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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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2009 Press Releases

11/24/2009   The Cystic Fibrosis Foundation to Benefit from Holiday Film Promotion
10/08/2009   NIH Director Francis Collins to Address 3,000 Cystic Fibrosis Experts at International Conference in Minneapolis
09/28/2009   More than 100 Organizations Support Bill to Boost Participation in Clinical Trials for Rare Diseases
09/25/2009   Cleveland Indians Manager Eric Wedge Urges Fans to Fight Cystic Fibrosis
09/22/2009   Cystic Fibrosis Patient Emily Schaller Begins 2,000-Mile Quest to Get on “The Ellen DeGeneres Show”
09/16/2009   Senate Introduces Bill to Boost Participation in Clinical Trials for Rare Diseases
08/12/2009   Cystic Fibrosis Foundation Receives Second 4-Star Rating from Charity Navigator for Exceptional Fiscal Management
07/09/2009   CF Foundation Supports President Obama’s Nomination of Francis Collins, M.D., Ph.D., as New NIH Director
07/07/2009   All Fifty States to Screen Newborns for Cystic Fibrosis by 2010
06/15/2009   New Legislation Seeks to Boost Participation in Clinical Trials for Rare Diseases
05/13/2009   Cystic Fibrosis Foundation Rings Bell to Close New York Stock Exchange
05/07/2009   Cystic Fibrosis Foundation Launches Great Strides Walks Nationwide at 600 Locations
05/05/2009   CW’s 7th Heaven Actress Mackenzie Rosman to Visit Birmingham Area High School to Honor Cystic Fibrosis Foundation Fundraising
03/18/2009   Cystic Fibrosis Foundation to Receive Prestigious Health Care Award
01/14/2009   Cystic Fibrosis Foundation Web Site Rated “Best of the Web”

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