No matter where you are in life — whether you’re a person with CF, parent, or caregiver — CF Peer Connect can connect you to a peer who has been through a similar situation.
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Caring for a child with CF can be a lot to juggle — from the many medications and daily treatments to the endless doctor's appointments. But I’ve found a system that helps me stay organized and stress-free so that I can focus on what really matters.
This competition provides one year of free lab and office space at Bakar Labs at the University of California Berkeley to awardees with emerging genetic medicines delivery technology that may be applied to CF.
Impact Grants provide guidance and funding to individuals or nonprofits that actively work with and empower the cystic fibrosis community.
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!
A brief overview of cystic fibrosis, how it can impact people who have it, and how you can help.
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.
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.