Magister Legum - LLM / In this research, I carefully and coherently examine Chapter 19 of the Children's Act 38 of 2005 as the first legislation to afford surrogate motherhood agreements legal recognition in South Africa. I argue that the application of Chapter 19 imposes a number of unwarranted limitations on several of the constitutional rights of the parties to a surrogacy agreement. In addition, I propose that Chapter 19 is not in accordance with the principal of the best interests of the child. I examine the history of surrogate motherhood in South Africa and establish that, prior to the enactment of Chapter 19, no legislation expressly afforded surrogate motherhood agreements legal recognition. Hence, prior to the enactment of Chapter 19, parties who entered surrogacy agreements could, first, not rely on the agreement to enforce contractual obligations, and secondly, the legal positions of the parties to the agreement were uncertain. Thirdly, a child born of a surrogacy agreement was seen as the child of the surrogate mother and not of the commissioning parents. / South Africa

This research contributes to understanding the attitudes of Russian politicians towards sex education in schools and the kind of argumentation styles they use to oppose it. The paper is based on a framing analysis of the arguments of two important opponents to sex education: Pavel Astakhov, a Russian politician and former Children’s Rights Commissioner from 2009 to 2016; and Yelena Mizulina, Chairman of the State Duma Committee on Family Affairs, Women and Children since 2008, using online media sources in a ten-year period (2011-2021). The analysis finds that Astakhov’s most used frames are the disapproval of children’s exposure to new, different attitudes, the interference in Russian traditions by the West and the spread of a gender discourse in Russia. Mizulina focuses mainly on the unfitness of teachers since sex education should only be addressed by parents, and on the “right age” to start talking about it with young people. From the results, both politicians seem to strongly oppose comprehensive sex education (CSE), but Astakhov proposes to adopt a type of abstinence-only curriculum (AO), while Mizulina tries to completely discourage sex education of any kind for school-aged children.

Thesis (M. Law. (Development and Management)) --University of Limpopo, 2019 / Like many other countries, South Africa has its own socio-economic challenges. For the past two decades, the country has been experiencing rapid population growth, yet in the same period, there has been a pervasive decline in social and economic stability, and in the end, stagnant human wellbeing. This has been as a result of diminishing access to basic services such as health care, quality housing, quality education and safe clean drinking water. Among other factors, unregulated and rapid population growth contribute to these socio-economic challenges. This study seeks to illustrate that overpopulation undermines and threatens social development, societal stability and survival of humanity. Therefore, the examines the possibility of enacting a legislation or policy that will regulate or limit procreation or the right to give birth. It also reflects on the Chinese experience to obtain some lessons from China’s One-Child Policy. It is submitted that South Africa must draft its own policy or legislation that will regulate population growth with the primary objective of aligning population with available state resources. Keywords: overpopulation, right to reproductive health, socio-economic rights, human wellbeing, social transformation.

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This paper uses a discourse analysis approach to analyze the political road to the Supreme Courts’ overturning of Roe v Wade and Casey. By using the theoretical framework by Fairclough and Fairclough (2012), the analysis is able to study the arguments which founded the historic decision, and its possible impact on women’s reproductive rights in the U.S. today.

