My Great Strides Story
My name is Julia, and I am 14. I was diagnosed with Cystic Fibrosis at just 3 weeks old. CF affects many things, mainly including the digestive system and lungs. As a little girl, I wasn’t sure how my future would look. The CF Foundation has helped to make many advancements in medication and treatments since I was first born. Looking back, I never would have thought I would be as healthy as I am now.
Thanks to the CF Foundation, Cystic Fibrosis has never gotten in the way of me being able to live life to its fullest. I am able to enjoy many activities such as orchestra, chorus, select chorus, dance, and school.
Donations towards our team helps to support finding a cure for Cystic Fibrosis and making CF stand for cure found. I am so grateful for Team Julia! We could not have gotten this far without you! Thank you for supporting our team!
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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.