CFF.org is the official website of the Cystic Fibrosis Foundation, a non-profit organization dedicated to finding a cure for cystic fibrosis and improving the quality of life for those with the disease. The site provides comprehensive resources for patients, families, and researchers, including information on treatment options, research updates, and ways to get involved in the fight against cystic fibrosis.
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A tool to help patients and families find cystic fibrosis care centers and specialized treatment options.
Latest news and findings from the cystic fibrosis research community.
Online forums for patients, families, and caregivers to share experiences and support.
Information on upcoming events and how to participate or donate.
Comprehensive guides and materials for understanding cystic fibrosis and its management.
Tools and information to help advocate for policies that benefit the cystic fibrosis community.
Information on current clinical trials and how to participate.
Resources and information on financial aid for cystic fibrosis treatment and care.
Subscription option for the latest news and updates from the Cystic Fibrosis Foundation.
Information on how to volunteer and make a difference in the cystic fibrosis community.
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.
A world without cystic fibrosis.
Bethesda, Maryland, United States.
Michael Boyle, MD (President and CEO), Preston W. Campbell, III, MD (Executive Vice President for Medical Affairs).
https://www.cff.org
Phone: 1-800-FIGHT CF (1-800-344-4823), Email: info@cff.org
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The Cystic Fibrosis Foundation has been recognized for its transparency and efficiency, receiving high ratings from charity watchdog organizations.
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