Cystic Fibrosis Foundation – Georgia Chapter

Cystic Fibrosis Foundation – Georgia Chapter We're helping to advance the Cystic Fibrosis Foundation’s mission to cure cystic fibrosis. Welcome to the official page of the Georgia Chapter!
(1)

Team bonding > our bowling scores. Grateful for an afternoon spent striking the perfect balance between hard work and su...
07/28/2026

Team bonding > our bowling scores. Grateful for an afternoon spent striking the perfect balance between hard work and summer fun. 💥🎳

Last month was the CF Foundation’s Teen Advocacy Day! Georgia was proud to have two teens represent us and advocate on b...
07/27/2026

Last month was the CF Foundation’s Teen Advocacy Day! Georgia was proud to have two teens represent us and advocate on behalf of all those living with CF. Thank you to Catherine and Joshua for being a voice and sharing your stories to help create a brighter future for the CF community. We are so proud of your leadership and dedication!

Have your voice be heard: https://act.cff.org/action_center/

🚨 FINAL CALL - BERLIN MARATHON! 🚨The Cystic Fibrosis Foundation has 2 remaining bibs for the Berlin Marathon, and we're ...
07/20/2026

🚨 FINAL CALL - BERLIN MARATHON! 🚨
The Cystic Fibrosis Foundation has 2 remaining bibs for the Berlin Marathon, and we're looking for passionate runners to join our Breathe Team!

If you've dreamed of running one of the World Marathon Majors while making a meaningful impact in the lives of people with cystic fibrosis, this is your chance.
Interested? Contact Danielle Driggers at [email protected] as soon as possible. Deadline to register is Friday, July 24.

Please share with friends, family, and local runners who may be interested!

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!

A huge congratulations to the Northside Hospital Peachtree Road Race Breathe Team members who participated in this year’...
07/08/2026

A huge congratulations to the Northside Hospital Peachtree Road Race Breathe Team members who participated in this year’s race, both in person and virtually!

Despite the heat, humidity, and challenging hills, our team showed incredible determination and heart as they crossed the finish line in honor of loved ones and individuals who inspired their journey. We are deeply grateful for the many ways they showed up, not only on race day, but throughout the weeks leading up to it.

Through sharing their personal stories, raising critical funds, and bringing awareness to our mission, these dedicated participants have helped move us one step closer to a cure. Their passion, perseverance, and commitment make a meaningful difference, and we could not be more thankful.

Please join us in celebrating and congratulating our amazing Breathe Team members!

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 Catherine Hawkins and Joshua Corrigan for representing the cystic fibrosis community at the Cy...
06/24/2026

We’re incredibly proud of Catherine Hawkins and Joshua Corrigan for representing the cystic fibrosis community at the Cystic Fibrosis Foundation’s 18th annual Teen Advocacy Day.

Catherine is 16 and has a younger brother living with cystic fibrosis. Joshua is also 16 and has CF.

They are sharing their stories with Senator Reverend Raphael Warnock, Senator Jon Ossoff, and Congressman Buddy Carter 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.

Address

57 Executive Park S, Suite 380
Atlanta, GA
30329

Opening Hours

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

Telephone

+14043256973

Website

Alerts

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

Contact The Organization

Send a message to Cystic Fibrosis Foundation – Georgia Chapter:

Shortcuts

Featured

Share

Category