May 21 is the annual Cystic Fibrosis fundraising walk. This fundraiser helps support the Foundation's mission to cure Cystic Fibrosis (CF) and raise awareness for this rare, genetic life shortening disease. Though no cure has yet to be found, great progress has been made in improving the lives of those afflicted through research and medical advancements fund by the CF Foundation.
My beautiful grandaughter, Ava Winter, has been living with this disease for 14 years. Ava has a rare mutation and the new medication advancements does not meet her needs YET. Your contribution will help accelerate the Foundations pursue of more new therapies and provide vital support to meet the needs of those with CF.
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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.