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.
OUR
LEGISLATIVE VISION
Read the paper
The State of Lyme Disease Research in the United States:
An Educational Paper from Center for Lyme Action
How You Can Get Involved
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 $106 per patient. Less common diseases such as West Nile has 190 times and Malaria has 1000 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 Impact Starts Here
Virtual LYME Fly-In Events
Active advocates across the US
Million dollar Increase in federal funding
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.
Get in Touch. Get Involved.
Lyme patients need your help.
