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our journey.
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The mission of the Cystic Fibrosis Foundation, a nonprofit donor-supported organization, is to assure the development of the means to cure and control cystic fibrosis and to improve the quality of life for those with the disease.
The Foundation is the leading organization in the United States devoted to cystic fibrosis. It has more than 80 chapters and branch offices nationwide and funds and accredits 115 CF care centers across the country, including 94 adult care programs, which provide patients and families with vital treatment and other CF resources. In addition, 54 affiliate programs provide multi-disciplinary care for CF with Foundation support.
The Foundation is one of the most efficient organizations of its kind. In 2006, nearly 90% of every dollar of revenue raised was available for investment in CF research, care and education programs. The National Institutes of Health and many prominent publications, including Forbes and USAToday , have heralded our innovative business model, which fuels drug discovery and development programs.
The Cystic Fibrosis Foundation Is...Hope in Action
Until we conquer this disease, our team will work tirelessly to extend and enhance life for those with cystic fibrosis by functioning as:
The Cystic Fibrosis Foundation Is...Building on Success