Walk with our team to Cure Cystic Fibrosis

Elara’s AirForce

Fundraising for Washington, DC Great Strides

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Elara’s AirForce

Welcome to Elara’s Air Force, a team created with love and hope for our brave baby girl, Elara, who was born with cystic fibrosis (CF)—a genetic condition that affects the lungs, pancreas, and other organs. Though her diagnosis was a shock, Elara has shown us nothing but strength, resilience, and joy. She is our fighter, our light, and the reason we’re walking, fundraising, and pushing for a cure.

Why We Fight

Cystic fibrosis is a progressive, life-shortening disease that makes it difficult to breathe and digest food. But thanks to medical advances and the power of community, people with CF are living longer, healthier lives than ever before. Still, there is no cure—yet. Every step we take and every dollar we raise brings us closer to that day.

We’re walking and fundraising not just for Elara, but for every child, teen, and adult living with CF. We believe in a future where CF stands for Cure Found.

Join Elara’s Air Force

Whether you walk beside us, donate, or simply share our story, you’re part of Elara’s Air Force—a squad of family, friends, neighbors, and even strangers who believe that every breath matters.

Together, we can lift up Elara and thousands of others like her. Together, we can fight for more tomorrows. 💜

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$1,614
raised of $100 goal
 

30 Participants

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Attendance Policy

The CF Foundation is committed to providing a safe, inclusive, and healthy experience for individuals attending Foundation Events. Individuals attending CF Foundation events must abide by the Foundation's Attendance Policy and accompanying guidelines, which include guidance for event attendee's living with cystic fibrosis.