Megan was diagnosed with Cystic Fibrosis when she was 4 years old! The life expectancy then was 25 years old. 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. We walk for them and Megan and hope you will support us in our 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. By walking today, We are helping add tomorrows to the lives of people living with cystic fibrosis. Will you join us? Join us for the walk in Annapolis on June 1st or support us by making a donation to our Great Strides fundraising campaign today!
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 got married to Kohl Early and they live in Norton, Ohio. Meg continues to benefit from medications and therapies that have been developed with your generous donations.
Help us reach our fundraising goal by joining our team or donating to our Great Strides fundraising campaign. Your gift will help add tomorrows to the lives of people with cystic fibrosis by supporting life-saving research and medical progress. Your gift is 100-percent tax deductible.
Connect With Us
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.