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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 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:
- Scientific pioneers, blazing new trails in CF research;
- Fund-raisers, securing the money needed to support our efforts;
- Advocates, keeping CF a top priority in government, industry and research;
- Investors, funding drug discovery and development;
- Caregivers, linking patients and families to specialized CF care; and
- Family, offering support, information and resources.
The Cystic Fibrosis Foundation Is...Building on Success
- When the Foundation was established in 1955, children with CF were not expected to live long enough to attend elementary school. Due in large part to the Foundation's aggressive investments in innovative research and comprehensive care, the predicted median survival age for people with this disease is now more than 37 years.
- In 1989, CF Foundation-supported scientists discovered the defective gene that causes cystic fibrosis--a monumental breakthrough on the road to a cure.
- The Foundation has played an integral role in the development and FDA approval of four therapies that are now a routine part of treatment regimens for many with CF. The Foundation is actively supporting more than 30 potential new treatments currently in development--that's more than in the entire history of the disease. Our challenge is to find enough patients to join clinical trials to keep the research moving forward.
- Anna Frumes
- (323) 655-8525
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