
Family caregivers of children with cystic fibrosis need more than just medical information. The informational needs of family caregivers for children with cystic fibrosis (CF) in a public hospital were explored, focusing on the role of Patient and Family-Centered Care (PFCC). Thirteen caregivers participated in interviews, revealing three key themes: types and sources of information and the need for emotional support and family involvement. The study emphasizes the importance of PFCC, highlighting the need for information sharing and emotional support in CF management.
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