Survey on Advanced Practice Providers

The CF Foundation’s Community Partnerships is seeking input from patients and families regarding advanced practice providers for CF patients. Here is the text of the announcement: The Cystic Fibrosis Foundation […]

Breathe for Bea Foundation Scholarship

The Breathe for Bea Foundation recently opened their cystic fibrosis scholarship program to people living with CF regardless of their state of residence. The foundation also offers other financial assistance […]

38th Kit Taylor Lecture Recap

The presentation by Dr. Steven Freedman at the 38th Kit Taylor Memorial Lecture met the high expectations we have developed for this annual event. His discussion, Beyond the Lungs – […]

Survey Opportunity: Pain Management

Cystic Fibrosis Foundation, through their Community Voice program, has announced a survey relating to pain management. Here is the text of the announcement: Researchers at Johns Hopkins University are interested […]

Clinical Trial Alerts – March 2018

Cystic Fibrosis Foundation distributed the following clinical trial updates during the month of March. Click the trial title to get more details. The following alert was issued on March 1: […]

Transplant Booklets from Cystic Fibrosis Trust

Cystic Fibrosis Trust, an organization similar to Cystic Fibrosis Foundation that serves the United Kingdom, recently published three booklets that provide information on the various aspects of transplant. Although lung […]

CF Health Guides for Women

The Boston CF Center and Center for Young Women’s Health at Boston Children’s Hospital has produced a series of health guides written specifically for adolescent and young adult women. According to […]