What happens when children with disabilities age out of the systems meant to support them? And what can families do to ensure their futures are protected? In this episode, anthropologists and authors Faye Ginsburg and Rayna Rapp explore the often-overlooked experiences of disabled caregivers and families navigating complex systems during and beyond the pandemic. We talk about how policy falls short, what protections families should expect, and the creative forms of resilience and care that disabled communities have built in the face of systemic neglect.

This conversation offers both a critical lens and a hopeful one—rooted in the power of community, advocacy, and the enduring brilliance of disabled lives.

In this episode, journalist Melody Schreiber breaks down what you really need to know about the recent measles outbreaks—including who should consider an MMR booster. We also unpack the growing information void from federal agencies and how to stay informed when the government isn’t stepping up—especially in potential crisis moments like bird flu and other emerging health threats.

In this episode, Dr. Kavita Patel breaks down how the current administration’s policies are reshaping public health, what parents might notice at their next pediatrician visit, and concrete ways to advocate for stronger protections for children and families.

CMV affects 1 in 200 babies, and 20% of them experience serious health complications. But a breakthrough is on the horizon—a CMV vaccine. Join us as we speak with Dr. Sallie Permar, a leading researcher in the fight against CMV.