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Get Assistance - Cox Boys
We are here to help people with CF get the insurance coverage they need. Hear how the Foundation helped the Cox family.

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News & Events

07/11/14   CF Foundation Featured at Congressional Hearing on Patients’ Involvement in Drug Development
07/02/14   Updated Infection Prevention and Control Guidelines for Cystic Fibrosis Now Published Online
07/01/14   CF Foundation Teen Advocates Share Their CF Stories with Members of Congress
06/24/14   Phase 3 Combination Studies of Ivacaftor (Kalydeco) and Lumacaftor (VX-809) Show Positive Results in Most Common CF Mutation
06/16/14   Georgia Wine and Roses Gala Raises more than $347,000 to Support CF Foundation’s Mission

Check this Out!

Letter to the Community on Exciting Vertex Clinical Trials Results
Foundation President and CEO Robert J. Beall, Ph.D., and Executive Vice President for Medical Affairs, Preston W. Campbell, III, M.D., share their thoughts on the results of Phase 3 clinical trials of ivacaftor (Kalydeco) in combination with lumacaftor (VX-809) for people with two copies of the F508del mutation.

Tips for Traveling with CF
What’s the best way to have a great trip? Be prepared! Check out our list of what to do before you hit the road.

In the Spotlight

Mike Hart
Mike Hart
Mike Hart is a dedicated CF Foundation volunteer who has been inspired to support the search for a cure by his best friend, Jill, who has CF.

Cycle 2014

The Cystic Fibrosis Foundation is an accredited charity of the Better Business Bureau.