My Great Strides Story
Finley was born on January 19th, 2024.
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 meconium ileus.
Cystic fibrosis affects the lungs, pancreas, and other organs. The symptoms can vary from person to person.
There is currently no cure for cystic fibrosis.
Your support makes a difference. Please help us fight for funding to ensure our little girl who deserves the world lives a long, happy, healthy life. She is everything.
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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.