Academic literature on the topic 'AIDS (Disease) – Social aspects – Canada'
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Journal articles on the topic "AIDS (Disease) – Social aspects – Canada"
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Orchard, Treena. "Strategies for Sustainability Among HIV/AIDS-Related NGOS in Canada and India." Practicing Anthropology 24, no. 2 (April 1, 2002): 19–22. http://dx.doi.org/10.17730/praa.24.2.kn11l2l008657371.
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Anthropologists have been involved in the implementation of culturally appropriate HIV/AIDS intervention programs since the advent of the disease. The tradition of applied research in areas like health in "developing" countries and urban "street cultures" (e.g., homeless and low income people, various drug scenes) since the 1950s make it a discipline well-suited to the study of HIV/AIDS, which is often associated with poor and socially marginalized groups. However, the stigma connected to the disease and the lack of political will to initiate structural changes to effectively deal with HIV/AIDS are two key factors prohibiting the establishment of long-term social and policy changes for communities at risk. These conditions have attributed to the growth of HIV/AIDS- related non-government organizations (NGOs), which have been instrumental in dealing with many aspects of the disease. Yet these groups are often faced with the challenge of balancing their clients' needs with program requirements of funding agencies. My involvement with NGOs in a western Canadian city and rural south India exposed some of the tensions these groups experience as they try to meet the demands of clients and funders. Some of these tensions reveal similar problems within NGO environments and others highlight different strategies for sustainability that reflect local constraints as well as strengths. Thus, the comparison of these cases should be of use to a discussion of HIV/AIDS research within applied anthropology and the broader discourse of NGO responses to the epidemic.
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Roger, Kerstin Stieber, Javier Mignone, and Susan Kirkland. "Social Aspects of HIV/AIDS and Aging: A Thematic Review." Canadian Journal on Aging / La Revue canadienne du vieillissement 32, no. 3 (August 13, 2013): 298–306. http://dx.doi.org/10.1017/s0714980813000330.
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RÉSUMÉIl manque de recherche spécifique qui décrit les aspects sociaux du vieillissement avec le virus de l’immunodéficience humaine/syndrome d’immunodéficience acquise (VIH/SIDA) au Canada, malgré une augmentation globale de la population viellissante et l’augmentation du nombre de ceux qui vieillissent avec le VIH/SIDA. Une revue systématique de la littérature été menée en se focalisant sélectivement sur les aspects sociaux aux personnes âgées vivant avec le VIH/SIDA. Les thèmes principaux qui se dégagent dans la littérature sont l’âgisme et la stigmatisation, le sexe, la santé mentale et les soutiens sociales. On présente des recommandations sur la recherche à l’avenir, les modèles théoriques, et le programmatisation.
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Frank, Pauline, and Emma Sasse. "Experiences and Support Needs of Caregivers of Patients with Higher-Risk MDS: Qualitative Insights Via Online Bulletin Board in the US, UK, and Canada." Blood 136, Supplement 1 (November 5, 2020): 21–22. http://dx.doi.org/10.1182/blood-2020-138670.
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Higher-risk MDS patients and caregivers can face many challenges in the course of the disease and disease management. Patients with advanced cancer and their caregivers can both experience physical, emotional, social, spiritual, and functional issues. Research on the burden of caring for advanced cancer patients suggest that there is insufficient support for caregivers, which might be due to the lack of knowledge about their needs and burdens (Friðriksdóttir et al. 2011; Chambers et al. 2012; Sklenarova et al. 2015). The overall experience of caregivers for MDS patients has not been evaluated to date. Our key research questions are related to: Caregiver role before, during, and after diagnosis; and along the disease journeyImpact on the caregiver's life and well-being; consequently their areas of need for supportImpact of decisions made, including treatments We used the online bulletin board (OBB) as the qualitative research methodology for this research. OBB enables data collection via a web-based platform. This innovative type of online focus group, can generate more meaningful and impactful insights compared to traditional focus groups (Reid et al. 2005). A mix of moderator-led Q&A and participant discussion will provide the caregiver insights as online dialogue. OBB is especially advantageous when participants are located in various geographic locations, time zones, and with differing availabilities (Rolland et al. 2013; Nyumba et al. 2018). This methodology will guide the caregiver discussions, optimize the gathering of caregiver insights, and facilitate interactive activities, including appropriate probes and follow up questions. Since it would be challenging to identify caregivers of higher-risk MDS patients, the research uses convenience sampling with the support of patient organizations. Fifteen participants were targeted for recruitment by patient organizations in their respective countries - Myelodysplastic Syndromes (MDS) Foundation in the US, Aplastic Anemia & Myelodysplasia Association of Canada, and MDS UK Support Group - through outreach to their membership. Participants were to be selected based on the inclusion and exclusion criteria, with additional screening by the researchers. Inclusion criteria Caregiver of patient diagnosed with high or very high risk MDS as diagnosed per IPSS-R category or high-risk MDS as per IPSS (intermediate-risk patients on hypomethylating agents (HMAs) will be considered only if it is challenging to recruit caregivers of high and higher-risk patients) Aged 18+ Able to communicate