Gigi and Miles love to READ!
At 3 weeks old, our little grandson Miles was diagnosed with Cystic Fibrosis. Miles is a powerhouse and the family has a great team at Dell Children's Hospital supporting him.
Miles and all of the 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 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.
Please join us in raising money for the Cystic Fibrosis Foundation between now and May 6th, 2023 when we will walk and run Great Strides for Miles!
Thank you, and we can't wait to see you there, supporting MILES FOR MILES and a Cystic Fibrosis cure.
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.