Alternate Title

Twenty-one days to die

Author

Hochstetler, Linda

Place of Publication

Manotick, ON,

Publisher

Sumeru Press Inc.,

Publication Date

2021

Physical Description

161 pages : illustrations ; 24 cm

Subjects

Popular Work

Attitude to Death

Palliative Treatment

Terminal Care

Hospice Care

Grief

Death and dying

Abstract

"This is a guide to end of life in the Canadian context. Chapters deal with issues such as palliative care, hospice, advanced care plans, how to recognize and respond to the stages of dying during the last 21 days, conversations to have, disposal of the body, and grief. Also included are many useful lists, websites, books and other resources for Canadians, presented in an easy-to-access form for sharing at a difficult time. Many of the resources include QR codes."-- Provided by publisher

ISBN

9781896559728

Language

English

Material Type

Book

Audience

Patient or Public

Location

Abbotsford Cancer Info Ctr

Vancouver Library

Victoria Cancer Info Ctr

Call Number

BF789 D7 H685c 2021

Copies

Alternate Title

Patient experience program : best practices for engagement

Corporate Author

BC Cancer, Patient & Family Engagement

Place of Publication

[Vancouver, BC?]

Publisher

BC Cancer Agency

Publication Date

2020

Subjects

Culturally Competent Care

Cultural Diversity

Patient Participation - methods

Decision Making

Caregivers

Professional - Patient Relations

Professional - Family Relations

Abstract

Contents:

Best Practices for Successful Engagement -- Diversity in Patient Engagement -- Engagement Methods -- How to Request Patient and Family Partners -- Matching Partners -- Planning Engagement -- Presenting With Patient Partners -- Reimbursing Partners.

Language

English

Material Type

Online

Audience

Professional

Location

Internet

Website Notes

Tip sheets in PDF format and more patient and family engagement resources available at link

Corporate Author

BC Cancer, Patient & Family Engagement

Place of Publication

[Vancouver, BC?]

Publisher

BC Cancer Agency

Publication Date

2020

Subjects

Patient Participation

Decision Making, Organizational

Caregivers

Professional - Patient Relations

Professional - Family Relations

Culturally Competent Care

Cultural Diversity

Policy

Practice Guideline

Notes

Also available : Engaging patients and families In projects, committees and organizational decision making procedure

Language

English

Material Type

Online

Audience

Professional

Location

Internet

Corporate Author

BC Cancer, Patient & Family Engagement

Place of Publication

[Vancouver, BC?]

Publisher

BC Cancer Agency

Publication Date

2020

Subjects

Patient Participation

Decision Making, Organizational

Caregivers

Professional - Patient Relations

Professional - Family Relations

Culturally Competent Care

Cultural Diversity

Practice Guideline

Notes

Also available :

Engaging patients and families in projects, committees and organizational decision making policy

Language

English

Material Type

Online

Audience

Professional

Location

Internet

Author

Fersko-Weiss, Henry

Tisdale, Sallie

Place of Publication

Newburyport, MA

Publisher

Red Wheel

Publication Date

2020

Subjects

Terminally Ill

Doulas

Hospice Care - psychology

Terminal Care

Attitude to Death

Advance Care Planning

Caregivers

Popular Work

Notes

Previously published as Caring for the dying in 2017 by Conari Press"--Title page verso.

