Cystic Fibrosis Foundation - Northern California Chapter

Cystic Fibrosis Foundation - Northern California 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.

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

For families affected by cystic fibrosis, an early diagnosis can make all the difference.During Newborn Screening Awaren...
09/25/2026

For families affected by cystic fibrosis, an early diagnosis can make all the difference.
During Newborn Screening Awareness Month, we're honored to highlight Dr. Martin Kharrazi, whose leadership helped bring cystic fibrosis newborn screening to California in 2007.

Today, countless families benefit from earlier diagnosis and access to life-changing care because of efforts like his. We are grateful for the individuals who have worked to ensure every child has the best possible start.

💙 Thank you, Dr. Kharrazi, for helping create a brighter future for people with CF.

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.

We're excited to share some of the incredible eateries serving up delicious bites at the 7th annual Taste for a Cure. Fr...
09/22/2026

We're excited to share some of the incredible eateries serving up delicious bites at the 7th annual Taste for a Cure. From savory favorites to sweet treats, these culinary stars are helping make this event unforgettable.

Don't miss out on this tasty event! Get your tickets today. https://events.cff.org/tasteforacure

Only one week until we stride! 💜 Santa Rosa Great Strides 2026 is happening at Howarth Park Sunday, Sept. 27, and we can...
09/20/2026

Only one week until we stride! 💜

Santa Rosa Great Strides 2026 is happening at Howarth Park Sunday, Sept. 27, and we can't wait to celebrate the incredible community working to make CF stand for Cure Found. We hope to see you there! https://fundraise.cff.org/santarosa2026

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

We are proud to honor Dr. Sheena Maharaj at this year's Taste for a Cure. Dr. Maharaj is a pediatric pulmonologist who h...
09/17/2026

We are proud to honor Dr. Sheena Maharaj at this year's Taste for a Cure.

Dr. Maharaj is a pediatric pulmonologist who has dedicated her career to helping children with cystic fibrosis live longer, healthier, and fuller lives, while supporting their families every step of the way. She serves as the medical director of the pediatric pulmonary and cystic fibrosis center at Sutter Medical Center, where she collaborates with patients, families, and a multidisciplinary team to provide comprehensive, evidence-based, and compassionate care.

Please join us in celebrating Dr. Maharaj at Taste for a Cure Oct. 11! https://events.cff.org/tasteforacure

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

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1540 River Park Drive Suite 116
Sacramento, CA
95815

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