More Federal Funding for Lyme

With nearly 500,000 people in the United States getting Lyme disease each year, current federal funding for research and prevention programs is simply not enough. Help us fight for more funding for Lyme.

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OUR LEGISLATIVE VISION

 

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Center for Lyme Action Membership

Join now as an individual member or encourage your local Lyme organization to join.

Lyme Cases Increasing

476,000 estimated cases of Lyme disease reported in 2019 by the CDC.  Reported total cases in 2019 are nearly 5 times the number reported in 1991.

476,000 cases in 2019

Low Per Patient Funding

Per patient federal funding for Lyme disease is incredibly low at $170 per patient. Less common diseases such as West Nile has 200 times and Malaria has 800 times the amount of per patient funding.

More Funding required

No Working Diagnostic or Therapy

Current diagnostics don’t work – at best 38% accurate.  Current treatments are insufficient for chronic patients and work for approximately 85% of acute patients.

Need diagnostic and therapy

Your Action – Starting Now

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What We Do

Center for Lyme Action sponsors educational sessions for the executive and legislative branches of the US federal government.  We work to bring more attention to Lyme disease, the human suffering, and the need for better diagnostics and treatments.  We then work to advocate for increases in federal funding for preventing and battling Lyme.

Our Mission

Center for Lyme Action is a member-supported 501(c)4 organization dedicated to increasing federal funding for Lyme disease. 

Become a Member. Get Involved.

We are seeking help from the Lyme community — Lyme foundations, Lyme advocacy organizations, Lyme patients and their family and friends.

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Lyme patients need your help.

611 Penn Ave SE Suite 126 Washington, DC 20003

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