in written English Caregiver is able to provide consent to participate in research Exclusion criteria Caregiver of patient diagnosed with low or very low risk MDS as diagnosed per IPSS-R category or low-risk as per IPSS Caregiver of patients currently active in a clinical trial Paid caregiver who is a nurse or aide We present in this abstract an interim report of the research, which is still ongoing. A total of 16 caregivers participated in the OBB with additional recruitment to cover any potential drop outs or withdrawals - 5 from the US, 6 from the UK, and 5 from Canada. There are 14 female and 2 male caregivers whereby 13 are spouses of the patient, 2 are children of the patient, and 1 is a friend of the patient. Full content analysis will be conducted at the completion of the research. However the interim findings already indicate there are unmet patient and caregiver needs in higher-risk MDS. For example, although the caregiver role for more recently diagnosed patients (≤ 1 year) is perceived as minimal effort, their role increases significantly if a stem cell or bone marrow transplant occurs, and/or if there are changes in the patient's health status (e.g. infection, medication change, managing side effects like nausea). The implications of this vary depending on the personal situation of the caregiver - the ability to continue in any employment and financial consequences if not; the demand on their time if they are balancing family and other commitments; and the impact on their own health particularly if they have their own health issues to manage. Most caregivers can manage the physical and functional aspects of care, however, many state that the bigger unmet need for both patient and caregiver is emotional support, which has not typically been part of the standard of care provided to MDS patients. Disclosures Frank: Novartis Pharma AG: Current Employment, Current equity holder in publicly-traded company. Sasse:Novartis Pharma AG: Current Employment, Current equity holder in publicly-traded company.
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Schlebusch, Lourens, and Michael J. Cassidy. "Stress, Social Support and Biopsychosocial Dynamics in HIV-AIDS." South African Journal of Psychology 25, no. 1 (March 1995): 27–30. http://dx.doi.org/10.1177/008124639502500104.
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Research trends in psychosocial aspects of HIV-AIDS are reviewed, exploring the role of psychosocial cofactors in disease progression. This is undertaken within a biopsychosocial model and gives cognisance to the role of psychosocial stress, social support, and emotional adjustment. Research data from a study of biopsychosocial interrelationships in a sample of HIV-positive patients show a significant correlation between social support and emotional adjustment and that social support exerts a mediatory, stress-buffering effect in these patients. Some observations are made on aspects of the social conditions of South Africans with HIV-AIDS.
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Selwyn, Peter A. "Tuberculosis and AIDS: Epidemiologic, Clinical, and Social Dimensions." Journal of Law, Medicine & Ethics 21, no. 3-4 (1993): 279–88. http://dx.doi.org/10.1111/j.1748-720x.1993.tb01252.x.
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In little more than a decade, the AIDS epidemic has exerted a profound effect on morbidity and mortality among young adults and children in many parts of the world. One of the more dramatic aspects of AIDS is that it seems to have arisen almost spontaneously as a new epidemic, spreading rapidly within at-risk populations in a way that is unprecedented for the serious infectious diseases of recent memory. Tuberculosis, on the other hand, had only recently been considered a disease of historical importance but of diminishing relevance to current public health priorities, especially in industrialized countries. Over the past decade, however, and in parallel with the AIDS epidemic, there has been a resurgence of tuberculosis in many of the same populations most affected by HIV infection. This has had important implications for clinical practice, public health, and the development of appropriate health policy. A number of elements have converged to promote the development of HIV-related tuberculosis, including biologic, social, and environmental factors. These will be discussed both to provide a context for understanding the relationship between the two epidemics, and as a basis for suggesting strategies for tuberculosis control in the AIDS era.
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Atta, Kouame. "Reflexion Sur Les Enjeux Epistemologique Et Methodologique De L’approche Anthropologique Sur La Maladie Chronique En Contexte Africain A Travers L’exemple Du VIH/Sida." European Scientific Journal, ESJ 13, no. 29 (October 31, 2017): 344. http://dx.doi.org/10.19044/esj.2017.v13n29p344.
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Our practical experience of anthropology in the field of HIV/AIDS and many researchers’ commitment in such scientific programs showed that social sciences’ approach of chronic disease in African cultural context includes relevant epistemological and methodological issues. The purpose of this article is to give an overview of these issues while showing the contribution of the anthropological approach to the comprehension of the health phenomena related to the AIDS in the African environment. The approach to this was to review the literature on fieldwork already done on HIV / AIDS in the social sciences. The results of our analysis indicate that medical research on HIV / AIDS in African cultural context has mobilized social sciences mainly anthropology in its various specialties which alongside Biology, Epidemiology and Clinic have led to the development of an inclusive approach of the disease. This interactive approach between social sciences and medical sciences allowed fulfilling the limits of medicine’s quantitative approaches and thus to grasp the AIDS pandemic in these epidemiological, behavioral and representational aspects.
