Dylan was born with Cystic Fibrosis – a rare, genetic, life-shortening disease that makes it difficult to breathe and digest foods. Dylan has faced many obstacles in his life. More than anyone ever should. Regardless of these challenges, he continues to be the happiest and strongest kid that we know!
The Great Strides walk will be held in Huntington Beach on May 20th. Participation in the walk is completely optional and free! Donations are welcome! If you would like to walk, please click “JOIN THIS TEAM”.
If you would ONLY like to donate, please click "DONATE TO A TEAM MEMBER". You can choose any team member below! All donations will benefit the Cystic Fibrosis Foundation.
With supporters like you by our side, the Cystic Fibrosis Foundation continues to lead the way in the fight against CF, fueling extraordinary medical and scientific progress. The life expectancy of someone born with CF has doubled in the last 30 years. Despite this progress, many people with CF do not benefit from existing therapies either because their disease is too advanced or because their specific genetic mutations will not respond. They are moms, dads, sisters, brothers, daughters, sons, friends, and co-workers who struggle every day in the face of this devastating disease.
We walk in Great Strides for them.
Will you join us?
Great Strides is a fun event that provides a fantastic opportunity for family, friends, students, and colleagues to come together to make a difference in the lives of people with CF.
To participate, just click on the "Join our Team" button. From there, you can make a donation and start fundraising.
By joining our Great Strides team and making a donation, you will be part of a tenacious and passionate group of people committed to ending this disease. Together, let’s make CF stand for Cure Found!
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.