Complications of cystic fibrosis affect everyone with the disease, regardless of their mutation. We are supporting research into CF complications, such as infections, inflammation, excessive mucus, and gastrointestinal issues, to develop better treatments and improve outcomes for people with CF.
Site Search
The Cystic Fibrosis Foundation would like to recognize and thank the following members of the CF community for providing their time, expertise, and insights to inform the content on this site.
We have about 70 chapters and offices across the country that work diligently to raise funds and support our community in the search for a cure. They host events (including virtually and outdoors) and serve as a hub for the CF community. Get to know them!
By using or visiting the website, services, mobile applications, or content provided by www.cff.org (“Site”), a service of the Cystic Fibrosis Foundation (“CFF”), including auction.cff.org, you are agreeing to be bound by the following Terms of Agreement (“Terms”). If you don't agree to these Terms, you may not register, visit, or use the Site.
The 19th annual Volunteer Leadership Conference (VLC), was held in Denver, CO from March 23-25, 2023. It was a special moment to reunite, share stories, and receive updates on the medical progress being made for those living with cystic fibrosis.
The Patient Registry is an invaluable tool for researchers conducting observational studies about people with CF in the U.S. About 50,000 individuals have been followed in the Registry since its inception in 1986; many of them have been included for over 20 years.
The Success with Therapies Research Consortium helps the clinical study of interventions so people with cystic fibrosis can improve the consistency of their day-to-day management of their CF to optimize health outcomes and quality of life.