A WEBINAR SERIES PROVIDING INFORMATION ABOUT CYSTIC FIBROSIS, THE CF FOUNDATION, AND AVAILABLE RESOURCES
This new series discusses different topics related to cystic fibrosis. You'll hear directly from people with a wide range of connections to cystic fibrosis - including local community members living with CF, clinicians, Foundation staff, and advocates - about their experiences and journeys, while getting information and resources available to all members of the CF community. These sessions are for everyone - whether you've just received a diagnosis, know someone with CF and want to learn more, or have been part of the CF community for years.
Session 1: “What I Wish I Knew About Cystic Fibrosis”
This session will host a discussion from two people living with cystic fibrosis and a mother of a daughter with CF about 'things they wish they knew' when they received their diagnosis. Hear from a local care center team about the resources, information, and next steps they share after a new diagnosis.