Cystic Fibrosis Foundation - Louisiana Chapter, New Orleans

Cystic Fibrosis Foundation - Louisiana Chapter, New Orleans Welcome to the official page of the Greater New Orleans Chapter! More than 10 million Americans are unknowing, symptomless carriers of a defective CF gene.

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.

Plan your Legacy, Transform Lives...Your legacy can make a difference in the lives of people with cystic fibrosis. Disco...
05/29/2026

Plan your Legacy, Transform Lives...

Your legacy can make a difference in the lives of people with cystic fibrosis. Discover how easily you can leave a lasting impact.

https://www.cff.org/legacy-giving

Plan your Legacy, Transform Lives...Your legacy can make a difference in the lives of people with cystic fibrosis.  Disc...
05/28/2026

Plan your Legacy, Transform Lives...

Your legacy can make a difference in the lives of people with cystic fibrosis. Discover how easily you can leave a lasting impact.

https://www.cff.org/legacy-giving

We are so proud to announce the installment of our 2026 Chapter Board Co-Presidents:  BRENT GUILBEAU & STEVEN ROMERO.  J...
05/12/2026

We are so proud to announce the installment of our 2026 Chapter Board Co-Presidents: BRENT GUILBEAU & STEVEN ROMERO. JIM CRANE has faithfully served as our State Board President for over 30 years and will transition to the role of Director Emeritus leaving a legacy of enduring friendship, leadership and dedication.
Brent Guilbeau, State Board Co-President, Cystic Fibrosis Foundation – Louisiana-Mississippi Chapter
Brent Guilbeau has been a lifelong advocate for the Cystic Fibrosis Foundation, dedicated to finding a cure in honor of his late brother, Brian (1971–2009).
Throughout his involvement with the Foundation, Brent has served on numerous fundraising committees—including Cycle for Life, Great Strides, and Capital City’s Finest—but he is most proud to be the founder and co-chair of Shoot for the Cure – BR, now in its 12th year of raising both funds and awareness within the Capital Region.
Brent’s commitment has been recognized with the Cystic Fibrosis Foundation’s Breath of Life Award, the Jim Crane Lifetime Achievement Award, and the Family of the Year Award, shared with his wife, Leslie, and their children, Julianna and Evan. He has also been spotlighted by the Foundation’s national chapter during their National Volunteer Week for his sustained impact. In addition, Brent served as a member of the 2023 National Volunteer Leadership Council.
Professionally, Brent is a Partner at Coleman Partners Architects, a multi-faceted architecture and interior design firm with a portfolio spanning the United States and the Caribbean. Deeply involved in his professional community, he also serves on the Board of Directors for both the Baton Rouge and Louisiana State chapters of the American Institute of Architects (AIA).
“Being able to give back to the Cystic Fibrosis community in honor of my big brother has been a tremendous privilege.”
Steven Romero, State Board Co-President, Cystic Fibrosis Foundation – Louisiana-Mississippi Chapter
Steven Romero has been a passionate advocate for the Cystic Fibrosis Foundation since 2012, driven by a deep personal commitment to finding a cure. Steven is a proud husband to his wife Jennifer and father to their four children. Steven & Jennifer we honored for their work with our organization as Hero of Hope recipients for our chapter.
Over the years, Steven has been proudly involved in our cause — from being recognized as a member and top earner of Capital City's Finest in 2017, to co-founding Shoot for the Cure Baton Rouge, which has raised over $300,000 toward research development. He joined the CF Foundation State Board in 2018 and now proudly steps into the role of State Board Co-President.
Outside of his CF work, Steven serves as Vice President of Operations and Co-Owner of BUILD Commercial Construction in Baton Rouge, where he helps leads the operational team with resolve and honesty.
"I am humbled and honored to continue my service to the CF community. We are committed to continuing this work and providing comfort and care to those living with CF."

We are SO excited to announce Capital City's Finest Class of 2026!  Please support these amazing young professionals in ...
05/12/2026

We are SO excited to announce Capital City's Finest Class of 2026! Please support these amazing young professionals in their efforts to go All In For A Cure for CF! finest.cff.org/batonrouge

We are here for our friends in Mississippi.
05/07/2026

We are here for our friends in Mississippi.

SIXTEEN TEAMS HAVE REGISTERED TO DATE!!!  We are so excited to welcome you to this year's Great Strides New Orleans walk...
05/06/2026

SIXTEEN TEAMS HAVE REGISTERED TO DATE!!!

We are so excited to welcome you to this year's Great Strides New Orleans walk.

Join Us SATURDAY, September 19th at The Batture for Great Strides presents 65 Roses Fest New Orleans!!! 🌹🎵 Great Strides 2026 is coming—music vibes, community spirit, and a walk with purpose. Let’s turn up the volume and take strides toward a cure!

Haven't registered yet?

Register: https://fundraise.cff.org/neworleans2026

04/22/2026

We enjoyed celebrating All of our Wonderful Volunteers at our Annual Awards Dinner.

03/05/2026

Hi everyone! I’m Renee, and I’m so excited to be your Great Strides Ambassador! I am 12 years old and have cystic fibrosis. CF is only part of my life; I love to ride horses, participate on swim team, and ride four wheelers. It’s important for me to say active and compliant with all of my CF medications and treatments so I can stay active and healthy. But that’s not always enough. CF can creep up on you and knock you down quickly. That’s why my family and I are passionate to continue fundraising for the Cystic Fibrosis Foundation!

Yay! Go Renee! Go Great Strides!

This Valentine’s Day, show your love and support for people with cystic fibrosis by becoming a monthly donor. When you j...
02/14/2026

This Valentine’s Day, show your love and support for people with cystic fibrosis by becoming a monthly donor. When you join the 65 Roses Club, you’ll join thousands of community members driving breakthroughs in research, treatments, and care — and ultimately — a cure.

Steady, monthly support helps advance critical progress, giving people with cystic fibrosis the opportunity to live longer, fuller lives. There is no better time than now to show your love for people with CF and the CF community. Join today:
https://give.cff.org/csust/donate?rbref=VDAY26chapter&donate=35&unitid=Louisiana%20-%20New%20Orleans

We want to hear from YOU! How are you making Great Strides in the fight against cystic fibrosis? What is your Great Stri...
02/13/2026

We want to hear from YOU! How are you making Great Strides in the fight against cystic fibrosis? What is your Great Strides team name and how are you helping to fund the mission?

Laissez les bons temps rouler! has gone all in this Mardi Gras season and partnered with Caywood & Randazzo's who donated 100 king cakes for a fundraiser AND a very special golf tournament "Golfing for Gabi"! Way to geaux Team Gabi on your efforts in the fight against CF. See you on September 19th at The Batture!

Address

3900 N. Causeway Boulevard , Ste 1200
Metairie, LA
70002

Opening Hours

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

Telephone

+15044555194

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