's mission. Visit us on social media or learn more at GLA.org
LymeDisease.org is 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. We believe in the importance of patient involvement at all levels of decision-making. Patients must have a voice whenever policymakers make decisions about Lyme disease.
Our mission is simple. We want to make our community a healthier place by protecting people from contracting Lyme and other tick-borne diseases and connecting patients and their families to helpful resources.
Lyme Connection is a unique community-based organization. We offer tick-borne disease prevention programming year-round as well as patient-support services. Lyme patients and their families enjoy our free monthly support groups, educational seminars, newsletters and health fairs. Run by caring individuals who have directly experienced the impact of tick-borne diseases, our organization understands the beneficial role wellness activities and educational resources play in recovery. We connect people to the fellow patients and professionals who can help make what is often a lonely and complicated experience less daunting. Hundreds have come to us for support since the group was created in 2003 as the Town of Ridgefield's Lyme Disease Task Force (RLDTF). RLDTF is a 501(c)(3) nonprofit under the Friends of Ridgefield Community Programs. We welcome your questions, support and participation. Visit LymeConnection.org for more information.
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