Evan Noelle Veto is small but mighty! She was diagnosed with cystic fibrosis soon after she was born on March 8, 2022. After 52 days in the NICU, Evan was able to go home to be with her mom, dad, sister, grandma and circus of pets.
Today she's busy growing, learning to walk and talk (her favorite thing to say is uh-oh!), and finding new ways to keep her family on their toes. Every day is an adventure and we're so proud of our girl!
Our team is driven by a dream that one day, every person with cystic fibrosis will have the chance to live a long, healthy life. You can help us reach that goal!
Please donate or join our team to help make a difference in the lives of all people living with CF.
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.