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

Cystic Fibrosis Foundation - Mississippi Chapter

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Ridgeland, MS
Cystic Fibrosis Foundation - Mississippi Chapter

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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.

10/29/2026

What a team!

BIG THANKS to staffers from the UMMC CF Care Center for volunteering at the CF Golf Classic yesterday!! UMMC Cystic Fibrosis Center

10/14/2026

Oh what a night! THANK YOU LAUREL!
We’re missing the summer already, and having fun at Bowl for Breath!

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.

10/07/2026

As we prepare for the upcoming Isaias in Alabama and Mississippi, we’re here to help ensure people living with cystic fibrosis and their families get the care they need.

Our Compass team can help with getting emergency access to medications and medical devices that were left behind, lost, or damaged. If you or a loved one needs help, please contact Compass at [email protected] or 844-COMPASS.

10/02/2026

Thank you Dr. Miller for your tireless dedication.

Your are truly an icon in the fight against cystic fibrosis. 🌹

https://www.facebook.com/share/1NLrW8W72N/?mibextid=wwXIfr

It is with heavy hearts that we share the passing of Dr. Suzanne Miller, a true pioneer of our CF Center and a beloved part of our CF family for many decades.
Dr. Miller cared for so many of our CF patients throughout the years, dedicating countless hours to their care and helping lay the foundation for the center we know today. She was known for her loving, compassionate care and for the genuine relationships she built with her patients and their families.
For many of her CF patients, they knew Dr. Miller was coming before they ever saw her. The familiar sound of her shuffling feet making their way down the hall during her late-night rounds became a comforting reminder that she was there, checking on them and making sure they were cared for.
Her impact on our center and on the lives of our patients cannot be measured. We are so thankful for the decades she devoted to caring for our CF community and for the role she played in helping build our center from the beginning.
Dr. Miller will be deeply missed, but her legacy of loving care will continue to live on in the countless patients, families, and colleagues whose lives she touched.
We are forever grateful for all she gave to our center and our patients. 🤍

10/01/2026

The cystic fibrosis community comes together during 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 to watch three plenaries, select symposia, and participate in interactive Q&A opportunities with experts and researchers.

Can't tune in live? 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://www.nacfconference.org/

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.

09/08/2026

Let's hear it for our sponsors!

The Bowl for Breath is one week away, and we're so grateful for the sponsors who have stepped up to support this incredible event and the mission of the Cystic Fibrosis Foundation.

09/03/2026

Thank you to our local sponsors for supporting Bowl for Breath. Your commitment to our cause brings us one step closer to a cure for cystic fibrosis. We're thrilled to have you participating in this year's event.

08/27/2026

Our teams are stepping up, hitting the lanes, and making every frame count in support of our mission to cure cystic fibrosis.

Meet the teams bowling for loved ones, friends, and a future without CF. Their efforts raise critical funds to advance research, high-quality care, and essential programs for people with CF.

Thank you for helping make CF stand for Cure Found.

Address

Ridgeland, MS
39157

Opening Hours

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

Telephone

+16019813100

Website

https://www.cff.org/chapters/louisianamississippi-chapter-jackson-office

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