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Umadevi, K. R., E. Blignaut, M. Glick, E. Nasir, V. Yengopal, F. Younai, and P. G. Robinson. "Social Aspects of HIV and Their Relationship to Craniofacial Problems." Advances in Dental Research 23, no. 1 (March 25, 2011): 117–21. http://dx.doi.org/10.1177/0022034511400223.
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The oral research community needs an understanding of the social causes, consequences, and costs of disease in relation to oral health. This workshop concluded that HIV infection constitutes a special dental need requiring specific arrangements to facilitate oral care for infected persons. Oral manifestations of HIV infection affect everyday life, but more evidence is needed on the effects of interventions to alleviate these impacts. Other oral health habits add to the burden of HIV/AIDS-associated oral diseases and compete with them for resources. These problems are most acute where the prevalence of HIV is high and resources are scarce. Effective health promotion is therefore important in these areas. Without data on the utility of oral health care in developing countries, practical approaches are guided by societal and multidisciplinary principles. There are also important ethical considerations
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Sargazi, Atefeh, Zahra Sepehri, Prigil Kumar Nadakkavukaran Jim, Negar Aali, Masoomeh Danesh, and Aliyeh Sargazi. "The Global Burden of Acquired Immune Deficiency Syndrome (AIDS) in Tuberculosis Infected Patients and Related Financial Aspects." International Journal of Basic Science in Medicine 3, no. 4 (June 18, 2018): 140–46. http://dx.doi.org/10.15171/ijbsm.2018.25.
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The acquired immune deficiency syndrome (AIDS) is an infectious disease caused by human immunodeficiency virus (HIV). Approximately about 37 million people are infected by this virus with the rate of 1.2 million deaths per year. The mortality rate is high among HIV infected patients in the first 6 months of treatment.1 Immune deficient cases are at the high risk of any opportunistic infection. AIDS has been closely linked with tuberculosis (TB) disease, so almost one third of total mortality is related to this co-infection. In this regard, tuberculosis is used as a diagnostic index for AIDS.2 AIDS is not only associated with high mortality and morbidity, but it affects social life with related stresses and anxieties.3 Considering vast influence of HIV-TB over peoples’ lives, the present study aimed to estimate direct global burden of HIV infection on the patients with TB in a one-year period in 2014.
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Gulyamov, Shodibek, Nigina Sharapova, and Yuriy Krivoruchko. "CLINICAL AND SOCIAL ASPECTS OF HEROIN ADDICTION: MODERN STATE OF ISSUE." Avicenna Bulletin 22, no. 1 (March 1, 2020): 112–19. http://dx.doi.org/10.25005/2074-0581-2020-22-1-112-119.
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The article provides a brief overview of the literature, which deals with the issues of heroin addiction, its history, prevalence, statistics, clinical characteristics, diagnostics, prevention and countermeasures, as well as programs aimed at social rehabilitation and harm reduction from injecting drug use. Issues such as physiological foundations and features of disease and remission formation, withdrawal, motivational attitudes of drug users, structure users of narcotic substances, the impact of pre-morbid features, socio-demographic, clinical-dynamic, regional and gender aspects of heroin addiction, and also existing approaches to therapeutic and preventive measures are considered in narcology. Medical and social consequences expressed in the form of the spread of hemo-contact infections, such as HIV/AIDS and viral hepatitis; risky behavior and its impact on the growth of sexually transmitted infections; reducing and completely losing social status; suicide-aggressive actions have been studied. The analysis of data on the study of the prognostic value of the socio-demographic and clinical-dynamic characteristics of heroin addiction and its effect is provided on the outcome of the disease. Keywords: Drugs, drug addiction, heroin addiction, opioids, addiction treatment
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Graeff, Samara Vilas-Bôas, Renata Palópoli Pícolli, Rui Arantes, Vivianne De Oliveira Landgraf de Castro, and Rivaldo Venâncio da Cunha. "Epidemiological aspects of HIV infection and AIDS among indigenous populations." Revista de Saúde Pública 53 (February 7, 2019): 71. http://dx.doi.org/10.11606/s1518-8787.2019053000362.
