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AIDS Activism, Science and Community Across Three Continents

https://libcat.nshealth.ca/en/permalink/provcat41412
Robert Lorway. --Cham: Springer , 2017.
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This book critically examines the many complex entanglements between AIDS activism and HIV science. It takes readers on a medical anthropological expedition across time and space that highlights the stakes from the perspective of those most affected by the epidemic. Author Robert Lorway reveals how early in the HIV epidemic, amid inadequate government leadership, communities of people living with and directly affected by HIV and AIDS rose to become a vital force at the forefront of prevention r…
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Author
Lorway, Robert
Responsibility
Robert Lorway
Place of Publication
Cham
Publisher
Springer
Date of Publication
2017
Physical Description
1 online resource (xxiv, 153 pages) : 14 illus.
Series Title
Social aspects of HIV
ISBN
9783319421995
9783319421971 (print ed.)
ISSN
2509-6559
Subjects (MeSH)
Acquired Immunodeficiency Syndrome - psychology
Community Health Services
HIV infections - psychology
Patient Advocacy
Sociological Factors
Abstract
This book critically examines the many complex entanglements between AIDS activism and HIV science. It takes readers on a medical anthropological expedition across time and space that highlights the stakes from the perspective of those most affected by the epidemic. Author Robert Lorway reveals how early in the HIV epidemic, amid inadequate government leadership, communities of people living with and directly affected by HIV and AIDS rose to become a vital force at the forefront of prevention responses. Yet now, more than three decades later, HIV prevention and treatment is increasingly being placed under the jurisdiction of clinical, epidemiological, and management scientific expertise. In this kind of context, where does activism figure into the possibility of more democratized collaborations between affected communities, scientists, and policy makers? Coverage draws upon the findings from an array of community research projects conducted in Canada, India, and Kenya over a 22-year period. It weaves together rich, original data sources that range from in-depth qualitative interviews, field notes, and primary and secondary archival document retrievals in these three regions. Offering a rich diversity in perspectives, this book tackles the broader themes related to global health policy, science, and transnational activism at the same time as it highlights the experiences and local arenas where debates about activism and science play out. In the end, Lorway questions the growing expectation for affected communities themselves to produce sound evidence to legitimize their advocacy projects. He calls for the planners and implementers of biomedically oriented HIV research and interventions to more meaningfully engage with communities in ways that de-monopolize decision making as a matter of ethics and improved scientific practice.
Contents
Introduction -- Section I. Canada: Professionalization -- 1. A Vital Response -- 2. Treatment Rebellions -- Section II. India: Techno-Bureaucratization -- 3. Geographies of Intervention -- 4. Documenting Sovereignty -- III. Kenya: Bioexperimentalization -- 5. A South-to-South Collaboration -- 6. The Logic of Verification -- Conclusion.
Format
e-Book
Location
Online
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Canadian patient's book of rights, The : a consumer's guide to Canadian health

https://libcat.nshealth.ca/en/permalink/provcat52960
[by] Lorne E. Rozovsky. (rev. and updated) --Toronto, ON: Doubleday Canada , 1994.
Call Number
W 32.5 DC2 R893 1994
Location
IWK Health Sciences Library
Call Number
W 32.5 DC2 R893 1994
Author
Rozovsky, Lorne E.
Responsibility
[by] Lorne E. Rozovsky
Edition
rev. and updated
Place of Publication
Toronto, ON
Publisher
Doubleday Canada
Date of Publication
1994
Physical Description
242 p.
ISBN
385254490
Subjects (MeSH)
Patient Advocacy - legislation & jurisprudence
Legislation, Medical
Ethics, Medical
Consumer Satisfaction
Patient Satisfaction
Canada
Notes
Consumer health information.
"Endorsed by the Canadian Pharmaceutical Association".
Format
Book
Location
IWK Health Sciences Library
Copies
1
Loan Period
2 weeks
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Children's rights in the practice of family law

https://libcat.nshealth.ca/en/permalink/provcat53026
edited by Barbara landau. --Toronto, ON: Carswell , 1986.
Call Number
WA 320 DC2 L16 1986
Location
IWK Health Sciences Library
Call Number
WA 320 DC2 L16 1986
Author
Landau, Barbara
Responsibility
edited by Barbara landau
Place of Publication
Toronto, ON
Publisher
Carswell
Date of Publication
1986
Physical Description
378 p.
ISBN
459390406
Subjects (MeSH)
Patient Advocacy - legislation & jurisprudence
Child Welfare - legislation & jurisprudence
Canada
Format
Book
Location
IWK Health Sciences Library
Copies
1
Loan Period
2 weeks
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Human Trafficking Is a Public Health Issue : A Paradigm Expansion in the United States

