Cystic Fibrosis Foundation - Oregon Chapter

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Cystic Fibrosis Foundation - Oregon Chapter We're helping to advance the Cystic Fibrosis Foundation’s mission to cure cystic fibrosis. Welcome to the official page of the Oregon Chapter!

Choosing a health insurance plan isn't always straightforward, and there isn't a perfect option. If you're feeling overw...
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

Did you know you can support the Cystic Fibrosis Foundation through a donor-advised fund (DAF)? A DAF is a charitable gi...
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.

Living with cystic fibrosis can bring financial challenges that go beyond medical bills and insurance premiums. From car...
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

Get ready to hear from leading voices shaping the future of cystic fibrosis research and care at .This year's plenary s...
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

Help us in wishing Joe a very happy birthday! He leads with heart and purpose and we are so grateful for his dedication!
09/23/2026

Help us in wishing Joe a very happy birthday! He leads with heart and purpose and we are so grateful for his dedication!

We’re committed to developing a transformative treatment — and ultimately, a cure — for all people with cystic fibrosis....
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.

Congratulations to Sarah Giambuzzi as she sets off to tackle the 2026 BMW Berlin Marathon as part of the CF Foundation's...
09/23/2026

Congratulations to Sarah Giambuzzi as she sets off to tackle the 2026 BMW Berlin Marathon as part of the CF Foundation's Breathe Team. Running in memory of her longtime friend, Jon, Sarah will tackle 26.2 miles this Saturday in support of our mission. Thank you Sarah!

The cystic fibrosis community comes together at the North American Cystic Fibrosis Conference (NACFC) each year to learn...
09/18/2026

The cystic fibrosis community comes together at the North American Cystic Fibrosis Conference (NACFC) each year to learn and connect, and you can be part of it from anywhere!

Join the virtual NACFC Oct. 8-10 for livestreamed plenaries, select symposia, and interactive Q&A opportunities with experts and researchers.

Can't make every session? Additional conference content, including slides and audio recordings, will be available on the CF Foundation's YouTube channel after the event.

Register now and join us virtually for NACFC 2026. https://events.ringcentral.com/events/virtual-north-american-cystic-fibrosis-conference-2026/registration

Join us for the CF Foundation’s signature Get Salty Comedy Show, streaming live Sept. 24 at 7:30 p.m. ET! Enjoy unforget...
09/17/2026

Join us for the CF Foundation’s signature Get Salty Comedy Show, streaming live Sept. 24 at 7:30 p.m. ET! Enjoy unforgettable laughs while helping us bring hope to people living with cystic fibrosis.

Don’t miss your chance to see an incredible line-up of comedians, including Kirsten Cills, a Philadelphia-born comedian living with CF who is known for her morbid sense of humor and the oxygen tank that often accompanies her on stage.

All proceeds will benefit the Cystic Fibrosis Foundation. Purchase your virtual ticket for $25 today: https://events.cff.org/rosesandthorns

Address

9755 SW Barnes Road , Suite 510
Portland, OR
97225

Opening Hours

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

Telephone

+15032263435

Website

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