Tag Archives: CHILDREN’S PALLIATIVE CARE

Interventions at the end of life in children: Where evidence meets experience

Posted on July 26, 2021 by pallcare

NEW SERIES: EXPLORING NEW DIMENSIONS AT #EAPC2021 … There are just 73 days to the 17th World Congress Online of the European Association for Palliative Care (EAPC). With live sessions on 6 to 8 October, and lots of on-demand content … Continue reading →

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Becoming a research expert in paediatric palliative care: 10 top tips at the Meet-the-Experts session #EAPC2020

Posted on September 14, 2020 by pallcare

Only 23 days to #EAPC2020 … The 11th World Research Congress of the European Association for Palliative Care which, for the first time, will take place online with live interactive sessions on 7 to 9 October. Professor Joanne Wolfe (USA) and Professor … Continue reading →

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Together We Can: Free resources to help you set up a volunteering support service for families of sick children

Posted on February 7, 2018 by pallcare

Lizzie Chambers, Development Director, Together for Short Lives, UK, rolled up her sleeves to volunteer in the home of a family caring for a child with a life-limiting condition. Lizzie explains how her organisation has developed the Family Support Volunteering … Continue reading →

Posted in CHILDREN'S PALLIATIVE CARE, VOLUNTEERING IN PALLIATIVE CARE | Tagged , | Leave a comment

What it means to be a parent of a dying child

Posted on December 9, 2016 by pallcare

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 →

Posted in CHILDREN'S PALLIATIVE CARE, EAPC-LINKED JOURNALS, Palliative Medicine: Editor's Choice | Tagged , | Leave a comment

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

Posted on November 28, 2016 by pallcare

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'S PALLIATIVE CARE, EAPC Task Forces/Reference Groups | Tagged | 1 Comment