Cystic Fibrosis Foundation - North Texas Chapter

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Cystic Fibrosis Foundation - North Texas Chapter We're helping to advance the Cystic Fibrosis Foundation’s mission to cure cystic fibrosis.

Our chapter covers the Dallas, Fort Worth, Lubbock, Tyler, Shreveport, LA and the surrounding areas. About CF:
Cystic fibrosis is a life-threatening genetic disease that affects the lungs and digestive system of approximately 40,000 children and adults in the United States. More than 10 million Americans are unknowing, symptomless carriers of a defective CF gene.

🎸 Three Weeks Until Breathe Easy Concert! 🎸The countdown is on! Join us on November 1 at the Granada Theater for an unf...
10/11/2026

🎸 Three Weeks Until Breathe Easy Concert! 🎸

The countdown is on! Join us on November 1 at the Granada Theater for an unforgettable evening of an intimate song swap performance featuring Rhett Miller, Jamie Lin Wilson , and Joshua Ray Walker , with The O's kicking off the night. It's a rare opportunity to hear some of Texas' most celebrated singer-songwriters share the stories behind their songs in a unique, collaborative format.

And we're not done with surprises yet. Our final special guest announcement is coming in just two weeks! Any guesses?

Get your tickets today and help us make CF stand for Cure Found!

https://events.cff.org/breatheeasydallas

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.

Choosing a health insurance plan isn't always straightforward, and there isn't a perfect option. If you're feeling overw...
10/05/2026

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

Get ready to hear from leading voices shaping the future of cystic fibrosis research and care at .This year's plenary s...
10/02/2026

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

YOU can help us unlock every dollar of this $40,000 match!DONATE HERE ➡ https://give.cff.org/north-texas With help from...
10/02/2026

YOU can help us unlock every dollar of this $40,000 match!
DONATE HERE ➡ https://give.cff.org/north-texas

With help from donors like you, we’ve already reached $13,059 toward the 2026 match but that means we have $26,941 left to go by November 28 to fully unlock these matching funds.

Every dollar counts, and we’re counting on YOU!

Every new or increased gift to our Annual Fund before November 28 is doubled while matching funds last.

That’s double the impact for care and support for people with cystic fibrosis and their families and for research that gets us closer to a cure.

The North Texas Chapter is excited to announce that the Harriman Family, Kendrick Oil and an anonymous donor have kindly offered a $40,000 local matching gift opportunity! Beginning August 1, 2026, all gifts in the amount of $1 to $9,999 in support of the North Texas Chapter's Annual Fund will be matched dollar for dollar up to $40,000 by November 28, 2026, or when the match is completed, whichever comes first. Donations received in excess of the matching goal of $40,000 will be used to support the CF Foundation's mission.

🌍 Congratulations to the 2026 BMW Berlin Marathon Breathe Team! We had 2 local runners, Ivan Calil & Shawn Talbott, repr...
10/01/2026

🌍 Congratulations to the 2026 BMW Berlin Marathon Breathe Team! We had 2 local runners, Ivan Calil & Shawn Talbott, represent the North Texas Chapter in Germany this past weekend.

As a team, they have raised over $189,000 and counting to help fund critical research and care for people living with CF. Every step brought us closer to a future where everyone with CF can live long, healthy lives.

💙 Thank you for turning your passion into purpose and making every mile matter!

Living with cystic fibrosis can bring financial challenges that go beyond medical bills and insurance premiums. From car...
09/28/2026

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://cff.zoom.us/meeting/register/JeksMf8gTAyXReaE-df0gw #/registration

The cystic fibrosis community comes together at the North American Cystic Fibrosis Conference (NACFC) each year to learn...
09/25/2026

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/.../virtual.../registration

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.

Address

125 E. John Carpenter Freeway, Ste. 255
Irving, TX
75062

Opening Hours

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

Telephone

+12148712222

Website

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