Gigi and Miles love to READ!
At 3 weeks old, our grandson Miles was diagnosed with Cystic Fibrosis. Miles is a tough guy and the family has a great team at Dell Children's Hospital supporting him.
Miles and the entire CF community deserve medical and scientific progress and a cure, and YOU can help!
Over the last 30 years, life expectancy with CF has doubled, and we hope in Miles' lifetime that it will continue to increase and that a cure will be found.
Join our Miles 4 Miles team and help us get one step closer to a cure for cystic fibrosis – a rare, genetic, life-shortening disease that makes it difficult to breathe.
Help us raise funding for the Cystic Fibrosis Foundation between now and May 4th, 2024 when we will walk and run Great Strides for Miles!
You will not see the miles I walk in this dashboard because I don't use a fitness tracker!
Thank you, and we can't wait to see you there, supporting MILES FOR MILES and a Cystic Fibrosis cure.
Until CF stands for CURE FOUND!
Gigi (Kalí ) Rourke
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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.