https://libcat.nshealth.ca/en/permalink/provcat41588
Makini Chisolm-Straker, Hanni Stoklosa, editors. --Cham: Springer , 2017.
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Online
This clear-sighted reference examines the public health dimensions of labor and sex trafficking in the United States, the scope of the crisis, and possibilities for solutions. Its ecological lifespan approach globally traces risk and protective factors associated with this exploitation, laying a roadmap towards its prevention. Diverse experts, including survivors, describe support and care interventions across domains and disciplines, from the law enforcement and judicial sectors to community h…
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Other Authors
Chisolm-Straker, Makini
Stoklosa, Hanni
Responsibility
Makini Chisolm-Straker, Hanni Stoklosa, editors
Place of Publication
Cham
Publisher
Springer
Date of Publication
2017
Physical Description
1 online resource (xxxvii, 457 pages) : 15 illus., 13 illus. in color
ISBN
9783319478241
9783319478234 (print ed.)
Subjects (MeSH)
Crime Victims
Health Policy
Human Trafficking - prevention & control
Patient Advocacy
Sex Offenses
Other Subjects
United States
Abstract
This clear-sighted reference examines the public health dimensions of labor and sex trafficking in the United States, the scope of the crisis, and possibilities for solutions. Its ecological lifespan approach globally traces risk and protective factors associated with this exploitation, laying a roadmap towards its prevention. Diverse experts, including survivors, describe support and care interventions across domains and disciplines, from the law enforcement and judicial sectors to community health systems and NGOs, with a robust model for collaboration. By focusing on the humanity of trafficked persons, a public health paradigm broadens our understanding of and ability to address trafficking while adding critical direction and resources to the criminal justice and human rights structures currently in place. Human Trafficking Is a Public Health Issue is a sobering read; a powerful call to action for public health professionals, including social workers and health care practitioners providing direct services, as well as the larger anti-trafficking community of advocates, prosecutors, taskforce members, law enforcement agents, officers, funders, and administrators. "An extraordinary collection of knowledge by survivors, academics, clinicians, and advocates who are experts on human trafficking. Human Trafficking is a Public Health Issue is a comprehensive offering in educating readers on human trafficking through a multi-pronged public health lens." Margeaux Gray: Survivor, Advocate, Artist, Public Speaker.
Contents
1. Introduction to Human Trafficking: Who Is Affected? -- 2. Sex Trafficked and Missed -- 3. The Lost Boy: How a Forgotten Child Became a Victim of Labor Trafficking -- 4. Sex Trafficking in the USA -- 5. The Ignored Exploitation: Labor Trafficking in the United States -- 6. Trafficking of Children Within the United States -- 7. Children at Risk: Foster Care and Human Trafficking -- 8. Sex Trafficking in Indian Country -- 9. LGBTQ Youth and Vulnerability to Sex Trafficking -- 10. The Multimodal Social Ecological (MSE) Approach: A Trauma-Informed Framework for Supporting Trafficking Survivors’ Psychosocial Health -- 11. Physical Health of Human Trafficking Survivors: Unmet Essentials -- 12. Trauma-Informed Treatment of Substance Use Disorders in Trafficking Survivors -- 13. The Development and Psychology of Young Minds: Communities Can Prevent Exploitation and Facilitate Rehabilitation -- 14. Legal Supports for Trafficked Persons: Assisting Survivors via Certification, State/Federal Benefits, and Compensation -- 15. NGOs and the Anti-Trafficking Movement: Advocacy and Service -- 16. The Role of Faith-Based Organizations in the US Anti-Trafficking Movement -- 17. Research Informing Advocacy: An Anti-Human Trafficking Tool -- 18. Caring for Survivors Using a Trauma-Informed Care Framework -- 19. Sex Trafficking in One US City: Traditional Policing and Boston’s Shift to a Survivor-Centered Response -- 20. The Role of Community Health Centers in Addressing Human Trafficking -- 21. The Media and Human Trafficking: A Discussion and Critique of the Dominant Narrative -- 22. Human Trafficking: Perspectives on Prevention -- 23. Combating Modern Bondage: The Development of a Multi-Disciplinary Approach to Human Trafficking -- 24. Moving Forward: Next Steps in Preventing and Disrupting Human Trafficking.
Format
e-Book
Location
Online
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Living donor advocacy : an evolving role within transplantation