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OBJECTIVE: To describe the epidemiological aspects of HIV infection and AIDS among indigenous peoples of the state of Mato Grosso do Sul, Brazil. METHODS: This is a descriptive epidemiological study on the occurrence and distribution of HIV infection and AIDS in the indigenous population assisted by the Distrito Sanitário Especial Indígena (Indigenous Special Health District) Mato Grosso do Sul between 2001 and 2014, based on three secondary databases. Annual rates of HIV and AIDS detection and prevalence were calculated, considering case distribution according to village, Health Base Pole and sociodemographic variables. Accumulated rates of detection, mortality and case fatality were calculated by ethnic group and for the Health Base Pole with the highest number of cases. RESULTS: The HIV detection rate fluctuated between 0.0 and 18.0/100 thousand people in the study period. For AIDS, there was no notification before 2007, but in 2012 its rate reached 16.6/100 thousand. HIV prevalence grew between 2001 and 2011, and it continuously grew for AIDS starting from 2007. The highest HIV detection rates occurred among Guarani peoples (167.1/100 thousand) and for AIDS, among the Kaiowá peoples (79.3/100 thousand); mortality and fatality rates were higher among the Kaiowá. Regarding the Dourados Health Base Pole, the AIDS detection rate increased, and the mortality and fatality rates decreased. CONCLUSIONS: HIV infection and AIDS have been increasing among indigenous peoples, with distribution of the disease mainly in the Health Base Poles of the southern region of the state, where greater economic and social vulnerability are also observed. The endemic character of HIV and AIDS can become epidemic in some years given the existence of cases in other villages in the state. Its occurrence among the Guarani and Kaiowá populations indicates the need for expanded diagnosis, access to treatment and prevention measures.
Dissertations / Theses on the topic "AIDS (Disease) – Social aspects – Canada"
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Strader, Scott C. "A causal model examining AIDS prejudice : AIDS attitudes and homophobia as latent variables." Virtual Press, 1994. http://liblink.bsu.edu/uhtbin/catkey/917830.
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Prejudice and discrimination against people infected with Acquired Immune Deficiency Syndrome (AIDS) is widespread. A significant body of research has examined what personality and demographic characteristics appear to be related to discriminatory behavior, in an attempt to suggest who might be more likely to express prejudicial attitudes and discrimination against people with AIDS. This study tested two causal models which attempted to verify existing theories explaining the influences of demographic and attitudinal factors on the evaluation of a person with AIDS. Specifically, these models sought to answer questions related to what personality characteristics and demographic information are most important to AIDS educators and counselors when examining prejudice and discrimination towards persons with AIDS. Three hundred university undergraduates participated in the study. Structural equations modeling was used to analyze the extent to which the models fit the data. Results showed that both models adequately explained the data, with the model establishing a direct causal link between homophobic attitudes and AIDSbased prejudice as the preferred model. Alternative models were also considered in a post-hoc fashion. Implications of the results are discussed, with specific emphasis given to the potential ramifications to further research, counseling practice, and AIDS education.Department of Counseling Psychology and Guidance Services
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Steele, Derek G. "The evolution of the Canadian AIDS Society : a social movement organization as network, coalition and umbrella organization." Thesis, McGill University, 2000. http://digitool.Library.McGill.CA:80/R/?func=dbin-jump-full&object_id=37844.
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This study presents a history of the Canadian AIDS Society (CAS), which began as an informal network of 16 local AIDS Service Organizations (ASOs) in 1986 and grew to 120 member organizations by the time of the renewal of Phase III of the National AIDS Strategy in late 1998. There are two main objectives of the study: (1) to look at why the organizational forms of the collection of groups evolved as they did; (2) to examine the outcomes and effectiveness of these organizational forms for CAS and its member organizations.Interviews were conducted with founding members of CAS and later staff and activists. Members of a subsection of local General Service Organizations (GSOs) were interviewed regarding group relationships to CAS and involvement with other organizations in their communities. Documentary research on materials produced by CAS (now publicly available in the AIDS Committee of Toronto library) was carried out. Some documentation was also available for local organizations. The Globe and Mail index was used to research CAS national level work.
This dissertation uses the concepts network, coalition and umbrella organization to develop an understanding of why CAS formalized and the positive and negative outcomes of this for member groups and the organization itself. The issues of insider/outsider organization, motivation, identity, framing and ideology are discussed in relation to their impact on both CAS and a subsection of member organizations.
CAS developed as a network, coalition, and umbrella organization. This evolution was in response to the purpose and goals of CAS at a national level, Ottawa based representative of member organizations interacting with the government and gathering and producing information useful to local work. CAS became increasingly formalized over the period under study, seeking and gaining access to government and other elites, as at least a semi-insider organization.
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Johnson, Lauri Sue. "An examination of moral boundaries associated with legal and social changes in response to the AIDS epidemic." PDXScholar, 1992. https://pdxscholar.library.pdx.edu/open_access_etds/4320.
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This thesis explores the relationship between law and society and various forms of causality: (1) legal change leading to social change; (2) social change leading to legal change; and (3) the interdependent interaction between social change and legal change. It is proposed that a multi-directional approach would be the most useful in examining the moral boundaries exemplified in the law identified with legal and social changes that have resulted in response to the AIDS epidemic.
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Lo, Yuk-ping, and 盧鈺苹. "The securitisation of HIV/AIDS: China and India." Thesis, The University of Hong Kong (Pokfulam, Hong Kong), 2012. http://hub.hku.hk/bib/B4832968X.
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Securitisation theory has made significant contributions to security studies. However, the theory is not without theoretical and empirical shortcomings. Notably, a lack of operationalisation and differentiation has led to a binary classification of results as either ‘securitised or not’. In addition, the presence of Euro-centric assumptions has weakened the theory’s applicability in non-Western contexts.
