The goal of this dissertation was to explore aging lesbian and gay individuals living in rural communities, in terms of their social networks and the relationships between these networks, identity, health, and quality of life. Guiding the study were three overarching questions. Using a multi-method design, the research was grounded within a socio-ecological context and focused on how structural systems create pathways for health and are affected by social position (intersectionality). Participants (n=25) were recruited from Kentucky (n=20), West Virginia (n=3), and Tennessee (n=2). Thirteen participants self-identified as gay and twelve as lesbian. Findings highlight the complexity of the aging experience and the difficulty in parsing out the influence of a rural location, the aging process, and being a lesbian or gay male, on social network development, identity, health, and quality of life. Findings indicate that rural gay and lesbian individuals develop networks based on need with limited consideration for network members’ acceptance of their identity. The findings also indicate that networks are primarily composed of heterosexual members. Social isolation and loneliness remain a pervasive issue in the rural gay and lesbian aging community. Finally, network size does not affect the overall health and quality of life for rural aging lesbian and gay individuals, but identity congruence does. Conclusions point to the greater need for research to understand the factors affecting aging lesbian and gay individuals in rural environments. Opportunities abound for developing further research addressing social isolation among this population and exploring the positive relationship between identity congruence and quality of life. The findings highlight the collective need to continue research into sexual minority aging and rural sexual minority aging.

Background: Digital primary care is expanding rapidly in Sweden and access is unevenly distributed and affected by socioeconomic status (SES) and digital exclusion. The COVID-19 pandemic further highlighted this problem as digital care removes risk of infection. Research is lacking on digital visits by traditional health care providers (HCP) during the COVID-19 pandemic and a risk exists that socially vulnerable groups are multiple afflicted by the current situation and that health policy goals are not achieved. Objectives: To investigate the effect of the COVID-19 pandemic on digital visits by traditional HCP, the distribution of visits and correlations to SES in Malmö municipality. Method: Ecological retrospective observational cross-sectional study with comparisons between the years 2020 and 2021. Descriptive analysis of changes between the years and distribution of visits and logistic regression for the correlation to Care Need Index (CNI) as a proxy for SES. Results: Physical visits decreased more than digital visits increased. Privately operated HCP and HCP in areas with higher income better compensated the decrease of physical visits with digital visits. There were major differences between HCP in use of digital visits and high CNI and private operation negatively affected this. Conclusion: Among traditional HCP in Malmö municipality the COVID-19 pandemic may have increased digital visits and the access was unevenly distributed. This risks increased inequality in health and not achieving set health policy goals. Further studies and efforts are needed to achieve a digital primary care with equal access and patient’s autonomy, participation, and empowerment in focus. / <p>Betyg i Ladok 220617.</p>

Os povos indígenas vivem há mais de 500 anos na luta pela superação do colonialismo interno. Com a homogeneização das formas de vida, estes povos são sistematicamente produzidos como não existentes nas políticas integracionistas. A Constituição Federal de 1988 rompe com esta prática garantindo o direito do reconhecimento de suas identidades e modos de vida, expressos pela sua cultura, e o direito à saúde. O direito dos povos originários à saúde pautou três Conferências de Saúde Indígena que estabeleceram as diretrizes para a criação do Subsistema de Atenção à Saúde Indígena em 1999. Desde o início de sua estruturação nos 34 Distritos Sanitários Especiais Indígenas (DSEI), foram organizados os Conselhos Distritais de Saúde Indígena (CONDISI) e o Fórum de Presidentes de CONDISI no nível central. Este estudo tem como objetivo analisar a participação e o protagonismo dos povos indígenas no processo de construção e implementação da Política Nacional de Saúde Indígena, após a Constituição Federal de 1988, a partir das Epistemologias do Sul. Foi utilizada a metodologia qualitativa com diversas fontes e materiais: análise documental das atas de reuniões, legislações, relatórios das cinco Conferências Nacionais de Saúde Indígena e 24 entrevistas em profundidade com indígenas, gestores, indigenistas e representante do MPF. A análise das legislações reconhecidas como pertinentes ao tema indicam uma grande quantidade e diversidade de normas que tratam de forma segregada as temáticas indígenas e as normas do Sistema Único de Saúde. Demonstram, para além da fragmentação legal e normativa, algumas iniciativas que avançam na integralidade da assistência, bastante pontuais, como a criação de incentivos financeiros específicos. Destaca-se a complexidade e a fragilidade da articulação interfederativa, que se torna mais complexa