What’s actually happening in Washington for Lyme and tick-borne diseases—and does it ever really move the needle?

In this episode of the Lyme+ Podcast, host Kenzie Vath sits down with Megan Bradshaw, Government Relations Manager for Center for Lyme Action, to pull back the curtain on how federal funding, legislation, and advocacy campaigns are changing the landscape for Lyme patients and their families.

Megan shares her personal “patient-to-advocate” story, how a virtual congressional briefing from her parents’ recliner turned into a full-time mission on Capitol Hill, and why she believes we’re entering the “golden age” of Lyme and tick-borne disease advocacy.

Megan Bradshaw is the Government Relations Manager at Center for Lyme Action, where she leads federal advocacy efforts to secure funding and drive policy change for Lyme and tick-borne diseases. A patient herself, Megan channels her lived experience into strategic work on Capitol Hill—coordinating with agencies like HHS, CDC, NIH, and DoD, and helping build one of the largest Lyme advocacy networks in the country.

Learn more about Center for Lyme Action and get involved at centerforlymeaction.org

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