Alternate Title

National Comprehensive Cancer Network guidelines for patients : distress during cancer care

Corporate Author

National Comprehensive Cancer Network (NCCN)

Place of Publication

Plymouth Meeting, PA

Publisher

National Comprehensive Cancer Network

Publication Date

2024

Physical Description

36 p. : col. ill. ; 29 cm

Series

NCCN guidelines for patients

Subjects

Popular Work

Neoplasms - psychology

Psychological Distress

Life Change Events

Adaptation, Psychological

ISBN

9781960388308

Language

English

Material Type

Book

Online

Audience

Patient or Public

Location

Internet

Abbotsford Cancer Info Ctr

Victoria Cancer Info Ctr

Vancouver Library

Call Number

QZ201 N277d 2024

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

British Columbia Ministry of Health Patients as Partners Initiative

Place of Publication

[Victoria, BC?]

Publisher

Province of British Columbia, Ministry of Health

Publication Date

2019

Subjects

Health Services for the Aged

Multiple Chronic Conditions

Patient Participation - methods

Decision Making

Caregivers

Professional - Patient Relations

Professional - Family Relations

Notes

May 2019

Language

English

Material Type

Online

Audience

Professional

Location

Internet

Corporate Author

British Columbia Ministry of Health Patients as Partners Initiative

Place of Publication

[Victoria, BC?]

Publisher

Province of British Columbia, Ministry of Health

Publication Date

2019

Subjects

Culturally Competent Care

Cultural Diversity

Patient Participation - methods

Decision Making

Caregivers

Professional - Patient Relations

Professional - Family Relations

Notes

May 2019

Language

English

Material Type

Online

Audience

Professional

Location

Internet

Corporate Author

British Columbia Ministry of Health Patients as Partners Initiative

Place of Publication

[Victoria, BC?]

Publisher

Province of British Columbia, Ministry of Health

Publication Date

2018

Subjects

Patient Participation - methods

Decision Making

Caregivers

Professional - Patient Relations

Professional - Family Relations

Notes

May 2018

Language

English

Material Type

Online

Audience

Professional

Location

Internet

Corporate Author

British Columbia Ministry of Health Patients as Partners Initiative

Place of Publication

[Victoria, BC?]

Publisher

Province of British Columbia, Ministry of Health

Publication Date

2018

Subjects

Patient Participation - methods

Decision Making

Caregivers

Professional - Patient Relations

Professional - Family Relations

Language

English

Material Type

Online

Audience

Professional

Location

Internet

Author

Weigler, Will

Place of Publication

[Victoria, BC?]

Publisher

Weigler, Will

Publication Date

2018

Subjects

Neoplasms - psychology

Adaptation, Psychological

Hope

Optimism

Storytelling

Personal Narratives

Popular Work

Abstract

A collection of messages or 'healing updates' which the author shared with a small circle of friends after cancer diagnosis and during cancer treatment.

Language

English

Material Type

Book

Online

Audience

Patient or Public

Location

Internet

Website Notes

Free online book may be downloaded at link.

Editor

Thomas, Keri

Lobo, Ben

Detering, Karen

Edition

2nd ed.

Place of Publication

Oxford, UK

Publisher

Oxford University Press

Publication Date

2018

Series

EBSCOhost eBook

Subjects

Advance Care Planning

Advance Care Planning - organization & administration

Decision Making

Terminal Care

Right to Die

Abstract

Table of Contents :

Introduction to advance care planning -- Overview and introduction to advance care planning -- What are the benefits of advance care planning and how do we know? -- An introduction to advance care planning: practice at the frontline -- Person-centred care: how does advance care planning support this and what are the economic benefits? -- Advance care planning for an ageing population -- Spiritual and ethical aspects of advance care planning -- Advance care planning: a personal view and stories from the frontline -- Context and experience of advance care planning in the UK -- Advance care planning in the UK: update on policy and practice -- Advance decisions to refuse treatment and the impact of wider legislation -- Discussions and decisions about cardiopulmonary resuscitation -- The implications of the Mental Capacity Act (MCA) 2005 for advance care planning and decision making -- Experience of use of advance care planning in care homes -- Advance care planning in the community -- Advance care planning in hospices and palliative care -- Advance care planning in hospitals -- Advance care planning: thinking ahead for parents, carers, children, and young people -- Advance care planning and people with dementia -- Experience of advance care planning internationally -- Advance care planning in Australia -- Advance care planning in Canada -- Advance directives and advance care planning: the US experience -- Advance care planning in New Zealand: our Voice--to tatou reo -- Advance care planning in Germany: on track for nationwide implementation -- Advance care planning in an Asian country -- Practicalities and areas of common ground -- Communication skills and advance care planning -- Advance care planning in chronic disease: finding the known in the midst of the unknown -- Planning ahead in all areas -- A population-based approach to end-of-life care and advance care planning.

