There are approximately 30,000 Americans living with cystic fibrosis. They are kids like Milla and Rhys. They are moms, dads, sisters, brothers, daughters, sons, and friends who face numerous challenges every day. Maintaining health, access to medication, food costs, treatment management, and the ability to breathe freely, I walk for them. Will you join us in support of Milla, Rhys, and the thousands of individuals like themespecially those who lack the resources?
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 team Tiny and Mighty!!
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!
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.