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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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 News and Events

 

03/14/12   CF Foundation Advocates “March on the Hill” to Attract Support from Members of Congress
12/22/11   CF Advocates Advance Research and Preserve Access to Care in 2011
11/09/11   New Online Library Helps CF Patients Navigate the Challenges of Health Care Coverage
10/14/11   Foundation Launches New Policy Bulletin
10/10/11   Influential Congressional Committee Recognizes the Importance of Cystic Fibrosis Research
06/24/11   Teens Travel to Washington, D.C., to Speak Out for Cystic Fibrosis
06/14/11   CF Foundation Drug Development Model Showcased at Congressional Briefing
04/04/11   “Improving Access to Clinical Trials Act” Takes Effect
03/23/11   Volunteers “March on the Hill” During the CF Foundation’s Annual Advocacy Effort
12/21/10   CF Advocates Make Their Voices Heard in 2010
10/08/10   President Obama Signs “Improving Access to Clinical Trials Act” Into Law, Finalizing a Major Achievement for CF Advocates
09/23/10   “Improving Access to Clinical Trials Act” Passes U.S. House, Heads to President for Signature
08/20/10   Michigan Teens Give U.S. Senator a Glimpse of Life with CF
08/06/10   “Improving Access to Clinical Trials Act” Passes U.S. Senate in Victory for CF Advocates
06/30/10   Teens Make Their Voices Heard on Capitol Hill, Urging Support for Siblings with CF
05/24/10   CF Foundation Drug Development Model is “Proof of Principle” for Other Diseases, says NIH Director in U.S. Senate Briefing
04/01/10   New Health Coverage Regulations Beneficial to People with CF to Take Effect In September 2010
03/22/10   New Health Reform Bill Includes Provisions that Impact People with CF
12/29/09   Cystic Fibrosis Foundation 2009 Successes: Advocating For and With Patients on Many Fronts
10/26/09   Teens Visit Capitol Hill to Urge Support for their Siblings with CF
09/28/09   Foundation Leads Coalition of More than 100 Organizations in Support for Clinical Trials Bill
09/16/09   U.S. Senate Introduces Bill to Increase Participation in Clinical Trials for Rare Diseases
09/16/09   Voices of CF Community Help CF Services Pharmacy Continue Operations in NY
09/15/09   CF Advocates Make Every Breath Count
08/18/09   NIH Director Francis Collins Steps into New Role
08/13/09   Cystic Fibrosis Foundation's Statement on Health Care Reform
07/09/09   CF Foundation Supports President Obama’s Nomination of Francis Collins, M.D., Ph.D., as New NIH Director
07/07/09   All 50 States to Screen Newborns for Cystic Fibrosis by 2010
06/18/09   CF Foundation Testifies Before Congress on Improving Rare Disease Research
06/15/09   Obama Cites Cincinnati CF Center as an Example of “Outstanding” Care
06/15/09   New Legislation Seeks to Boost Participation in Clinical Trials for Rare Diseases
05/28/09   Senator Shelby and Acting NIH Director Raynard Kington Praise CF Foundation at Hill Hearing and Call for Ongoing Funding
05/11/09   Texas Legislature to Fund CF Newborn Screening – All 50 States Soon to be Screening for CF
05/04/09   Connecticut Legislature Unanimously Approves CF Newborn Screening Bill
04/15/09   North Carolina Begins Screening Newborns for CF
04/13/09   As Health Care Reform Takes Center Stage, Foundation Asks Washington to Consider CF Patients
01/28/09   Senator Highlights CF During Children's Health Insurance Debate
01/16/09   U.S. House Passes Measure to Ensure Health Care for Millions of Children
01/08/09   Utah Begins CF Newborn Screening
11/18/08   Patients and Families Asked to Share Their Experiences About AZLI
10/14/08   New Law Ensures Health Coverage for College Students with CF
09/19/08   New Information Available About Health Coverage & Income Assistance
09/02/08   Summer Advocacy Campaign Connects CF Community with Congress
08/26/08   North Carolina and Nevada Step up Efforts to Screen Newborns for Cystic Fibrosis
07/15/08   House Passes Resolution to Recognize Cystic Fibrosis
07/11/08   Five States Step Up Efforts to Screen Newborns for Cystic Fibrosis
05/13/08   Alabama Begins Screening Newborns for CF
05/01/08   Genetic Non-Discrimination Act and Newborn Screening Laws Pass Congress
04/29/08   Senate Declares May National CF Awareness Month
04/24/08   CF Foundation Lauds Congress for Passage of Small Business Innovation Research Program
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