ISBN

9780198802136

9780192542359

9780192542366

Language

English

Material Type

Ebook

Audience

Professional

Location

Internet

Website Notes

This EBSCO 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.

Corporate Author

Canadian Partnership Against Cancer

Place of Publication

[Toronto, ON]

Publisher

Canadian Partnership Against Cancer

Publication Date

2018

Physical Description

50 p.

Series

System performance reports

Subjects

Neoplasms

Neoplasms - psychology

Patient Satisfaction

Patient Navigation

Cancer Survivors

Adaptation, Psychological

Uncertainty

Integrative Oncology

Health Services Accessibility

Delivery of Health Care, Integrated

Continuity of Care

Quality of Health Care

Statistics

Canada

Abstract

Living with Cancer: A Report on the Patient Experience, is the first in a series looking at Canadian cancer care exclusively from the patient perspective, illustrating the experience of those individuals and families living with and beyond cancer. This groundbreaking report includes data drawn from multiple sources, including Patient Reported Outcomes partners, the Ambulatory Oncology Patient Satisfaction Survey, and initial results from the first Canada-wide study of cancer survivors on the experience of 13,000 Canadians with cancer. - website

Notes

January 2018

ISBN

9781988000343

9781988000350

Language

English

Material Type

Report

Online

Audience

Professional

Location

Internet

Author

Gruman, Jamie A.

Healey, Deirdre

Place of Publication

Charlotte, NC

Publisher

Information Age Publishing

Publication Date

2018

Physical Description

xv, 193 p. : 24 cm.

Series

EBSCOhost eBook

Subjects

Stress, Psychological - prevention & control

Adaptation, Psychological

Burnout, Psychological - prevention & control

Work-Life Balance

Abstract

Table of contents:

1.ReNU -- 2.HOW TO REAP THE BOOSTING BENEFITS OF NATURE -- 3.CUTTING THE VIRTUAL CORD -- 4.QUALITY TIME WITH THE SANDMAN -- 5.VOLUNTEERING -- 6.MEDITATION, MINDFULNESS, AND MORE -- 7.FAMILY AND FRIENDS -- 8.EXERCISE -- 9.HOBBIES -- 10.VACATIONS DONE RIGHT -- EPILOGUE

Notes

Surrey CIC keep 2022

ISBN

9781641133029

9781641133043

9781641133036

Language

English

Material Type

Book

Ebook

Audience

Professional

Location

Internet

Surrey Cancer Info Ctr

Call Number

WM172.4 G887 2018

Website Notes

This EBSCO 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.

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.

Copies

Author

Wassersug, Richard J

Walker, Lauren M

Robinson, John W

Edition

2nd ed.

Place of Publication

New York, NY

Publisher

Demos Health

Publication Date

2018

Physical Description

xxvi, 203 p. ; 26 cm.

Series

Proquest Ebook Central

Subjects

Prostatic Neoplasms - therapy

Prostatic Neoplasms, Castration-Resistant

Neoplasms - psychology

Androgen Antagonists - therapeutic use

Androgen Antagonists - adverse effects

Prostatic Neoplasms - diet therapy

Exercise Therapy

Sexual Partners

Family Relations

Adaptation, Psychological

Popular Work

Notes

Surrey CIC keep 2022 (F0002681, F0002507)

ISBN

9780826183910

0826183913

9780826183927

Language

English

Material Type

Book

Ebook

Audience

Patient or Public

Location

Vancouver Library

Abbotsford Cancer Info Ctr

Kelowna Cancer Info Ctr

Prince George Cancer Info Ctr

Surrey Cancer Info Ctr

Vancouver Cancer Info Ctr

Victoria Cancer Info Ctr

Internet

Call Number

WJ762 W322 2018

Website Notes

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

Patients and the public of BC and the Yukon can access this title by emailing library@bccancer.bc.ca or calling 1.888.675.8001 x 7000 (toll-free) to obtain a username and password.

Copies

Corporate Author

Canadian Breast Cancer Network

Place of Publication

[Ottawa, ON]

Publisher

Canadian Breast Cancer Network

Publication Date

2018

Physical Description

60 p. ; 22 cm.

