Cystic Fibrosis Foundation - Washington Chapter

10/14/2026

Just one month until the Seattle Breath of Life Gala! ✨

We're looking forward to an incredible evening with our community, and tickets and tables are nearly sold out. If you've been meaning to join us, now is the time.

Be part of a night that makes a lasting impact. Secure your place before it's too late. https://events.cff.org/breathoflifegala

10/09/2026

✨ Get ready to raise your paddle! ✨

These are just some of the exclusive items and experiences that will be featured at this year's Seattle Breath of Life Gala. Join us Nov. 14 for an evening of celebration and friendly competition, all in support of the Cystic Fibrosis Foundation! https://events.cff.org/breathoflifegala

10/09/2026

Choosing a health insurance plan isn't always straightforward, and there isn't a perfect option. If you're feeling overwhelmed, are unsure where to start, or want a second opinion, Compass can help you compare plans, understand trade-offs, and choose the option that best supports you or your child’s healthcare needs.

Learn more and prepare now: https://www.cff.org/support/choosing-insurance-coverage-cystic-fibrosis

10/08/2026

Did you know you can support the Cystic Fibrosis Foundation through a donor-advised fund (DAF)? A DAF is a charitable giving account that allows you to contribute cash, stocks, or other assets, receive an immediate tax deduction, and recommend grants to the causes you care about most. It's a flexible and easy way to support the CF Foundation with a one-time or recurring gift, or in the future as a beneficiary.

Learn more about giving through a DAF: https://www.cff.org/get-involved/other-ways-give

Please consult your DAF sponsor and financial or legal advisor regarding DAF giving. The Cystic Fibrosis Foundation cannot provide tax or legal advice.

10/05/2026

Thank you to VLACK MEDIA, Aaron Briggs and KISW 99.9 "The Rock" for the wonderful photos of the Seattle CF StairClimb!

10/05/2026

Living with cystic fibrosis can bring financial challenges that go beyond medical bills and insurance premiums. From career decisions to long-term savings goals, many people with CF and their families face difficult financial decisions along the way.

Join a peer-led conversation Oct. 13 about the financial realities of life with CF. This virtual CF Circle is a supportive space to share experiences, learn from one another, and connect with people who understand the journey. Register today: https://on.cff.org/CF-Circles-October-2026

10/01/2026

Get ready to hear from leading voices shaping the future of cystic fibrosis research and care at .

This year's plenary sessions will explore:
🔹 Gene Editing at the Frontier: Advancing Precision Medicine & Delivery Science
🔹 Trusted Voices, Transformative Research: Advancing CF Research Together
🔹 Liver Disease in Cystic Fibrosis Across the Lifespan: Where We Are & Where We're Going

Whether you're joining us in person or virtually, these plenary sessions will be available to all NACFC participants. Register today and be part of the conversation. https://events.ringcentral.com/events/virtual-north-american-cystic-fibrosis-conference-2026/registration

09/30/2026

As we count down to the 43rd annual Seattle Breath of Life Gala, we're honored to recognize the sponsors helping make this special evening possible.

Their generosity and belief in our mission help create an unforgettable event while accelerating progress toward a future free from cystic fibrosis. We appreciate their partnership and all they do for our community.

Please join us in thanking these incredible supporters! https://events.cff.org/breathoflifegala

09/29/2026

09/23/2026

We’re committed to developing a transformative treatment — and ultimately, a cure — for all people with cystic fibrosis. With the generous support of people like you, and our national peer to peer sponsor, Vertex, we’re confident we can continue to make meaningful progress toward this goal.