Category Archives: CHILDREN’S PALLIATIVE CARE

What it means to be a parent of a dying child

Kristina Thomas, Senior Research Fellow and Anna Collins, Research Fellow, Centre for Palliative Care, St Vincent’s Hospital Melbourne, Australia, explain the background to their longer article selected as ‘Editor’s choice’ in the December issue of Palliative Medicine.  We have been … Continue reading

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2016 – the year we raised more awareness about children’s palliative care in Norway

Continuing our series of posts, in collaboration with the European Association for Palliative Care (EAPC) Paediatric Taskforce, about children’s palliative care with examples of initiatives that aim to improve care for children, young people and their families. Today, Natasha Pedersen, … Continue reading

Posted in ADVOCACY & POLICY, Children and young people, CHILDREN'S PALLIATIVE CARE, EAPC Taskforces/special projects | Tagged | 1 Comment

The ICPCN – networking palliative care globally

Contininuing our series of posts, in collaboration with the European Association for Palliative Care (EAPC) Paediatric Taskforce, about children’s palliative care with examples of initiatives that aim to improve care for children, young people and their families. Today, Professor Julia … Continue reading

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New development for Irish children’s palliative/complex care nursing

Continuing our series of posts, in collaboration with the European Association for Palliative Care (EAPC) Paediatric Taskforce, about children’s palliative care with examples of initiatives that aim to improve care for children, young people and their families.  Today, Claire Quinn, … Continue reading

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Please don’t get my Independence confused with my Ability . . .

Continuing our series of posts, in collaboration with the European Association for Palliative Care (EAPC) Paediatric Taskforce, about children’s palliative care with examples of initiatives that aim to improve care for children, young people and their families. Today, we hear … Continue reading

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Paediatric Comfort Teams – a step forward in realising paediatric palliative care in the Netherlands

Continuing our series of posts, in collaboration with the European Association for Palliative Care (EAPC) Paediatric Taskforce, about children’s palliative care with examples of initiatives that aim to improve care for children, young people and their families. Today we hear … Continue reading

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The Trieste Charter – The Charter of the Rights of the Dying Child

Continuing our series of posts, in collaboration with the European Association for Palliative Care (EAPC) Paediatric Taskforce, about children’s palliative care with examples of initiatives that aim to improve care for children, young people and their families. Today, Giovanna Abbiati … Continue reading

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