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Bakgrund Gynekologisk cancer drabbar många kvinnor globalt och är ett samlingsnamn för äggstockscancer, vulvacancer, livmoderhalscancer och livmodercancer. Vanliga behandlingsmetoder inkluderar strålbehandling, cellgiftsbehandling (cytostatika) och kirurgi. Dessa behandlingsmetoder kan leda till påtagliga biverkningar som kan påverka den sexuella funktionen. Sexualitet utgör en viktig del av människans välbefinnande och har betydelse för övergripande hälsa. Det är dock viktigt att notera att upplevelsen av sexualitet är subjektiv och variationer kan förekomma bland individer. Rätten till sexuell och reproduktiv hälsa är universell, och hälso- och sjukvården bör sträva efter att tillgodose och främja denna rättighet genom att tillhandahålla information och resurser på ett personcentrerat sätt. Syfte Syftet var att beskriva upplevelser av sexuell hälsa vid gynekologisk cancer. Metod ​​En allmän litteraturöversikt som undersökt vetenskapliga originalartiklar från databaserna Cinahl Complete och PubMed. För att hitta dessa artiklar användes Mesh-termer och Cinahl Subject Headings och sökord relaterade till sexuell hälsa och gynekologisk cancer. Sökningen resulterade i elva utvalda artiklar som användes till resultatet. Resultat Denna litteraturöversikt fann att gynekologisk cancer och dess behandling negativt påverkar kvinnors sexualitet genom fysiska och känslomässiga förändringar, inklusive minskad sexlust och påverkan på relationer. Bristande informationsutbyte och stöd från sjukvårdspersonal ökar osäkerhet och lidande. Denna litteraturöversikt identifierade fyra teman relaterade till kvinnor som diagnostiseras och behandlas för gynekologisk cancer: sexuell funktion, kroppsbild och kvinnlig identitet, relationstillfredsställelse och kontakt med vården. Slutsats ​​Kvinnors sexualitet påverkades i olika grad av en gynekologisk cancerdiagnos och medföljande behandling. Det framkom dock att dessa upplevelser skiljde sig från person till person vilket förtydligar vikten av ett personcentrerat och holistiskt perspektiv i mötet med dessa personer. Ytterligare forskning krävs för att vidare undersöka kulturella skillnader, åldersskillnader och upplevelser hos dessa kvinnor. / Background Gynecological cancer affects many women worldwide and encompasses ovarian cancer, vulvar cancer, cervical cancer, and uterine cancer. Common treatment methods include radiation therapy, chemotherapy (cytostatics), and surgical interventions. These treatment modalities may entail challenging side effects that can impact sexual functioning. Sexuality is a crucial aspect of human life and influences overall health. However, sexuality is subjective, and cultural differences in the experience of sexuality may exist. Everyone has the right to sexual and reproductive health, and it is essential for healthcare to meet and promote these needs through, among other things, personalized information and resources.​ Aim The aim was to describe experiences of sexual when effected with gynecological cancer​. Method A general literature review that examined scientific original articles from the Cinahl Complete and PubMed databases. To find these articles, Mesh terms and Cinahl Subject Headings, as well as keywords related to sexual health and gynecological cancer, were used. These resulted in eleven selected articles. Results This literature review found that gynecological cancer and its treatment negatively impact women's sexuality through physical and emotional changes, including decreased libido and effects on relationships. Insufficient information exchange and support from healthcare professionals increase insecurity and suffering. This literature review identified four themes related to women diagnosed and treated for gynecological cancer: sexual function, body image and female identity, relationship satisfaction, and healthcare communication. Conclusions Women's sexuality was variably affected by a diagnosis of gynecological cancer and its accompanying treatments. However, it became evident that these experiences differed among individuals, underscoring the significance of a person-centered and holistic perspective when engaging with these individuals. Further research is warranted to explore cultural variations, age-related differences, and the unique experiences of these women.​

