May is Neurofibromatosis (NF) Awareness Month. In honor of that, we are re-releasing a deeply moving episode that focuses on a truly incredible foundation—and the powerful story behind it.Leslie sits down with Kate Doerge, founder of Penny’s Flight Foundation. Kate shares the powerful story of her daughter, Penny, who passed away in November 2022 from NF—the most common genetic disorder in children, and one that still has no cure.In the wake of unimaginable loss, Kate, her husband Chad, and their community turned grief into action. They founded Penny’s Flight Foundation, a growing national movement dedicated to raising awareness and funding for NF research.In this heartfelt conversation, Kate reflects on Penny’s joyful spirit, the mission of the foundation, and the boundless energy fueling efforts to find a cure. Her story is one of resilience, love, and the power of community.Tune in and be inspired by the legacy of Penny and the incredible work being done in her name.If you’re moved by this episode, please consider subscribing and leaving a review on your favorite platform. And if you haven't already, be sure to follow us on Instagram @TheInterviewWithLeslieHosted by Ausha. See ausha.co/privacy-policy for more information.
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3ª PARTE | 17 DIC 2025 | EL PARTIDAZO DE COPE
01 Jan 1970
El Partidazo de COPE
13:00H | 21 DIC 2025 | Fin de Semana
01 Jan 1970
Fin de Semana
12:00H | 21 DIC 2025 | Fin de Semana
01 Jan 1970
Fin de Semana
10:00H | 21 DIC 2025 | Fin de Semana
01 Jan 1970
Fin de Semana
13:00H | 20 DIC 2025 | Fin de Semana
01 Jan 1970
Fin de Semana
12:00H | 20 DIC 2025 | Fin de Semana
01 Jan 1970
Fin de Semana