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You may have a lot of questions, and may not know where to start. While there is a wealth of information available, we pulled together a few of the key things you should know, and sources of help and support, right here on this page. Keep reading. You're in the right place.
Hearing from diverse voices is critical as we continue our journey to listen, learn, and take action against racism and discrimination.
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3 min read
To request use of trademarked or copyrighted material from the CF Foundation, please complete this materials permission request form.
Since 2011, the Foundation has awarded $2.5 million across 35 different projects to improve cystic fibrosis newborn screening across the country.
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4 min read
Welcome to the Cystic Fibrosis Foundation! We're glad you're here.
Every spring, the cystic fibrosis community comes together for National Volunteer Week. We are so grateful for our incredible volunteers and their dedication to the CF community.
Funding will support a Phase 2b trial of phage therapy for chronic Pseudomonas aeruginosa lung infections.
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2 min read
The mission of the Cystic Fibrosis Foundation is to cure cystic fibrosis and to provide all people with CF the opportunity to lead long, fulfilling lives by funding research and drug development, partnering with the CF community, and advancing high-quality, specialized care.
This year’s program marked the largest in-person advocacy event in the Foundation’s history.
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3 min read
Learn how we fund research, how to navigate our grants management system as both an applicant and awardee, and key research priorities to keep in mind to maximize your potential for being funded.