This photovoice study explored the lived experiences of nine Puerto Rican mental health professionals who provided postdisaster counseling services to children. Due to the complex and multilayered experiences of Puerto Rican mental health professionals, this study used intersectionality as the theoretical lens to facilitate thematic analysis of the data. Results from coresearchers' narratives and photographs generated seven major themes: (a) la politiquería of disasters; (b) the impact of compounding disasters; (c) Puerto Rico se levanta: strategies for collective healing; (d) impact of disasters on children; (e) experiences with clients; (f) awareness, action, change; and (g) supporting, connecting, and transforming. The results and discussion provide awareness into the experiences of Puerto Rican clinicians who formed part of disaster response efforts in their own community. Clinical, educational, and research implications are drawn from coresearchers' narratives and insight.

People with intellectual/developmental disabilities experience exclusion from social spaces. In this dissertation, I address social inclusion in: a) research and b) peer relationships in the context of mental health services. To address inclusion in research, we conducted key informant interviews with academic researchers (n = 8) and co-researchers with intellectual disability (n = 6) who have expertise in inclusive research (study 1). Using principles of grounded theory we analyzed the data and developed a conceptual model describing the contextual factors and team-level factors that coalesce to foster and maintain inclusive research collaborations. We found that team members’ values and characteristics influence inclusive research collaborations and drive a commitment to accessibility. Additionally, perceived personal and societal benefits contribute to co-researcher involvement. Contextual factors, including funding and partnership duration, influence teams’ processes and structures. These processes and structures influence the extent to which co-researchers perceive the inclusive research team to be co-facilitated or academic-facilitated. This model describes how contextual and team-level factors and processes may be optimized to support co-researcher engagement in inclusive research. To address peer relationships in the context of mental health services, I used a stakeholder-driven approach to develop a peer mentoring intervention for young adults with intellectual/developmental disabilities and co-occurring mental health conditions (study 2). This approach included partnership with 3 young adults with intellectual/developmental disabilities and co-occurring mental health conditions and a 7 member advisory board composed of self-advocates and professionals. In addition, I conducted focus groups with mental health clinicians (n = 10), peer support specialists (n = 9), and transition specialists (n = 20) to identify the desired peer mentoring outcome and intervention components and content that may facilitate these outcomes. The focus group participants identified several relationship-driven and outcome-driven actions peer mentors may use to support outcome achievement. Stakeholders also identified five components relevant to the intervention: safety considerations, mentor matching, degree of intervention structure, mentor training and support, and collaboration with mentees’ support teams. These findings draw attention to the importance of social relationships and individualization of both mentoring and supports for mentors. Together, these two studies highlight the importance of valuing the unique strengths of people with disabilities and the need for task and environmental adaptations to foster social inclusion of people with intellectual/developmental disabilities. / 2021-06-18T00:00:00Z

The purpose of this participatory action research study was to explore queer womxn of color's experiences of microaggressions in therapy. Due to the multifaceted and complex experiences of queer womxn of color, this study was informed by intersectionality theory and utilized photovoice methodology to answer the following question: How do queer womxn of color experience microaggressions in therapy? The seven queer womxn of color who participated in this study provided vivid, honest, and courageous portrayals of their experience of microaggressions in therapy. Six major themes were prominent in their photographs and narratives: (a) collective and pervasive experiences of oppression, (b) therapy as a tool of oppression, (c) impact of oppression in therapy, (d) strategies for survival, (e) healing for queer womxn of color, and (f) the power of sharing mi historia. Overall, co-researchers provided insight into their experiences of oppression in therapy, while highlighting clinical and research practices that may be healing and liberatory for queer womxn of color. Additionally, implications and conclusions drawn from the experiences of co-researchers provide recommendations for mental health professionals, educational programs, and researchers to consider when working with queer womxn of color.

Background: Obesity disproportionately affects Pakistani women and rates of obesity related conditions are high in Bradford. Research priority setting can guide the development of policy and practice, resulting in more relevant research. There are no research prioritisation exercises targeted at obesity in Pakistani women. Aim: To develop an obesity research agenda with Pakistani women living in deprived inner-city areas of Bradford. Methods: Using a feminist participatory action research design, a five stage process was adopted involving the following: (i) A systematic review to identify the gaps in knowledge (ii) face-to-face interviews with 21 Pakistani women to generate their health concerns (iii) focus groups to explore the obesity concerns of 23 Pakistani women (iv) survey to identify unmet obesity needs of Pakistani women according to 160 local, multisectoral stakeholders (v) adapted consensus method involving 32 Pakistani women to rank their identified concerns and unmet needs in order of importance. Results: The study identified needs related to cultural and language constraints, including barriers in obtaining health promotion information and the social isolation of women. Education needs and misconceptions surrounding diet and physical activity were also identified. Highest rankings were given to concerns and needs surrounding the mental health of Pakistani women, education needs for a healthy diet, and the benefits of physical activity. Conclusion: Pakistani women’s unmet obesity needs highlight the existence of wider determinants of health that are structural in nature. Considering these barriers, a research agenda was developed from the findings and reflect the obesity health needs of this population. / Funding through Born in Bradford / The full text will be available at the end of the embargo: 21st Sept 2022

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