Our first walk was 25 years ago to the day. My name is Elizabeth Clark, I am the mother of three beautiful children, two have Cystic Fibrosis. The years since their diagnosis have been filled with promise, largely due to the generosity of those who contribute to fundraisers like this. Cystic Fibrosis is too small a disease to attract corporate funding and relies heavily on the generosity of friends, families, neighbors and coworkers. We walk today to continue the hope for a cure. While a tremendous amount of progress has been made in the past 25 years there, we are not yet there. Donate, come walk or keep may family and other families with CF in your thoughts and prayers. 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.