Walk with our team to Cure Cystic Fibrosis

Fighting For Futures

Fundraising for Seattle Great Strides 2026

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Fighting for Futures

We invite you to take part in Great Strides by joining our team. We promise, you belong here! This event promises to be a fun-filled day where you can help advance the care and research needed to cure cystic fibrosis. By walking with us, you’ll enjoy not only the natural camaraderie (yes, lots of laughter!), but the important impact we are making together.

Anna and Nikki are waiting for an impactful treatment option to give them longer futures and a greater quality of life. While the CF Foundation has made incredible progress, around 11% of CFers like Anna and Nikki can not use the latests and most impactful treatment options that have given many more tomorrows to people and families with CF. We are not dismayed...we will not give up! And, we believe in the human potential to find a cure for everyone with cystic fibrosis regardless of what kind of CF you may have. A cure that will someday mean that having a CF gene doesn't change your life like it does today. This will require time, funding, and persistence – but with you on our team – we are ready to go the distance.

Anna dances for you as she reminds you that it is time for us to "BREAK FREE" from having CF with no cure. Let's break free from this limiting and life-taking health situation to be in a place of resiliency, treatment options, and bright futures to live like others around us....free from machines and pills and hospital stays.  

break free with me.
touch the stars with me.
loose time with me.

-butterflies rising

Our team is committed to providing every person with CF the opportunity to live a long, healthy life. Will you join us?

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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.