2022 Team
My Great Strides Story
Nearly 40,000 people in the United States have cystic fibrosis: a progressive, genetic disease that affects the lungs, pancreas, and other organs. They are moms, dads, sisters, brothers, daughters, sons, and friends who face the sobering prospect of a shortened lifespan. I walk for them.
We walk for our son, Kevin, who battles CF. He is 20 years old and was diagnosed at the age of 3. His obstacles include respiratory infections, nasal polyps, breathing, coughing, and poor weight gain. A normal day includes multiple breathing treatments, digestive enzymes, vitamins, and tube feeding at night for extra calories.
You can support me!
By supporting my fundraising goal, you have an opportunity 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.