Celia is one of the 30,000 Americans living with cystic fibrosis. Right now there is no cure for cystic fibrosis, but there is HOPE. Real progress has been made in the search for a cure, but the lives of people with CF are still cut far too short (currently avg life expectancy is around 50), and we want Celia around for a long time. By supporting us, you will fund the search for a cure and add tomorrows to the lives of people with cystic fibrosis, like Celia.
IMPORTANT NOTE ON ATTENDANCE AT FOUNDATION EVENTS:
Updated July 5th, 2023
The CF Foundation is committed to ensuring the health and wellbeing of individuals attending Foundation events. Individuals attending CF Foundation events must abide by the Foundation's Event Attendance Policy www.cff.org/attendancepolicy, which includes guidance for event attendees living with cystic fibrosis.