Onder het oppervlak van alledaagse zorg (deel II)

KWALON ◽  
2016 ◽  
Vol 21 (2) ◽  
Author(s):  
Michael Kolen ◽  
Guus Timmerman ◽  
Frans Vosman

Below the surface of everyday care (Part II): Working with the underwater screen in the analysis of research on interaction between lvb youth and their caregivers In our qualitative research project we look at the everyday interaction between young people with a mild intellectual disability and their caregivers, and we are interested in the institutional impact on the everyday dealings. We have developed an analysis tool that helps identify these institutional influences. In addition, we have used the research methodology Institutional Ethnography. This tool also offers opportunities for other areas of research, because it sensitizes the researchers for the ruling relations that shape the everyday interaction between people. In Part 1 of this article (KWALON 2015, 3), we describe the development of our underwater screen. In this article (Part 2), we discuss the operation of the instrument.

KWALON ◽  
2015 ◽  
Vol 20 (3) ◽  
Author(s):  
Michael Kolen ◽  
Guus Timmerman ◽  
Frans Vosman

Under the surface of everyday care. On the development of an underwater screen, an instrument that identifies institutional influences on the everyday care relationship Under the surface of everyday care. On the development of an underwater screen, an instrument that identifies institutional influences on the everyday care relationship In our qualitative research project we look at the everyday interactions between young people with a mild intellectual disability and their caregivers, and we are interested in the institutional impact on the everyday dealings. We have developed an analysis tool that helps to identify these institutional influences. In addition, we have used the research methodology institutional ethnography. This tool also offers opportunities for other areas of research, because it sensitizes the researchers for the ruling relations that shape the everyday interaction between people.


2021 ◽  
Author(s):  
Lise Ludwig Mogensen ◽  
Nicole Sharp ◽  
Jenny McDonald ◽  
Gabrielle Drake

Abstract Background: An increasing body of evidence suggests that transitioning from school to adult life can be challenging for young people with intellectual disability. Transition from secondary school includes preparation of students before leaving school and may continue several years into adult life. Transition challenges may include isolation, mental health problems, and reduced participation in employment and tertiary education. Some literature indicate links between poor post-school outcomes, and ineffective collaboration between school systems, disability services, and employers. Yet, consolidated evidence to understand how young people themselves experience transition from school is needed. The aim of this scoping review is to draw together current literature reporting what is important to young people with intellectual disability about transitioning to life after school. Methods: Using the Joanna Briggs scoping review methodology, a systematic strategy will identify peer-reviewed qualitative research and grey literature reporting the voices of young people with intellectual disability to better understand personal experiences of transition to life after school. The review will explore scope and foci of topics, identify gaps in current evidence, and highlight approaches and methods used by investigators to include young peoples’ own views.Database searches for relevant qualitative research will include ERIC via Proquest, Ovid MEDLINE, selected EbscoHost databases, and Web of Science. Non-indexed and grey literature such as policies and reports will be searched via TROVE, ProQuest Dissertations & Theses, and Google (with URL control and by crawling key agency websites). Studies will be selected using a three-step process: i) managing search results and removing duplicates, ii) title and abstract screening by two independent reviewers, and iii) full text review of included articles against inclusion criteria by two independent reviewers. Data will be tabulated, and presented in a narrative summary, aligning with the objectives and scope of this review.Discussion: Review findings will inform policy makers, educators and disability support organisations of transition experiences of young people with intellectual disability. Their identification of transition challenges and enablers will inform the design and implementation of participatory transition processes, ensuring that future guidelines reflect the views of those they intend to support.Registration with OSF DOI: 10.17605/OSF.IO/YHCDG


2018 ◽  
Vol 66 (6) ◽  
pp. 1209-1225 ◽  
Author(s):  
Sarah Wilson

This article focuses on the representation of qualitative sociological research to academic and non-academic audiences. It argues that a broader, ethically informed consideration of the communication of findings is required, rather than the current, audit-shaped approach, to do justice to complex (affective) data and to research participants. An important catalyst for this article is the concern that the current predominance of peer-reviewed articles may contribute, however unintentionally, to the maintenance of stigmatizing social imaginaries of groups including marginalized young people. This article draws on interdisciplinary sources to extend Avery Gordon’s work on haunting to the representation of research. It contends that research ‘outputs’ can ‘haunt’, or stay with and produce empathy in their audience, by communicating the ‘seething absences’ that trace the everyday effects of power affectively and by highlighting the ‘complex personhood’ of those affected. The possibilities of such an approach are illustrated through consideration of textual and visual representations of findings from a project that explored understandings of ‘belonging’ among young people in state care, and particularly a short film, co-produced with, and featuring, a participant. While ‘representation’ is employed here primarily in an everyday sense, this article discusses ‘non’ or ‘more than’ representational approaches, while advocating a strategic negotiation with representation in relation to social justice.


