Learn about cystic fibrosis, a genetic lung disorder that affects the pancreas and other organs, and how to treat and live with this chronic disease.
CF is a rare genetic disease found in about 30,000 people in the U.S. If you have CF or are considering testing for it, knowing about the role of genetics in CF can help you make informed decisions about your health care.
If you or your child has just been diagnosed with cystic fibrosis, or your doctor has recommended testing for CF, you may have many questions.
Diagnosing CF is a multistep process. A complete diagnostic evaluation should include a newborn screening, a sweat chloride test, a genetic or carrier test, and a clinical evaluation at a CF Foundation-accredited care center.
Raising a child with cystic fibrosis can bring up many questions because CF affects many aspects of your child’s life. Here you’ll find resources to help you manage your child’s daily needs and find the best possible CF care.
Living with cystic fibrosis comes with many challenges, including medical, social, and financial. By learning more about how you can manage your disease every day, you can ultimately help find a balance between your busy lifestyle and your CF care.
People with CF are living longer, healthier lives than ever before. As an adult with CF, you may reach key milestones you might not have considered. Planning for these life events requires careful thought as you make decisions that may impact your life.
People with cystic fibrosis are living longer and more fulfilling lives, thanks in part to specialized CF care and a range of treatment options.
Cystic Fibrosis Foundation-accredited care centers provide expert care and specialized disease management to people living with cystic fibrosis.
We provide funding for and accredit more than 120 care centers and 53 affiliate programs nationwide. The high quality of specialized care available throughout the care center network has led to the improved length and quality of life for people with CF.
The Cystic Fibrosis Foundation provides standard care guidelines based on the latest research, medical evidence, and consultation with experts on best practices.
As a clinician, you’re critical in helping people with CF maintain their quality of life. We’re committed to helping you partner with patients and their families by providing resources you can use to improve and continue to provide high-quality care.
As part of the Cystic Fibrosis Foundation's mission to help improve the lives of people living with cystic fibrosis, the PSDC initiative taps the CF community to inform key efforts to support the management of daily care.
Your cystic fibrosis care team includes a group of CF health care professionals who partner with you to provide specialized, comprehensive CF care.
Many cystic fibrosis patients and families face complicated issues related to getting the care they need. But CF Foundation Compass makes sure that no one has to do it alone.
For many people with cystic fibrosis, dealing with insurance is as much a part of living with the disease as nebulizers and vests. Many people with CF and their families face issues related to getting the care they need, but no one has to do it alone.
The Cystic Fibrosis Foundation is the world’s leader in the search for a cure for CF and supports a broad range of research initiatives to tackle the disease from all angles.
The CF Foundation offers a number of resources for learning about clinical trials and treatments that are being developed to improve the treatment of cystic fibrosis.
Our understanding of CF continues to evolve as scientists study what causes the disease and how it affects the body. These insights drive the development of new and better treatments and bring us one step closer to a cure.
Researchers, supported by the CF Foundation, have made tremendous advances to improve the health and quality of life of people with CF. We are committed to providing the tools and resources you need to continuously build upon this work.
Our goal is to educate policy makers about the needs of people with cystic fibrosis so that they make smart decisions about CF-related research, treatment, and access to care.
We recognize the value of tapping into the expertise that only people with CF and their families have. We invite you to share insights to help improve and develop programs and services that support the daily lives of people with CF.
Our mission is to find a cure for cystic fibrosis and improve the quality of life for those living with the disease. We can't do it alone. Help us add tomorrows by giving today.
In addition to working for a cure, the CF Foundation supports programs and policies to improve the lives of people with CF. Help us by raising awareness of CF, participating in a fundraising event, or volunteering with your local chapter.
4600 Park Road, Suite 100
The Carolinas Chapter - Charlotte Office of the Cystic Fibrosis Foundation welcomes you! Volunteers are the key to our success and the lifeblood of our organization. We have many opportunities for you to get involved. Your participation in any way will help us achieve our mission – finding a cure for all people with CF. Take a moment to check out our upcoming events and learn more.
Fashion Breathes Life
6:30 PM, January 27, 2018
Mint Museum - Expansion Space
Carolinas - Charlotte
The 3rd Annual Fashion Breathes Life will feature top fashions presented by prominent designers, elegant dining, a unique auction and the chance to mix and mingle with some of the Queen City's elite.
An Evening with the Master Chefs
6:30 PM, March 3, 2018
Quail Hollow Club
Join us for An Evening with the Master Chefs!
18th Annual Guys & Dolls Auction Gala
6:30 PM, March 24, 2018
Hilton Charlotte Center City
The Guys & Dolls Auction Gala is Charlotte's premier event for young professionals. Coming up on its 18th year, the event features fabulous Live Auction Packages which Charlotte's most dedicated "Guys" and "Dolls" put together, up for auction to the highest bidder.
Charlotte Spring Xtreme Hike 2018
April 21, 2018
The Charlotte Chapter of the Cystic Fibrosis Foundation is proud to present the 2018 XTREME HIKE to Cure Cystic Fibrosis. In just one day, a dedicated team of Xtreme Hikers will hike a 30.1 mile stretch of the famed Appalachian Trail to raise funds and awareness for the CF Foundation's mission to find a cure for cystic fibrosis.
Charlotte CF Cycle for Life 2018
6:30 AM, August 18, 2018
The Foundry/Draught Restaurant & Bar
Get your wheels in motion and join us for the 7th Annual CF Cycle for Life (CFL)! We will be starting and ending the ride at The Foundry, right beside Bank of America Stadium, and riding through the cycle friendly outskirts of Charlotte.
Charlotte Fall Xtreme Hike 2018
September 29, 2018
In just one day, a dedicated team of Xtreme Hikers will hike a 30.1 mile stretch of the famed Appalachian Trail to raise funds and awareness for the CF Foundation's mission to find a cure for cystic fibrosis.
Follow Us On
With more than 70 chapters and offices across the country, it’s easy to find and join a local Cystic Fibrosis Foundation chapter near you.
Cystic Fibrosis Foundation
4550 Montgomery Ave.
Suite 1100 N
Bethesda, MD 20814
800-344-4823 (toll free)
Sign up for our emails