A few weeks ago, while contemplating the trip I was about to take to Washington D.C. to join my fellow advocates for the Cystic Fibrosis Foundation's tenth annual March on the Hill, I challenged myself to "think big." So I sat down in front of the computer and wrote a letter to the President of the United States.
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Katrina Young
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5 min read
Our federal and state advocacy efforts support our mission of ensuring that everyone with cystic fibrosis has access to high-quality, specialized care. We evaluate policies and legislation through one lens: How would this impact people with CF and their families?
Galapagos and Cystic Fibrosis Foundation Therapeutics Sign €1.3 million* Agreement
Press Release
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April 14, 2005
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4 min read
Press Release
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Oct. 3, 2005
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5 min read
The Cystic Fibrosis Foundation's Greater New York Chapter recently recognized leading journalist Scott Pelley at the 14th annual Breath of Life Gala for his unwavering dedication to those living with CF.
News
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Dec. 19, 2017
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2 min read
Cystic Fibrosis Foundation Therapeutics to Provide Alnylam with $1.5 Million in Funding for Discovery Efforts
Press Release
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March 16, 2005
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5 min read
Press Release
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Jan. 12, 2006
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6 min read
Press Release
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Feb. 14, 2006
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3 min read
Press Release
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Jan. 18, 2006
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3 min read
How do you define passion? For me, it's simple. It's the things that I enjoy, the things that I love and the things that I want to do continuously. However, trying to figure out what those things are is not so simple.
Nicholas Kelly
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4 min read