Dylan was diagnosed with Cystic Fibrosis (CF) at birth and had heart surgery 3 weeks after birth. Dylan is the definition of a miracle. He fights everyday by enduring multiple breathing treatments daily, taking enzymes with every meal, and going to numerous doctor appointments. To Dylan, this is all he knows and is just part of his daily routine. He never complains about it and acts like a normal ten-year-old kid.
Some of Dylan's favorites are:
- Favorite Superpower: To Fly
- Favorite Color: Purple
- Favorite Food: Donuts
- Favorite Ice Cream Flavor: Wild and Reckless Sherbet
- Favorite Sport: Skateboarding
- Favorite Car: Bugatti Bolide
- Favorite Season: Winter
- Favorite School Subject: Math & Science
If you ask Dylan what his one wish in life is, he will tell you it is to not take enzymes every time he eats something.
Join us on June 8th to walk for Dylan the 2024 Ambassador of Southern California and Nevada against CF! I know Dylan would love to see his friends, family, and classmates at the walk supporting him!
Our Great Strides Story
Join our team to help make a difference in the lives of all people living with CF. To become a member, click the "Join this team" button. From there, you can donate and start fundraising.
As a member of our team, you are joining a growing community of people committed to finding a cure for cystic fibrosis. Together, we can make CF stand for Cure Found.
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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.