My Great Strides
As a two year old with cystic fibrosis: a progressive, genetic disease that affects the lungs, pancreas, and other organs. My mom, dad, sister and brother help me extend my life everyday thru medication and will also walk for me.
I have started my life with a challenge but know I can do anything with my family by my side. Running, jumping, laughing and encouragement is how i spend my days. Thank God for my family!
The CF Foundation vision is a cure for every person with cystic fibrosis – a life free from the burden of this disease – and we will not leave anyone behind.
You can support Me!
By supporting Leah and help reach her fundraising goal, you have an opportunity in your lifetime to be part of ending this disease. Please consider joining us and help make medical history.
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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.