Hi everyone!!
Welcome to our pack!
We have organized this Great Strides team to support Ryan, Brittany, and their son Pax.
Pax Francis was born on May 13th, 2023 and his family learned that he had Cystic Fibrosis when he was just 9 days old.
Cystic Fibrosis is a rare, genetic disease that affects the lungs, the digestive system, and the liver.
Please consider joining our team as a walker (on September 30th in Sarasota), a virtual walker (that’s right you don’t need to be near to be on our team), or by donating to one of our pack members so we can continue to stride towards a cure for cystic fibrosis. Soon we know CF will stand for Cure Found!
Let’s make Pax proud!
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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.