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Orientadores: Eliana Amaral, Maria Yolanda Makuch / Tese (doutorado) - Universidade Estadual de Campinas, Faculdade de Ciências Médicas / Made available in DSpace on 2018-11-07T13:33:28Z (GMT). No. of bitstreams: 1 Rossi_AndreadaSilveira_D.pdf: 2215950 bytes, checksum: c190d83a71722140f11b48daa634163e (MD5) Previous issue date: 2010 / Resumo: Objetivo: Identificar quais Serviços de Reprodução Assistida (SRA) e Serviços de Assistência Especializada em HIV e Aids (SAE) do Sistema de Saúde Pública do Brasil, que oferecem atendimento a pessoas vivendo com HIV com desejo reprodutivo e descrever as vivências, informações adquiridas e barreiras encontradas pelos gestores de programas, profissionais de saúde e usuários, relacionados a essa demanda. Metodologia: Estudo descritivo, de corte transversal através de entrevistas telefônicas com 69 gestores dos programas de saúde da mulher (PSM) e 69 de DST/Aids, estaduais e municipais associado a estudo de casos através de entrevistas semi-estruturadas com profissionais e usuários soropositivos de um serviço de reprodução assistida (SRA) e um serviço de atenção especializada em HIV/Aids (SAE) por região geográfica do país. Foi realizada análise descritiva dos dados quantitativos e análise temática do conteúdo para os dados qualitativos. Resultados: Foram realizadas 64 entrevistas com gestores dos PSM, sendo identificado apenas um SRA universitário que atendia casais soropositivos. Nas 63 entrevistas realizadas com gestores dos Programas de DST/Aids, constatou-se que 64% dos SAE estaduais e 73% dos municipais ofereciam orientação reprodutiva. As dificuldades relatadas pelos gestores para não oferecimento de apoio à reprodução incluíram falta de decisão política, de recursos humanos e financeiros. Nas entrevistas com os profissionais dos seis SAE visitados, foi observado que o foco dos atendimentos era na prevenção, principalmente através do uso do preservativo. A falta de encaminhamentos apropriados e a desatualização do conhecimento científico foram frequentes nos relatos dos profissionais dos serviços. A dificuldade em falar sobre o desejo reprodutivo nas consultas foi observada nas falas dos profissionais e também dos usuários. Para os últimos, isso esteve associado ao medo da discriminação e do preconceito. Entretanto, através da 47 entrevistas realizadas com usuários, o desejo de ter filhos foi vivenciado de maneira natural e expresso independentemente de se ter ou não parceiro fixo, mas, para aqueles que possuem parceiros fixos, o fato de não ter filhos da atual união pareceu aumentar a intenção reprodutiva. Conclusão: Os resultados sugerem a existência de demanda reprimida para reprodução de casais vivendo com HIV, a falta de aconselhamento reprodutivo nos SAE e de investimento em SRA que atenda a essa população, havendo um único SRA universitário no país que oferece esse tipo de atendimento. A falta de integração entre os vários setores sugere a ausência de políticas públicas voltadas para o aconselhamento reprodutivo e a necessidade de diretrizes nacionais específicas voltadas para a redução da transmissão do HIV durante todo o contexto reprodutivo / Abstract: Objective: To identify assisted reproductive services(ARS) and specialized HIV/AIDS services within the Brazilian public health system that provide care to people living with HIV who desire a child and describe the experience, the information, and the barriers encountered by program managers, healthcare professionals and users with respect to this demand. Methods: A descriptive, cross-sectional study in which 69 women's healthcare program managers and 69 STD/AIDS program managers at both state and municipal level were interviewed by telephone, in association with a case study conducted through semistructured interviews with professionals and users of one ARS service and one HIV/AIDS service in each geographical region of the country. Descriptive analysis of the quantitative data and thematic content analysis of the qualitative data were performed. Results: Sixty-four interviews were conducted with women's healthcare program managers. Only one university ARS provided care to seropositive couples. Of the 63 interviews carried out with STD/AIDS program managers, 64% of the state and 73% of the municipal HIV/AIDS services were found to offer reproductive counseling. The difficulties offered by managers as reasons for not providing reproductive support included a lack of political decision and of human and financial resources. At the six HIV/AIDS services the professionals revealed that the focus of consultations was on the prevention, lack of appropriate referrals and outdated scientific knowledge were frequently reported. Difficulty in discussing reproductive issues was perceived in the interviews with the professionals and also with the users. In the latter case, this was associated with a fear of discrimination and prejudice. Nevertheless, as shown in the 47 interviews conducted with users, the desire to have a child was experienced as a natural part of life and was expressed irrespective of whether the individual had a steady partner or not; however, in the former case, the fact of not having a child with the individual's current partner appeared to increase the desire for a child. Conclusion: These findings suggest the existence of a repressed demand for reproduction of PLWHA and lack of reproductive counseling was observed at all HIV/Aids specialized services, as well as investment in ART services to be provided to HIV-positive couples, based on the finding that only one university ART service in the country offers this type of care. Lack of integration between the various sectors suggests an absence of public policies on reproductive counseling and a need for specific national guidelines aimed at reducing HIV transmission within the whole context of reproduction / Doutorado / Ciencias Biomedicas / Doutor em Tocoginecologia