Update on “Five Feet Apart”

In November, we shared opposing viewpoints concerning the upcoming movie Five Feet Apart. The Cystic Fibrosis Foundation (CFF) has been receiving comments and inquiries reflecting the variations in reactions to […]

Survey Opportunity: Exercise and Airway Clearance

The CF Foundation Community Voice team shared information regarding a new survey opportunity. Their announcement follows. The Evidence Based Child Health Group at the University of Nottingham is working with […]

Active Community Voice Projects

CF Foundation’s community Voice is looking for input on a variety of topics. Here is the text of their request. We wanted to make sure you were aware of the […]

Clinical Trial Alerts – December 2018

Cystic Fibrosis Foundation distributed the following clinical trial updates in December. Click the trial title to get more details. OPTION: Study of AzurRx MS1819 in people with cystic fibrosis and […]

A Daughter’s Perspective on Transplant

We have added a new page to the Our Lung Transplant Story section of the site. A Daughter’s Perspective presents an essay written by the daughter of the transplant recipient. […]

Two Opportunities for Input Regarding Your Care

CFF’s Community Voice has issued requests for input on two different aspects of CF care. Here are the announcements including links to the online surveys. ENT Guidelines – Deadline November […]