My three-year-old nephew Sidney is one of approximately 30,000 Americans living with cystic fibrosis--moms, dads, sisters, brothers, daughters, sons, and friends who struggle every day just to breathe.
The Cystic Fibrosis Foundation had been instrumental in funding CF Care Centers, where Sid and others receive specialized treatment, and providing funding for the research and development of drugs that are literally extending the life expectancy and lung capacity of people living with CF. Sidney takes medications every day that were developed through funding from the Cystic Fibrosis Foundation.
There is still no cure for this devastating disease and many lives are cut far too short. There's still so much work to do. We will not stop striding until all those with cystic fibrosis have a cure. We will not leave anyone behind.
Please support me!
With your help, we can invest our resources in research today, while raising funds for tomorrow, to ensure we have what it takes to reach the finish line. Together, we can make CF stand for Cure Found. Please help me reach my fundraising goal!
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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.