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
Many Ways to Give
Volunteer
Become a Corporate Partner
Foundation Events
Give Us Your Ideas
Become an Advocate
Public Policy Agenda
Tell Your Story
Take Action Now
Action Alert!
Advocacy Toolkit
Call Your Member
Write Your Member
Visit Your Member
Thank Your Member
Tips to Tell Your Story
You Can Do This!
Advocacy Achievements
News and Events
Congressional CF Caucus
Newborn Screening
Make Every Breath Count
Participate In A Clinical Trial
Improve Your CF Care
Shop the Marketplace
Buy Limited Collectibles
Request Mailing Labels
65 Roses Collection Store
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

 Lewis Black and others in the CF community share their dreams of a cure for CF. Click to watch.
 Lewis Black and others in the CF
 community share their dreams of
 a cure 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

Senator Shelby and Acting NIH Director Raynard Kington Praise CF Foundation at Hill Hearing and Call for Ongoing Funding

May 28, 2009

Senator Richard Shelby (R-AL), a champion of CF research, spoke at length about advances in CF research during a Senate Appropriations Committee hearing last week. He addressed the critical need for increased research funding for rare diseases like CF.

During the hearing, Acting NIH Director Raynard Kington, M.D., Ph.D., and other NIH institute directors, praised the work of the CF Foundation and the CF community. “The CF community is in many ways held up as a good example of how a community affected by a disease can work collaboratively with the research community to facilitate translation,” said Kington.

Also during the hearing, Shelby, Kington and Elizabeth G. Nabel, M.D., director of the National Heart, Lung, and Blood Institute, suggested that NIH mirror the Foundation’s successful clinical trials network (also known as the Therapeutics Development Network), and its research model to gain better results for rare disease research.

“If we take a minute and reflect on the progress that’s been made in cystic fibrosis, it’s been remarkable over the past decade,” Nabel said. Nabel also cited recent media coverage the CF Foundation received in the The New Yorker.

Make a donation to the Cystic Fibrosis Foundation.
Sign up to get the latest news and information.
It's Time to Take GREAT STRIDES! Your steps TODAY will help find a cure for cystic fibrosis. Register for a walk near you!
Help discover and develop potential new treatments for CF by enrolling in a clinical trial.
The Cystic Fibrosis Foundation is an accredited charity of the Better Business Bureau.   The Cystic Fibrosis Foundation has a 4-star rating from Charity Navigator, America's largest independent evaluator of charities.