Bloomsbury Studies in Health Communication – serie
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32 produkter
32 produkter
Häftad, Engelska, 2020
534 kr
Skickas inom 10-15 vardagar
Challenging Reproductive Control and Gendered Violence in the Américas: Intersectionality, Power, and Struggles for Rights utilizes an intersectional Chicana feminist approach to analyze reproductive and gendered violence against women in the Américas and the role of feminist activism through case studies including the current state of reproductive justice in Texas, feminicides in Latin America, raising awareness about Ni Una Más and anti-feminicidal activism in Ciudad Juárez, and reproductive rights in Latin America amidst the Zika virus. Each of these contemporary contexts provides new insights into the relationships between and among feminist activism; reproductive health; the role of the state, local governments, health organizations, and the media; and the women of color who are affected by the interplay of these discourses, mandates, and activist efforts.
Inbunden, Engelska, 2018
1 149 kr
Skickas inom 10-15 vardagar
Communication Studies and Feminist Perspectives on Ovarian Cancer examines the embodied experience of ovarian cancer by critically analyzing impacts of normative social and medical discourses—including discourses of risk, choice, early detection, lack of reliable screening tests for ovarian cancer, feminine beauty, and self-advocacy—on women’s communicative responses to the disease and treatments. It argues that these discourses help discredit some ovarian cancer experiences, encourage a one-dimensional perspective on the disease, and divert attention from larger issues such as society’s disregard for women’s complaints about disease symptoms. Blanket promotion of these discourses essentializes women’s experiences of the disease, pointing out how normative beliefs about women’s health and illness are often flipped and repackaged as standard language to discuss women’s experiences.Using interview data and scholarly work from communication studies, feminist studies, critical/cultural studies, anthropology, critical psychology, and other disciplines, this book suggests we give equal importance to personal experiences and medical/scientific research to advance knowledge about ovarian cancer. Ovarian cancer is a disease specific to women; as such, women’s experiences cannot be minimized in attempts to understand the disease.
Inbunden, Engelska, 2017
1 221 kr
Skickas inom 10-15 vardagar
Reifying Women's Experiences with Invisible Illness: Illusions, Delusions, Reality provides a platform that recognizes that the experience of invisible illness is greatly influenced by context and personal circumstance. The contributors to this book include women who exude diversity as it relates to race and ethnicity, career, religious experience, education, social support, and interpersonal relationships. From recent college graduates to senior level professionals, these women share stories that create a space to advocate on behalf of the individual who is chronically ill rather than focusing on the often privileged perspective of medical professionals.
Inbunden, Engelska, 2017
1 149 kr
Skickas inom 10-15 vardagar
Discoveries of Medically Themed Media: Pediatric Patients and Parents’ Journeys of Sense-making examines the information needs and sense-making processes of pediatric patients through ethnographic accounts of 14 children undergoing craniofacial, neurological, and neurosurgical treatment. It contends that children rely on information—much of which is not delivered in an age-appropriate manner but rather geared toward adults—for the navigation of their medical experiences, and proposes medically themed media as a significant avenue by which greater understanding and sense-making are possible for pediatric patients.
Inbunden, Engelska, 2017
1 221 kr
Skickas inom 10-15 vardagar
More and more women are searching the Internet for medical information. Women who have been diagnosed with breast cancer search for information and participate in online communities—groups that “gather” in established online spaces to interact about their diagnoses of breast cancer. They share their own struggles and emotions with their own language: the rhetoric of breast cancer. They ask questions, share experiences, create friendships, discuss their disease processes, and present their illness narratives. However, they also create ethical dilemmas for online researchers and privacy issues as they share information that is legally protected through HIPAA.Online communities will only increase as research of online information expands through big data and predictive analytics, and more than ever before, women need to be aware of the information they share. Researchers also need to be aware, as they share the data they gather, and seek to preserve the privacy of the creators of the online data that they investigate and report.The Rhetoric of Breast Cancer provides a discussion of the complex structures of online communities, particularly those focused on medical diagnoses, and is a valuable read for patients, theorists, physicians, and researchers.
Häftad, Engelska, 2020
550 kr
Skickas inom 10-15 vardagar
Politics, Propaganda, and Public Health: A Case Study in Health Communication and Public Trust takes an in-depth look at Merck Pharmaceutical's groundbreaking launch of the Gardasil vaccination and ways in which new trends in pharmaceutical marketing affect public health awareness efforts. Prior to receiving FDA approval for Gardasil, Merck built up concern around the human papillomavirus through early awareness messaging. Though Merck's approach may have promoted inoculation efforts, the company seemingly crafted a product endorsement for Gardasil through its social marketing strategy and nationwide lobbying. The question is, do the ends justify the means? Crosswell and Porter use a unique combination of eye tracking data, in-depth interviews, and rhetorical analysis as they examine what happens to public trust when Big Pharma combines product marketing with awareness messaging. This book offers a platform for cross-disciplinary debate on the effects of direct-to-consumer advertising and proposes future courses of action for Big Pharma regulators and media scholars.
Inbunden, Engelska, 2019
1 578 kr
Skickas inom 10-15 vardagar
Ten years after the adoption of the HITECH Act of 2009, eMessaging and the Physician/Patient Dynamic: Practices in Transition examines the complex, interlocking forces at play when mandates for electronic health records (EHRs) and electronic messaging within secured health portals forced an unprecedented transformation of the healthcare environment. Technological, sociological, medical, economic, political, governmental, legal, and communication issues converged, forever altering the “medicological environment,” a space within which health professionals and patients alike strive towards efficacious, satisfying transactions that lead to improved health. Susan M. Wieczorek’s analysis discusses the layers of policies and regulations that thrust healthcare users—often unwillingly—into the newly required practice of online communication between physicians and patients. Wieczorek also compares and contrasts rural and urban early adoption practices through the use of surveys, critical incident reports, and oral histories and anticipates future trends in data mining of electronic messaging by demonstrating a content analysis of over 60,000 electronic medical transactions within secured health portals. This book identifies the key converging influences that affected the real-life, early adopters amid this transformation process and provides a practical foundation for current, on-going practice applications while anticipating the inevitable challenges of future health communication technologies. Scholars of communication, health, and media studies will find this book particularly useful.
