Background: Parents of children with life-limiting illnesses experience considerable burden
and distress, yet few interventions have targeted their well-being. Objectives: Evaluate the …

Introduction Despite palliative care being offered to paediatric cancer patients, it has limited
utilisation and often excludes parental support. Therefore, this review aims to consolidate …

Objective To identify the perceptions of parents of children who died from cancer regarding
the palliative and supportive care they received in hospital and in community settings …

Aims: This feasibility study aimed to systematically identify and address the support needs of
parents of children with life-limiting illnesses and to assess whether the systematic approach …

Objective To obtain feedback from parents of children who died from cancer about their
understanding of palliative care, their experiences of palliative and supportive care received …

Context 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 …

Background: Provision of paediatric palliative care is complex and optimally covers meeting
the individual needs of a heterogenous population of children and their parent caregivers …

Background: Having a child with a life-limiting illness is a situation that is relatively rare and
represents a multidimensional burden on the family. Paediatric palliative care (PPC) aims to …

Purpose The National Consensus Project (NCP) published a set of standards for quality
palliative care delivery. A key step before applying these guidelines to pediatric oncology is …

Background This study examined care needs and utilisation of psychosocial support
services among parents of children who had received specialist paediatric palliative care, as …