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

Cystic Fibrosis Foundation - South Florida

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Cystic Fibrosis Foundation - South Florida

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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.

10/13/2026

Congratulations to Joe DiMaggio Children’s Hospital Care Center on receiving the 2026 Outstanding Care Center Partnership Award! 🏆

This well-deserved recognition celebrates your team’s compassion, expertise, and unwavering commitment to the cystic fibrosis community. We are incredibly grateful for a team that goes above and beyond to support patients and families, advance care, and make a meaningful difference every day.

Thank you for your continued collaboration, dedication, and shared passion for improving the lives of those affected by CF. We are so proud to see your team recognized on a national level!

Congratulations on this outstanding achievement!

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.

10/01/2026

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.

08/17/2026

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: https://cff.zoom.us/meeting/register/0CYmF5JjRzq7qSTfdjjCfg #/registration

08/11/2026

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

08/10/2026

Let's Build Our Legacy Together.

This Make-A-Will Month, we're inviting our community to take a powerful step toward a future beyond cystic fibrosis.
Creating a will helps protect the people you love while giving you the opportunity to support the causes closest to your heart. By including a gift to the Cystic Fibrosis Foundation in your estate plans, you can help fuel research, care, and advocacy for generations to come.

Together, we're building a legacy of hope, progress, and possibility. Start building your legacy today at cff.org/legacy-giving.

08/05/2026

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

07/21/2026

Nominations STILL OPEN! Help us honor South Florida’s finest professionals by submitting a nomination for the 2026 class today, serving Miami, Broward, Palm Beach, Indian River, St. Lucie, and Martin counties.

South Florida’s Finest is a 12-week fundraising initiative that honors exceptional professionals throughout the region for their professional accomplishments and dedication to their communities. Through personalized meetings and weekly initiative, honorees develop a deeper awareness of cystic fibrosis and the impact it has on individuals and families. The CF Foundation’s South Florida’s Finest Professional Program is proud to share that nominations are now open for two upcoming classes: Miami-Dade/Broward and Palm Beach/Treasure Coast.
Sign up today! https://afasignup.formstack.com/forms/flfinestnomination2026

07/16/2026

Because of the support of people like you and our national peer-to-peer sponsor, Vertex, people with CF are achieving dreams for themselves, not limited by their disease. Thank you for all you do!

Address

3201 W. Commercial Boulevard #237
Fort Lauderdale, FL
33309

Opening Hours

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

Telephone

+19547395006

Website

https://www.cff.org/chapters/southeast-florida-chapter-fort-lauderdale-office, https://give.cff.org/ftlauderdale/donate?

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