Cystic Fibrosis Foundation - North Texas Chapter

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.

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...
08/27/2026

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

While many people with cystic fibrosis have benefited from life-changing therapies, others are still waiting.For individ...
08/27/2026

While many people with cystic fibrosis have benefited from life-changing therapies, others are still waiting.

For individuals whose unique genetic mutations don't respond to today's modulators, the search for new treatments continues.

YOU can help ensure no one is left behind.

Donate today to double the impact of your gift: https://give.cff.org/north-texas

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.

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

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

Every day, people living with cystic fibrosis hold onto hope—hope for brighter futures, more milestones to celebrate, an...
08/20/2026

Every day, people living with cystic fibrosis hold onto hope—hope for brighter futures, more milestones to celebrate, and ultimately, a cure.

YOU can give hope.

Donate today and double your impact: https://give.cff.org/north-texas

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.

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

CF Dads, this one’s for you! ⚾️💙Join us for a night at the ballpark as we cheer on the Texas Rangers and connect with ot...
08/19/2026

CF Dads, this one’s for you! ⚾️💙

Join us for a night at the ballpark as we cheer on the Texas Rangers and connect with other CF dads!

📅 September 4th
⏰ 7:05 PM
📍 Globe Life Field

Come hang out, enjoy the game, and spend some time with other dads who understand the CF journey.

Tickets are limited, so sign up today 👇www.signupgenius.com/go/10C0F4EAAAA23A6FBC70-65121749-cfdads

Questions? Reach out to [email protected] or call 214-871-2222.

We need items for our upcoming live & silent auctions to help make our North Texas Chapter fall events unforgettable! We...
08/18/2026

We need items for our upcoming live & silent auctions to help make our North Texas Chapter fall events unforgettable!

We're seeking items such as:
✈️ Travel Packages
🍽️ Dining Experiences
🌴 Vacation Homes
🎟️ Entertainment & Event Tickets
🛍️ Retail Gift Cards
🏡 Home Goods
💖 Beauty & Spa Items
✨ Unique Experiences

If you're interested in donating an item or connecting us with a business or individual who may be able to help, send us a DM or email us at [email protected].

Every donation, big or small, helps create memorable experiences for our guests while supporting life-changing research, care, and advocacy for those living with CF.

Thank you for helping make our fall events a success and for supporting the CF community!

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

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