Book edited by Marie Fallon and Bill O'Neill. User friendly guide to the palliative care of patients with incurable diseases, taking a practical, easy to follow approach to this complex subject.
Book by Tim Albert. The purpose of this book is to help doctors and other health professionals with their writing problems. It consists of several hundred topics, from the process of writing to authorship, and from the use of semi–colons to the law of late literals. These are arranged alphabetically, with extensive cross referencing and, where appropriate, lists of books that the author has read and recommends. The book will provide concise, practical information about how to tackle any form of writing required of health care professionals.
Article by John D Springer.
Charity providing information and support for new and established befriending projects, helping them to develop effectively and efficiently by sharing experience and practice between projects.
Authoritative report from the Department for Business, Enterprise and Regulatory Reform; of benefit to those working with low income families and providing money-management and debt advice.
Membership organisation setting standards for therapeutic practice and provides information for therapists, clients of therapy, and the general public.
Book by David Jeffrey. When a patient needs specialised palliative care, the GP can lose touch, and can feel divorced from the palliative care system. Using many actual quotes from practising GPs, this book highlights the dilemmas faced by GPs struggling to provide high standards of palliative care in the community.
Families and Communities: a Caring System on Your Side, a Life of Your Own. 2008 Department of Health publication outlining the role played by carers in society, the role of government & health services, and the future of the relationship between them.
Carers Direct Review 2012: "Review of national arrangements for providing information and advice to carers"
Published August 8th 2012; Department of Health assessment of the online information resource, Carers Direct.
Practical guide to effective communication between health professionals and cares of older people, reflecting their specific needs.
Book by Keri Thomas. Aiming to strengthen the role, confidence, systems and skills of primary health care teams (PHCTs) for the delivery of palliative care and patient support, this is a comprehensive resource book to support and enable primary care professionals to make improvements in the care provided for their patients.
Delivery materials for the carer support programme, now hosted by the NHS Choices website.
The Centre for Death and Society (CDAS) is the UK\\\'s only centre devoted to the study and research of social aspects of death, dying and bereavement. Established in September 2005, CDAS is an interdisciplinary centre of regional, national and international importance. It provides a centre for the social study of death, dying and bereavement and acts as a catalyst and facilitator for research, education and training, policy development, media, and community awareness.
Centre for Mental Health - No health without mental health: guides for local services
This series of briefings aim to help develop better local mental health services. Following the publication of the implementation framework for the government’s mental health strategy, these briefings set out the steps that local authorities, CCGs, and those involved with Healthwatch and health and wellbeing boards can take to improve mental health care, treatment and support:
- CCG briefing
- Local Healthwatch briefing
- Health and wellbeing board briefing
- Directors of Public Health briefing
- Local authorities briefing
- Overview and scrutiny committees briefing
- Centre for Mental Health - press release
By the American College of Chest Physicians. Practical guide for professionals on dealing with relatives of the dying.
News and information for everyone working with children, young people, and families.
Book edited by Sheila Payne and Caroline Ellis-Hill. Holistic approach to care, for professionals.
Book by Jean Lugton. Exploring the emotional problems patients, relatives, close friends and professionals experience and the support they need when someone is dying, this book focuses on the skills required to support the patient and to provide pre- and post-bereavement counselling for relatives.
National specialist infrastructure and membership organisation, focusing on the development and support of LGBT groups, organisations and projects; so they can deliver direct services and campaign for individual rights.
National Autistic Society information for police officers, solicitors, barristers, magistrates, justices of the peace, the judiciary and the courts etc on recognizing autism and strategies for dealing with people affected by it.
Book by David Barnard et al. Case narratives following individual patients and families throughout the course of illness and death in the context of hospice and palliative care. Using a variety of qualitative research methods, including participant-observation, interviews, and journal-keeping, the experiences, perceptions, and feelings of the patient, the family and a range of caregivers are recorded, providing multi-textured narratives.
Article by Leah Abramowitz. Perspectives on end of life by palliative care professionals.
Promoting high quality care for all adults at the end of life. (2008)
From the Department of Health; The aim of this document is to help local mental health services develop support services for carers of people with mental health problems. It contains guidance on developing and sustaining mental health carer support services and also includes a sample job description for carer support workers.
DVD and booklet by Connie Wiskin. Visual, interactive training experience, linking with supportive care frameworks to improve this difficult and highly sensitive area of communication. The DVD contains filmed scenes illustrating a range of challenging dialogues between health workers and a patient and his family through the journey of his terminal illness, the accompanying booklet highlights communication issues with suggested exercises, reflection points and advice.
