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Mary Rose Van Kesteren

Biographic Data

ID355255
NAMEMary Rose Van Kesteren
GIVEN NAMESMary Rose
FAMILY NAMEVan Kesteren
SIGNATUREVAN KESTEREN M R
AFFILIATIONSCentre for Addiction and Mental Health
VERIFIEDNo
TOTAL WORKS7
TOTAL CITATIONS0
AUTHOR COUNT7
EDITOR COUNT0
FIRST PUBLICATION YEAR2023
LATEST PUBLICATION YEAR2026
H-INDEX0
  • “A sense of community.” A qualitative descriptive study on how to build relationships and rapport with people with lived/living experience and caregivers engaged in mental health and substance use hea…

    Open Access•Diana Kaliza, Wuraola Dada-Phillips et al.•ARTICLE•Social Sciences & Humanities Open•2026

    Engaging people with lived/living experience (PLLEX) and caregivers (-C) is becoming more widely adopted in mental health and substance use health research. Their engagement meaningfully improves the relevance and impact of research outcomes. Yet, authentic engagement can be difficult to achieve without building and maintaining strong relationships with PLLEX-C. This qualitative descriptive study explores the perspectives of PLLEX-C engaged in me…

  • Writing Patient Engagement Effectively Into Grant Applications

    Open Access•Lisa D Hawke, Katie Upham et al.•ARTICLE•Health Expectations•2026

    Engaging people with lived/living experience and caregivers in research (also known as ‘patient engagement’ or ‘patient and public involvement’) has many benefits to research, to the community, and to the people involved in the process [1]. Engagement is increasingly valued by many funding bodies [2, 3] as being best practice when possible. However, funding barriers have been described as getting in the way of authentic engagement [4]. It is ther…

  • Strengthening the Delivery of Physical Healthcare for Adults Living With Serious Mental Illness – A Qualitative Description of Patient and Family Member Perspectives

    Open Access•Munazzah Ambreen, Christopher Canning et al.•ARTICLE•Health Expectations•2025

    BACKGROUND: Individuals with serious mental illness (SMI) have higher rates of comorbid physical health conditions, poorer associated health outcomes, and die on average 10-20 years earlier than the general population. This qualitative study aimed to explore the perspectives and experiences of adults living with SMI and family members with accessing physical healthcare within primary and mental health settings in Canada. METHODS: We conducted a q…

  • Gaps in the Engagement of People With Lived and Living Experience and Caregivers in Mental Health and Substance Use Health Research

    Open Access•Lisa D Hawke, Jingyi Hou et al.•ARTICLE•Health Expectations•2025

    BACKGROUND: People with lived/living experience and family/caregivers (PLLEX-C) can be engaged in mental health and substance use health research in roles such as advisors, collaborators, and co-researchers. While there is a substantial body of research describing the barriers and facilitators to effective lived experience engagement, the actual contributions that PLLEX-C are making to the research remains under-explored. This qualitative descrip…

  • Co‐Authoring and Reporting on Lived Experience Engagement in Mental Health and/or Substance Research

    Open Access•Natasha Y Sheikhan, Kerry Kuluski et al.•ARTICLE•Health Expectations•2025

    INTRODUCTION: There is a move towards engaging people with lived experience and families (PWLE/F)-also referred to as PWLE/F engagement-in mental health and/or substance use research. However, PWLE/F engagement is inadequately reported on in mental health and/or substance use research papers. OBJECTIVE: To understand what PWLE/F and researchers perceive are important components to report on related to engagement in mental health and/or substance …

  • Walking Alongside

    Open Access•Hamer Bastidas-Bilbao, Vicky Stergiopoulos et al.•ARTICLE•Qualitative Health Research•2023

    Medical assistance in dying (MAiD) was introduced into Canadian federal legislation in 2016. Mental illness as the sole underlying medical condition (MI-SUMC) is currently excluded from eligibility; such exclusion is scheduled to expire on March 17, 2024. Irremediability, capacity, quality of life, autonomy, family involvement, and healthcare system constraints have been debated intensively. Recent studies have not explored the views of family me…

  • Searching for relief from suffering

    Open Access•Hamer Bastidas-Bilbao, Vicky Stergiopoulos et al.•ARTICLE•Social Science & Medicine•2023•References: 39

    Medical assistance in dying (MAiD) was introduced into Canadian legislation in 2016. Mental illness as the sole underlying medical condition (MI-SUMC) is excluded from eligibility; this is expected to change in 2024. Incurability, intolerable suffering, capacity to make healthcare decisions, and suicidality have been publicly debated in connection with mental illness. Few studies have explored the views of persons with mental illness on the intro…

No prominent works on this page.

