Our Great Strides Story
Finley was born on January 19th, 2024. She is everything.
Three days before her arrival we found out news that changed our life. Sadly, our little girl had an extremely dilated bowel and was showing signs of CF. Once here she was transported to the best Children's hospital in the nation and was officially diagnosed with CF. She is currently still in the NICU where she is battling many bowel complications and fighting each day.
There is currently no cure for cystic fibrosis.
Your support makes a difference. Please help us fight for funding to make sure Finley and all others battling this terrible disease live long, happy, and healthy lives.
#FinleysVillage
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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.