Pediatric Cystic Fibrosis (CF) | Pediatric Pulmonology

UNC CF Patient Family Advisory Board (PFAB)

The UNC CF clinic invites all parents of children with CF to participate in the Patient Family Advisory Board (PFAB). The PFAB is a group of staff and parents working together to improve to clinic experience and foster connection. The PFAB meets monthly to share ideas, build community, and work on projects to benefit children and families served in our center. The parents on the PFAB offer their experiences and ideas for improvement. They help educate clinic staff about ways to improve the patient and family experience.

Find Family-Centered Care at UNC

At UNC Children’s, you’ll find friendly, compassionate staff who are experts at working with children and families. We’ll do our best to ease your anxiety, help you understand your child’s medical condition so you can make informed choices about their care, and offer whatever additional support you need. You can help make your experience go as smoothly as possible by exploring our patients and visitors section to learn about:

Preparing for your child’s stay
Services and amenities, including play areas
Visiting hours

UNC Cystic Fibrosis Family Newsletter

We are always looking for ways to keep you better informed. Take a look at the CF Family Newsletter, published quarterly. You can help make the newsletter even better but sharing any ideas for the next newsletter or submitting an article to include. If you have a contribution, please contact Kelly Moormann.