The International Children’s Palliative Care Network (ICPCN) is the only global organisation working to improve access to palliative care for the more than 21 million children worldwide who need it. ICPCN is recognised as the world leader in children’s palliative care (CPC) and has a globally renowned expert leadership, a wealth of educational resources and a network of members in over 140 countries.
Through its network, ICPCN are uniquely placed to advise, educate and support at a national, regional and international level on best practice in CPC. As a central repository for information relating to CPC, and with a global perspective of what is happening in the field, ICPCN are in an ideal position to strategically advocate for the development and improvement of services, the creation of palliative care policies, that include children and their families, and the implementation of these policies, thus increasing access to CPC.
Established in 1988, The European Association for Palliative Care (EAPC) is a membership organisation committed to supporting the promotion and development of palliative care throughout Europe and beyond. Recognised by the Council of Europe, EAPC aims to speak with ‘one voice and one vision’ on matters that are important in palliative care. To do so, we recognise the definition of palliative care set out by the World Health Organisation.
Respectful of the cultural and political diversity of our members, the EAPC provides a forum for all of those either working or with an interest in palliative care. EAPC works in close collaboration with our members, research partners and other European and international agencies. Through our significant networks, we advocate, anticipate and proactively shape EU health and research policies on palliative care issues. We raise awareness about palliative care and the value and benefits it can have for individuals, healthcare services and communities.
The EAPC represents and is open to members from associations and individuals in Europe and throughout the world. Members are engaged in palliative care across the lifespan and trajectories from a range of perspectives: specialist and generalist clinical practice, professional groups and public, education, advocacy, and research.