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A wealth of advocacy tools for health and mental health professionals at all levels of training and practice are included in this clear and comprehensive volume. Written by medical, legal, and policy experts, it fills a void in the literature by addressing multiple topics in advocacy in the health field as a whole. The text addresses the legislative process, provides step-by-step approaches for using the media, and discusses when to seek an attorney, when to litigate, working with family and community, and funding strategies. It also covers such seldom-addressed topics as leveraging research f
Patient advocacy --- Advocacy, Health care --- Advocacy, Patient --- Health care advocacy --- Nonlegal patient advocacy --- Social patient advocacy --- Medical care --- Advance directives (Medical care) --- Patients' associations --- Quality control
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Most professionals working in health or social care will be required to act as advocates as part of their work. A social worker or community nurse may need to obtain extra benefits or a particular service for a client; a housing official may need to help a tenant whose benefit has been delayed thus placing them at risk of homelessness; a voluntary body may decide to challenge a statement of special educational needs for a child. This is a practical guide to advocacy skills specifically written for those in the health and social care professions. Neil Bateman examines the function of advocacy w
Social advocacy. --- Patient advocacy. --- Advocacy, Health care --- Advocacy, Patient --- Health care advocacy --- Nonlegal patient advocacy --- Social patient advocacy --- Medical care --- Advance directives (Medical care) --- Patients' associations --- Advocacy, Social --- Social service advocacy --- Social work advocacy --- Social service --- Quality control
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Advocacy for people with disabilities is widely practised, but what about self-advocacy? How often do parents or carers speak 'for' you and prevent you being heard? Do you know your rights within advocacy law? The four books in the Speaking Up set were conceived and written specifically to promote self-advocacy to disabled individuals who want to learn how to speak up for themselves. This first book in the series introduces the concept of advocacy and explores appropriate advocacy models, for example peer group supportive models, and examines different forms of advocacy such as campaign advoca
Social advocacy. --- Patient advocacy. --- Advocacy, Health care --- Advocacy, Patient --- Health care advocacy --- Nonlegal patient advocacy --- Social patient advocacy --- Medical care --- Advance directives (Medical care) --- Patients' associations --- Advocacy, Social --- Social service advocacy --- Social work advocacy --- Social service --- Quality control
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Dementia --- Patient advocacy. --- Advocacy, Health care --- Advocacy, Patient --- Health care advocacy --- Nonlegal patient advocacy --- Social patient advocacy --- Medical care --- Advance directives (Medical care) --- Patients' associations --- Patients --- Care. --- Quality control
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Biomedical research today has a high public profile, largely because of patient advocacy. Following in the footsteps of HIV/AIDS activists, advocates representing an array of patient groups are now vocal partners in the research enterprise. This book shows how advocates have transformed health research, often - but not always - for the better. Dresser is the first to examine patient advocacy through the lens of research ethics. She exposes the bright and dark sides of patients' expanded opportunities to enroll in clinical trials and join researchers in planning and evaluating studies. She considers the virtues and drawbacks of giving patients more influence over how the government invests its research dollars. She argues that advocates should do more to promote ethical human studies and responsible media reporting about research. Patient advocates can help make research more ethical, but advocacy raises ethical issues of its own. This book clearly and vividly recounts the advocacy contribution to research and explores the thorny ethical issues facing research advocates. This volume shows how advocates have transformed health research, often - but not always - for the better. Dresser examines patient advocacy through the lens of research ethics. Her book recounts the advocacy contribution to research and explores the thorny ethical issues facing research advocates.