ISBN

9781590035023

Language

English

Material Type

Book

Audience

Patient or Public

Location

Vancouver Library

Victoria Cancer Info Ctr

Call Number

BF789 D4 F399f 2020

Copies

Editor

Silbermann, Michael

Berger, Ann

Place of Publication

New York

Publisher

Oxford University Press

Publication Date

c2022

Series

Proquest Ebook Central

Subjects

Neoplasms - therapy

Neoplasms - psychology

Spiritual Therapies

Spirituality

Cultural Diversity

Religion and Medicine

Abstract

"With cancer ranking as the primary or secondary cause of premature death in almost 100 countries worldwide, the World Health Organization recognized a high level of investment in cancer control and treatment (including palliative care) in 2019. At that time, governments at the World Health Assembly (WHA) unanimously adopted a new cancer resolution (Universal Health Coverage: Moving Together to Build a Healthier World). The resolution noted the potential for cancer prevention to reduce cancer burden in the future, while reducing the suffering from cancer in the communities.As most countries are facing an overall increase in the absolute number of cancer cases, large geographical diversity in cancer occurrence and variations in the magnitude and profile of the disease still continue between and within world regions. Specific types of cancer dominate globally: lung, female breast, and colorectal cancer. The regional variations in common cancer types signal the extent to which societal, economic, and lifestyle changes interplay to differentially impact the profile of this most complex group of diseases.Although survival rates for cancer have improved significantly over the past few decades, for each individual, the diagnosis and treatment of cancer are still devastating, affecting the family and community as well. The care of a person with cancer must be more than just the treatment of the cancer itself. Understanding the cultural, psychological, social, and spiritual dimensions of the cancer sufferer and their family and community will ensure the best care.In order to treat individuals with cancer and understand how to give the best possible care to underserved populations, we need to understand cultural diversity. Understanding that cultural aspects of a society may be intertwined with finances and other resources can improve adherence and access to care. Culture is made up of language, religion, cuisine, social norms, history, ancestry, music, arts, and spirituality. In order to improve cancer care outcomes, patients' diverse spiritual and cultural beliefs must be recognized. In addition, available methods must be utilized to improve access and adherence to treatment modalities and regimens.In this book, we focus on numerous diverse cultures, traditions, and faiths. Many parts of the world are composed of indigenous cultures, with unique spiritual beliefs in addition to the region's primary religion. We present chapters on indigenous religions as well as indigenous traditional healers. People everywhere experience trouble, sorrow, need, and sickness, and they develop skills and knowledge in response to these adversities. This book provides insightful models of these parameters and serves as a valuable resource for health care providers and policymakers by taking a global approach to cultural diversity in the world. By understanding this multiculturalism and the many aspects of psychological, social, and spiritual dimensions of health and healing, we can learn from one another." --publisher

ISBN

9780197551349

Language

English

Material Type

Ebook

Audience

Professional

Location

Internet

Website Notes

This title is licensed for one user at a time on BC Cancer-network computers. If you are denied access while on a network computer, try again later.

This Proquest title is licensed for ONE BC Cancer staff user at a time. If you are denied access while on a network computer, please try again later.

Authentication via HealthBC sign in required. Use your BC Cancer staff username and ID when prompted.

Author

Kanarek, Robin Bennett

Place of Publication

Baltimore, MD

Publisher

Johns Hopkins University Press

Publication Date

2023

Physical Description

209 p. ; 22 cm.

Series

Johns Hopkins Press health book

Subjects

Quality of Life

Palliative Care

Terminal Care

Adaptation, Psychological

Advance Care Planning

Caregivers - psychology

Popular Work

Abstract

This book was written to educate individuals diagnosed with a serious medical condition along with their loved ones about the importance of palliative care. The work outlines what palliative care is, provides communication strategies for getting the type of support and care that you want and need (and not just medications), outlines successful coping strategies, and discusses family dynamics, grieving, emotional support, and spirituality. Although palliative care is often associated with hospice and end-of-life planning, the author argues for a more expanded definition that includes improved quality of life at early as well as later stages of the disease process.

Notes

This resource was purchased with a donation from the Order of the Eastern Star.

ISBN

9781421445984

Language

English

Material Type

Book

Status

Processing

Audience

Patient or Public

Location

Vancouver Library

Abbotsford Cancer Info Ctr

Kelowna Cancer Info Ctr

Victoria Cancer Info Ctr

Call Number

WB310 K16 2023

Copies

Editor

Congress, Elaine

González, Manny

Edition

4th ed.

