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A hub of information for journalists interested in writing about the CF Foundation that includes direct links to learn more about CF, the Foundation, and our latest news.
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.
Welcome to the Cystic Fibrosis Foundation! We're glad you're here.
Child just diagnosed? You may have a lot of feelings and questions, and may not know where to start. We've 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.
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.