How far would you go for a cure?

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    We can't wait to bring the CF community together for Xtreme Hike!

    To reduce the risk of COVID-19 the Foundation is taking steps to host safe events for our community. Please be advised that events may be subject to change at any time based on guidance from the Centers for Disease Control and Prevention and local health officials. Please review the attendance policy for CF Foundation events.

    Register today and stay up to date on how your chapter plans to safely bring the community together and make CF stand for Cure Found.

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    Help Us Find a Cure.

    We've made incredible progress in the fight against cystic fibrosis, but we still have a long way to go.

    Far too many lives are being cut short by this devastating disease.

    Learn More

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    Find a Hiker and Donate

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    Go Mobile!

    Take your Xtreme Hike fundraising everywhere you go with our new mobile app!

    Get Started

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    Fundraise Through Your Passion

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National Fundraising Goal

Help us get to our goal of $27,500,000 for Great Strides, CF Cycle for Life, CF Climb, Xtreme Hike, and Team CF.
This amount is updated on a weekly basis

These lists are updated on a weekly basis.

2022 National Ambassadors

Lauren Luteran National Ambassador for CFF

Lauren Luteran

Lauren Luteran is 22-years old with cystic fibrosis from Orlando, Florida. She is a full-time student at the University of Central Florida working on her bachelor’s degree in journalism with a minor in sociology. She was seen on season 16 of “So You Think You Can Dance” in 2019 when she was a contestant on the show, spreading awareness for CF. “One thing I am most excited about taking on in the role of a national ambassador is to give back to the Foundation that has given me so much. Paying it forward is what feels like my life’s purpose.”

Saiul Merrero National Ambassador for CF

Saiul Marrero

Saiul Marrero is a 5-year-old living with cystic fibrosis from Atlanta, Georgia. Although he had two CF mutations and experienced CF-related symptoms at birth, doctors were sure he did not have cystic fibrosis because of his Latino ethnicity. After time in the hospital and because his mother and grandmother advocated for him, they were able to confirm his diagnosis a month after he was born. His family is ready to advocate so children like Saiul do not have to travel down that same road.