Cystic Fibrosis Foundation - Arizona Chapter

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

Whether you're heading back to the classroom, campus, or workplace, back-to-school season means more exposure to germs, ...
08/30/2026

Whether you're heading back to the classroom, campus, or workplace, back-to-school season means more exposure to germs, but a few simple habits can help reduce your risk.

From handwashing and covering your cough to cleaning and disinfecting your nebulizer, there are simple tips and routines you can do to lower your risk of getting sick. Explore ways to protect your health every day: https://www.cff.org/managing-cf/8-ways-guard-against-germs-everyday-life

Have 10 minutes? Take the Annual CF Insights survey to share what’s working, what’s hard, and what would make a real dif...
08/28/2026

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

Please join us in welcoming Karen Bisko, CFRE to the Cystic Fibrosis Foundation, Arizona Chapter!With more than 25 years...
08/27/2026

Please join us in welcoming Karen Bisko, CFRE to the Cystic Fibrosis Foundation, Arizona Chapter!

With more than 25 years of nonprofit fundraising and leadership experience across health care, higher education, and community organizations, Karen brings a wealth of expertise and a passion for building meaningful relationships with donors, volunteers, and community partners.

A Certified Fund Raising Executive (CFRE), Karen has held development leadership roles with organizations including Dignity Health St. Joseph’s Hospital, The Leukemia & Lymphoma Society, American Diabetes Association, Banner Health Foundation, Arizona State University, and Children’s Hospital of Pittsburgh.

We are thrilled to welcome Karen to the CFF Arizona team and look forward to all we will accomplish together for the CF community. Welcome, Karen!

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...
08/26/2026

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

Know a young professional who is making an impact through their leadership, career, and community involvement? Nominate ...
08/25/2026

Know a young professional who is making an impact through their leadership, career, and community involvement? Nominate them for Arizona’s Finest, happening Dec. 3.

Nominations close Oct. 1. Help us recognize Arizona's next generation of leaders. Nominate today: https://afasignup.formstack.com/forms/2026_azsfinest_nomination_form

Join a peer-led, small-group discussion for Hispanic adults with cystic fibrosis and parents or caregivers of Hispanic i...
08/24/2026

Join a peer-led, small-group discussion for Hispanic adults with cystic fibrosis and parents or caregivers of Hispanic individuals with CF Sept. 22 at 9 p.m. ET. You’ll have an open space to connect, share experiences, and support one another. Discussion groups will be available in English and Spanish.

Participe en una conversación en un grupo pequeño facilitada por personas con experiencias similares, enfocada en la experiencia de los adultos hispanos que viven con fibrosis quística y de padres, madres y cuidadores de personas hispanas con fibrosis quística. La conversación se llevará a cabo el 22 de septiembre a las 9 p.m. (hora del Este). Tendrá la oportunidad de conectarse con otras personas, compartir experiencias y apoyarse mutuamente. Habrá grupos de conversación disponibles en inglés y en español.

Únase a la conversación!

As a parent of a child with cystic fibrosis, you are an important advocate for their success at school. Accommodations s...
08/23/2026

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

Starting college is an exciting milestone, and having cystic fibrosis shouldn't stand in the way of your goals. From hou...
08/20/2026

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

Calling all CF Fighters!We want to celebrate the hopes, dreams, and futures of our CF community at the 2026 65 Roses Gal...
08/18/2026

Calling all CF Fighters!
We want to celebrate the hopes, dreams, and futures of our CF community at the 2026 65 Roses Gala. Share a photo and a short quote about where you see yourself in the future, or for our younger fighters, what you want to be when you grow up. Deadline: Sept. 14. https://afasignup.formstack.com/forms/consent?Chapter=6

Not everyone can benefit from CFTR modulators like Alyftrek, Trikafta, Symdeko, Kalydeco, or Orkambi — and that can feel...
08/14/2026

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.

Address

4742 North 24th Street, Suite 360
Phoenix, AZ
85016

Opening Hours

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

Telephone

+16022240068

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