Subjects

Breast Neoplasms - psychology

Social Adjustment

Social Support

Adaptation, Psychological

Young Adult

Popular Work

Notes

Surrey CIC keep 2022

Language

English

Material Type

Booklet

Online

Audience

Patient or Public

Location

Abbotsford Cancer Info Ctr

Kelowna Cancer Info Ctr

Prince George Cancer Info Ctr

Surrey Cancer Info Ctr

Vancouver Cancer Info Ctr

Victoria Cancer Info Ctr

Internet

Call Number

WP870 C215n 2018

Website Notes

PDF may be downloaded at URL.

Copies

Editor

Jones, Keith

Edition

2nd ed.

Place of Publication

Detroit, MI

Publisher

Omnigraphics

Publication Date

2017

Series

Health reference series

EBSCOhost eBook

Subjects

Cancer Survivors

Neoplasms - psychology

Neoplasms - rehabilitation

Neoplasms - therapy

Quality of Life

Adaptation, Psychological

Popular Work

Abstract

Cancer survivorship sourcebook : basic consumer health information about the physical, educational, emotional, social, and financial needs of cancer patients from diagnosis, through cancer treatment, and beyond, including facts about researching specific types of cancer and learning about clinical trials and treatment options, and featuring tips for coping with the side effects of cancer treatments and adjusting to life after cancer treatment concludes ; along with suggestions for caregivers, friends, and family members of cancer patients, a glossary of cancer care terms, and directories of related resources

Table of contents:

Part I If Your Doctor Says It's Cancer -- Part II Making Treatment and Cancer Care Decisions -- Part III Clinical Trials and Cancer Research Updates -- Part IV Coping with Side Effects and Complications of Cancer Treatment -- Part V Emotional, Cognitive, and Mental Health Issues in Cancer Care -- Part VI Maintaining Wellness during and after Cancer Treatment -- Part VII Information for Friends, Family Members, and Caregivers -- Part VIII Additional Help and Information

ISBN

9780780815490

9780780815506

Language

English

Material Type

Ebook

Audience

Patient or Public

Location

Internet

Website Notes

Patients and the public of BC and the Yukon can access this title by emailing library@bccancer.bc.ca to obtain a username and password from the Library.

Corporate Author

Canadian Agency for Drugs and Technologies in Health

Edition

4th ed.

Place of Publication

[Ottawa, ON]

Publisher

Canadian Agency for Drugs and Technologies in Health (CADTH)

Publication Date

2017

Physical Description

76 p. ; 28 cm.

Series

CADTH methods and guidelines

Subjects

Technology Assessment, Biomedical - economics

Technology Assessment, Biomedical - methods

Cost-Benefit Analysis

Decision Making

Guidelines

Canada

Notes

In April 2006 Canadian Coordinating Office for Health Technology Assessment (CCOHTA) changed to Canadian Agency for Drugs and Technologies in Health (CADTH)

Language

English

Material Type

Report

Online

Audience

Professional

Location

Vancouver Library

Internet

Call Number

W 82 G946 2017

Copies

Continues / Continued By

Continues:

Getting through : a teacher resource for understanding student(s) affected by cancer in the family

Getting through : a student resource for sorting out school when cancer affects the family

Corporate Author

BC Cancer Agency. Patient and Family Counselling

Place of Publication

[Vancouver, BC?]

Publisher

BC Cancer Agency. Psychosocial Oncology

Publication Date

2016

Subjects

Neoplasms - psychology

Family Relations

Adaptation, Psychological

Life Change Events

Schools

Adolescent

Child

Popular Work

Language

English

Material Type

Booklet

Online

Audience

Patient or Public

Professional

Location

Internet

Alternate Title

How to win a tickle fight : a true story about what can go right, even when things have gone terribly wrong

Author

Lang, Mike

Bryant, Aaron

Corporate Author

Survive & Thrive Cancer Programs

Family Lines

Canadian Cancer Society

Publisher

Common Language Storytelling

Hands On Films

Publication Date

2016

Physical Description

50 min.