com a gestão federal e a territorialização dos DSEI, que não coincidem com os territórios de estados e municípios. No que tange à participação, pode-se afirmar que a maioria dos entrevistados reconhecem o CONDISI como espaço legítimo de diálogo entre indígenas e governo para debater a política de saúde e sua execução nas aldeias indígenas. Contudo, é evidente o predomínio das pautas de interesse da gestão e a repercussão nas reuniões de CONDISI de temas já discutidos no Fórum de Presidentes. Nas pautas do CONDISI Litoral Sul, que foram objeto deste estudo, por exemplo, a discussão da divisão territorial do DSEI, de interesse dos indígenas, não ganhou espaço e reconhecimento pela gestão. Chama a atenção à ausência de discussão nos espaços formais de temas que predominam nas entrevistas com os indígenas, como a valorização da medicina tradicional e a atenção diferenciada. Esta última é a justificativa central para existência do Subsistema e pauta-se nas desigualdades em saúde, na necessidade de modos de produção de cuidado que articulem as medicinas indígenas e a biomedicina e na diversidade cultural dos mais de 300 povos. O predomínio da biomedicina como forma científica e legítima do saber sobre a saúde acaba por interditar as pautas referentes às medicinas indígenas. Esta lógica perpetua a relação colonial do governo com os povos originários, principalmente sobre o saber, comprometendo a efetivação da atenção diferenciada, e, por consequência, do direito à saúde. Esta política, para ser efetiva, deveria se organizar na perspectiva da Ecologia de Saberes, considerando os modos de existência destes povos, principalmente sua relação com a terra, e sua construção como sujeitos coletivos. / Indigenous Peoples have been living for more than 500 years in the struggle to overcome internal colonialism. With the homogenization of the way of life, these peoples are systematically considered as non-existent in integrationist policies. The Federal Constitution of 1988 breaks with this logic assuring them the right to their identities and their ways of life, expressed by their culture, and also their right to health. The Indigenous Peoples\' right to health established three Indigenous Health Conferences that set the guidelines for the creation of the Indigenous Health Care Subsystem, in 1999. Since its beginning, along with the establishiment of the 34 Special Indigenous Sanitary Districts (DSEI), participatory Councils were organized (CONDISI), and also the CONDISI Presidents\' Forum at the central level. Based on Epistemologies of the South, this study aims to analyze the participation and the protagonism of Indigenous Peoples in the construction and implementation processes of the National Indigenous Health Policy, after the Federal Constitution of 1988. The qualitative methodology used with several sources and materials: documenta analysis of minutes of meetings, legislations, reports of the five National Indigenous Health Conferences and 24 in-depth interviews with Indigenous Peoples, managers, indigenists and Federal Prosecution Service. Relevant legislation analyzed showed great quantity and diversity of norms that separate the indigenous themes and the norms of the Unified Health System. They demonstrate, in addition to legal and normative fragmentation, some initiatives towards care integrality quite specific ones, such as the creation of financial incentives. We highlight the complexity and fragility of the interfederative articulation, which becomes more complex with federal management and territorialisation of the DSEI, which do not match with the limits of states and municipalities territories. Regarding participation, it can be said that most interviewees recognize the CONDISI as a legitimate space for dialogue between Indigenous Peoples and the government to discuss the health policy and its implementation in indigenous communities. However, there is a clear predominance of agendas in the interest of the management representatives and the repercussions on the CONDISI meetings of topics already discussed in the Presidents\' Forum. For example, on the agenda of the CONDISI Litoral Sul, object of this study, the discussion of the territorial division of the DSEI, on the interest of the indigenous representatives, did not gain space and recognition by the management representatives. What also draws attention is the absence of discussions of topics that were predominant on the interviews with Indigenous Peoples on formal spaces, such as traditional medicine and differentiated care. This last one is central to the existence of the Subsystem and it is based on inequalities in health, the need for care production methods that articulate traditional indigenous medicine and biomedicine, and the cultural diversity of more than 300 tribes. The predominance of biomedicine as a scientific and legitimate way of health knowledge inhibits the agenda related to traditional indigenous medicine. This logic perpetuates the colonial relationship of the government upon the Indigenous Peoples, especially regarding knowledge, compromising the effectiveness of differentiated care and, consequently, the right to health. This policy, in order to be effective, should be organized in the perspective of the Ecology of Knowledges, considering the ways of existence of these peoples, especially their relationship with the land, and their construction as collective subjects.

