Cystic Fibrosis is a life shortening genetic disease of the lungs and the digestive system - and there is NO CURE! We need YOUR help in finding one!
Together, we ARE adding tomorrows to the lives of all people living with CF!
Thank you for your support!!!!!
The J Team -Jenn, John, Jackson, and Jacob Miller
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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.