  • Walking Alongside

    Open Access•Hamer Bastidas-Bilbao, Vicky Stergiopoulos et al.•ARTICLE•Qualitative Health Research•2023

    Medical assistance in dying (MAiD) was introduced into Canadian federal legislation in 2016. Mental illness as the sole underlying medical condition (MI-SUMC) is currently excluded from eligibility; such exclusion is scheduled to expire on March 17, 2024. Irremediability, capacity, quality of life, autonomy, family involvement, and healthcare system constraints have been debated intensively. Recent studies have not explored the views of family me…

  • Searching for relief from suffering

    Open Access•Hamer Bastidas-Bilbao, Vicky Stergiopoulos et al.•ARTICLE•Social Science & Medicine•2023•References: 39

    Medical assistance in dying (MAiD) was introduced into Canadian legislation in 2016. Mental illness as the sole underlying medical condition (MI-SUMC) is excluded from eligibility; this is expected to change in 2024. Incurability, intolerable suffering, capacity to make healthcare decisions, and suicidality have been publicly debated in connection with mental illness. Few studies have explored the views of persons with mental illness on the intro…

  • Strengthening the Delivery of Physical Healthcare for Adults Living With Serious Mental Illness – A Qualitative Description of Patient and Family Member Perspectives

    Open Access•Munazzah Ambreen, Christopher Canning et al.•ARTICLE•Health Expectations•2025

    BACKGROUND: Individuals with serious mental illness (SMI) have higher rates of comorbid physical health conditions, poorer associated health outcomes, and die on average 10-20 years earlier than the general population. This qualitative study aimed to explore the perspectives and experiences of adults living with SMI and family members with accessing physical healthcare within primary and mental health settings in Canada. METHODS: We conducted a q…

  • Gaps in the Engagement of People With Lived and Living Experience and Caregivers in Mental Health and Substance Use Health Research

    Open Access•Lisa D Hawke, Jingyi Hou et al.•ARTICLE•Health Expectations•2025

    BACKGROUND: People with lived/living experience and family/caregivers (PLLEX-C) can be engaged in mental health and substance use health research in roles such as advisors, collaborators, and co-researchers. While there is a substantial body of research describing the barriers and facilitators to effective lived experience engagement, the actual contributions that PLLEX-C are making to the research remains under-explored. This qualitative descrip…

  • Co‐Authoring and Reporting on Lived Experience Engagement in Mental Health and/or Substance Research

    Open Access•Natasha Y Sheikhan, Kerry Kuluski et al.•ARTICLE•Health Expectations•2025

    INTRODUCTION: There is a move towards engaging people with lived experience and families (PWLE/F)-also referred to as PWLE/F engagement-in mental health and/or substance use research. However, PWLE/F engagement is inadequately reported on in mental health and/or substance use research papers. OBJECTIVE: To understand what PWLE/F and researchers perceive are important components to report on related to engagement in mental health and/or substance …

  • “A sense of community.” A qualitative descriptive study on how to build relationships and rapport with people with lived/living experience and caregivers engaged in mental health and substance use hea…

    Open Access•Diana Kaliza, Wuraola Dada-Phillips et al.•ARTICLE•Social Sciences & Humanities Open•2026

    Engaging people with lived/living experience (PLLEX) and caregivers (-C) is becoming more widely adopted in mental health and substance use health research. Their engagement meaningfully improves the relevance and impact of research outcomes. Yet, authentic engagement can be difficult to achieve without building and maintaining strong relationships with PLLEX-C. This qualitative descriptive study explores the perspectives of PLLEX-C engaged in me…

  • Writing Patient Engagement Effectively Into Grant Applications

    Open Access•Lisa D Hawke, Katie Upham et al.•ARTICLE•Health Expectations•2026

    Engaging people with lived/living experience and caregivers in research (also known as ‘patient engagement’ or ‘patient and public involvement’) has many benefits to research, to the community, and to the people involved in the process [1]. Engagement is increasingly valued by many funding bodies [2, 3] as being best practice when possible. However, funding barriers have been described as getting in the way of authentic engagement [4]. It is ther…

Mental health (6 works) · Mental Health and Patient Involvement (6 works) · Qualitative research (6 works) · Medicine (5 works) · Psychiatry (5 works) · Psychology (5 works) · Family Caregiving in Mental Illness (4 works) · Sociology (4 works) · Thematic analysis (4 works) · Mental illness (3 works)

Ethnos_APP • Open Source Project • MIT License • Frontend v2.0.0 • Privacy and Cookies • API Documentation: api.ethnos.app/docs • API Source Code: GitHub • DOI: 10.5281/zenodo.17049435 • Frontend Source Code: GitHub • DOI: 10.5281/zenodo.17050053 • cruz.rio.br • Expectantes Misericordiae