Our granddaughter Evelyn Yonke was born on Valentine's Day in 2020, and was diagnosed with cystic fibrosis at one month old. We quickly learned of the support of the Cystic Fibrosis Foundation. Their research has resulted in new medications, treatments, and therapies that are already impacting Evelyn's life in a positive way, as they do all other CF kids and adults. A cure is within the realm of possibility.
Evelyn is one of approximately 30,000 Americans living with cystic fibrosis. We walk for Evelyn - and for all of them. Will you join us and support our fundraising goal? Gary and I have donated $2,500 and are hoping to double that through donations from family and friends.
Please support Evelyn!
We are at a pivotal moment in the history of cystic fibrosis and your support matters. With your help, we can invest our resources in research today, while raising funds for tomorrow, to ensure we have what it takes to reach the finish line. Together, we can make CF stand for Cure Found. Please help me reach my fundraising goal!
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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.