Inside Cystic Fibrosis: A Conversation with Kate Hylan of the Cystic Fibrosis Foundation

SHOEMAKER LAB

What does it take to find a cure for a rare disease like Cystic Fibrosis? In this episode, we sit down with Kate Hylan, Director of Development for the Cystic Fibrosis Foundation, to discuss the foundation's mission and the challenges of raising awareness for this orphan disease. We dive into the genetic nature of CF, its impact on patients, and the groundbreaking work being done to improve their quality of life. Kate also shares personal stories and highlights the importance of advocacy and fundraising. Tune in to learn more about how the CFF is fighting to make a difference!

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