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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

07/31/14   Vertex Announces Phase 2 Results of Combination Treatment in People with One Copy of the F508del CF Mutation
07/22/14   CF Foundation Provides New Health Education Resources on Infection Prevention and Control for CF Community
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

Check this Out!

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Speak out for CF in your state!
Inspire action in the fight against CF by meeting with your member of Congress in your hometown. Join Make Every Breath Count, the Cystic Fibrosis Foundation’s national advocacy campaign.

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Get Germ Smart!
Germs are everywhere, but there are plenty of things you can do to reduce the risk of getting or spreading them. Check out our new resources to help you get germ smart!

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.