This thesis develops a new framework featuring a typology with eight branches of securitisation. The thesis then uses that framework to study HIV/AIDS securitisation in two Asian countries: China and India.
The process of HIV/AIDS securitisation in both countries is illustrated chronologically. Following the international HIV/AIDS securitisation obtained in 2000, the study shows that HIV/AIDS has been fully securitised by both national governments since 2004. However, the Chinese government addressed HIV/AIDS through a stand-alone programme, whereas India’s national HIV/AIDS programme was integrated into its primary health care system.
Six cities were included in the detailed empirical analysis: Beijing, Shanghai, and Kunming in China, and New Delhi, Mumbai, and Imphal in India. Semi-structured interviews were conducted amongst 62 individuals working in HIV/AIDS-related non-governmental organisations, and 10 officials working in government agencies. Chinese respondents were receptive to framing the threat and handling of HIV/AIDS, yet many grassroots organizations lacked opportunities to participate in the national HIV/AIDS programme. In contrast, such groups were strongly involved in national HIV/AIDS interventions; however, Indian government efforts in fully securitising HIV/AIDS were largely faded out.
The thesis therefore responds to the major theoretical and empirical shortcomings identified by security scholars. The thesis also advances the existing knowledge of security studies in general, and HIV/AIDS securitisation processes in the non-Western world in particular.published_or_final_version
Humanities and Social Sciences
Doctoral
Doctor of Philosophy
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Scheibe, Kim. "AIDS anxiety and sexual behavior: a comparative study." Thesis, Virginia Polytechnic Institute and State University, 1988. http://hdl.handle.net/10919/52073.
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Questionnaire responses of 214 college students at Virginia Polytechnic & State University regarding AIDS anxiety and how it affects sexual behavior were analyzed. Results indicated that women tend to have more AIDS anxiety than do men. Fifty-three percent of the male respondents reported their AIDS anxiety to be low/very low, and 15.7% reported high/very high, while 44.9% of the women responded low/very low, and 22.5% as being high/very high.
Both males and females reported an increase in the number of sexual encounters a month, however, the number of different partners has decreased when data from 1986 and 1988 were compared. In 1986, 36.9% of the males reported being sexually active 3+ times a month, while in 1988, 51.5% of the males were sexually active 3+ times a month. In 1986, 50.2% of the females reported being sexually active 3+ times a month, whi1e 56.6% of the females in 1988 indicated that frequency. In 1986, 36.2% of the males and 31.5% of the females responded that they had 3+ different partners while 22.9% of the males and 14.1% of the females responded this way in 1988.
Those who reported experiencing high anxiety concerning AIDS were less likely to use birth control than those who reported a low AIDS anxiety. Seventy-one percent of the respondents reported using some form of birth control, with 35.5% reporting the use of condoms.Master of Science
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Ritter, Nicola. "Terminal sliding mode control for rigid robotic manipulators with uncertain dynamics." Thesis, Edith Cowan University, Research Online, Perth, Western Australia, 1996. https://ro.ecu.edu.au/theses/932.
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This thesis presents two new adaptive control laws that use the terminal sliding mode technique for the tracking problem of rigid robotic manipulators with non-linearities, dynamic couplings and uncertain parameters. The first law provides a robust scheme which uses several properties of rigid robotic mauipulators and adaptively adjusts seven uncertain parameter bounds. The law ensures finite time error convergence to the system origin and is simple to implement The second law treats the manipulator as a partially known system. The known dynamics are used to build a nominal control law and the effects of unknown system dynamics arc compensated for by use of a sliding mode compensator. The resulting control law is robust, asymptotically convergent, has finite time convergence to the sliding mode and allows for bounded external disturbances. It is easy to implement and requires no bounds on system parameters, adaptively adjusting only three bounds on system uncertainties. Both laws are extended to include a reduction of chattering by use of the boundary layer technique. They are tested via application to a two-link robot simulated using MatLab.
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Suwisith, Nongluck. "The lived experiences of people living with HIV infection." Thesis, Edith Cowan University, Research Online, Perth, Western Australia, 1996. https://ro.ecu.edu.au/theses/937.
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This phenomenological study was undertaken to describe the meaning of living with HIV infection. Descriptive phenomenology was utilised to investigate the lived experiences of persons who had human immunodeficiency virus infection (HIV/ AIDS), describe common elements, themes or patterns of lived experiences of persons with HIV / AIDS, and analyse the meaning of lived experiences of persons with HIV/ AIDS. Twelve Australians, experiencing HIV infection and participating in the community support groups in Perth, volunteered as participants. Two participated in the pilot study. The other ten participants were interviewed individually for the main study. Intensive open-end questions pertaining to the experiences of living with HIV infection were asked during interviews which were audiotaped, transcribed verbatim, and analysed using Colaizzi's (1978) method of analysis. Significant statements were gathered and clustered into themes. Validity and reliability was confirmed during data analysis. The phenomenon of living with HIV infection emerged as experiences of social discrimination, emotional disturbances, changes, losses, suicide attempts, and dealing with the difficulties. The experiences of living with HIV were influenced by chronic illness, terminal illness, and social stigmatisation towards people with HIV. Roy's (1984) Adaptation Model was utilised as a second level for analysis. The Model was able to be applied to explain the experiences of living with IDV to a certain degree. Human responses to a variety of situations showed similar patterns in people living with HIV infection.