2012 ◽  
Vol 18 (3) ◽  
pp. 309-321 ◽  
Author(s):  
Tlakale Nareadi Phasha ◽  
Doris Nyokangi

Following qualitative research methodology, this article presents school-based sexual violence experiences of female learners with mild intellectual disability. A total of 16 learners aged 16 to 24 years participated in the study. The findings revealed that learners with intellectual disability are not immune to school-based sexual violence. Modes of behavior that occurred frequently included touching, threats, and intimidation. School practices that reinforced school-based sexual violence are identified. The findings contradict common misconceptions that people with intellectual disability do not understand what is happening to them. The study recommends that school policies for sexual violence be intensified and learners receive developmentally appropriate sex education.


2007 ◽  
Vol 191 (6) ◽  
pp. 484-492 ◽  
Author(s):  
Eve C. Johnstone ◽  
David G. C. Owens ◽  
Peter Hoare ◽  
Sonia Gaur ◽  
Michael D. Spencer ◽  
...  

BackgroundThere is evidence to suggest that among young people with mild intellectual disability there are those whose cognitive difficulties may predict the subsequent manifestation of a schizophrenic phenotype. It is suggested that they may be detectable by simple means.AimsTo gain adequate cooperation from educational services, parents and students so as to recruit a sufficiently large sample to test the above hypothesis, and to examine the hypothesis in the light of the findings.MethodThe sample was screened with appropriate instruments, and groups hypothesised as being likely or not likely to have the phenotype were compared in terms of psychopathology and neuropsychology.ResultsSimple screening methods detect a sample whose psychopathological and neuropsychological profile is consistent with an extended phenotype of schizophrenia.ConclusionsDifficulties experienced by some young people with mild and borderline intellectual disability are associated with enhanced liability to schizophrenia. Clinical methods can both identify those with this extended phenotype and predict those in whom psychosis will occur.


Author(s):  
Anna Gutowska

Current scientific publications present different paradigms of masculinity, but research in this area is a relatively new perspective. However, the specific nature of the everyday experience of people with intellectual disability is still neglected and unrecognised. The aim of this article is to show the concept of masculinity from the perspective of men with intellectual disability. The research is placed in the stream of qualitative research using a case study as a method. The subject of the research covers the statements of men with intellectual disability concerning masculinity. The analysis of the research material obtained from 12 interviews allowed for the identification of four types of masculinity.


Author(s):  
Marzena Buchnat ◽  
Aneta Wojciechowska

The situation of the pandemic of SARS-CoV-2 virus that causes COVID-19 disease is a new and unknown situation for everyone, causing fear and uncertainty. It is also a situation that has led to numerous changes in the everyday life of many people, including students who had to adapt to the new reality of distance education from day to day. The paper concerns with the situation of online education of students with mild intellectual disability and autism spectrum disorder. It is an attempt to indicate the difficulties encountered by this group of students in the situation of distance learning from a perspective of both the student and the teacher. The paper also indicates the issues which should be considered in this education, the way of its adaptation to the possibilities of the discussed group of students, as well as elementswhich are really important in this education.


Politeia ◽  
2020 ◽  
Vol 39 (1) ◽  
Author(s):  
Lloyd Pswarayi

This article draws on qualitative research that was conducted in four areas in Zimbabwe, namely, Lupane, Bulawayo, Chipinge and Mutare. The aim was to extend the use of the concept of “resilience” in relation to working with the youth and preventing violence. Through the concept of “the everyday” it analysed how the youth was surviving in an environment that had undergone nearly two decades of socio-economic and political decline, resulting in high levels of unemployment. The methods used to obtain data were focus-group discussions and individual interviews. The findings showed that the youth applied all the elements associated with resilience (e.g. adapting to the environment, absorbing the pressures that the environment posed, and employing transformative elements) in an effort to emerge in a better position despite having to contend with an environment fraught with many difficulties and risks, which included drug and substance abuse as well as being coopted to participate in violence. Gaining an understanding of the ways the youth navigated environmental, political and social factors was difficult; consequently it was problematic in such a developmental context to define resilience. Nevertheless, the study provided some insights into how young people’s decisions about violence participation were informed. Contrary to dominant current discourses that portray the youth as violent, this study showed that many young people avoided relationships that carried the risk of their being mobilised to take part in violence.


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