Cystic Fibrosis Foundation - Central Texas Chapter

Cystic Fibrosis Foundation - Central Texas 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.

💙 Get to know Austin’s Finest Honoree Tiffany!Tiffany is among an incredible group of young professionals being recogniz...
08/31/2026

💙 Get to know Austin’s Finest Honoree Tiffany!

Tiffany is among an incredible group of young professionals being recognized for their leadership, success and commitment to giving back. We’re honored to celebrate her impact at this year’s Backyard Ball in support of the Cystic Fibrosis Foundation.

Meet Tiffany! https://finest.cff.org/austin/TiffanyFigueroa

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

✨ Congratulations to Matt, one of this year’s Austin’s Finest honorees!Matt is being recognized for his accomplishments,...
08/28/2026

✨ Congratulations to Matt, one of this year’s Austin’s Finest honorees!

Matt is being recognized for his accomplishments, leadership and philanthropic spirit. We’re excited to celebrate him at the Backyard Ball alongside an outstanding group of young professionals making an impact in Austin.

Learn more about Matt! https://finest.cff.org/austin/mattduke

Have 10 minutes? Take the Annual CF Insights survey to share what’s working, what’s hard, and what would make a real dif...
08/27/2026

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

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

08/24/2026

Thanks to our incredible CFF accredited care team for hosting this lunch and learn for our Finest Honorees!

💙 Get to know Austin’s Finest Honoree Coral!Coral is among an incredible group of young professionals being recognized f...
08/24/2026

💙 Get to know Austin’s Finest Honoree Coral!

Coral is among an incredible group of young professionals being recognized for their leadership, success and commitment to giving back. We’re honored to celebrate her impact at this year’s Backyard Ball in support of the Cystic Fibrosis Foundation.

Meet Coral! https://finest.cff.org/austin/coraldraper

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

Address

3316 Bee Caves Road, Ste A
Austin, TX
78746

Opening Hours

Monday 9am - 7pm
Tuesday 9am - 7pm
Wednesday 9am - 7pm
Thursday 9am - 7pm
Friday 9am - 3pm

Telephone

+15123381744

Website

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