NOW IS THE TIME

CF Climb

Help us find a cure for CF

Please review the attendance and pet policies for CF Foundation events.

NOW IS THE TIME

CF Climb

Help us find a cure for CF

Climb to Cure Cystic Fibrosis

CF Climb is the Cystic Fibrosis Foundation’s premier climbing event. Each year, thousands of participants take steps to raise funds for people living with cystic fibrosis, a progressive genetic disease that affects the lungs, pancreas, and other organs. While progress has been made, we still lose precious lives to CF every day. 


Get ready for an unforgettable experience that’s more than just a climb—it’s a chance to make a real impact! Imagine the thrill of reaching the top of an iconic building or arena, the sense of accomplishment, and the breathtaking views that await you—all while knowing you’ve made a difference in the lives of those who need it most. 


Join a community of climbers eager to make a difference while embracing the joy, challenges, and personal triumphs that come with reaching new heights. Whether you're an experienced climber or a first-timer, this event is designed for everyone. Challenge yourself, connect with others, and be inspired by the stories of those who benefit from your support. Don’t miss out on this unique opportunity to elevate your fitness, your spirit, and your impact. 


Your participation is crucial in helping us achieve our shared dream of a CF cure. To achieve this goal, more research is essential, requiring a very substantial investment. Even after a cure is found, customized care will be needed for generations to treat long-lasting health problems, making continued donor support vital. Fundraising is critical to advance our mission, and now is the time to act. Sign up today and take the first step towards changing lives! Help us find a cure for cystic fibrosis.

Step Up Your Fundraising

Become a 65 Roses Champion

by raising $1,000 or more

Create a National Team

Join up with friends, family, and colleagues across the country and locally to participate in multiple events, make sub-teams, and get fundraising support to grow your impact.

2025 National Ambassadors

Meet your 2025 National Ambassadors, Alexis Vargas and Caroline Lewis!

KENTUCKY-WEST VIRGINIA CHAPTER

Alexis Vargas

Alexis was not diagnosed with cystic fibrosis until she was 5 years old. Despite chronic lung infections and violent coughing episodes, the military hospital where she was born never tested her for CF. After receiving her diagnosis, the Vargas family walked in their first Great Strides. This is Alexis’ 14th year participating, and she now walks in the Lexington/Winchester walk.

NORTH CAROLINE CHAPTER

Caroline Lewis

Caroline was diagnosed with cystic fibrosis at 10 days old. She is a champion for the North Carolina Xtreme Hike community, and has participated in three Xtreme Hikes since she was able to start hiking at 14. When she was an infant in 2010, her dad participated in the inaugural North Carolina Xtreme Hike while she did nebulizers from the car.



Thank you to our National Sponsors!

National Peer to Peer Sponsors

Outstanding Corporate Supporter

AbbVie has been a proud supporter of the Cystic Fibrosis Foundation for over 30 years.

Vertex is a longstanding supporter of the Cystic Fibrosis Foundation and proud National Peer to Peer Event Sponsor.

Proud supporters of the Cystic Fibrosis Foundation and Title Sponsors of American Airlines Celebrity Ski, with more than $45M raised over the last 40 years.

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.