Cystic Fibrosis Foundation - Click here for homepage
 | Stay Informed  |  Volunteer  |  Clinical Trials
ABOUT CYSTIC FIBROSIS ABOUT THE CYSTIC FIBROSIS FOUNDATION LIVING WITH CYSTIC FIBROSIS TREATMENTS RESEARCH OVERVIEW GET INVOLVED!
In This Section
Message from the President
Foundation Leadership
Annual Report & Financial Statements
Publications & Videos
News Room
News & Events
2012 News Archive
2011 News Archive
2010 News Archive
2009 News Archive
2008 News Archive
2007 News Archive
2006 News Archive
2005 News Archive
About 65 Roses
Locations
Governance & Policies
Milestones II Campaign
Employment Opportunities
Contact Us
Quick Links
Find A Chapter
Great Strides
Become a Corporate Partner
Volunteer
Employment Opportunities
Become an Advocate
Find A Clinical Trial
Care Center Network
Drug Development Pipeline
CF Services Pharmacy
Make a Donation
Find a Chapter
Get Connected

 Watch National Advocacy Co-chairs, Amy & Peter Barry, and learn how easy it is to be an advocate for CF. 
 Watch National Advocacy Co- 
 chairs, Amy & Peter Barry, and
 learn how easy it is to be an
 advocate for CF.
 

Join us on YouTube at http://www.youtube.com/CysticFibrosisUSA Join us on YouTube





Join us on Facebook at www.facebook.com/CysticFibrosisFoundation Join us on Facebook





Follow us at twitter.com/CF_Foundation Follow us on Twitter
Display a Printer Friendly Version This Page

Cystic Fibrosis Foundation 2009 Successes: Advocating For and With Patients on Many Fronts

December 29, 2009

As the year closes, the Foundation and its advocates nationwide can point to many successes on critical CF-related issues. Here is a list of significant 2009 milestones that will help improve the lives of people with CF:

  • 102 Members of the U.S. House of Representatives co-sponsored the Improving Access to Clinical Trials Act of 2009 (H.R. 2866), which will remove financial barriers that discourage participation in clinical research. The Foundation continues to work with the House and the Senate to pass the bill.

  • 20 new Representatives became members of the House Congressional Cystic Fibrosis Caucus – bringing the total to 147 and making the CF Caucus one of the largest in Congress.

  • In September, funding was restored to New York’s CF Adult care program after it had been targeted for elimination. 

  • In October, New York CF patients’ ability to use the Cystic Fibrosis Services Pharmacy was protected. New York Governor Paterson signed legislation to allow people with CF in that state to continue getting their medications through the pharmacy

  • In June, all 50 states, along with Washington, D.C., began requiring that all newborns be automatically screened for cystic fibrosis – a big win for CF advocates. 

  • In May, in a Senate Appropriations Committee hearing on biomedical research, Senator Richard Shelby (R-AL) and Acting NIH Director Raynard Kington, M.D., Ph.D., acknowledged the CF Foundation as a leader in rare disease research

  • In April, the Idaho Adult CF program was protected from funding cuts that would have reduced healthcare services for people with CF in the state. 

  • In January, Senator Patty Murray (D-WA) spoke of the importance of the Children’s Health Insurance Program to Brenna Krug, a 6-year-old child with CF from Marysville, Wash., during a Senate debate. In February, President Obama signed the bill into law, expanding the healthcare program to an additional 4 million children, including many with CF.
Drug Development Pipeline
Cystic Fibrosis Services Pharmacy
The Cystic Fibrosis Foundation is an accredited charity of the Better Business Bureau.