Submitted by Gentil Jeorgina (jeorgina@icict.fiocruz.br) on 2013-10-09T16:15:12Z No. of bitstreams: 1 Valéria Hartt.pdf: 1919843 bytes, checksum: 68a6cd38069d53b02f4eb969f570af19 (MD5) / Made available in DSpace on 2013-10-09T16:15:12Z (GMT). No. of bitstreams: 1 Valéria Hartt.pdf: 1919843 bytes, checksum: 68a6cd38069d53b02f4eb969f570af19 (MD5) Previous issue date: 2013 / Fundação Oswaldo Cruz. Instituto de Comunicação e Informação Científica e Tecnológica em Saúde. Rio de Janeiro, RJ, Brasil / Nesse recorte de pesquisa, o conceito de conhecimento leigo é ponto de partida e fio condutor para compreender as práticas de participação e ativismo de uma organização de pacientes de câncer, aqui na experiência da International Myeloma Foundation no Brasil (IMF). É a perspectiva informacional que ancora a meta de identificar os contornos do conhecimento leigo da representação brasileira da IMF para dar relevo aos sentidos de equidade em saúde na atenção oncológica. Os resultados apontam para uma forma de mobilização cidadã capaz de abrigar a produção social do conhecimento científico, mas mostram que a prática de advocacia em saúde ainda precisa avançar no Brasil como reflexo dessa nova forma de construção do conhecimento. / In this research outline, the concept of lay knowledge is a starting point and guideline for understanding the practices of participation and activism of a cancer patients organization, here through the experience of the International Myeloma Foundation (IMF) in Brazil. It is the informational perspective that anchors the goal of identifying the contours of lay knowledge of Brazilian representation of the IMF to emphasize the senses of equity in health in cancer care. The results point to a form of citizen mobilization able to shelter the social production of scientific knowledge, but show that the practice of health advocacy still needs to advance in Brazil as a result of this new form of knowledge construction.

OBJETIVOS: Determinar la desigualdad de la prevalencia de desnutrición crónica infantil en función a algunos determinantes sociales en países de América Latina y el Caribe (ALC)  MÉTODOS: Se realizó un estudio ecológico con los indicadores de desarrollo de la base de datos del Banco Mundial. Se analizaron los indicadores de 19 países (acceso a electricidad y servicios básicos de agua en población rural, PBI per cápita, gasto en salud per cápita). La desigualdad absoluta y relativa se determinó mediante el Índice de Kuznets absoluto, y relativo, la gradiente de la desigualdad a través de índice de las gradientes de la desigualdad, y para la desigualdad proporcional se usó el (índice de concentración de salud) ICS y la curva de concentración. RESULTADOS: la brecha de las desigualdades en la prevalencia de desnutrición crónica infantil entre los países de ALC se mantuvo prácticamente sin cambios significativos a lo largo del periodo estudiado. El 20% de los países con mayor desventaja concentran el 40% de la prevalencia de desnutrición crónica mientras que el 20% de los países con mayor ventaja solo el 7-8%, medido a través del ICS. CONCLUSIONES: A pesar de que en los Objetivos de Desarrollo del Milenio se encontraban eliminar la desnutrición, ésta permanece. La brecha de desigualdad ha disminuido respecto a la gradiente de desigualdad (desigualdad absoluta), sin embargo, la desigualdad proporcional se ha mantenido igual. Para eliminar esta brecha en ALC se deben generar políticas para distribuir de forma más eficiente y equitativa los recursos destinados al gasto en salud y los sectores relacionados, para de esa forma enfocarse en los determinantes sociales debidos. / OBJECTIVES: determinate the inequality of the prevalence of chronic childhood malnutrition according to some social stratifiers in the countries of Latin America and the Caribbean (LAC) METHODS: An ecological study was carried out at the country level with the development indicators of the World Bank database. The indicators of 19 countries will be analyzed (access to electricity and basic water services in rural areas, GDP per capita, health expenditure per capita). The absolute and relative inequality was determined by the absolute and relative Kuznets index, gradient of the inequality through the graduation index of the inequality, in addition, the proportional inequality was