Episode 467: LIVE from ILADS: Megan Bradshaw - Advocating for Tick-Borne Disease Patients

Key Points: Megan Bradshaw shares her personal recovery journey and how it led her to pursue a master's in public health at UNC Chapel Hill. She discusses her new role as Government Relations Manager for the Center for Lyme Action, a 501(c)(4) nonprofit dedicated to increasing federal funding for tick-borne disease research and policy. The Center for Lyme Action organizes "fly-in" events, where patients and advocates virtually meet with members of Congress to share their stories and push for increased Lyme disease funding. Megan highlights the power of grassroots advocacy, explaining how patient voices influence legislative change despite bureaucratic hurdles. She explores opportunities within the current administration's focus on chronic illnesses and the potential role of federal agencies in tackling Lyme disease. Megan encourages patients and caregivers to participate in the upcoming virtual "fly-in" event, offering training and support to help them make a difference. Advocacy is not just about policy—it can be an empowering part of the healing journey, providing patients with purpose, connection, and a platform for change. Resources & Links: 🔗 Follow the latest ILADS updates at ILADS.org 🔗 Learn more about Megan Bradshaw: Instagram @mcbradshaw 🔗Center for Lyme Action Website: CenterForLymeAction.org 🔗 Stay connected with Tick Boot Camp: Website | Instagram | Facebook | YouTube | TikTok | Twitter (X)