Place of Publication

New York, NY

Publisher

Springer Publishing Company, LLC

Publication Date

[2021]

Series

R2 Library

Subjects

Cultural Diversity

Social work - methods

Counselling

Family Therapy - methods

Sexual and Gender Minorities

Culturally Competent Care

United States

Abstract

Contents:

I Overview-- 1. Using the Culturagram and an Intersectional Approach in Practice With Culturally Diverse Families -- 2. Practice With Multiracial Individuals and Families -- 3. Transracial Adoption and Transracial Socialization: Clinical Implications and Recommendations -- 4. The DSM-5 From a Multicultural Perspective -- 5. Evidence-Based Practice With Ethnically Diverse Clients -- II: ADMINISTRATIVE AND LEGAL PERSPECTIVES -- 6. Managing Agencies for Multicultural Services -- 7. Legal Issues in Practice With Immigrants and Refugees -- III: LIFE CYCLE PERSPECTIVES -- 8. The Multicultural Triangle of the Child, the Family, and the School: Culturally Competent Approaches -- 9. Cross-Cultural Perspectives on Working With Adolescents -- 10. Working With Culturally Diverse Older Adults -- IV: PRACTICE WITH INDIVIDUALS AND FAMILIES FROM DIFFERENT RACIAL/ETHNIC BACKGROUNDS AND GENDER ORIENTATION -- 11. Practice With African American Families -- 12. Practice With Hispanic Individuals and Families -- 13. Practice With Asian Immigrant Families and Intergenerational Issues -- 14. Practice With Native American Families -- 15. Practice With Arab American Families -- 16. Practice With Lesbian, Gay, Bisexual, and Transgender People and Their Families -- V: PHYSICAL AND MENTAL HEALTH ISSUES WITH MULTICULTURAL FAMILIES -- 17. Health Beliefs, Care, and Access of Individuals and Families From Diverse Backgrounds -- 18. Spirituality and Culturally Diverse Families: The Intersection of Culture, Religion, and Spirituality -- 19. HIV/AIDS and Latinx Families: Practice Considerations -- 20. Substance Abuse --21. Practice With Immigrant Victims of Domestic Violence -- 22. Culture, Intersectionality, and Suicide -- VI ETHICAL ISSUES AND FUTURE DIRECTIONS -- 23. Ethical Issues and Future Directions

ISBN

082615414X

9780826154149

9780826154156

Language

English

Material Type

Ebook

Audience

Professional

Location

Internet

Website Notes

This R2 title is licensed for one BC Cancer staff user at a time only. Authentication via HealthBC sign in required. Use your BC Cancer staff username and ID when prompted.

Alternate Title

Palliative medicine

Editor

Cherny, Nathan I.

Fallon, Marie T.

Kaasa, Stein

Portenoy, Russell K.

Currow, David C.

Edition

6th ed.

Place of Publication

New York, NY

Publisher

Oxford University Press

Publication Date

2021

Physical Description

xxi,1386 p. : ill. ; 28 cm.

Subjects

Neoplasms - complications

Palliative Care

Pain - therapy

Terminal Care

ISBN

9780198821328

Language

English

Material Type

Book

Audience

Professional

Location

Victoria Library

Abbotsford Library

Vancouver Library

Kelowna Library

Call Number

WB310 O98 2021

Copies

Alternate Title

Psycho-oncology care

Editor

Kissane, David W.

Watson, Maggie

Breitbart, William

Place of Publication

New York, NY

Publisher

Oxford University Press

Publication Date

2023

Series

Proquest Ebook Central

Psycho oncology care

Subjects

Neoplasms? psychology

Palliative Care

Terminal Care

Professional-Patient Relations

ISBN

9780197615935

9780197615942

Language

English

Material Type

Ebook

Audience

Professional

Location

Internet

Website Notes

This title is licensed for one user at a time on BC Cancer network computer. If you are denied access while on a network computer, try again later.

This Proquest title is licensed for ONE BC Cancer staff user at a time. If you are denied access while on a network computer, please try again later.

Authentication via HealthBC sign in required. Use your BC Cancer staff username and ID when prompted.

Author

Green, Stephanie

Place of Publication

New York, NY

Publisher

Scribner

Publication Date

2022

Physical Description

295 pages ; 22 cm

Subjects

Right to Die

Advance Care Planning

Terminal Care

Euthanasia

Suicide, Assisted

Popular Work

ISBN

9781668004784

Language

English

Material Type

Book

Audience

Patient or Public

Location

Vancouver Library

Victoria Cancer Info Ctr

Call Number

W85.5 G795 2022

Copies