calculated through the index of concentration in health and the curve of concentration. RESULTS: the gap of inequalities in the prevalence of chronic child malnutrition in the LAC countries, remained practically without significant changes throughout the period studied. In addition, 20% of the countries with the greatest disadvantage accounted for 40% of the prevalence of chronic malnutrition compared to 20% of the countries with the greatest advantage, which presented 7-8% of the prevalence through the index of concentration on health. CONCLUSIONS: Although the Millennium Development Goals were to eliminate malnutrition, it was not possible to do so. However, the inequality gap has partially decreased. To eliminate it In LAC, wealth should be distributed more efficiently, and equitable resources allocated to health spending and related sectors. As well as generating Policies to address inequalities in and between countries. / Tesis

Bakgrund: Narkotikamissbruk har sedan 1960-talet ansetts vara ett allvarligt samhällsproblem som ökar risken för sjukdom och social utsatthet. Varje år dör omkring 900 personer i Sverige av läkemedels- och narkotikaförgiftningar. Personer som utvecklat ett narkotikamissbruk kan hamna i en ond spiral där de negativa konsekvenserna ökar och medför en risk att förlora allt så som jobb, hem och familj. Detta kan i sig öka de socioekonomiska skillnaderna i befolkningen. När en person bryter sitt missbruk sker en process som i denna studie förklarats utifrån modellen Stages of change. Syfte: Syftet med studien är att skildra betydelsefulla faktorer i förändringsprocessen för individer som tagit sig ur narkotikamissbruk. Metod: Studien var av kvalitativ karaktär och genomfördes med semistrukturerade intervjuer. I studien kombinerades induktiv och deduktiv ansats. Resultat: Resultatet visade att socialt stöd var en viktig faktor genom förändringsprocessen, framförallt under faserna action och maintenance. Olika strategier som att bryta gamla beteenden och mönster var betydande. Den egna viljan ansågs vara essentiell för att inleda och genomföra en förändring. Genom behandling fick informanterna verktyg att hantera sin vardag. De jobbade hårt med sig själva genom de olika förändringsfaserna i Stages of change för att uppnå ett vidmakthållande och minimera risken för återfall. Konklusion: Studiens resultat visar att när en person är i behov av hjälp, och uttrycker detta, då behöver familj och samhälle erbjuda stöd. För de individer som inte har det sociala nätverket bakom sig, där synliggörs ett större behov av att samhällsinsatser måste finnas tillgängliga för att bidra till jämlik hälsa. / Background: Since the 1960s, drug abuse has been considered a serious societal issue that increases the risk of illness and social exclusion. In Sweden approximately 900 people die from drug intoxication annually. People who develop a drug addiction can end up in a negative spiral with consequences such as loss of work, home and family. Consequences that can increase the socio-economic differences within the population. When a person decides to end their addiction a process of change takes place, in this study explained using the Stage of change model. Purpose: The purpose of the study is to describe significant factors during the process of change within individuals who have recovered from drug abuse. Method: The study design was qualitative and was conducted using a semi-structured interview guide. The study combined inductive and deductive analysis. Results: The results indicated that social support was an important factor throughout the process of change, especially during the phases action and maintenance. Various strategies such as breaking old habits and patterns were also significant. Self-determination was considered essential to initiate and implement change. During treatment, the informants were given coping strategies to handle their everyday lives. They worked hard with themselves throughout the various stages in Stages of change to achieve sustainability and minimize the risk of relapse. Conclusion: The study's result implies that when a person is in need of help, and expresses this, family and community need to offer support. Individuals who do not have the social network requires more interventions from the community to enable a healthy life.

