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.
Individuals with cystic fibrosis require more energy to breathe normally, fight lung infections and compensate for poor digestion. For these reasons, they need more calories than people without CF.
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.
Theratyping matches therapies, or medications, to specific types of mutations. The primary goal of theratyping is to identify which mutations respond to certain CFTR modulators, thereby helping people with rare CFTR mutations gain access to already approved modulators quickly and safely.
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.