Subjects

Terminally Ill - psychology

Neoplasms - psychology

Parent-Child Relations

Family Relations

Adaptation, Psychological

Young Adult

Personal Narratives

Canada

Popular Work

Abstract

How to Win a Tickle Fight is a true story that follows one young father, Brock, and his family for two years as they strive to live full, meaningful lives despite the metastatic cancer diagnosis they are navigating. Brock desperately wants to leave a legacy for his 7 year old son and be remembered as more than a 'sick person'. Kristen, Brock's wife, wants to maintain a closeness with her husband even while he is dying. And their son Ben... he just wants to have fun with his mom and dad. Through their difficult journey, the family comes to realizes that many things can still go right even when things have gone terribly wrong.

Notes

The complete documentary can be viewed online.

Language

English

Material Type

Video

Online

Audience

Patient or Public

Location

Internet

Corporate Author

Openlab, University Health Network

Place of Publication

[Toronto, ON]

Publisher

Openlab, University Health Network

Publication Date

2016

Physical Description

87 p.

Subjects

Inpatients - psychology

Aged

Hospitalization

Adaptation, Psychological

Consumer Health Information

Patient Satisfaction

Patient Navigation

Patient Participation

Guidebooks

Patient Education Handout

Notes

"This Handbook is a product of OpenLab's Stuff Patients Want initiative. Stuff Patients Want is a participatory design initiative in which patients come together to share health care experiences they find frustrating. These patients are then armed with the tools (e.g. design, production)they need to bring their practical and inspired solutions to life. Stuff Patients Want is carried out in the Scandinavian participatory design tradition, driven by the idea that the people destined to use a product or service should play a critical role in designing it, and characterized by active collaboration between users and designers throughout the participatory process."

ISBN

9780995281509

Material Type

Book

Online

Audience

Patient or Public

Location

Internet

Website Notes

E-book available in PDF format

Corporate Author

Vancouver Coastal Health Community Engagement

Place of Publication

[Vancouver, BC?]

Publisher

Vancouver Coastal Health

Publication Date

2015

Subjects

Patient Participation - methods

Community Participation - methods

Delivery of Health Care

Decision Making

Professional - Patient Relations

Professional - Family Relations

Language

English

Material Type

Online

Audience

Professional

Location

Internet

Author

Katz, Anne

Place of Publication

Pittsburgh, PA

Publisher

Oncology Nursing Society

Publication Date

2015

Series

R2 Library

Subjects

Neoplasms - psychology

Adolescent

Young Adult

Survivors - psychology

Neoplasms - rehabilitation

Adaptation, Psychological

Employment

Workplace

Life Change Events

Popular Work

ISBN

1935864645

9781935864646

9781935864653

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.

Editor

Rehmann-Sutter, Christoph

Gudat, Heike

Ohnsorge, Kathrin

Place of Publication

Oxford, UK

Publisher

Oxford University Press

Publication Date

2015

Series

EBSCOhost eBook

Subjects

Right to Die - ethics

Suicide, Assisted - ethics

Euthanasia

Patient Participation

Attitude to Death

Palliative Care - psychology

Advance Care Planning

Terminal Care

Decision Making

Ethics, Clinical

Abstract

Table of Contents :

PART I: Introduction -- Why it is important to know about patients? wishes to die -- PART II: Research --Illness narratives, meaning making, and epistemic injustice in research at the end of life -- Expressed desire for hastened death in seven patients living with advanced cancer: a phenomenologic inquiry -- Expressed desire for hastened death: a phenomenologic inquiry? 10 years later -- Euthanasia (requests) after the implementation of the euthanasia law in Belgium in 2002. Results of empirical studies in Flanders, Belgium -- The journey to understanding the wish to hasten death -- The desire for hastened death in patients in palliative care -- Intentions, motivations, and social interactions regarding a wish to die -- Acting on a wish to die at the end of life: the Swiss situation -- Understanding older people?s wish to die -- Dialogue intermezzo: I -- PART III: Ethics -- Caring and killing in the clinic: the argument of self-determination -- Towards responsive knowing in matters of life and death -- Dealing with dilemmas around patients? wishes to die: moral case deliberation in a Dutch hospice -- End-of-life ethics from the perspectives of patients? wishes -- Dialogue intermezzo: II -- PART IV: Practice -- Issues of palliative medicine in end-of-life care -- Spirituality at the bedside: negotiating the meaning of dying -- Communication of wishes to die -- From understanding to patient-centred management: clinical pictures of a wish to die -- What does the wish to hasten death mean for the palliative patient? Clinical implications -- PART V: Conclusion -- Concluding dialogue.

ISBN

9780191023330

9780198713982

Language

English

Material Type

Ebook

Audience

Professional

Location

Internet

Website Notes

This EBSCO 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.