International Charter of Rights

The International Children's Palliative Care Network (ICPCN) has published a Charter of Rights for children with life-limiting or life threatening conditions, which they wish to see accepted and ratified by governments and health departments around the world.

The ICPCN Charter is to be launched to coincide with World Hospice and Palliative Care Day on 11 October 2008.  The theme of this day is "Palliative Care – A Human Right".

According to the United Nations Convention on the rights of the child, every child and young person has the right to the enjoyment of the highest attainable standard of health.  Governments are also required to do everything in their power to ensure that they enjoy full and holistic development.  Children have the right to be protected against abuse, neglect and all forms of ill-treatment.  

In the spirit of the UN Convention, the ICPCN Charter sets out the international standard of support that is the right of all children living with life limiting and life threatening illnesses worldwide, and their families.

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Palliative care action plan for Scotland

Living and Dying Well, the new national action plan for palliative care and end of life care in Scotland (published by NHS Scotland) has been launched by Health Secretary Nicola Sturgeon today (2 October 2008).

ACT, the UK children’s palliative care charity, although disappointed that the action plan does not directly highlight nor recognise the specific needs of children and young people with life-limiting or life-threatening conditions, welcomes the plan’s commitment to ensure that good palliative care and end of life care is available to all patients and families who need it.   ACT says that there are currently about 1200 children in Scotland will not live to reach adulthood.

Although children‘s needs have not been highlighted within the plan, ACT is heartened that the action plan has identified a range of further work that will need to take place in the next two years in order to develop an accessible and cohesive approach to palliative and end of life care, and this includes developing recommendations on appropriate service configurations to meet the needs of adolescents and young people with palliative and end of life care needs.

You can access the Scottish Government Press Release about the action plan here http://www.scotland.gov.uk/News/Releases/2008/10/02113708

You can also download a PDF of the action plan here: http://www.scotland.gov.uk/Publications/2008/10/01091608/0

 
Volunteer nurses needed to support disabled children in Bulgaria

Volunteer nurses urgently required to help in a social care home for disabled children and young adults in Bulgaria.  This is a demanding yet rewarding placement for those who want to care for abandoned and neglected children. Volunteers will spend their time helping the staff to look after the children i.e. feeding and dressing, as well as interacting with them, playing games and providing one on one attention and care. All the children at the home are physically disabled and many of them are bed-ridden and have very complex needs.   Nurses experienced in palliative care or working with disabled children and young adults are sought for a minimum of one month from October as part of a volunteer team of 6.   Accomodation and travel will be arranged by TBACT.

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National Framework for Assessing children’s Continuing Care

The Department of Health has launched its consultation on proposals for a National Framework for assessing children and young people’s continuing care. The Framework is intended to assist Primary Care Trusts to apply a consistent and transparent approach to assessing the healthcare needs of children and young people and to work jointly with local authorities to provide services in the light of those needs.  This Framework will apply in respect of children and young people under the age of 18 years. The closing date for the consultation is 31 December 2008.


You can view the consultation here:

http://www.dh.gov.uk/en/Consultations/Liveconsultations/index.htm

 
Children must not be forgotten in Scotland Action Plan

ACT has welcomed the Audit Review of Palliative Care in Scotland and is encouraged to see that some information about children’s palliative care services had been included, however is disappointed that its primary focus had been on adult palliative care. Information about two of Scotland’s hospices for children, run by CHAS (Children’s Hospice Association Scotland) were included, however the diverse range of non-hospice based services were not audited or included and the Review process has failed to acknowledge the gaps in services for children, young people and their families.

ACT hopes that the forthcoming National Action Plan for Scotland, due to be published by the Scottish Government, in October 2008, will provide an opportunity to redress this imbalance, and a forum to highlight the urgent need for appropriate services for children, young people and their families.  ACT will be working with the Scottish Children’s Palliative Care Network to influence the plan; lobbying to raise awareness of the needs of life-limited children, to highlight the differences between children’s and adult services, and to raise awareness of the need to plan for those young people who need to make the transition from children’s to adult services.  

Lizzie Chambers, Chief Executive of ACT said: “The new Action Plan for Scotland is a real opportunity to move children’s palliative care to the top of agenda, and develop a national strategy for children and young people with life-liming conditions and their families.  We must ensure that these children in Scotland have the same opportunities, support, and policy framework as those life-limited children who live in Wales, England and Northern Ireland.”  

 
ACT launches Networks Project

ACT has launched a new National Networks Project designed to support the roll-out of the Government’s first Children’s Palliative Care Strategy for England, Better Care: Better Lives.

Working alongside the Department of Health, ACT will play a key role in supporting and informing children’s palliative care networks, and has just appointed a dedicated National Networks and Policy Officer to help kick-start the project. The development of a web-based “Network’s Hub” to support this work is also underway.

In some areas dedicated children’s palliative care multi-agency networks already play a key role in improving the outcomes and experiences of children and young people who have complex health conditions or disabilities that will shorten their lives. One of the major recommendations of Better Care: Better Lives is to reinforce the value and strengthen the role of these networks.  The aim of these regional networks is to bring together health and local authority commissioners with all the voluntary and statutory agencies that deliver services to children and their families. ACT believes that these networks should be locally owned and driven by leads in Strategic Health Authorities.   

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