21 research outputs found

    Epistolary Labours: Reading Childbirth and the Politics of Reproductive Medicine in Two Eighteenth-Century Women’s Letters

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    Birth stories, as numerous scholars have observed, are central aspects of maternal identity. Such stories build community, enabling women to navigate what Fiona Nelson (2009) has referred to as the “culture of motherhood.” In this essay, I offera detailed analysis of two eighteenth-century birth stories. I argue that these two narratives, both written by elite women during the second half of the eighteenth century, allow the contemporary reader a window not only into eighteenth-centuryexperiences of childbirth, but more importantly, into the tensions that sometimes arose between labouring women and the medical personnel who were meant to support them

    Sleep Solutions for Your Baby, Toddler and Preschooler

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    In the Other Room: Entering the Culture of Motherhood

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    Le nƓud lui-mĂȘme : L'enchevĂȘtrement du multiculturalisme

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    Multiculturalism has defined Canadian identity, both within and beyond its borders, for fifty years. Supporters laud the policy’s celebration of unity through difference. Critics, meanwhile, argue that this celebration is superficial. Canada’s multiculturalism policy, they say, obscures the workings of power in processes entrenching structural inequalities. Taking a reflexive approach, we—a mixed-race settler immigrant who arrived in Canada as a young child in 1975, and a White settler Canadian born in Halifax in the 1990s—interrogate our experiences and understandings of multiculturalism. Using collaborative autoethnography and found poetry, we examine our affective encounters and engagements with settler multiculturalism. In the process, we tangle with questions of (non)arrival, belonging, migration, branding and identities. Ultimately, we suggest that thinking through the knot and knottiness of multiculturalism can offer a path towards more nuanced and complicated futures.Le multiculturalisme dĂ©finit l'identitĂ© canadienne, tant Ă  l'intĂ©rieur qu'Ă  l'extĂ©rieur de ses frontiĂšres, depuis cinquante ans. Les partisans de cette politique louent la cĂ©lĂ©bration de l'unitĂ© dans la diffĂ©rence. Les critiques, quant Ă  elles, affirment que cette cĂ©lĂ©bration est superficielle. La politique de multiculturalisme du Canada, disent-ils, masque les rouages du pouvoir dans les processus d'enracinement des inĂ©galitĂ©s structurelles. En adoptant une approche rĂ©flexive, nous—une immigrante mĂ©tisse arrivĂ©e au Canada dans son enfance en 1975 et une Canadienne blanche nĂ©e Ă  Halifax dans les annĂ©es 1990—interrogeons nos expĂ©riences et notre comprĂ©hension du multiculturalisme. En utilisant l'auto-ethnographie collaborative et la poĂ©sie retrouvĂ©e, nous examinons nos rencontres affectives et nos engagements avec le multiculturalisme des colons. Dans ce processus, nous abordons les questions de (non-)arrivĂ©e, d'appartenance, de migration, d'Ă©tiquette et d'identitĂ©. Ultimement, nous suggĂ©rons que la rĂ©flexion sur le nƓud et le caractĂšre noueux du multiculturalisme peut offrir une voie vers un avenir plus nuancĂ© et compliquĂ©

    The Intro Course: A Pedagogical Toolkit

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    AbstractThis article offers ideas and strategies for teaching introductory-level courses in Gender and Women’s Studies by providing the responses of eleven experienced educators who were asked two questions: What main theme or idea do you hope students will learn in the introductory class you teach? And what practical strategies do you use in the classroom to achieve that learning objective?RĂ©sumĂ©Cet article propose des idĂ©es et des stratĂ©gies pour enseigner les cours d’introduction aux Études sur le genre et les femmes en fournissant les rĂ©ponses d’onze Ă©ducatrices chevronnĂ©es Ă  qui l’on a posĂ© deux questions : Quel thĂšme ou quelle idĂ©e principale espĂ©rez-vous que les Ă©tudiants apprennent dans la classe d’introduction que vous enseignez? Et quelles stratĂ©gies pratiques utilisez-vous en classe pour atteindre cet objectif d’apprentissage

    Validation of activity questionnaires in patients with cystic fibrosis by accelerometry and cycle ergometry

