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)
