Cystic Fibrosis Foundation - West Florida Chapter

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Cystic Fibrosis Foundation - West Florida Chapter We're helping to advance the Cystic Fibrosis Foundation’s mission to cure cystic fibrosis.

Faced with insurmountable odds, but determined to save the lives of their children, a group of concerned parents came together in 1955 to form the Cystic Fibrosis Foundation. At the time, very little was known about cystic fibrosis, but the tenacity and strength of CF families laid the groundwork for monumental progress in research, care, and treatment of a rare disease. Today, because of their hard work and the support of generous volunteers and donors, many people with CF are living into adulthood. Yet, we still lose precious young lives every day and will not be satisfied until there is a cure for all those living with this disease.

We’re moving to a new home on social! 💜 Follow us at Cystic Fibrosis Foundation - North Florida Chapter for the same con...
08/25/2026

We’re moving to a new home on social! 💜 Follow us at Cystic Fibrosis Foundation - North Florida Chapter for the same connection, support, and Cystic Fibrosis Foundation updates. We look forward to staying connected with you there!

Whether you're heading back to the classroom, campus, or workplace, back-to-school season means more exposure to germs, ...
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

Let's Build Our Legacy Together.This Make-A-Will Month, we're inviting our community to take a powerful step toward a fu...
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.

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

Because of the support of people like you and our national peer-to-peer sponsor, Vertex, people with CF are achieving dr...
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!

Research funded by the National Institutes of Health (NIH) has driven decades of progress in cystic fibrosis. It led to ...
06/25/2026

Research funded by the National Institutes of Health (NIH) has driven decades of progress in cystic fibrosis. It led to the discovery of the CFTR gene and deepened our understanding of the disease, laying the foundation for today’s treatments and future therapies in development. Despite this progress, significant unmet needs remain. There is still no cure, and many people with CF cannot benefit from existing therapies.

Today, teens from across the country are advocating on Capitol Hill and online for the Foundation’s 18th annual Teen Advocacy Day. They are sharing their personal stories and asking members of Congress to increase funding for the NIH to sustain a robust research pipeline, support innovation, and accelerate progress toward treatments for every person with CF and, ultimately, a cure.

Help amplify their voices. Urge your members of Congress to increase NIH funding.
https://act.cff.org/campaign/increasefundingNIH/

We’re incredibly proud of everyone representing the cystic fibrosis community at the Cystic Fibrosis Foundation’s 18th a...
06/18/2026

We’re incredibly proud of everyone representing the cystic fibrosis community at the Cystic Fibrosis Foundation’s 18th annual Teen Advocacy Day.

Our Florida community will be sharing their stories with Lois Frankel & Rep. María Elvira Salazar to highlight the urgent need to increase funding for the National Institutes of Health to sustain a robust research pipeline, support innovation, and accelerate progress toward treatments for every person with CF — and ultimately, a cure.

This 65 Roses Day (6/5), join the 65 Roses Club: a dedicated group of monthly donors committed to helping cure cystic fi...
06/05/2026

This 65 Roses Day (6/5), join the 65 Roses Club: a dedicated group of monthly donors committed to helping cure cystic fibrosis.

As a monthly donor, you can spread your support into smaller gifts that add up to real progress. This steady, reliable stream of revenue helps enable the Foundation to fund innovative research, drug development, and provide high-quality, specialized care so that we can get closer to a cure for cystic fibrosis.

Joining is easy — set up automatic monthly giving through the donation page and know your support is working for people with CF every month, without any extra steps.

https://give.cff.org/65rosesclub/donate?rbref=65RD26ch&donate=35&unitid=Florida%20-%20West%20-%20Tampa

Join the next CF Circle for a virtual, small-group discussion about the Black CF Experience. On June 23 at 7 p.m. ET, Bl...
06/04/2026

Join the next CF Circle for a virtual, small-group discussion about the Black CF Experience. On June 23 at 7 p.m. ET, Black adults with CF, as well as parents and caregivers of Black children with CF, are invited to talk openly with peers about shared experiences like misdiagnosis, delays in treatment, self-advocacy in medical settings, and navigating life with CF.

https://on.cff.org/CF-Circles-June-2026

Address

1614 North 19th Street
Tampa, FL
33605

Opening Hours

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

Telephone

+18133749041

Website

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