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Bitangaro, Barbara Kagoro. "The role of gender relations in decision-making for access to antiretrovirals. A study of the AIDS Support Organisation (TASO) clients, Kampala district, Uganda." Thesis, University of the Western Cape, 2005. http://etd.uwc.ac.za/index.php?module=etd&.
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The way gender relations influence access to care and treatment particularly access to antiretroviral medicines is a challenge to HIV/AIDS programmes and to the individuals and families with HIV. Gender norms that push women and men to adhere to dominant ideals of femininity and masculinity may restrict women's access to economic resources, health care and fuel the spread of HIV. The aim of this study was to determine the role of gender relations in influencing decision-making for access to antiretroviral medicines between partners and in the family.
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Mechar, Kyle William. "The cultural logic of dis-ease : difference andas displacement in popular discourses of the AIDS crisis." Thesis, McGill University, 1995. http://digitool.Library.McGill.CA:80/R/?func=dbin-jump-full&object_id=23229.
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This thesis investigates the cultural and social production of AIDS in popular discourse, particularly film and mass media, and offers a critical consideration of the ways in which the proliferation and dispersion of these discourses function in our current episteme to rearticulate and reinscribe traditional value systems of sexuality, familialism, and nationalism. Taking the lead of the work of Michel Foucault on the body in various historical regimes, the author here will posit a theoretical analysis of the "discursive formation" of AIDS, how the body of AIDS is put into discourse, to provide a matrix for establishing the various disciplinary and regulatory apparatuses structuring the epidemic--that is, the affirmation of certain kinds of pleasures and bodies and the strategic circumvention of other pleasures and bodies. Under what the author refers to as the cultural logic of dis-ease, the investigations that follow will be animated by the central question: Whose pleasure and/or power is served by these representations and discourses of the body of AIDS in popular cultural practices?
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Beetge, Lijahne. "Themes related to children living with HIV/AIDS." Thesis, Stellenbosch : Stellenbosch University, 2007. http://hdl.handle.net/10019.1/21549.
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Assignment (MA)--University of Stellenbosch, 2007.ENGLISH ABSTRACT: This review examines themes related to children, especially children under the age of fifteen, living with HIV/Aids. For review purposes themes include defining children living with HIV/Aids as a vulnerable population, the psychological impact of HIV/Aids on children, children’s coping with and perceptions of HIV/Aids. The global HIV/Aids pandemic has caused major worldwide social change. The impact, especially the psychological impact of HIV/Aids on children appears to be vast and at times disastrous in nature. HIV/Aids is estimated to affect the lives of several generations of children and the impact of the pandemic will therefore characterize their communities for decades to come as the numbers of affected and infected children are on the increase. It has been noted by research done that children living with HIV/Aids become impoverished, their insecurities worsen and their psychosocial and psychological problems increase. In addition their educational and work opportunities decline, their nurturing and support systems disintegrate, and child mortality rates rise. The necessity of psychological support for children affected and infected by HIV/Aids is directly linked to the rights of children listed in the United Nations Convention on the Rights of the Child and the South African Constitution. Research reviewed points out that a child’s physical and psychological health is intertwined and therefore a child cannot be physically healthy without also being psychologically secure. Research reviewed also points out that it is of the utmost importance that the voices of children who live with HIV/Aids are heard, their involvement in decision making and planning related to HIV/Aids is allowed and that their needs are met, especially their psychological needs in relation to the pandemic. Overall the literature reviewed in the past four years (2003-2006) highlights the significantly under-investigated, under-researched themes such as psychological aspects related to children living with HIV/Aids, both in South Africa and internationally. These aspects surrounding HIV/Aids, as previously mentioned, also seem to be the least tangible and the most difficult for adults to address or comprehend fully and yet they impinge on all aspects of developing children - hence the identified need in this area for adequate research and psychological support, such as program implementation.