https://libcat.nshealth.ca/en/permalink/provcat33408
Jennifer Steel, editor. --New York: Springer , c2014.
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Location
Online
The inadequate supply of organs in the United States and other countries continues to drive the reliance on living donor transplantation. Representatives of the transplant community convened for a meeting on living donation in an effort to provide guidelines to promote the welfare of living donors. The consensus statement that resulted from this meeting recommended that transplant centers retain an Independent Living Donor Advocate (ILDA) to focus on the best interest of the donor. Over a decad…
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Other Authors
Steel, Jennifer
Responsibility
Jennifer Steel, editor
Place of Publication
New York
Publisher
Springer
Date of Publication
c2014
Physical Description
1 online resource (xv, 362 pages)
ISBN
9781461491439 (electronic bk.)
9781461491422
Subjects (MeSH)
Living Donors - ethics
Patient Advocacy - ethics
Patient Advocacy - standards
Transplantation - ethics
Transplantation - standards
Subjects (LCSH)
Living related donor transplantation
Transplantation of organs, tissues, etc. - Moral and ethical aspects
Transplant Surgery
Abstract
The inadequate supply of organs in the United States and other countries continues to drive the reliance on living donor transplantation. Representatives of the transplant community convened for a meeting on living donation in an effort to provide guidelines to promote the welfare of living donors. The consensus statement that resulted from this meeting recommended that transplant centers retain an Independent Living Donor Advocate (ILDA) to focus on the best interest of the donor. Over a decade later, nearly every transplant center in the United States, performing living donor surgeries, has incorporated an ILDA into their living donor screening and/or evaluation process, however there are no guidelines with regard to the ILDA's qualifications, clinical practice, or how address ethical challenges.
Contents
Part I: Living Donation -- 1. The Medical Selection of Live Donors -- 2. Kidney Paired Donation Programs for Incompatible Living Kidney Donors and Recipients -- 3. Living Donor Liver Transplantation -- 4. Intestinal Transplantation from Living Donors -- 5. Living Donor Lung Transplantation -- 6. Live Donor Pancreas Transplantation -- Part II: Living Donor Advocacy -- 7: The History of Living Donor Advocacy in Living Donor Transplantation -- 8. Findings from a National Survey of Living Donor Advocates -- 9. The Independent Donor Advocate and the Independent Donor Advocate Team -- 10. Classification of Living Organ Donors -- 11. Unrelated Donors -- 12. Education of the Donor by the ILDA (Psychosocial Aspects) -- 13. Components and Timing of the ILDA Evaluation -- 14. Contraindications to Living Donation from an ILDA Perspective -- 15. Management of Conflict Between the Independent Living Donor Advocate and the Transplant Team -- 16. Story Behind the Story -- 17. Living Donor Experience -- Part III: Living Donor Ethics -- 18. Informed Consent for Living Organ Donation -- 19. Pressure and Coercion -- 20. Financial Considerations -- 21. Autonomy, Agency, and Responsibility: Ethical Concerns for Living Donor Advocates -- 22. A Practical Guide: Role of the Independent Living Donor Advocate: Protect or Advocate or Is It Both/And? -- 23. Racial Disparities in Kidney Transplant and Living Donation -- 24. The Evolution of the Role of the Independent Living Donor Advocates: Recommendations for Practice Guidelines.
Format
e-Book
Location
Online
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Patients' rights : ethical and legal issues in health care and nursing

https://libcat.nshealth.ca/en/permalink/provcat54107
[by] Janet Storch. --Toronto, ON: McGraw-Hill , 1982.
Call Number
W 50 DC2 S76 1982
Location
IWK Health Sciences Library
Call Number
W 50 DC2 S76 1982
Author
Storch, Janet
Responsibility
[by] Janet Storch
Place of Publication
Toronto, ON
Publisher
McGraw-Hill
Date of Publication
1982
Physical Description
249 p.
ISBN
75484773
Subjects (MeSH)
Patient Advocacy
Nurse-Patient Relations
Physician-Patient Relations
Ethics, Medical
Legislation
Canada
Format
Book
Location
IWK Health Sciences Library
Copies
1
Loan Period
2 weeks
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Speaking for patients and carers : health consumer groups and the policy process

