Our vision is that every child, regardless of their health condition, receives the palliative care support they need to live life to the fullest. Our mission is to catalyse change, scale investments, and build a supportive community to advance paediatric palliative care globally.

Together, we’re building a community of locally rooted, globally connected initiatives to transform children’s palliative care worldwide.

What do we mean by children’s palliative care?


Children’s palliative care is the full continuum of care for children with life-limiting and life-threatening conditions, giving them and their families space, be that emotional or physical, to enjoy the best possible quality of life. Palliative care includes pain management, relief from distressing symptoms, respite breaks for families, care at the end of life, and bereavement support. It can be provided in children’s hospices, hospitals, tertiary care facilities, community health centres, and children’s own homes.



Access to children’s palliative care is a human right. According to the United Nations Committee on the Rights of the Child, "children are entitled to quality health services, including prevention, promotion, treatment, rehabilitation and palliative care services.’’

Children’s palliative care is an essential part of the continuum of care for all patients. The UN Sustainable Development Goal 3 and the World Health Assembly also affirm this central principle.