No description available.

McMaster University DOCTOR OF PHILOSOPHY (2019) Hamilton, Ontario (Health Research Methods, Evidence, and Impact) TITLE: Measuring International Health Inequalities and Socioeconomic Status Using Household Survey Data AUTHOR: Mathieu J.P. Poirier, B.Sc., M.P.H. (McMaster University) SUPERVISOR: Dr. Michel Grignon NUMBER OF PAGES: xii, 231 / The methods underlying the quantification of health inequalities have profound consequences for measuring progress in achieving health for all. In Chapter two, associations between household wealth indices, income, and consumption were systematically compiled and different methods of wealth index calculation were evaluated for appropriateness of use in a variety of settings. Researchers are presented with a synthesis of existing evidence about the appropriateness of use of wealth indices in urban and rural areas, their robustness to changes in the asset mix, future applications, and advantages and disadvantages of primary competing methods of quantifying SES using household survey data. In Chapter three, international microdata were analyzed to evaluate how magnitudes of health inequality are affected by different methods of quantifying household socioeconomic status (SES), including income, consumption, and asset wealth. In Chapter four, the need for a transnational approach to measuring health inequalities was justified and the new method was developed using an empirical example. Substantively, these chapters develop the most complete evaluation of the association between the asset wealth, consumption, and income using both critical interpretive synthesis and microdata analysis, as well as the first meta-analysis evaluating changes in health inequality magnitudes according to the SES measure used over time and across country-income levels. The transnational analysis of health inequalities uncovered previously hidden health disparities in the island of Hispaniola, and detailed instructions for all methodological aspects of the new method were presented. The distribution of disease between nations, subnational regions, and urban-rural areas in Hispaniola were analyzed from 1994 to 2013, and the first relative geospatial wealth ranking between Haiti and the Dominican Republic was presented. Global health researchers should strive to measure the equity of health between people, and this sometimes requires analyzing populations that are not neatly contained by national boundaries. / Thesis / Doctor of Philosophy (PhD) / This thesis investigates social inequalities in health and how to measure socioeconomic status (SES) using household surveys in a way that is robust across jurisdictions. It examines how wealth indices compare to income and consumption, and develops a new method to calculate transnational health inequalities. Chapter two conducts a comprehensive evaluation of evidence surrounding the use of wealth indices in urban and rural areas, robustness to changes in assets, future applications, and the advantages and disadvantages of the primary competing methods for quantifying household SES. The third chapter systematically evaluates how health inequality magnitudes evolve over time and across country-incomes according to SES measure. Finally, a transnational measurement of health inequalities was calculated for the island of Hispaniola in chapter four, uncovering the distribution of disease between nations, subnational regions, and urban-rural areas. Detailed instructions for all methodological aspects of the new transnational method are presented.

Utilizing a mixed methods approach in assessing cities and metropolitan areas with the highest rates of breast cancer disparities in African-American communities, this study presents the Affiliate perspective of the Susan G. Komen non-profit organization in combination with available socioeconomic data and academic literature. Analyzed through an anthropological lens, qualitative and quantitative data illuminate the lived experiences and dynamic circumstances in which breast cancer disparities are disproportionately experienced in 21 of the nation’s populations of African-Americans. Two main recommendations arose from this research: prioritization of granting to activities such as patient navigation, usage of patient narrative messaging, community-based participatory research methods of program development and implementation, mobile mammography delivery, usage of lay health educators, and self-advocacy education to alleviate barriers to healthcare and supplementation of the current educational activities of the Komen Affiliates through program sharing and leverage of current assets with consideration of current Affiliate capacity. These recommendations may help in alleviating breast cancer disparities present in African-American communities with the highest levels of disparities in the nation.

