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 Watch Charlotte, whose son Trey has CF, talk about her dream for the future. 
 Watch Charlotte, whose son
 Trey has cystic fibrosis, talk
 about her dream for the future.
 

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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”
Drug Development Pipeline
Cystic Fibrosis Services Pharmacy
The Cystic Fibrosis Foundation is an accredited charity of the Better Business Bureau.