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Voices from 25 Years of Hospice Care

Voices from 25 Years of Hospice Care
Author: Neil Gadsby
Publisher:
Total Pages: 79
Release: 2016
Genre: Hospices (Terminal care)
ISBN: 9780955519512

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Hospice Voices

Hospice Voices
Author: Eric Lindner
Publisher: Rowman & Littlefield Publishers
Total Pages: 235
Release: 2013-10-08
Genre: Medical
ISBN: 1442220600

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As a part-time hospice volunteer, Eric Lindner provides “companion care” to dying strangers. They’re chatterboxes and recluses, religious and irreligious; battered by cancer, congestive heart failure, Alzheimer’s, old age. Some cling to life amazingly. Most pass as they expected. In telling his story, Lindner reveals the thoughts, fears, and lessons of those living the ends of their lives in the care of others, having exhausted their medical options or ceased treatment for their illnesses. In each chapter, Lindner not only reveals the lessons of lives explored in their final days, but zeroes in on how working for hospice can be incredibly fulfilling. As he’s not a doctor, nurse, or professional social worker, just a volunteer lending a hand, offering a respite for other care providers, his charges often reveal more, and in more detail, to him than they do to those with whom they spend the majority of their time. They impart what they feel are life lessons as they reflect on their own lives and the prospect of their last days. Lindner captures it all in his lively storytelling. Anyone who knows or loves someone working through end of life issues, living in hospice or other end of life facilities, or dealing with terminal or chronic illnesses, will find in these pages the wisdom of those who are working through their own end of life issues, tackling life’s big questions, and boiling them down into lessons for anyone as they age or face illness. And those who may feel compelled to volunteer to serve as companions will find motivation, inspiration, and encouragement. Rather than sink under the weight of depression, pity, or sorrow, Lindner celebrates the lives of those who choose to live even as they die.


The Hospice Heritage

The Hospice Heritage
Author: Inge B. Corless
Publisher: Routledge
Total Pages: 0
Release: 1999
Genre: Hospice Care
ISBN: 9780789008473

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Practitioners celebrate the 25th anniversary of the movement in the US and the 20th anniversary of the National Hospice Organization. In 19 essays they trace the origins and history, then look at such issues as symptom control, spirituality, and access to care and current efforts such as hospice versus palliative care, patient and family voices in measuring quality of care, and documenting impact. They also include personal reflections and reminiscences. Paper edition (unseen), $29.95. The anthology is published simultaneously as The Hospice Journal vol. 14, nos. 3/4 (1999). Annotation copyrighted by Book News, Inc., Portland, OR


Hospice Voices

Hospice Voices
Author: Eric Lindner
Publisher: Rowman & Littlefield
Total Pages: 233
Release: 2013-10-08
Genre: Medical
ISBN: 1461742056

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As a part-time hospice volunteer, Eric Lindner provides “companion care” to dying strangers. They’re chatterboxes and recluses, religious and irreligious; battered by cancer, congestive heart failure, Alzheimer’s, old age. Some cling to life amazingly. Most pass as they expected. In telling his story, Lindner reveals the thoughts, fears, and lessons of those living the ends of their lives in the care of others, having exhausted their medical options or ceased treatment for their illnesses. In each chapter, Lindner not only reveals the lessons of lives explored in their final days, but zeroes in on how working for hospice can be incredibly fulfilling. As he’s not a doctor, nurse, or professional social worker, just a volunteer lending a hand, offering a respite for other care providers, his charges often reveal more, and in more detail, to him than they do to those with whom they spend the majority of their time. They impart what they feel are life lessons as they reflect on their own lives and the prospect of their last days. Lindner captures it all in his lively storytelling. Anyone who knows or loves someone working through end of life issues, living in hospice or other end of life facilities, or dealing with terminal or chronic illnesses, will find in these pages the wisdom of those who are working through their own end of life issues, tackling life’s big questions, and boiling them down into lessons for anyone as they age or face illness. And those who may feel compelled to volunteer to serve as companions will find motivation, inspiration, and encouragement. Rather than sink under the weight of depression, pity, or sorrow, Lindner celebrates the lives of those who choose to live even as they die.


