Each year, researchers and care team members gather at the North American Cystic Fibrosis Conference to share their research on how to improve the lives of people with cystic fibrosis. The three ...

Balancing college and working full-time while managing my cystic fibrosis can be challenging. However, I have tips and insights that have helped me juggle my academic and professional responsibilities ...

Through grants, advocacy, and the development of a consensus guideline, the Cystic Fibrosis Foundation continues to advance its Newborn Screening Initiative, pushing for better newborn screening ...

This site contains general information about cystic fibrosis, as well as personal insight from the CF community. Opinions and experiences shared by members of our community, including but not limited ...

Have you ever wondered if there was something else going on with you? Something else affecting you that you were not aware of? Well, I felt that way. Ever since I was young, I have always struggled ...

I imagine most people have vivid memories of the first date they went on with their spouse. Emily took me on a hike through Will Rogers State Park in Los Angeles. It was a perfect, blue-sky, Southern ...

The Delaware Valley Chapter - Philadelphia Office of the Cystic Fibrosis Foundation welcomes you! Volunteers are the key to our success and the lifeblood of our organization. We have many ...

Help make CF stand for Cure Found. Give Once Give to a Walker Other Ways to Give ... Footer Life with CF Intro to CF Managing CF Research & Clinical Trials CF Community ...

All 15 centers focus on improving the transplant journey for people with CF, including transplant referrals and post-transplant care management. The consortium helps support the Lung Transplant ...

The Gateway Chapter of the Cystic Fibrosis Foundation welcomes you! Volunteers are the key to our success and the lifeblood of our organization. We have many opportunities for you to get involved.

As a person with cystic fibrosis who can’t benefit from modulators, I believe it is my responsibility to use my position on a Cystic Fibrosis Foundation research committee to advocate for others like ...