Introduction : Les droits en matière de santé sexuelle et reproductive (SSR) sont essentiels pour parvenir à une couverture sanitaire universelle pour tous, y compris les personnes handicapées. L'Ouganda a émergé d'un conflit armé de 20 ans qui a engendré à la fois des handicaps et des dommages aux systèmes de santé, en particulier au nord du pays. Une personne sur cinq vit avec un handicap en Ouganda où plusieurs lois et politiques ont été adoptées promouvant les droits des personnes handicapées. Or, leur accès aux services de SSR demeure limité. Les rôles genrés restent omniprésents et les hommes et les jeunes handicapés sont moins ciblés par les programmes de SSR (article 1). Les politiques de santé et leur mise en œuvre nécessitent donc une analyse contextuelle plus approfondie pour protéger le droit à la santé des personnes handicapées. Cette thèse visait à examiner les relations perçues et empiriques entre la législation, les politiques de santé et l'utilisation des services de SSR par les personnes handicapées dans la région post-conflit au nord l'Ouganda. Méthodes : Un devis séquentiel exploratoire de méthodes mixtes s'est appuyé sur le cadre d’analyse des politiques basée sur l'intersectionnalité (IBPA). 1) Nous avons mené une étude de cas multiples auprès de cinq groupes d'acteurs des politiques (personnes handicapées, prestataires de services, organisations de personnes handicapées, organisations nationales et internationales, et décideurs politiques nationaux), thématiquement analysé 45 entretiens approfondis et neuf groupes de discussion, et observé sept structures de santé en matière d'accessibilité. 2) Nous avons analysé des données secondaires provenant des enquêtes démographiques et sanitaires ougandaises de 2006, 2011 et 2016 à l'aide de régressions logistiques multivariées. Le but était d’analyser l'utilisation des services de SSR chez 15 739 personnes au cours de la décennie qui a suivi l'adoption de la Loi sur le handicap en Ouganda. 3) Une revue systématique a été réalisée pour examiner les relations entre la législation, les politiques de santé et l'utilisation des services de SSR parmi les populations vulnérables en Afrique subsaharienne (1994-2019). Résultats : Cette thèse met en exergue quatre résultats principaux. 1) Le cadre de l’IBPA a mis en évidence des relations complexes entre la législation, les politiques de santé et l'utilisation des services de SSR chez les personnes handicapées au nord de l'Ouganda. Ces relations ont été marquées par des défis de mise en œuvre des politiques, la violation des droits des personnes handicapées, et des vulnérabilités croisées vécues par les personnes handicapées, exacerbées par les structures de pouvoir sociétales sous-jacentes. Les perceptions des différents groupes d'acteurs des politiques convergeaient en soulignant les iniquités persistantes en matière de SSR auxquelles sont confrontées les personnes handicapées (articles 2 et 3). L'utilisation des services de SSR s’est accrue au fil du temps. Cependant, elle ne s'est pas améliorée de la même manière pour tous. L'évolution de l'utilisation des services de SSR sur une décennie a révélé des tendances d’utilisation des services nuancées chez les personnes vivant avec différentes incapacités; notamment, les femmes plus nanties avec une incapacité auditive étaient moins susceptibles d'avoir utilisé les services de maternité comparativement aux femmes pauvres non handicapées (article 4). 2) Les cinq groupes d’acteurs des politiques ont identifié des défis en matière de mise en œuvre des politiques et ont émis plusieurs recommandations concrètes et complémentaires pour lever les barrières et rendre opérationnelles les mesures transformatrices, telles que la budgétisation et la collecte de données sur le handicap (articles 2 et 3). 3) Les résultats au niveau local (Ouganda) ont permis de contextualiser ceux au niveau régional (Afrique subsaharienne), et vice versa. Une revue systématique sur une période de 25 ans a montré que les personnes handicapées restent dans l’angle mort de la recherche sur l'analyse des politiques en matière d’utilisation des services SSR (article 5). 4) La pratique de la réflexivité tout au long de la recherche a mis en lumière les tensions dans l'application des normes éthiques dans le contexte de la recherche qualitative en santé mondiale avec des personnes handicapées menée dans le Sud (article 6). Conclusion : Ces résultats permettent aux acteurs des politiques à différents niveaux d'agir – maintenant – pour aborder et corriger les iniquités sociales de santé vécues par les personnes handicapées. Le cadre de l'IBPA s'est avéré un outil analytique et théorique utile pour mieux comprendre les questions complexes liées aux politiques et aux vulnérabilités intersectionnelles auxquelles font face les personnes handicapées. Ce cadre pourrait enrichir d’autres cadres existants d’analyse des politiques. La thèse propose deux adaptations théoriques, soit le cadre du IBPA combiné au « Multiple Streams Framework» de