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This chapter outlines the successful development of a women’s initiative from a grass roots organization to a firmly established institution within our medical school. Championed by a group of dedicated women leaders, the mission of the Alliance for Women in Medicine and Science (AWIMS) is to provide a supportive forum to promote honest discussion and positive change in the realms of gender equity, career advancement, work-life balance, and community service, and to champion professional development and promotion of women in medicine and science. What started as an informal gathering within Southern Illinois University (SIU) School of Medicine’s Department of Medicine in 2015, led by Dr Vidhya Prakash, first morphed into a robust, vital organization called Women in Medicine that contributed meaningfully to SIU Medicine and to the community before it broadened its focus to women in medicine and science and expanded its reach to the entire SIU system. In January of 2018, the initiative was firmly institutionalized as AWIMS, an organization open to ALL members of the SIU community. AWIMS seeks to advance women’s rights through various initiatives. This chapter is co-authored by AWIMS director Dr Vidhya Prakash, and Dr Anne Scheer, a qualitative sociologist in the medical school’s Department of Population Science and Policy, who hopes to help tell the story of AWIMS and translate the Alliance’s successful development process into a narrative accessible to other professionals interested in creating innovations to promote women’s interests in traditionally male-dominated professional settings.

This chapter outlines methodological difficulties and ethical dilemmas encountered during my fieldwork at a high-poverty, high-minority U.S. inner-city school. Using a qualitative research design informed by the “new” sociology of childhood and constructivist grounded theory, I conducted child-centered research at the school for four months, including participant observations and interviews with 50 students. This chapter argues that good ethnographic research not only depends on solid research design but also requires researchers to be flexible, adaptable, and diplomatic. Especially regarding the “least adult” role, the dilemma of objectivity, lying in interviews, and the ethical predicament of students sharing sensitive information, I argue that ethnographic studies often require the researcher to act more like a diplomat maneuvering the stormy waters of contradictory interests than the objective observer described in the methodological literature. First-hand accounts of research exploring children’s own perspectives are scarce. Particularly difficulties and dilemmas encountered in the field are often mentioned only in passing, if they are mentioned at all. Novice researchers thus struggle to find information to guide their own endeavors and may set themselves up for frustration if they expect their research to be as predictable as the methodological literature suggests. The paucity of discussion of real-life difficulties encountered in the field also hinders scholarly dialog and obstructs the advancement of methodological and ethical questions surrounding research with children. This chapter hopes to help fill this gap.

The purpose of this study is to explore rural children’s own perspectives on health, well-being, and nutrition to better understand how they approach, navigate, and make sense of these topics.

This study uses a qualitative ethnographic research design theoretically informed by the “new” Sociology of Childhood and methodologically informed by constructivist grounded theory. This ongoing study with fifth-grade students in an elementary school in a small rural school district in central Illinois consists of ethnographic observations conducted at the school, in-depth interviews with students, and participatory tools that seek to involve students more fully in the process of data collection.

Preliminary findings of this pilot study suggest that many aspects often discussed in the context of childhood obesity, especially in rural settings, including knowledge or education about healthy eating, increasing physical activity levels, or access to healthy foods, are complex and multifaceted and do not easily lend themselves to standard interventions. Findings also indicate that children’s ideas about healthy eating deviate from their own eating practices.

Conceptualized as a grounded theory study, the research is not intended to be generalizable or reproducible. Instead, the study seeks to develop hypotheses directly from the field and study participants’ views and voices. These perspectives will inform a more in-depth study of childhood obesity in rural settings planned for 2019.

Findings from this pilot study will inform innovative, informed interventions that are guided by children’s own experiences and perspectives. Study findings will also be of benefit to practicing pediatricians and other child health professionals as they understand how to better think about and address challenges of health and weight management of patients and their families.

Departing from an online interactive Gender Café on the topic of Knowledge Management (KM), jointly hosted by a UN agency and the Society of Gender Professionals, this chapter seeks to provide gender practitioners and others with practical examples of how to “gender” KM in international development. Through analyzing the travel of feminist ideas into the field of KM with inspiration from Barbara Czarniawska’s and Bernard Joerge’s (1996) theory of the travel of ideas, the chapter explores the spaces, limits, and future possibilities for the inclusion of feminist perspectives. The ideas and practical examples of how to do so provided in this chapter originated during the café, by the participants and panellists. The online Gender Café temporarily created a space for feminist perspectives. The data demonstrate how feminist perspectives were translated into issues of inclusion, the body, listening methodologies, practicing reflection, and the importance to one’s work of scrutinizing underlying values. However, for the feminist perspective to be given continuous space and material sustainability developing into an acknowledged part of KM, further actions are needed. The chapter also reflects on future assemblies of gender practitioners, gender scholars and activists, recognizing the struggles often faced by them. The chapter discusses strategies of how a collective organizing of “outside–inside” gender practitioners might push the internal work of implementing feminist perspectives forward.

This chapter presents the broad themes of this special issue by introducing the contributions and connections among the chapters in the volume. Recent theoretical constructions of childhood have positioned children as social actors resulting in a growth of child- and youth-centered empirical research. Yet, there is a continued importance for researchers to discuss ethical issues that arise in research with youth, contend with the competing constructions of children as social agents and in need of protection, and explore innovative methodological strategies used in research with youth.

This paper aims at revealing the process of identity reconstruction for individuals who have acquired sensory disabilities, as well as the contribution of consumption to this process.

The data was collected through both interviews conducted in France and autobiographical accounts.

When disability occurs, individuals go through a rite of passage that shapes their identity reconstruction process. Two forms of liminality appear: acute and sustained liminality. These phases can foster or hamper individuals’ identity reconstruction.

The mechanisms leading from one stage of the identity reconstruction process to another should be deepened through further research.

Given the fluctuating behaviors of consumers with disabilities, especially in view of their identity reconstruction process, this research encourages retailers and public policy actors not to consider them as a homogeneous consumer segment.

While scholars dealing with consumers with disabilities have mainly focused on the accessibility of the marketplace, this research disentangles their identity issues.