Kylea's Great Strides Story
Kylea was diagnosed with CF December 2, 2008, at three months old. At the time of her diagnosis the life expectancy was just 35.
Over the past 15 years, we have made it our priority to educate ourselves and live life to the fullest. It's been my goal for Kylea not to ever feel as though she can't because of CF and let me tell you she lets nothing get in her way! From dance and gymnastics, karate, t-ball, horseback riding, paddle boarding in Mexico and most recently representing Texas Children's Hospital as the Children's Miracle Network champion.
Kylea truly is an inspiration!
Our family is eternally grateful for the work of the CFF, the volunteers and all of those who donate each day, each, month, each year to help add tomorrow's, because of your dedication and the brilliant researchers, the median life expectancy is now mid-50's.
Until it's done.
Connect With Us
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.