Interviewees characterized their mothers and childhoods as different, yet ordinary. Understanding the social context, including but not limited to the availability of informal support, is critical to understanding the experience of children growing up with mothers with intellectual disability.
In this qualitative study, I offer a feminist reflection on motherhood from the perspectives of 25 women with various types of physical and sensory disabilities. Disability was treated not only as an individual experience but also as a social construct. I conducted 25 non-standardised narrative interviews with women with various types of physical disabilities. Using grounded theory method, with a particular emphasis on symbolic interactionism, I identified three important themes from the nonstandardised narrative interviews: the effects of insufficient health care on pregnant women, the lack of acceptance and support for mothers, and a welfare system inadequate to the needs of mothers. These themes affect the way Polish women with disabilities experience motherhood. Findings highlight the different ways that mothers with disabilities challenge the prevailing normative categories of gender and disability and, in so doing, demythologise and delegitimise the traditional Polish model of motherhood. While this study points to needed reforms in Poland to support women with disabilities, it also reveals a model of motherhood based on interdependence and mutual care. The women with disabilities in this study identify new possibilities for all families.
The author analyses how intellectual disability and social and system conditions related to it influence decisions, reproductive rights and ways of experiencing motherhood. She asks questions about motherhood models of intellectually disabled women, the role of informal social support in parenthood and the ways of building, negotiating and crossing the norms of care practices of such women. She verifies the assumptions of participatory research, attempts to recognize the scope and possibilities of engaging women with intellectual disability in the research process.
This article analyses the representation of femininity in school textbooks in search of elements that discourage girls from taking up scientific educational paths. Quantitative content analysis and elements of the constant comparison method were used to examine the content of 75 Polish textbooks. Significant differences were identified in the number of male and female characters, their ages, financial resources, occupations, family roles and mental characteristics. Interestingly, the authors of the analysed textbooks are mostly women, which seems to indicate a manifestation of self-discrimination. These results indicate the existence of mechanisms discouraging females from a scientific career and are discussed in light of Hofstede’s masculinity-femininity theory.
The main goal of this study was to identify the impact of a narrative construction of a life challenge - discovering to have a child with autism - on the meaning of life and on resources for coping depending on the challenge’s novelty, i.e., the number of years from the diagnosis. Three hundred and sixty four mothers of children with autism participated in a long-term 3 × 2 experiment. Half of the mothers had children with autism at the age of 9–12 years. For the remaining half, having children with autism was a new and stressful life situation. Their children were 2–3 years old and just diagnosed by a medical center as having autism spectrum disorder. The mothers were assigned to one of three study conditions: they were either asked to write stories of their motherhood or to describe their children’s behavior on a questionnaire or they did not participate in any tasks. One month and then 4 months after this task the participants completed measures of meaning of life and several well-being scales. The results indicated that following the narrative writing the participants had the highest scores on the meaning of life and well-being scales. This affect was sustained over 4 months and was significant only for mothers with older children. The mediation analysis showed that the effects of the experimental conditions on different well-being scales were mediated by the changes in perceived meaning of life. The results suggest that construction of self-narratives of difficult ongoing challenges facilitates meaning making and subsequently strengthens resources for coping. However, it seems that a meaning-making construction of such self-story may be blocked by the uncertainty and stress caused by novelty of the challenging situation.
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