There are approximately 30,000 Americans living with cystic fibrosis. They are moms, dads, sisters, brothers, daughters, sons, and friends who struggle every day just to breathe.
Our daughter Aubin was recently diagnosed with CF. The CFF is such a great organization that has made huge strides in finding a cure. They are the reason we have the genetic modifying medications to help her body work more normally. The hope that these medications give us personally is indescribable.
We are at a pivotal moment in the history of cystic fibrosis and your support matters. 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.
We would love to have you join our team and donate to help our mini but mighty girl!
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Our daughter Aubin was recently diagnosed with CF. The CFF is such a great organization that has made huge strides in finding a cure. They are the reason we have the genetic modifying medications to help her body work more normally. The hope that these medications give us personally is indescribable.
We are at a pivotal moment in the history of cystic fibrosis and your support matters. 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.
We would love to have you join our team and donate to help our mini but mighty girl!
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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.