Cystic Fibrosis Foundation - Missouri Chapter

Cystic Fibrosis Foundation - Missouri 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.

As a parent of a child with cystic fibrosis, you are an important advocate for their success at school. Accommodations s...
09/05/2026

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

09/04/2026

"One of the biggest misconceptions I encounter is that because I'm taking a CFTR modulator, my cystic fibrosis no longer affects my life. The reality is that while modulators have transformed my health and given me opportunities I never thought possible, they haven't erased my disease. My body is still healing from pregnancy and delivery while managing a chronic illness that requires daily attention. Each day is a balancing act.

There have been days when I've felt guilty for leaving the NICU to go home and complete my treatments. Days when exhaustion made me question whether I was doing enough. Days when I wished my body didn't need so much care while my heart wanted to be somewhere else. I've learned that caring for myself isn't taking time away from my babies — it's investing in the mother I want to be for them.

As more people with CF become parents, I hope we continue to talk about what happens after pregnancy. Thanks to groundbreaking therapies, more of us are reaching milestones that once seemed out of reach. But motherhood doesn't erase CF, and CF doesn't disappear after delivery.

The postpartum journey deserves more attention, research, and support, especially for parents balancing their own health while caring for medically complex or premature babies.

To anyone else with CF who finds themselves navigating postpartum recovery, a NICU stay, or simply the overwhelming transition into parenthood, I hope you know this: you are not alone."

Springfield Great Strides walkers, next week is Spirit Week! We will have a daily challenge Tuesday through Friday to he...
09/04/2026

Springfield Great Strides walkers, next week is Spirit Week!
We will have a daily challenge Tuesday through Friday to help you get into the Great Strides spirit and kickstart your fundraising. Each completed challenge earns you an entry to win our spirit pack (14 L black backpack, lung plushie pillow, and a Committed to the Cure hat)! If you still need to register for the walk, now's the time so that you can participate and have a chance to win:
https://fundraise.cff.org/springfield2026

This November, join us for an unforgettable evening celebrating a New Horizon of Hope for the cystic fibrosis community....
09/03/2026

This November, join us for an unforgettable evening celebrating a New Horizon of Hope for the cystic fibrosis community. At the Reach for a Star Gala, you'll hear firsthand stories that showcase the remarkable progress being made in CF care, research, and treatment.

⭐We're honored to welcome Patricia Burks, a dedicated CF mom and Senior Director of Clinical Trial Affairs at the Cystic Fibrosis Foundation whose work has helped advance care and clinical trials for people with cystic fibrosis across the country.

⭐You'll also hear from our Ambassadors, the Cullman family, whose experience highlights a breakthrough prenatal approach to cystic fibrosis treatment and offers a powerful glimpse into what's possible for future generations living with CF.

Nov. 14 | 6 p.m. | The Chase Park Plaza
Reserve your tickets or table today or visit our bio! https://events.cff.org/reachforastargala

We are deeply grateful to the businesses whose generous sponsorship makes our event possible. Your support does far more...
09/03/2026

We are deeply grateful to the businesses whose generous sponsorship makes our event possible. Your support does far more than bring people together—it strengthened our shared mission to cure cystic fibrosis and bring hope to every individual and family impacted by this disease.

Have 10 minutes? Take the Annual CF Insights survey to share what’s working, what’s hard, and what would make a real dif...
09/02/2026

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

"We're so grateful to all of our golfers, sponsors, every donor, support and volunteer that has come out today -- we're ...
09/01/2026

"We're so grateful to all of our golfers, sponsors, every donor, support and volunteer that has come out today -- we're all going to be the ones that help find that cure."
- Jillian Simpson, mother of ambassador Connor, age 3

Thanks to all of YOU for helping to make the 65 Roses Gateway Golf Classic a huge success, raising over $134,000 in its second year! Check out this video, recapping a day filled with fun and HOPE!

https://www.youtube.com/watch?v=6TKmeSIlD94&t=2s

It's not too late to join the momentum and donate in honor of Connor! https://events.cff.org/65rosesgatewaygolfclassic/Donate

"We're so grateful to all of our golfers, sponsors, every donor, su...

Join us for a live virtual event to celebrate our incredible ROSE UP community for coming together to raise money for a ...
08/31/2026

Join us for a live virtual event to celebrate our incredible ROSE UP community for coming together to raise money for a cure for cystic fibrosis in their own way. Join us Thursday, Sept. 17! Save your seat today: https://on.cff.org/4w5BTTz

Starting college is an exciting milestone, and having cystic fibrosis shouldn't stand in the way of your goals. From hou...
08/29/2026

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

We are truly thankful for the businesses whose generous sponsorship made this event possible. Your commitment not only b...
08/28/2026

We are truly thankful for the businesses whose generous sponsorship made this event possible. Your commitment not only brings our community together, but also strengthens our shared mission to cure cystic fibrosis and offer hope to every person and family affected by it.

Address

St. Louis, MO

Opening Hours

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

Telephone

+13147331241

Alerts

Be the first to know and let us send you an email when Cystic Fibrosis Foundation - Missouri Chapter posts news and promotions. Your email address will not be used for any other purpose, and you can unsubscribe at any time.

Share