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
Press Room
News & Events
2008 News Archive
2007 News Archive
2006 News Archive
2005 News Archive
2004 News Archive
About 65 Roses
Locations
Governance & Policies
Milestones 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 NIH Director Dr. Francis Collins sing a song he wrote for the CF community at the 2009 North American CF Conference.
 Watch NIH Director Dr. Francis 
 Collins sing a song he wrote for
 the CF community at the 2009
 North American CF Conference.

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
Bookmark and Share Display a Printer Friendly Version This Page

CF Foundation Hosts Successful 23rd Annual North American CF Conference

October 21, 2009

More than 3,500 CF researchers and medical professionals from around the world gathered at the CF Foundation’s 23rd annual North American Cystic Fibrosis Conference (NACFC) in Minneapolis, Minn., where they discussed progress and hope in the battle against cystic fibrosis.

Director of the National Institutes of Health (NIH), Francis Collins, M.D., Ph.D., who led the international effort to map the human genome and co-discovered the CF gene in 1989, kicked off the conference with a keynote address and wowed the audience by playing his guitar and singing a song he wrote about CF, “Dare to Dream.”

Robert J. Beall, Ph.D., president and CEO of the CF Foundation, noted the tremendous impact of the CF gene discovery and the progress it has spurred in CF research. Beall told the crowd that the CF community is making headlines around the world for its efforts to treat the basic defect and for advancements in improving the quality of CF care.

In his keynote, Collins reminded the audience of the unique approach the CF Foundation has used to better the lives of people with cystic fibrosis and advance the search for a cure. He noted how the Foundation fosters extraordinary teamwork that unites experts from multiple disciplines, uses cutting-edge technology for drug discovery and formed a clinical trial network to speed the study of drug candidates through clinical trials and to the marketplace.

Many disease organizations, explained Collins, as well as the NIH are following in the Foundation’s footsteps.

Highlights from this year’s NACFC include:

  • The completion of a number of clinical trials of CF therapies, from pancreatic enzyme replacements and new antibiotic treatments to compounds that repair the basic genetic defect.
  • Information on new ways of using old methods to battle the symptoms of CF.
  • A focus on the increasing age of the CF population and the new strategies to focus on the care that adults with CF need.
  • Quality improvement and its effect on health outcomes.

Check back later this week for in-depth conference highlights and video interviews of leading CF researchers and physicians.

 Click Play to View photos highlighting NACFC 2009


     

 

 

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. Click to learn more.
Cystic Fibrosis Services Pharmacy
Shop for gifts and -- at the same time -- support the mission of the CF Foundation.
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.