Medical ethics. --- Patient advocacy. --- onderzoeksethiek --- patient advocacy --- wetenschappelijk onderzoek --- éthique de la recherche --- recherche scientifique --- Medical ethics --- Patient advocacy --- Advocacy, Health care --- Advocacy, Patient --- Health care advocacy --- Nonlegal patient advocacy --- Social patient advocacy --- Biomedical ethics --- Clinical ethics --- Ethics, Medical --- Health care ethics --- Medical care --- Medicine --- Moral and ethical aspects --- Advance directives (Medical care) --- Patients' associations --- Bioethics --- Professional ethics --- Nursing ethics --- Social medicine --- Quality control
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Medical Sociology is the among the largest and first subdisciplines in Sociology. It is an area of ongoing work, advancing theory, method and our substantive understanding of social life. This series brings together the newest issues and most current concerns in Medical Sociology, in an ongoing collection of edited volumes. Each volume is edited by a medical sociologist with a particular expertise, bringing together contributions from sociologists working in different settings and nations, exploring one particular advance in Medical Sociology.
Consumers --- Patient advocacy. --- Patients' associations. --- Patients --- Attitudes. --- Patient associations --- Patient organizations --- Patients' organizations --- Advocacy, Health care --- Advocacy, Patient --- Health care advocacy --- Nonlegal patient advocacy --- Social patient advocacy --- Consumer attitudes --- Persons --- Sick --- Voluntary health agencies --- Patient advocacy --- Medical care --- Advance directives (Medical care) --- Patients' associations --- Market surveys --- Consumers' preferences --- Quality control --- Medical sociology. --- Medical --- Health Policy.
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Health. --- Comprehensive Health Care. --- Patient Advocacy. --- #GBIB:CBMER --- Clinical Ombudsman --- Patient Ombudsman --- Patient Ombudsmen --- Patient Representatives --- Advocacy, Patient --- Ombudsman, Clinical --- Ombudsman, Patient --- Ombudsmen, Patient --- Patient Representative --- Representative, Patient --- Representatives, Patient --- Commitment of Mentally Ill --- Patient Rights --- Comprehensive Healthcare --- Health Care, Comprehensive --- Healthcare, Comprehensive --- Family Practice --- Sociology of health --- Hygiene. Public health. Protection --- Health --- Comprehensive Health Care --- Patient Advocacy
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In examining how advocates have transformed health research, the author of this study examines patient advocacy through the lens of research ethics.
Patient advocacy. --- Medical ethics. --- Biomedical ethics --- Clinical ethics --- Ethics, Medical --- Health care ethics --- Medical care --- Medicine --- Bioethics --- Professional ethics --- Nursing ethics --- Social medicine --- Advocacy, Health care --- Advocacy, Patient --- Health care advocacy --- Nonlegal patient advocacy --- Social patient advocacy --- Advance directives (Medical care) --- Patients' associations --- Moral and ethical aspects --- Quality control --- Research --- Moral and ethical aspects.
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When Chicken Soup Isn't Enough brings together compelling personal narratives from a wide range of nurses from across the globe. The assembled profiles in professional courage provide new insight into the daily challenges that RNs face in North America and abroad--and how they overcome them with skill, ingenuity, persistence, and individual and collective advocacy at work and in the community.
Nursing. --- Nursing --- Communication in nursing. --- Patient advocacy. --- Advocacy, Health care --- Advocacy, Patient --- Health care advocacy --- Nonlegal patient advocacy --- Social patient advocacy --- Medical care --- Advance directives (Medical care) --- Patients' associations --- Society and nursing --- Clinical nursing --- Nurses and nursing --- Nursing process --- Care of the sick --- Medicine --- Social aspects. --- Quality control --- Verpleegkunde
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Medical law --- Netherlands --- Sick --- Patient advocacy. --- Legal status, laws, etc. --- Patient Advocacy. --- 316:61 --- -#GBIB:CBMER --- patiëntenrecht --- gezondheidsvoorlichting --- Ill persons --- Persons --- Diseases --- Patients --- Clinical Ombudsman --- Patient Ombudsman --- Patient Ombudsmen --- Patient Representatives --- Advocacy, Patient --- Ombudsman, Clinical --- Ombudsman, Patient --- Ombudsmen, Patient --- Patient Representative --- Representative, Patient --- Representatives, Patient --- Commitment of Mentally Ill --- Patient Rights --- Medische sociologie --- Legal status, laws, etc --- Patient advocacy --- 316:61 Medische sociologie --- Patient Advocacy --- #GBIB:CBMER
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