SCIE\\\'s Dignity in Care guide been designed for people who want to make a difference by improving standards of dignity in care.
Online training course and information toolkit. Accreditation demonstrates knowledge of who is classified \\\'carer\\\', carers\\\' rights, support available in the Dudley Borough etc.
Subscription required to view articles.
Developed by the Royal College of Nursing & Royal College of General Practitioners.
Supporting black and minority ethnic family carers; a resource for practitioners. This site has been funded by the Department of Health in order to provide an understanding of the needs of black and minority ethnic family carers and best practice support.
Book by Stephen C Lundin, Harry Paul and John Christensen. In this engrossing parable, a fictional manager has the responsibility of turning a chronically unenthusiastic and unhelpful department into an effective team, based on lessons learned from the world famous Pike Place Fish market in Seattle.
Provides education about life-threatening illness and end of life care. Growth House aims to improve the quality of compassionate care for people who are dying through public education and global professional collaboration. Our search engine gives you access to the Internet\\\'s most comprehensive collection of reviewed resources for end-of-life care.
Article by Richard Humphries et al.
Article by Jonathan Lawrence, Positive Health Online.
Supports health and social care staff working with people nearing the end of life (Policy, education, research, commissioning).
Umbrella charity for all those involved in palliative, end of life and hospice care in England, Wales and Northern Ireland. Believes everyone approaching the end of life has the right to the highest quality care and support, wherever they live, and whatever their condition. Works with government, health and social care staff and people with personal experience to improve end of life care for all.
DVD film by Amanda Waring. One of several DVD’s and training packs around dignity in care.
Book by Elisabeth Kubler-Ross. Compassionate discussion on communicating openly with the dying patient.
Book edited by D. J. Enright. An anthology of poems and prose.
Book by Richard Hain and Satbir Singh Jassal
Book by Derek Doyle and David Jeffrey
Book by Linda L Emanuel and S Lawrence Librach
Book edited by Declan Walsh
A project to collect and distribute digital stories of patients to develop more patient-shaped healthcare.
Book by George Gawlinski and Lois Graessie
Book by Rodger Charlton
Learning module; Professor Mayur Lakhani, chair of the National Council for Palliative Care, suggests 10 ways GP commissioners can improve care for their dying patients (site membership required).
Assisting commissioners and providers in defining who really is a \\\'quality provider\\\' of today\\\'s self management support services. Download introductory leaflet here.
Works with children and adults with learning disabilities, their families and supporters, aiming to lessen the effect of abuse or trauma, through psychotherapy, advocacy, campaigning and other support.
Gives voice to those with serious illness, who are often marginalised and isolated. The use of film and media for health advocacy is central to all Rosetta Life projects. A collection of Rosetta Life films can be viewed on the website. Useful evidence for training and care education.
Aims to reclaim grace and dignity for the dying, refocus attention on the spiritual aspects of the end-of-life process. Resources include vigil training, dispelling anger.
Article by S Bird et al, featured in Nursing Times. Discusses providing best environment for relatives of those hearing bad news or dealing with end of life issues.
Consortium of eight Shropshire based voluntary sector organisations, all of which provide support to other voluntary and community groups across Shropshire. Established to support, develop, coordinate and promote voluntary and community groups to help them to deliver their work more effectively.
Ensures that England\\\'s adult social care workforce has the appropriately skilled people in the right places working to deliver high quality social care. focussing on the attitudes, values, skills and qualifications people need to undertake their roles. Works closely with organisations that employ adult social care workers, together with people who use services, carers and other key partners to develop effective tools and resources that meet the workforce development needs of the sector.
Exists to promote best practice in bereavement care. Membership benefits include professional development, publications, training days etc.
An online paper outlining ways to identify and help carers through the GP surgery team.
Article by G Grande et al, featured in Palliative Medicine Vol.23 No.4, June 2009.
Book by David Jeffrey. Practical teaching techniques. Accessible, practical and easy-to-use, it should encourage busy clinicians to teach by increasing their confidence in their training abilities. It provides a resource of various tools and describes how to approach teaching in a team, planning, methods and evaluation.
Book by David Werner et al. Widely-used health care manual for work in developing countries. Information about recognising, treating and preventing common illnesses and injuries. Also covers home remedies, modern medicines, cleanliness, diet, vaccination, childbirth and family planning.