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The Foundation is here for you. Whether you're looking to talk to someone, find your local chapter or care center, or read some additional information, we have plenty of resources to help.
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.
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.
In addition to the typical travel headaches, people with cystic fibrosis must also consider other things related to their health. This section will discuss ways to be as prepared as possible for your trip so that you can spend less time on travel hassles and more time enjoying yourself.
La Fundación de Fibrosis Quística está buscando una cura para cada persona con FQ. No descansaremos hasta encontrarla. Mientras tanto, le ofrecemos apoyo y información para ayudarle a vivir lo mejor posible.
To request use of trademarked or copyrighted material from the CF Foundation, please complete this materials permission request form.
We hold ourselves accountable to our donors, volunteers, people with CF and their families, and the public. Learn about our governance and policies.
The CF Community Blog highlights voices from across the CF community, touching on all aspects of life with cystic fibrosis.
If your company would like to request an investment from the CF Foundation, please complete this form. Attach a non-confidential slide deck and up to three supporting non-confidential documents that describe the innovation and high-level business and development plan.
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.