Including pupils with special educational needs in secondary school physical education: a sociological analysis of teachers' views

This paper explores physical education (PE) teachers' views of the inclusion of pupils with special educational needs (SEN) in PE from a figurational sociological perspective. Starting from the premise that teachers' views cannot be adequately explained by studying the concept of inclusion or the teacher in isolation, it is argued that we can only begin to make sense of such views by locating teachers within the figurations of which they are a part and by exploring two particularly salient features of those figurations: namely, teachers' habituses and contexts. In doing so, the paper focuses upon the training teachers receive, the constraints imposed upon them by their colleagues and pupils, and, most importantly, the suitability of the National Curriculum for meeting the needs of pupils with SEN. The paper concludes by highlighting some of the unintended consequences of the inclusion of pupils with SEN in PE.     

#3: continuous labor support

In this position paper-one of six care practice papers published by Lamaze International and reprinted here with permission-the benefit of continuous labor support is discussed and presented as an evidence-based practice that helps promote, protect, and support normal birth. The paper is written for childbearing women and their families. Women with continuous support are less likely to have a cesarean, an instrument delivery, and regional anesthesia. They are also less likely to report dissatisfaction with or negatively rate their childbirth experience. The value of the doula for both the laboring woman and her labor partner is discussed. The accompanying commentary-written by a leading proponent of maternity care practices-supports evidence that promotes continuous labor support. Lamaze International encourages women to plan for a supportive birth environment that includes continuous support.     

Neurological impairment in maltreated children

The neurological competency of maltreated children was assessed by comparing physically abused children not known to have sustained serious head trauma, neglected children, and normally raised children from the same socioeconomic milieu. Each child underwent physical and neurological examinations including EEGs, supplemented by perceptual-motor tests devised to detect subtle evidence of neurological dysfunction. Obstetrical and developmental histories, as well as intelligence test protocols, were available. Blind ratings by a pediatric neurologist using all available information revealed significantly more impairment in the maltreated groups with more than 50% of the abused children in the moderate or severely impaired category. The complex relationship between the maltreating environment and neurological disorders in these populations is discussed including the need to routinely search for evidence of subtle neurological impairment when maltreatment is known or suspected.     

Contrasting disclosure practices and experiences of school support for Australian adolescents with cancer,cystic fibrosis and anorexia nervosa: parent perspectives

Schools in Australia are required to promote equitable access to education and provide support services to students with chronic health conditions (CHCs). This qualitative study was conducted to explore stakeholders’ experiences and perceptions regarding school-based support. In-depth interviews were conducted with 38 parents of upper secondary school students with cystic fibrosis, anorexia nervosa or cancer (which were illustrative of different types of severe congenital, mental health or somatic CHCs). This enabled comparison of findings to determine whether there were any patterns in perceptions and experiences that were tied to the different CHCs. Data were analysed using a modified grounded theory approach to identify themes. Even though analysis indicated that all cohorts of parents viewed informed educators as best placed to provide tailored school-based support, major cohort differences were reported in parental experiences of school-based support as well as parental diagnosis disclosure behaviour. This latter finding was associated with cohort-related perceptions of risk to their adolescent child. Barriers to school-based support were perceived as varying by condition, the advocacy experience of parents and the nature of health service supports. Taking these findings into account, modification of current policies and practices within education and health sectors may lead to more equitable educational outcomes.     

Peter rabbit hops into the twenty-first century

Summary Adults have tried to identify and to seek complex explanations for Potter's success. She explained it simply: “It is much more satisfactory to address a real live child. I often think that was the secret of the success of Peter Rabbit; it was written to a child—not made to order” (Lane, 1976, p. 183). She felt the more spontaneous the pleasure, the better the result. You are encouraged to heed Potter's advice. Address the real live child as you enjoy the pleasure of this adventure into the life and times of Beatrix Potter and all her animal friends.     

Finding a new kind of knowledge on the HeartNET website

Background: A website developed by the National Heart Foundation (WA Division) and Edith Cowan University, with the help of an Australian Research Council–Linkage grant, provides insight into the sense of isolation experienced by many heart patients which prompts them to engage in a relentless search to answer the fundamental question: why me? Objective: To discover whether an online community for people with heart conditions may help instil a sense of sharing a journey with others, and to assess the impact of this shared experience. Methods: The qualitative data constituted 50 in‐depth interviews with heart patients using the HeartNET website. This website, with its 600+ membership, also provides Discussion Board data to add depth to the analysis. Results: Patients describe how their unsatisfactory search for information in one ‘place’ (the Internet) led them to discover a new ‘place’ (an online community) where they could ‘ask difficult questions’, and ‘gain support and wisdom’ from others. Conclusion: This paper suggests that, when anxious patients seek health‐related information, for example in a library, they may benefit from being given contact points to communicate with others who find themselves in similar situations. Internet‐based social software (Web 2.0) can provide this kind of communication.     

Is open access affordable? Why current models do not work and why we need internet‐era transformation of scholarly communications

Progress to open access (OA) has stalled, with perhaps 20% of new papers ‘born‐free’, and half of all versions of record pay‐walled; why? In this paper, I review the last 12 months: librarians showing muscle in negotiations, publishers’ Read and Publish deals, and funders determined to force change with initiatives like Plan S. I conclude that these efforts will not work. For example, flipping to supply‐side business models, such as article processing charges, simply flips the pay‐wall to a ‘play‐wall’ to the disadvantage of authors without financial support. I argue that the focus on OA makes us miss the bigger problem: today’s scholarly communications is unaffordable with today’s budgets. OA is not the problem, the publishing process is the problem. To solve it, I propose using the principles of digital transformation to reinvent publishing as a two‐step process where articles are published first as preprints, and then, journal editors invite authors to submit only papers that ‘succeed’ to peer review. This would reduce costs significantly, opening a sustainable pathway for scholarly publishing and OA. The catalyst for this change is for the reputation economy to accept preprints as it does articles in minor journals today.