Kingdon et au « Policy Triangle Model» de Walt et Gilson pour de futures recherches en santé mondiale sensibles au handicap et axées sur l'analyse des politiques basées sur l'équité. / Introduction: Sexual and reproductive health (SRH) rights are essential to achieve universal health coverage (UHC) for all, including people with disabilities. Uganda emerged from a 20-year armed conflict which created both disability and damage to health systems, especially in the Northern region. One Ugandan in five lives with some disability. Uganda adopted a series of normative tools promoting the rights of people with disabilities. However, their access to SRH services remains limited. More broadly, ableist gendered roles remain pervasive and men and youth with disabilities are less targeted by SRH programmes (Article 1). Health policies and their implementation need deeper contextualised analysis to protect the right to health of people with disabilities. This thesis aimed to examine the perceived and empirical relationships among legislation, health policies, and SRH service utilisation among people with disabilities in post-conflict Northern Uganda. Methods: A sequential exploratory mixed methods design was informed by the Intersectionality-based Policy Analysis (IPBA) framework. First, I conducted a multiple case study with five groups of policy actors (people with disabilities, service providers, disabled people’s organisations, national and international organisations, and national policy-makers). I thematically analysed 45 in-depth interviews and nine focus groups and observed seven health facilities regarding accessibility. Second, I analysed secondary data with multivariable logistic regressions, from the 2006, 2011, and 2016 Uganda Demographic and Health Surveys regarding SRH service use among 15,739 individuals in the decade following the adoption of national legislation promoting the rights of people with disabilities. Third, I conducted a systematic review examining the relationships among legislation, health policies, and SRH service use among vulnerable populations in sub-Saharan Africa (1994-2019). Results: This thesis highlights four main findings. First, the IBPA framework revealed complex relationships among legislation, health policy, and the use of SRH services by people with disabilities in Northern Uganda. These relationships were marked by policy implementation challenges, disability rights violation through multiple barriers to access, and intersecting vulnerabilities experienced by people with disabilities, exacerbated by underlying societal power structures. On one hand, the perceptions of different groups of policy actors converged by emphasising the ongoing SRH inequities faced by people with disabilities (Articles 2 and 3). On the other hand, although SRH service use improved over time, it did not improve equally for everyone. The 10-year SRH service use trend showed nuanced patterns across people with different impairments; notably, richer women with hearing impairments were less likely than poor non-disabled women to have used safe motherhood services (Article 4). Second, despite identifying legislation and policy implementation challenges, the five groups of policy actors suggested several concrete and complementary recommendations to address barriers and operationalise transformative measures, such as disability data collection and budgeting (Articles 2 and 3). Third, research findings at the local level (Uganda) contextualised the findings at the regional level (sub-Saharan Africa), and vice versa. A 25-year systematic review showed that people with disabilities continue to be a blind spot in research on SRH service use and policy analysis (Article 5). Finally, the practice of reflexivity throughout the research revealed tensions in the application of ethics norms in the context of global health qualitative research with people with disabilities conducted in the Global South (Article 6). Conclusion: The IPBA framework proved to be a useful and transformation-oriented analytical tool to disentangle complex policy implementation issues and multiple intersecting vulnerabilities and barriers to SRH service access and utilisation by people with disabilities. This thesis proposes two adapted conceptual frameworks for future disability-sensitive research focusing on equity-focused policy analysis in global health, integrating IBPA with Kingdon’s Policy Streams framework to enhance sensitivity to equity and Walt and Gilson’s Policy Triangle model to enhance sensitivity to the multiple dimensions of (in)equity. The Sustainable Development Goals emphasise inclusiveness and accountability. UHC for all is only possible through transformative action and research to fill knowledge and programmatic gaps, focusing on equity and human and disability rights. This thesis provides evidence enabling policy actors at different levels to act – now – to address and redress the social health inequities experienced by people with disabilities.