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The mission of the Cystic Fibrosis Foundation is to cure cystic fibrosis and to provide all people with the disease the opportunity to lead full, productive lives by funding research and drug development, promoting individualized treatment, and ensuring access to high-quality, specialized care.
The Cystic Fibrosis Foundation is the world’s leader in the search for a cure for cystic fibrosis, a life-threatening genetic disease that affects 30,000 children and adults in the United States, and 70,000 people worldwide. The Foundation has raised and invested hundreds of millions of dollars to help develop CF drugs and therapies. Through our efforts, the life expectancy of a child with CF has doubled in the last 30 years, and research to find a cure is more promising than ever before.
- Amanda Hodge
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