https://libcat.nshealth.ca/en/permalink/provcat41080
Rob Baggott, Judith Allsop, and Kathryn Jones. --Houndmills [England]: Palgrave Macmillan , c2005.
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Location
Online
Speaking for Patients and Carers draws on original research and is based on a theoretical framework taken from sociology and politics. It examines health consumer groups in the context of specific conditions: arthritis and related conditions, cancer, heart and circulatory disease, maternity and childbirth, and mental health. It also analyzes their interaction with government, health professionals and the media, and assesses their impact on policy.
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Author
Baggott, Rob
Other Authors
Allsop, Judy, 1938-
Jones, Kathryn
Responsibility
Rob Baggott, Judith Allsop, and Kathryn Jones
Place of Publication
Houndmills [England]
Publisher
Palgrave Macmillan
Date of Publication
c2005
Physical Description
1 online resource (xvi, 349 p.)
ISBN
9780230801851
9780333968284 (hbk.)
9780333968291 (pbk.)
Subjects (MeSH)
Consumer Organizations
Health Policy
Patient Advocacy
Other Subjects
United Kingdom
Abstract
Speaking for Patients and Carers draws on original research and is based on a theoretical framework taken from sociology and politics. It examines health consumer groups in the context of specific conditions: arthritis and related conditions, cancer, heart and circulatory disease, maternity and childbirth, and mental health. It also analyzes their interaction with government, health professionals and the media, and assesses their impact on policy.
Contents
1. Health care politics and the policy process: concepts, theories and models -- 2. The policy context -- 3. The condition areas -- 4. Health consumer groups: formation and characteristics -- 5. Health consumer groups: social and political resources -- 6. Networks, and informal and formal alliances -- 7. Collaboration with health professionals -- 8. The pharmaceutical industry -- 9. Working with government -- 10. Working with parliament -- 11. Working with the media -- 12. Conclusion: speaking for patients and carers?
Format
e-Book
Location
Online
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Supportive Cancer Care

https://libcat.nshealth.ca/en/permalink/provcat39966
David Alberts, Maria Lluria-Prevatt, Stephanie Kha, Karen Weihs, editors. --Cham: Springer , c2016.
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Online
This textbook provides a highly coordinated, interdisciplinary model for future clinical cancer supportive care programs in National Cancer Institute (NCI)-designated Clinical and Comprehensive Cancer Centers and NCI Community Oncology Research Programs (NCORPs). At the same time, it is intended to serve as an up-to-date resource for oncologists and primary care providers that addresses the many aspects of supportive care associated with cancer survivorship. Accordingly, the book covers a wide …
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Other Authors
Alberts, David
Lluria-Prevatt, Maria
Kha, Stephanie
Weihs, Karen
Responsibility
David Alberts, Maria Lluria-Prevatt, Stephanie Kha, Karen Weihs, editors
Place of Publication
Cham
Publisher
Springer
Date of Publication
c2016
Physical Description
1 online resource (x, 346 p. : 27 illus., 19 illus. in color)
ISBN
9783319248141
9783319248127 (print ed.)
Subjects (MeSH)
Continuity of Patient Care
Neoplasms - therapy
Patient Advocacy
Social Support
Survivors - psychology
Abstract
This textbook provides a highly coordinated, interdisciplinary model for future clinical cancer supportive care programs in National Cancer Institute (NCI)-designated Clinical and Comprehensive Cancer Centers and NCI Community Oncology Research Programs (NCORPs). At the same time, it is intended to serve as an up-to-date resource for oncologists and primary care providers that addresses the many aspects of supportive care associated with cancer survivorship. Accordingly, the book covers a wide range of areas and topics, including but not limited to psychosocial oncology, patient and family education, lifestyle change counseling, palliative care, symptom management (eg. pain control), cancer risk and genetic counseling, financial planning, and patient navigation.
Contents
1. Introduction -- 2. Patient Navigation and Supportive Cancer Care -- 3. Psychosocial Oncology -- 4. Psychosocial Services/Management of Depression -- 5. Palliative Care -- 6. Survivorship Care Planning -- 7. Fundamentals of Cancer Pain Management -- 8. Breakthrough Cancer Pain -- 9. Delayed Nausea/Emesis -- 10. Fatigue -- 11. Changes in Cognitive Function Related to Chemotherapy -- 12. Sleep Disorders -- 13. Nutrition and the Cancer Survivor -- 14. Symptom Management: Weight Gain -- 15. Genetic Counseling and Risk Assessment -- 16. Cancer Survivorship in the Digital Age -- 17. Health Economic and Outcomes Research in Cancer -- 18. Hospitality Houses for Cancer Patients: The Editha House Perspective -- 19. Supportive Care: The Patient’s Perspective.
Format
e-Book
Location
Online
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8 records – page 1 of 1.