For too long, cystic fibrosis, a rare, genetic disease, has robbed people of tomorrows – progressively limiting their ability to breathe and tragically shortening life. There are approximately 30,000 Americans living with CF.
Real progress has been made for those who have CF, but there is still no cure for this devastating disease and many lives are cut far too short.
By walking with me or donating to the #65roseschallenge, you can help accelerate the Foundation’s pursuit of new therapies and provide vital support to meet the needs of the CF community.
Kinson was diagnosed at a month and 5 days old. We have been extremely lucky with his health so far, with only two quick hospital stays since he was 9 months old. Our daily life is filled with breathing treatments, vest sessions, pills, and other medicines, but Kinson is such a little champ and takes it all in stride! CF is just a tiny part of our perfect boy
Please support us!
Your participation will help us get one step closer to ending this terrible disease. Let’s make CF stand for Cure Found.
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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.