Cystic Fibrosis Foundation - West Tennessee Chapter

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Cystic Fibrosis Foundation - West Tennessee Chapter 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.

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.

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.

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.

Happy Grandparents Day! When someone you love is living with cystic fibrosis, every act of support matters. Today, we ce...
09/13/2026

Happy Grandparents Day! When someone you love is living with cystic fibrosis, every act of support matters. Today, we celebrate the grandparents and grandpersons whose unwavering love, encouragement, and dedication help make a difference in the lives of people with CF and their families.

Join us for the CF Foundation’s signature Get Salty Comedy Show, streaming live Sept. 24 at 7:30 p.m. ET! Enjoy unforget...
09/10/2026

Join us for the CF Foundation’s signature Get Salty Comedy Show, streaming live Sept. 24 at 7:30 p.m. ET! Enjoy unforgettable laughs while helping us bring hope to people living with cystic fibrosis.

Don’t miss your chance to see an incredible line-up of comedians, including Kirsten Cills, a Philadelphia-born comedian living with CF who is known for her morbid sense of humor and the oxygen tank that often accompanies her on stage.

All proceeds will benefit the Cystic Fibrosis Foundation. Purchase your virtual ticket for $25 today: https://events.cff.org/rosesandthorns

Tennessee, time is running out on our $100,000 match! Donate by Sept. 18, and your gift will be matched, dollar-for-doll...
09/02/2026

Tennessee, time is running out on our $100,000 match!

Donate by Sept. 18, and your gift will be matched, dollar-for-dollar, up to $100,000, thanks to a generous donor.

Your support can help rewrite the future of cystic fibrosis: from life-changing therapies to investing in genetic research that has the potential to benefit everyone with CF.

Don’t miss your chance to support our mission and have your gift doubled now: https://give.cff.org/tennessee/Donate?rbref=MSAM26social01&donate=100

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

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

Join a peer-led, small-group discussion for Hispanic adults with cystic fibrosis and parents or caregivers of Hispanic i...
08/17/2026

Join a peer-led, small-group discussion for Hispanic adults with cystic fibrosis and parents or caregivers of Hispanic individuals with CF Sept. 22 at 9 p.m. ET. You’ll have an open space to connect, share experiences, and support one another. Discussion groups will be available in English and Spanish.

Right now, your gift can go twice as far for people with cystic fibrosis.Thanks to a generous donor, gifts made to the T...
08/13/2026

Right now, your gift can go twice as far for people with cystic fibrosis.

Thanks to a generous donor, gifts made to the Tennessee Chapter 2026 Annual Fund will be matched, dollar-for-dollar, up to $100,000.

We’ve made important progress in CF research and care, but lives continue to be lost every year to this disease. This is your opportunity to help rewrite the future of cystic fibrosis.

Give now to support our mission and have your gift matched: https://give.cff.org/tennessee/Donate?rbref=MSAM26social01&donate=100

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

Address

5865 Ridgeway Center Pkwy, Ste 300
Memphis, TN
38120

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