AFRIKAANSE OPSOMMING: Hierdie literatuuroorsig bied ’n ondersoek na die wêreldwye sosiale verandering en uitwerking wat die globale HIV/vigs-pandemie tot gevolg het. Daar word veral gelet op temas wat verwantskap hou met kinders, veral kinders vyftien jaar oud en jonger wat leef met HIV/vigs. Temas sluit in die definiëring van kinders as weerloos, kinders se hantering van HIV/vigs, hulle persepsies van HIV/vigs en hulle sielkundige behoeftes en ander aspekte met betrekking tot HIV/vigs. Die trefkrag van HIV/vigs blyk omvattend en by tye rampspoedig te wees. Na beraming beïnvloed HIV/vigs verskeie geslagte van kinders en die uitwerking van die pandemie sal dus dekades lank nog deel vorm van hulle gemeenskappe soos die aantal kinders wat geïnfekteer en geaffekteer is, toeneem. Navorsing toon dat kinders wat met HIV/vigs leef, verarm. Verder vererger hulle onsekerhede en hulle psigososiale en sielkundige probleme neem toe. Ook neem die kinders se opvoedkundige en werkgeleenthede af, hulle versorgings- en ondersteuningsnetwerke disintegreer en sterftesyfers neem toe. Die noodsaaklikheid van sielkundige ondersteuning vir kinders wat deur HIV/vigs geïnfekteer en geaffekteer is, word direk in verband gebring met die regte van kinders soos gelys in die Verenigde Nasies se Konvensie oor die Regte van die Kind en die Suid-Afrikaanse Grondwet. Die literatuuroorsig toon dat ‘n kind se fisieke en sielkundige gesondheid ten nouste met mekaar verband hou en daarom kan ’n kind nie fisiek gesond wees sonder om ook sielkundig geborge te wees nie. Verder dui navorsing ook op die kardinale belang daarvan dat kinders wat leef met HIV/vigs se stemme gehoor word, hulle betrokkenheid by besluitneming en beplanning verseker word en al hulle behoeftes bevredig word, veral hulle sielkundige behoeftes wat met die pandemie verband hou. Oor die algemeen beklemtoon die literatuuroorsig wat oor die afgelope vier jaar strek (2003-2006) dat daar nie voldoende navorsing gedoen is met betrekking tot temas wat verwantskap hou met kinders en HIV/vigs nie, nie alleen in Suid-Afrika nie, maar ook internasionaal. Hierdie bevindings is kommerwekkend veral omdat Suid-Afrika ‘n land is met onrusbarende groot getalle kinders wat deur HIV/vigs geïnfekteer is. Dit wil ook voorkom of hierdie aspekte wat te make het met kinders en HIV/vigs nie baie duidelik is vir volwassenes nie en ook die moeilikste is om te hanteer of ten volle te verstaan, hoewel dit alle aspekte van die kind se ontwikkeling raak. Vandaar die behoefte op hierdie gebied aan voldoende navorsing en sielkundige ondersteuning, soos program implementering.
Books on the topic "AIDS (Disease) – Social aspects – Canada"
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Ornstein, Michael D. AIDS in Canada: Knowledge, behaviour and attitudes of adults. [North York, Ont.]: Institute for Social Research, York University, 1989.
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Understanding AIDS: A Canadian strategy. Toronto: Key Porter Bks, 1988.
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Replacing citizenship: AIDS activism and radical democracy. New York: Guilford Press, 1997.
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Willms, Sharon Manson. Choice, voice and dignity: Housing issues and options for persons with HIV infection in Canada : a national study. Vancouver: Centre for Human Settlements, University of British Columbia, 1991.
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Willms, Sharon Manson. Housing for persons with HIV infection in Canada: Issues, options and housing system impacts. Vancouver: University of British Columbia, School of Community & Regional Planning, 1990.
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Singh, Natasha. Facing the face of AIDS. [Toronto: s.n., 1995.
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Canada. Library of Parliament. Research Branch. AIDS: Medical and scientific aspects. Ottawa: Library of Parliament, 2000.
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Peter, Aggleton, Homans Hilary 1950-, and UK Conference on Social Aspects of AIDS (1st : 1986 : Bristol Polytechnic), eds. Social aspects of AIDS. London: Falmer Press, 1988.
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Nordquist, Joan. AIDS: Political, social, international aspects. Santa Cruz, CA, USA: Reference and Research Services, 1988.
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Peter, Aggleton, Hart Graham 1957-, Davies Peter, and UK Conference on Social Aspects of AIDS (2nd : 1987 : South Bank Polytechnic), eds. AIDS: Social representations, social practices. New York: Falmer Press, 1989.
Find full textBook chapters on the topic "AIDS (Disease) – Social aspects – Canada"
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Cohen, Mary Ann, and Joseph Z. Lux. "Palliative and Spiritual Care of Persons with HIV and AIDS." In Handbook of AIDS Psychiatry. Oxford University Press, 2010. http://dx.doi.org/10.1093/oso/9780195372571.003.0016.
