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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 News Archive

 

12/31/2009   Rosie O'Donnell, Lewis Black and Others Share Their Dreams for CF
12/29/2009   Cystic Fibrosis Foundation 2009 Successes: Advocating For and With Patients on Many Fronts
12/28/2009   Washingtonians Raise Monumental Millions for CF
12/22/2009   New York Times Says Cystic Fibrosis Foundation is Model for Other Chronic Diseases
12/18/2009   Rosie O’Donnell and Others Share Their Dreams for CF
12/16/2009   South Carolina Family Motivated by Challenge Match
12/15/2009   CF Foundation Urges Swift FDA Review of AZLI Antibiotic
12/15/2009   Cystic Fibrosis Guild Honors CF Foundation Volunteers in Seattle
12/10/2009   U.S. Food and Drug Administration Advisory Panel Rules in Favor of CF Antibiotic by Gilead Sciences
12/09/2009   Minnesotans Dine for a Cure
12/08/2009   Delaware Valley Breath of Life Celebration Honors Wawa, Inc.
12/07/2009   Ultimate Golf Experience Unites Friends to Support CF
11/24/2009   “How the Grinch Stole Christmas” and other Holiday Films for Sale at CVS/pharmacy to Benefit CF Foundation
11/20/2009   Volunteers Turn a Great Strides Effort into a CureFinders Miracle
11/19/2009   Voluntary Recall of Vicks Sinex Nasal Spray by Proctor & Gamble
11/18/2009   Pittsburgh’s 50 Finest Raises Record $220,000 for CF Foundation
11/16/2009   CF Foundation is Halfway to Receiving $6 Million Matching Gift
11/12/2009   World-Famous Harley Davidson Museum Hosts Wisconsin's Breath of Life Gala
11/10/2009   Connecticut Athletes Draw Major League Support for Cystic Fibrosis
11/09/2009   San Diego “Well Healed” Gala Celebrates 10th Anniversary
11/05/2009   CF Foundation Care Centers Receive Awards for Quality Care at 2009 NACFC
11/04/2009   Minnesotans Honored at North American CF Conference
11/02/2009   Drug Development News – 2009 NACFC
10/30/2009   Fixing the Faulty Protein in CF, CFTR – 2009 NACFC
10/29/2009   CF Treatment Adherence Can Improve Health Outcomes – 2009 NACFC
10/27/2009   The Importance of Quality Improvement – 2009 NACFC
10/26/2009   Expanding Adult Care for People with Cystic Fibrosis – 2009 NACFC
10/26/2009   Teens Visit Capitol Hill to Urge Support for their Siblings with CF
10/23/2009   Full Length Videos of the NACFC Plenary Sessions Now Available
10/21/2009   CF Foundation Hosts Successful 23rd Annual North American CF Conference
10/20/2009   Inspire Pharmaceutical's President Christy Shaffer Receives Cystic Fibrosis Foundation's Highest Award
10/19/2009   Cystic Fibrosis is "Proof of Principle" for Drug Development for Rare Diseases, says NIH Director on Minnesota Public Radio
10/16/2009   CF Foundation's Own American Idol: Director of NIH Gives Keynote Address and Sings at CF Foundation’s International CF Conference
10/16/2009   CF Foundation President & CEO Talks with Director of the NIH
10/15/2009   NIH Director Francis Collins Gives Keynote Address at NACFC
10/15/2009   CF Foundation Kicks Off the 23rd Annual North American CF Conference
10/14/2009   Oregon Firefighters Climb for a Cure
10/13/2009   CF Foundation Celebrates Tennessee’s ‘Top 30 Under 30’
10/09/2009   Great Strides Success in 2009
10/08/2009   NIH Director Francis Collins to Address 3,000 Cystic Fibrosis Experts at International Conference in Minneapolis
09/28/2009   Foundation Leads Coalition of More than 100 Organizations in Support for Clinical Trials Bill
09/28/2009   One-of-a-Kind Les Paul Gibson Guitar Auction to Benefit the CF Foundation
09/25/2009   Voluntary Recall on Children’s and Infants’ Tylenol
09/23/2009   Join Us on Twitter & Facebook!
09/23/2009   Research Shows Showerheads Harbor Bacteria
09/22/2009   CF Foundation Volunteer Bikes to East Coast for Twin Sons
09/22/2009   CF Foundation Provides Guidance on Seasonal and H1N1 Influenza
09/21/2009   Californians Lift Their Glasses for a Cure
09/17/2009   Marathon Golf Challenge Raises Support for CF
09/16/2009   U.S. Senate Introduces Bill to Increase Participation in Clinical Trials for Rare Diseases
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