There have been many days & weeks spent in the hospital. A lot traditions and holidays missed. A lot of family time split up, many missed parties and fun. In 2020, Kaidynce started Trikafta to better manage cystic fibrosis.
This year she is a freshman and navigating high school. She has gone through sports without having to take a break due to illness, excelling in school and enjoying being a "normal" kid. So proud of this litte woman and all the obstacles she has gotten through!
Cystic Fibrosis is the number one genetic, fatal disease that affects children in the US, yet CF receives ZERO financial support from the government!
Real progress has been made in the search for a cure, but the lives of people with CF are still cut far too short. There still is no cure for this devastating disease.
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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.