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Palliative care of persons with HIV and AIDS has changed over the course of the first three decades of the pandemic. The most radical shifts occurred in the second decade with the introduction of combination antiretroviral therapy and other advances in HIV care. In the United States and throughout the world, progress in prevention of HIV transmission has not kept pace with progress in treatment, thus the population of persons living with AIDS continues to grow. Furthermore, economic, psychiatric, social, and political barriers leave many persons without access to adequate HIV care. As a result, persons who lack access to care may need palliative care for late-stage AIDS while persons with access to AIDS treatments are more likely to need palliative care for multimorbid medical illnesses such as cardiovascular disease, cancer, pulmonary disease, and renal disease. Palliative care of persons with HIV and AIDS cannot be confined to the end of life. We present palliative care on a continuum as part of an effort to alleviate suffering and attend to pain, emotional distress, and existential anxiety during the course of the illness. We will provide guidelines for psychiatric and palliative care and pain management to help persons with AIDS cope better with their illnesses and live their lives to the fullest extent, and minimize pain and suffering for them and their loved ones. This chapter reviews basic concepts and definitions of palliative and spiritual care, as well as the distinct challenges facing clinicians involved in HIV palliative care. Finally, issues such as bereavement, cultural sensitivity, communication, and psychiatric contributions to common physical symptom control are reviewed. The terms palliative care and palliative medicine are often used interchangeably. Modern palliative care has evolved from the hospice movement into a more expansive network of clinical care delivery systems with components of home care and hospital-based services (Butler et al., 1996; Stjernsward and Papallona, 1998). Palliative care must meet the needs of the “whole person,” including the physical, psychological, social, and spiritual aspects of suffering (World Health Organization, 1990).
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Francis, Linda, Richard E. Adams, Alexandra König, and Jesse Hoey. "Identity and the Self in Elderly Adults with Alzheimer’s Disease." In Identities in Everyday Life, 381–401. Oxford University Press, 2019. http://dx.doi.org/10.1093/oso/9780190873066.003.0018.
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Alzheimer’s disease is characterized by the gradual loss of memory, ultimately progressing to forgetting who one is and has been. From a symbolic interactionist perspective, the progression of this disease raises the question of what happens to the “self” as part of an interactive social process with others. Our exploratory study of elders with mild to moderate Alzheimer’s indicates that, while identities grounded in memories and roles will fade as a person loses their ability to remember people and events, habitual and behavioral aspects of identity that reflect one’s personhood may persist longer. Thirty-two elders in Canada and the United States, plus 20 of their caregivers, participated in a qualitative interview. Results indicated that even people with very impaired memory still reacted to situations in ways congruent with their past identities, although they often did not remember the identities themselves. Viewing this phenomenon sociologically informs our understanding of the formation and disintegration of self.
Conference papers on the topic "AIDS (Disease) – Social aspects – Canada"
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Romić, Danijela, and Jelena Dujmović Bocka. "STRENGTHENING THE ACTIVITIES OF YOUTH ASSOCIATIONS IN THE EUROPEAN ENVIRONMENT: CERTAIN LEGAL AND SOCIAL MATTERS." In The recovery of the EU and strengthening the ability to respond to new challenges – legal and economic aspects. Faculty of Law, Josip Juraj Strossmayer University of Osijek, 2022. http://dx.doi.org/10.25234/eclic/22438.
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In the previous ten years in the EU, the youth have become one of the priority groups that is being strengthened for more intensive involvement in the life and development of society. Research has shown that the youth are quite uninterested in getting involved in political and social activities that contribute to the development of the community and society. The still current pandemic caused by Coronavirus Disease (COVID-19) has further “pushed” the youth into the virtual world because they are now forced to conduct their daily activities (for example, schooling, additional education) in an online environment. The youth, otherwise avid fans of technological achievements, are now trapped in their homes with computers, smartphones and other technological aids, thus losing direct contact with their peers and adults, remaining deprived of some of the socializing effects of the teaching process and are at risk of complete alienation. EU Youth Strategy 2019-2027 addresses youth organizations, as one of the key actors that strengthen the competencies of the youth and promote their social inclusion. Youth associations and associations for the youth, in addition to providing various services and programs for the youth, strengthen empathy among the youth, raise awareness of the youth on the needs of society and, through the development of additional competencies, empower them to actively participate in community life. This paper presents the results of the part of the research created within the Youth Activation Network project. The research was conducted using the focus group method, where the respondents were representatives of youth associations and associations for the youth from entire Croatia. Research questions were focused on trying to identify and differentiate youth associations and associations for the youth from other associations, ways to activate and involve the youth in the work of associations, and assess the current legal framework of associations. The results obtained from the implementation of focus groups were transcribed, processed in Dedoose computer program and presented in the paper according to main research issues. For results analysis, content analysis method was used, as well as comparison method and contrast method. The results of the research show that it is necessary to legally define work with the youth so that it can be used as one of the distinguishing criteria of youth associations and associations for the youth. Associations involve the youth as volunteers, users and service providers, and empower and motivate them to further engage in social activities. The biggest problems pointed out by the representatives of associations are related to the ways of financing the work of the associations. Although some respondents pointed out certain shortcomings, research results indicate that the existing legal framework for the work of the associations is satisfactory, while its amendments could further complicate the work of youth associations. The revocation of the complex consequences of the pandemic requires the active involvement of all factors in society, where active and engaged, socially responsible and empathetic youth can be the bearers of change and improvement.