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Caring for a child who will die from a life-limiting illness is one of the most difficult experiences a parent may face. Pediatric palliative care (PPC) has grown as a specialty service to address the unique needs of children and families with serious illness. However, gaps remain between the needs of families in PPC and the support received. The objective of this study was to explore the concerns of parents who have a child in home-based PPC. Semistructured interviews were conducted with 25 mothers and 10 fathers from 25 families short