Cystic Fibrosis Foundation - Tennessee Chapter

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

Did you know you can support the Cystic Fibrosis Foundation through a donor-advised fund (DAF)? A DAF is a charitable gi...
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.

A huge thank you to American Airlines for making Breath of Roses a memorable event. Your support and commitment to the c...
09/25/2026

A huge thank you to American Airlines for making Breath of Roses a memorable event. Your support and commitment to the cystic fibrosis community is helping us move closer to a day where CF stands for Cure Found.

We’re committed to developing a transformative treatment — and ultimately, a cure — for all people with cystic fibrosis....
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.

The cystic fibrosis community comes together during the North American Cystic Fibrosis Conference (NACFC) each year to l...
09/23/2026

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/

09/21/2026

The countdown to Guitars & Greens is on.

Get your team together and join us for a day of golf, great food, friendly competition, and meaningful impact in the fight against cystic fibrosis.

Purchase your foursome today. https://events.cff.org/guitarsandgreens

We did it!Thanks to a generous donor and the support of the cystic fibrosis community, we achieved our $200,000 match, m...
09/18/2026

We did it!

Thanks to a generous donor and the support of the cystic fibrosis community, we achieved our $200,000 match, moving us one step closer to a cure for CF.

We’re proud of the progress we’ve made, but our work isn’t done as lives continue to be lost to this disease. Together, let’s keep pushing forward and rewrite the future of cystic fibrosis.

Get ready to raise your paddle.This year’s Breath of Roses live auction features something for everyone, including a Gra...
09/18/2026

Get ready to raise your paddle.

This year’s Breath of Roses live auction features something for everyone, including a Grand Canyon glamping adventure, a hand-crafted 65 Roses quilt created by members of the Seymour Quilt Club, a custom Tennessee Volunteers fan table, and a Patricia Nash Designs postcards from Paris luxury travel set.

Every bid supports our mission and helps move us closer to a cure.

Join us Sept. 18 at Jackson Terminal.

Bruce and Lucy are championing the fight against cystic fibrosis in honor of their granddaughter, Evelyn Van Cleve. "Eve...
09/17/2026

Bruce and Lucy are championing the fight against cystic fibrosis in honor of their granddaughter, Evelyn Van Cleve.

"Every day is a blessing to share life with our granddaughter, Evelyn, a 9-year-old CF fighter. Watching her grow into a beautiful child who loves the Lord, builds friendships with her classmates, plays sports, loves the outdoors, is excited about going to school and learning as much as she can, and yet is still a goofy 9-year-old, all while navigating a daily regimen of breathing treatments, pills, and a healthy diet, is truly inspiring.

We have seen firsthand what the generosity of donors has made possible through research and new, advanced therapies that help people with CF live longer, healthier lives. This is why we are involved with the East Tennessee Chapter, and why we will continue supporting its mission of making CF stand for Cure Found."

Support Bruce and Lucy at: https://events.cff.org/rosesgala26/BruceLucyVanCleve

Jill is championing the fight against cystic fibrosis in honor of her niece, Bella Rocha. "My niece, Bella, has lived wi...
09/16/2026

Jill is championing the fight against cystic fibrosis in honor of her niece, Bella Rocha.

"My niece, Bella, has lived with cystic fibrosis her entire life, but CF does not define her. She is pure light, kind, joyful, empathetic, and always lifts up those around her.

As someone who has navigated chronic illness myself, I see the strength and resilience Bella carries every day. But more than that, I see possibility, hope, and an extraordinary young girl with a beautiful future ahead of her.

Bella inspires me to do more, love more deeply, and keep fighting for a day when every person with CF can live a long, full life free from this disease. Until then, I will keep hoping, keep fighting, and keep giving back what CF takes away.

Help me make the difference people with CF need and deserve."

Support Jill at: https://events.cff.org/rosesgala26/BellasAuntieJill

Sharon is championing people living with cystic fibrosis in honor of her close family friend, Kyle Blake. "My best frien...
09/15/2026

Sharon is championing people living with cystic fibrosis in honor of her close family friend, Kyle Blake.

"My best friend's son, Kyle, was diagnosed with cystic fibrosis at just 6 months old. For nearly 30 years, I've had the privilege of watching him and his family navigate life with CF, while also witnessing incredible progress in research, treatments, and care.

Over the years, I've seen the Cystic Fibrosis Foundation invest in groundbreaking science, help advance life-changing therapies, and transform what is possible for people living with CF. While we've come so far, our work is not done.

I'm committed to continuing this fight until a cure is found for Kyle, and for everyone living with cystic fibrosis. Together, we can help create a future free from CF."

Support Sharon at: https://events.cff.org/rosesgala26/Member/MyPage/10517879/Sharon-Bitzer

Address

4710 Charlotte Ave
Nashville, TN
37209

Opening Hours

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

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