There are approximately 30,000 Americans living with cystic fibrosis. They are moms, dads, sisters, brothers, daughters, sons, and friends who struggle every day just to breathe. My daughter Megan was diagnosed with CF when she was 4 years old. She is now 29. Megan has been an advocate for CF since her first walk 25 years ago. Meg is working as an Engineering Education Consultant serving the Kern Family Foundation in their Faculty Development Initiative while completing her dissertation research as a Phd candidate in Engineering Education. She recently married Kohl Early and they live in Norton, Ohio. Meg continues to benefit from medications and therapies that have been developed with your generous donations.
Will you join me and support my fundraising goal or join my team, the Westwood Walkers? We will be walking on Saturday, June 1st at the Navy Marine Stadium in Annapolis.
Real progress has been made for those who have CF, but there is still no cure for this devastating disease and many lives are cut far too short. We’ve come so far, but there’s still so much work to do. I will not stop striding until all those with cystic fibrosis have a cure. We will not leave anyone behind.
Please support me!
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.