There are approximately 30,000 Americans living with cystic fibrosis. They are moms, dads, sisters, brothers, daughters, sons, friends and co-workers who struggle every day just to breathe. I walk for them and hope you will support me in my efforts.
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.
Katie is my daily reminder that life is about living but she can only do this with the support of many agents: viable health care without pre-existing conditions, fantastic care at our local children's hospital, and the full support from the Cystic Fibrosis Foundation.
Katie has finally gone off to college and living her best life. I couldn't be happier and so much of it comes from the great care she's had.
Please help me help them by donating to my cause. The future depends on us helping each other.
Thank you!!!
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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.