Cystic Fibrosis Foundation - Washington Chapter

Cystic Fibrosis Foundation - Washington Chapter We're helping to advance the Cystic Fibrosis Foundation’s mission to cure cystic fibrosis.

About CF:
Cystic fibrosis is a life-threatening genetic disease that affects the lungs and digestive system of approximately 30,000 children and adults in the United States. More than 10 million Americans are unknowing, symptomless carriers of a defective CF gene.

As wildfires spread across the West, we’re standing by to help ensure people living with cystic fibrosis and their famil...
09/02/2026

As wildfires spread across the West, we’re standing by to help ensure people living with cystic fibrosis and their families get the care they need. Our Compass team can help with getting emergency access to medications and medical devices that were left behind, lost, or damaged. If you or a loved one needs help, please contact Compass at [email protected] or 844-COMPASS.

https://www.cff.org/support/get-help-cf-foundation-compass

As Make-A-Will Month comes to a close, there's still time to take an important step for your loved ones—and for everyone...
08/31/2026

As Make-A-Will Month comes to a close, there's still time to take an important step for your loved ones—and for everyone affected by cystic fibrosis.

By creating or updating your will and joining the Cystic Fibrosis Foundation Legacy Society, you can help ensure future generations benefit from the progress we make today.

And thanks to a special challenge from The Delaney Binker Family Cure Cystic Fibrosis Miami Foundation, every new Legacy Society member who joins through December 31, 2026, will inspire an additional $1,000 gift to the CF Foundation, up to $65,000.

Together, we're not just planning for the future—we're building it.

Join the Legacy Society and help unlock an additional $1,000 for the CF community. Learn more at cff.org/legacy-giving

As a parent of a child with cystic fibrosis, you are an important advocate for their success at school. Accommodations s...
08/28/2026

As a parent of a child with cystic fibrosis, you are an important advocate for their success at school. Accommodations such as an Individualized Education Program (IEP) or a 504 Plan can help support your child's health, learning, and overall well-being in the classroom.

Learn more about school accommodations and resources to help ensure your child has the support they need to thrive at school: https://www.cff.org/managing-cf/individualized-education-programs-ieps-and-504-plans

Have 10 minutes? Take the Annual CF Insights survey to share what’s working, what’s hard, and what would make a real dif...
08/25/2026

Have 10 minutes? Take the Annual CF Insights survey to share what’s working, what’s hard, and what would make a real difference for the CF community.

Results will help guide CF Foundation decisions around research, care, and support — and ensure researchers and clinicians have a clearer understanding of the evolving needs of the CF community.

The survey is open to everyone in the community and is available in English and Spanish. Share your anonymous insights by Sept. 7: https://cff.qualtrics.com/jfe/form/SV_cXQWcpMTUVgPDhA?Source=33

The countdown is on! 👟Join hundreds of climbers Sept. 16 for the 38th annual Seattle CF StairClimb. Whether you're looki...
08/24/2026

The countdown is on! 👟

Join hundreds of climbers Sept. 16 for the 38th annual Seattle CF StairClimb. Whether you're looking for a fitness challenge, a team-building experience, or a fun way to give back, this event has something for everyone.

Registration is still open, but event day will be here before you know it. Be sure to register in advance to save $10 on registration fees! https://fundraise.cff.org/seattleclimb

Starting college is an exciting milestone, and having cystic fibrosis shouldn't stand in the way of your goals. From hou...
08/21/2026

Starting college is an exciting milestone, and having cystic fibrosis shouldn't stand in the way of your goals. From housing accommodations and class flexibility to other support services, there are laws in place to help ensure your medical needs are met while you're on campus.

Learn to speak up for your needs, understand your rights, and prepare for a successful college experience with CF. Explore resources for navigating college with CF: https://www.cff.org/support/accommodations-college

Not everyone can benefit from CFTR modulators like Alyftrek, Trikafta, Symdeko, Kalydeco, or Orkambi — and that can feel...
08/18/2026

Not everyone can benefit from CFTR modulators like Alyftrek, Trikafta, Symdeko, Kalydeco, or Orkambi — and that can feel isolating.

If this is part of you or your loved one’s experience, join a virtual small-group discussion Aug. 18 at 7 p.m. ET to connect with others who understand what you’re going through. Together, you’ll have an open, honest space to connect and find support in one another.

Congratulations to our team fundraising challenge winners!These incredible teams have each raised over $2,500 and recrui...
08/17/2026

Congratulations to our team fundraising challenge winners!

These incredible teams have each raised over $2,500 and recruited 10 or more climbers, earning their team name on the official Seattle CF StairClimb T-shirt and a featured team photo on the Mariners Vision Board at the event.

Amazing work, teams!

It's not too late to get involved. There's still time to register, build your team, and raise funds to bring us one step closer to a cure for everyone with CF! https://fundraise.cff.org/seattleclimb

Every breakthrough is built on the generosity of those who came before us.Legacy gifts have helped advance research, imp...
08/17/2026

Every breakthrough is built on the generosity of those who came before us.

Legacy gifts have helped advance research, improve care, and create new possibilities for people with cystic fibrosis. When supporters include the CF Foundation in their estate plans, they're building the foundation for tomorrow's discoveries.

This year, you have the opportunity to make a big impact thanks to a generous donor challenge. When you join the Legacy Society between April 15 and December 31, 2026, The Delaney Binker Family Cure Cystic Fibrosis Miami Foundation will donate an additional $1,000 to the CF Foundation in your honor.

One decision today can help create lasting change tomorrow.

Let's build our legacy together. Join today at cff.org/legacy-giving

Address

400 University Street 3rd Floor
Seattle, WA
98101

Opening Hours

Monday 9am - 5pm
Tuesday 9am - 5pm
Wednesday 9am - 5pm
Thursday 9am - 5pm
Friday 9am - 5pm

Telephone

+12062824770

Website

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