Hospice and Palliative Care Handbook, Fourth Edition: Quality, Compliance, and Reimbursement

Hospice and Palliative Care Handbook, Fourth Edition: Quality, Compliance, and Reimbursement
Author: Tina M. Marrelli
Publisher: Sigma Theta Tau
Total Pages: 246
Release: 2023-06-23
Genre: Medical
ISBN: 1646480856

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“This book is a perfect blend of compassion and competence that addresses the core values of care, the interdisciplinary team, self-care of staff, and the needs of an aging society.” –Betty Ferrell, PhD, FAAN, FPCN, CHPN Professor and Director, Nursing Research, City of Hope Medical Center Principal Investigator, End-of-Life Nursing Education Consortium “A must-read for all hospice providers. It is a comprehensive overview of the core elements required to practice effectively, compliantly, safely, and compassionately. An indispensable addition to all hospice libraries.” – Kim Corral, MA Ed, BSN, RN, COS-C Director of Corporate Compliance, Quality and Education Bridge Home Health and Hospice “I have utilized Tina Marrelli’s home health and hospice handbooks to support training new clinical staff and students for decades and consider these resources to be the gold standard.” – Kimberly Skehan, MSN, RN, HCS-D, COS-C Vice President of Accreditation Community Health Accreditation Partner Hospice & Palliative Care Handbook, Fourth Edition, offers updated coverage of all aspects of hospice and palliative care for the entire healthcare team who provide important care while meeting difficult multilevel regulations. This edition includes examples and strategies covering key topics related to standards, guidelines, goals, and effective care planning. TABLE OF CONTENTS Prologue: Hospice and Covid-19: A Pandemic Part 1: Hospice Care: An Overview of Quality and Compassionate Care Part 2: Documentation: An Important Driver for Care and Coverage Part 3: Planning, Managing, and Coordinating Hospice Care Part 4: Hospice Diagnoses and Guidelines for Care Alzheimer’s Disease and Other Dementias Care Bedbound, Coma, and Skin Care Cancer Care Cardiac and Cerebrovascular Accident (Stroke) Care Frailty and Geriatric Care Liver Disease Care Neurological Disease Care Pediatric Care: A Very Special Patient Population Pulmonary Care Renal Disease Care Skin and Wound Care Resources ABOUT THE AUTHORS TINA. M. MARRELLI, MSN, MA, RN, FAAN, is the author of over 10 award-winning books. She is an international consultant specializing in home care and hospice and is the President of Marrelli & Associates, Inc., a publishing and consulting firm working in healthcare and technology for over 25 years. JENNIFER KENNEDY, EdD, BSN, RN, CHC, is the Vice President for Quality, Standards, and Compliance at Community Health Accreditation Partner (CHAP) and is a nationally recognized hospice expert. She has more than 35 years of experience as a leader and nurse in diverse healthcare settings and has worked in hospice and palliative care for more than 25 years.


Your Gift

Your Gift
Author: John M. Schneider
Publisher:
Total Pages: 149
Release: 2012
Genre: Self-Help
ISBN: 9780963898456

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This 25th anniversary third edition of Your Gift blends the voices of contributing authors and hospice volunteers working within increasingly complex health care systems. Your Gift reinforces the skill and art of hospice care with contributions from volunteers themselves and a new chapter on palliative music with harp at the bedside.


Congressional Record

Congressional Record
Author: United States. Congress
Publisher:
Total Pages: 2008
Release:
Genre: Law
ISBN:

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Collective Voices

Collective Voices
Author: Debra Parker Oliver
Publisher:
Total Pages:
Release: 2021-10-30
Genre:
ISBN: 9780578255729

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COLLECTIVE VOICES is a set of letters and notesfrom some of the many who have cared for loved onesduring their end-of-life journeys. It is the authors hope that thebrief stories will help support other caregivers as they tryto cope with challenging situations.


Integrating the Patient and Caregiver Voice into Serious Illness Care

Integrating the Patient and Caregiver Voice into Serious Illness Care
Author: National Academies of Sciences, Engineering, and Medicine
Publisher: National Academies Press
Total Pages: 101
Release: 2017-10-17
Genre: Medical
ISBN: 030946031X

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Millions of peopleâ€"infants, children, adults, and their familiesâ€"are currently coping with serious illness in the United States. Efforts are intensifying to improve overall care quality through the delivery of person-centered and family-oriented services, for patients of all ages and across disease stages, care settings, and specialties. While aging Baby Boomers are increasing the proportion of patients in the Medicare population over time, the sickest and most vulnerable patients needing health system support and other services to meet their complex needs can be found across the age spectrum and in a broad range of care settings, from perinatal care to geriatric care. Recognizing the need to thoughtfully consider and address the challenges and opportunities in efforts to improve care quality and value, the Roundtable on Quality Care for People with Serious Illness of the National Academies of Sciences, Engineering, and Medicine held the public workshop Integrating the Patient and Caregiver Voice into Serious Illness Care, on December 15, 2016, in Washington, DC. This workshop was the first in a series planned by the roundtable, and was designed specifically to bring together diverse personal perspectives and experiences about priorities and values that are important to patients and families coping with serious illness, and to consider solutions that support integration of these priorities and values in practice. This publication summarizes the presentations and discussions from the workshop.