We Are Adding Tomorrows.

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

    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. Please review the attendance policy for CF Foundation events.

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    I am the Reason.

      The life expectancy of a person with cystic fibrosis has doubled in the last 30 years, but there is still no cure.

    Learn More

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    I am Making a Difference.

    Find a participant and donate

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    We will not rest.

    We will not rest until we find a cure for all people with cystic fibrosis.

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

2023 Top Events

    2023 National Ambassadors

    Lauren Luteran National Ambassador for CFF

    Cru Aguinaga

    Cru Aguinaga was diagnosed with cystic fibrosis at 5 weeks old. He loves animals, playing with his siblings, Adair and Witten Rose, and eating — namely noodles, brownies, and strawberries. Cru’s support system consists of his brother and sister, his dog, Nala, his mom and dad, and all his friends and family. As a 2023 national ambassador for the Cystic Fibrosis Foundation, he looks forward to showing what CF means to him and his family.

    Saiul Merrero National Ambassador for CF

    Elle Kellner

    Elizabeth (Elle) Kellner was diagnosed with cystic fibrosis at 4.5 months old and is a double-lung and kidney transplant recipient. As a child, she remembers being told she couldn’t do some of the things her peers did because she wasn’t “strong enough” or she was too sick. However, she is not one to give up easily and never accepts no as an answer. In her free time, she loves yoga, cooking, dancing, and going to the beach. In 2007, following a toy drive she ran alongside her husband, she started a non-profit that benefits pediatric patients at her local hospital.