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    BACKGROUND: The objective of this study was to validate physical activity questionnaires for cystic fibrosis (CF) against accelerometry and cycle ergometry. METHODS: 41 patients with CF (12-42 years) completed the Habitual Activity Estimation Scale (HAES), the 7-Day Physical Activity Recall questionnaire (7D-PAR) and the Lipid Research Clinics questionnaire (LRC) and performed an incremental exercise test according to the Godfrey protocol up to volitional fatigue. Time spent in moderate and vigorous physical activity (MVPA) assessed objectively by accelerometry was related to the time spent in the respective activity categories by correlation analyses and calculating intraclass correlation coefficients (ICC). Furthermore, the results of the exercise test were correlated with the results of the questionnaires. RESULTS: Time spent in the categories 'hard','very hard' and 'hard & very hard' of the 7D-PAR (0.41 > r > 0.56) and 'active' (r = 0.33) of the HAES correlated significantly with MVPA. The activity levels of the LRC were not related to objectively determined physical activity. Significant ICCs were only observed between the 7D-PAR activitiy categories and MVPA (ICC = 0.40-0.44). Only the LRC showed moderate correlations with the exercise test (Wmax: r = 0.46, p = 0.002; VO2peak: r = 0.32, p = 0.041). CONCLUSIONS: In conclusion, the activity categories 'hard' and 'very hard' of the 7D-PAR best reflected objectively measured MVPA. Since the association was at most moderate, the 7D-PAR may be selected to describe physical activity within a population. None of the evaluated questionnaires was able to generate valid physical activity data exercise performance data at the individual level. Neither did any of the questionnaires provide a valid assessment of aerobic fitness on an invidual leve

    2018 Research & Innovation Day Program

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    A one day showcase of applied research, social innovation, scholarship projects and activities.https://first.fanshawec.ca/cri_cripublications/1005/thumbnail.jp

    Demographic, clinical, and service-use characteristics related to the clinician’s recommendation to transition from child to adult mental health services

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    Purpose: The service configuration with distinct child and adolescent mental health services (CAMHS) and adult mental health services (AMHS) may be a barrier to continuity of care. Because of a lack of transition policy, CAMHS clinicians have to decide whether and when a young person should transition to AMHS. This study describes which characteristics are associated with the clinicians’ advice to continue treatment at AMHS. Methods: Demographic, family, clinical, treatment, and service-use characteristics of the MILESTONE cohort of 763 young people from 39 CAMHS in Europe were assessed using multi-informant and standardized assessment tools. Logistic mixed models were fitted to assess the relationship between these characteristics and clinicians’ transition recommendations. Results: Young people with higher clinician-rated severity of psychopathology scores, with self- and parent-reported need for ongoing treatment, with lower everyday functional skills and without self-reported psychotic experiences were more likely to be recommended to continue treatment. Among those who had been recommended to continue treatment, young people who used psychotropic medication, who had been in CAMHS for more than a year, and for whom appropriate AMHS were available were more likely to be recommended to continue treatment at AMHS. Young people whose parents indicated a need for ongoing treatment were more likely to be recommended to stay in CAMHS. Conclusion: Although the decision regarding continuity of treatment was mostly determined by a small set of clinical characteristics, the recommendation to continue treatment at AMHS was mostly affected by service-use related characteristics, such as the availability of appropriate services

    Cohort profile : demographic and clinical characteristics of the MILESTONE longitudinal cohort of young people approaching the upper age limit of their child mental health care service in Europe

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    Purpose: The presence of distinct child and adolescent mental health services (CAMHS) and adult mental health services (AMHS) impacts continuity of mental health treatment for young people. However, we do not know the extent of discontinuity of care in Europe nor the effects of discontinuity on the mental health of young people. Current research is limited, as the majority of existing studies are retrospective, based on small samples or used non-standardised information from medical records. The MILESTONE prospective cohort study aims to examine associations between service use, mental health and other outcomes over 24 months, using information from self, parent and clinician reports. Participants: Seven hundred sixty-three young people from 39 CAMHS in 8 European countries, their parents and CAMHS clinicians who completed interviews and online questionnaires and were followed up for 2 years after reaching the upper age limit of the CAMHS they receive treatment at. Findings to date: This cohort profile describes the baseline characteristics of the MILESTONE cohort. The mental health of young people reaching the upper age limit of their CAMHS varied greatly in type and severity: 32.8% of young people reported clinical levels of self-reported problems and 18.6% were rated to be ‘markedly ill’, ‘severely ill’ or ‘among the most extremely ill’ by their clinician. Fifty-seven per cent of young people reported psychotropic medication use in the previous half year. Future plans: Analysis of longitudinal data from the MILESTONE cohort will be used to assess relationships between the demographic and clinical characteristics of young people reaching the upper age limit of their CAMHS and the type of care the young person uses over the next 2 years, such as whether the young person transitions to AMHS. At 2 years follow-up, the mental health outcomes of young people following different care pathways will be compared. Trial registration number: NCT03013595
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