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  • A House Called Helen: The Development of Hospice Care for Children

    A House Called Helen by Worswick, Jacqueline;

    The Development of Hospice Care for Children

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      • Publisher's listprice GBP 51.00
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    Product details:

    • Edition number 2
    • Publisher OUP Oxford
    • Date of Publication 30 November 2000

    • ISBN 9780192632357
    • Binding Paperback
    • No. of pages268 pages
    • Size 216x138x16 mm
    • Weight 367 g
    • Language English
    • Illustrations 36 black and white photographs
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    Short description:

    When the first edition of A House Called Helen was published in 1993, there were only a handful of children's hospices in existence, all of them within the UK. There are now more than twenty in operation, and a significant number at the project stage, in the UK alone, and children's hospices have been set up in Canada, the USA, Australia and continental Europe. The concept of a children's hospice, seen as innovative when the first, Helen House, opened in Oxford in 1982, is now well established and the growth in the number of children's hospices has seen corresponding important developments in the field of paediatric palliative care.
    This book provides an authoritative account of how Helen House came into being. It records the events surrounding the foundation of the hospice and how it stemmed directly from what was learnt from the events following the sudden illness of the author's eldest daughter Helen, after whom it was named. The book sets out the philosophy that underpinned the hospice, which was taken up as the guiding philosophy of children's hospice care. It describes the hospice's operational framework and details the service provided by Helen House, which is widely cited as a model for children's hospice care worldwide. It provides valuable insight into the needs of the families who use hospice services and touches both on the difficulties they face caring, often over a long period of time, for a child with a life-limiting illness, and on the role and attitudes of professionals and indeed of the public at large.
    In this new edition an additional chapter reviews the growth of children's hospices and reflects on the challenges they face in their maturity. It considers the development of children's hospice care in relation to wider service provision and examines current and future issues surrounding the care of children with life-limiting illness.
    "The book will be essential reading for individuals training in the field of palliative care and is important for any professional or lay person involved in the care of seriously ill children." Professor Clifford C. Bailey, Consultant Paediatric Oncologist, United Leeds Teaching Hospitals Trust and Director of Research and Development, NHS Executive, Northern and Yorkshire, UK

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    Long description:

    When the first edition of A House Called Helen was published in 1993, there were only a handful of children's hospices in existence, all of them within the UK. There are now more than twenty in operation, and a significant number at the project stage, in the UK alone, and children's hospices have been set up in Canada, the USA, Australia and continental Europe. The concept of a children's hospice, seen as innovative when the first, Helen House, opened in Oxford in 1982, is now well established and the growth in the number of children's hospices has seen corresponding important developments in the field of paediatric palliative care.
    This book provides an authoritative account of how Helen House came into being. It records the events surrounding the foundation of the hospice and how it stemmed directly from what was learnt from the events following the sudden illness of the author's eldest daughter Helen, after whom it was named. The book sets out the philosophy which underpinned the hospice, which was taken up as the guiding philosophy of children's hospice care. It describes the hospice's operational framework and details the service provided by Helen House, which is widely cited as a model for children's hospice care worldwide. It provides valuable insight into the needs of the families who use hospice services and touches both on the difficulties they face caring, often over a long period of time, for a child with a life-limiting illness, and on the role and attitudes of professionals and indeed of the public at large.
    In this new edition an additional chapter reviews the growth of children's hospices and reflects on the challenges they face in their maturity. It considers the development of children's hospice care in relation to wider service provision and examines current and future issues surrounding the care of children with life-limiting illness.

    Will be of interest to anyone involved in paediatric palliative care.

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    Table of Contents:

    Introduction
    Helen's illness
    Home from hospital
    Frances and Helen
    Planning the hospice
    The vision becomes reality
    After the opening
    The philosophy at work
    Reflections on years of caring
    Conclusion
    Into the new millennium

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