Apply for an Impact Grant to make your vision a reality. The best ideas come from personal experience, and no one knows the ins and outs of life with CF like the CF community!
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Learn more about KC White, chair of the CF Foundation’s Board of Trustees.
Find answers to questions about the COVID-19 pandemic while living with cystic fibrosis.
A brief overview of cystic fibrosis, how it can impact people who have it, and how you can help.
People with chronic diseases, such as cystic fibrosis, are at greater risk for developing clinical depression. When left untreated, depression can interfere with your ability to manage your CF effectively and experience a better quality of life.
The Drive is the Cystic Fibrosis Foundation’s ultimate golf experience, held in the fall at renowned golf courses around the United States.
ResearchCon is for everyone with a personal or professional connection to cystic fibrosis to learn and discuss CF-related science and care alongside others living with and studying the disease.
Learn more about previous CF Foundation community conferences.
The Cystic Fibrosis Foundation is aggressively pursuing potential treatments for people with CF who have nonsense and rare mutations who will not benefit from drugs known as modulators, which correct the malfunctioning cystic fibrosis transmembrane conductance regulator (
Newborn screening (NBS) is a program run by each state to identify babies born with certain health conditions, including cystic fibrosis. Although a sweat test should ultimately be done to rule out or confirm a CF diagnosis, NBS can help you and your health care providers take immediate steps to keep your child as healthy as possible.