Inbunden, Engelska, 2018
1 116 kr
Skickas inom 10-15 vardagar
Disability in the Media: Examining Stigma and Identity looks at how disabilities are portrayed within the media and how individuals with disabilities are affected by their representation. The effects of media representation can be seen both at the level of the individual, with effects on self-identity for those with a disability, and at the level of society as a whole, with these portrayals playing a role in the social construction of disability, often further stigmatizing individuals with disabilities. On all levels, research has ended with a call to media producers, asking those in the entertainment industry to think about how they are portraying disability, to hire actors with disabilities, and to realize that the “supercrip” may not always be the most positive portrayal of disability. This book looks at the current status of disability representation in television and the popular press, offering case studies that examine their effect on individuals with disabilities and making suggestions for improving media representation and battling the perpetuation of social stigmas.
Häftad, Engelska, 2020
499 kr
Skickas inom 10-15 vardagar
Disability in the Media: Examining Stigma and Identity looks at how disabilities are portrayed within the media and how individuals with disabilities are affected by their representation. The effects of media representation can be seen both at the level of the individual, with effects on self-identity for those with a disability, and at the level of society as a whole, with these portrayals playing a role in the social construction of disability, often further stigmatizing individuals with disabilities. On all levels, research has ended with a call to media producers, asking those in the entertainment industry to think about how they are portraying disability, to hire actors with disabilities, and to realize that the “supercrip” may not always be the most positive portrayal of disability. This book looks at the current status of disability representation in television and the popular press, offering case studies that examine their effect on individuals with disabilities and making suggestions for improving media representation and battling the perpetuation of social stigmas.
Inbunden, Engelska, 2020
1 219 kr
Skickas inom 10-15 vardagar
Non-suicidal self-injury (NSSI) is the deliberate harming of one's body without suicidal intent. NSSI tends to be secretive, often involving cutting, bruising, or burning on hidden parts of the body. While NSSI often occurs among adolescents, it is not limited to that age group. Communication and NSSI intersect in many ways, including conversation among family members, consultation with healthcare providers, representation in the media, discourse among people who self-injure, and even communication with oneself. Each chapter in Communicating With, About, and Through Self-Harm: Scarred Discourse addresses a different context of communication crucial to our understanding NSSI. An international group of clinicians and communication specialists describe, analyze, and explain how NSSI is communicated about, what NSSI is communicating, and how can we do a better job in communicating with others about NSSI. This book’s fundamental purpose is to empower individuals who self-injure as well as their families, friends, healthcare providers, and communities to better understand and deal with NSSI and the pressures that cause it.
Häftad, Engelska, 2022
492 kr
Skickas inom 10-15 vardagar
Non-suicidal self-injury (NSSI) is the deliberate harming of one's body without suicidal intent. NSSI tends to be secretive, often involving cutting, bruising, or burning on hidden parts of the body. While NSSI often occurs among adolescents, it is not limited to that age group. Communication and NSSI intersect in many ways, including conversation among family members, consultation with healthcare providers, representation in the media, discourse among people who self-injure, and even communication with oneself. Each chapter in Communicating With, About, and Through Self-Harm: Scarred Discourse addresses a different context of communication crucial to our understanding NSSI. An international group of clinicians and communication specialists describe, analyze, and explain how NSSI is communicated about, what NSSI is communicating, and how can we do a better job in communicating with others about NSSI. This book’s fundamental purpose is to empower individuals who self-injure as well as their families, friends, healthcare providers, and communities to better understand and deal with NSSI and the pressures that cause it.
Häftad, Engelska, 2020
534 kr
Skickas inom 10-15 vardagar
CTE, Media, and the NFL: Framing a Public Health Crisis as a Football Epidemic examines the central role of mediain constructing an entangled relationship between chronic traumatic encephalopathy (CTE) and the National Football League (NFL), challenging a predominately symbiotic sports/media complex. The authors of this book analyze more than a decade of media coverage, along with three prominent films, to unpack how media discourse resurrects CTE, a preventable degenerative brain disease linked to boxing in 1928, and subsequently frames it as a football epidemic dating back to 2005.The authors position CTE as a public health crisis, whereby media coverage of CTE and the NFL’s vigorous reliance on controversial published research by the Mild Traumatic Brain Injury (MTBI) Committee parallels the moral panic of the HIV/AIDS epidemic and Big Tobacco’s manufacturing of doubt through faulty science. This book argues that the continued aspiration and idolization of the NFL, and its lack of accountability for health concerns surrounding brain injuries, highlight the firm grasp of hegemonic masculinity on the ideology of American football - further problematizing media’s glorification of the sport. Scholars of sports media, health communication, and general media studies will find this book particularly useful to discuss longitudinal effects of media framing centered on critical health risks in sport and the challenge of translating accurate scientific knowledge to the public domain.
Inbunden, Engelska, 2019
1 623 kr
Skickas inom 10-15 vardagar
Communicating Mental Health: History, Contexts, and Perspectives explores mental health through the lens of the communication discipline. In the first section, contributors describe the major contributions of the communication discipline as it pertains to a broader perspective and stigma of mental health. In the second section, contributors investigate mental health through various narrative perspectives. In the third and fourth sections, contributors consider many applied contexts such as media, education, and family. At the conclusion, contributors discuss the ways in which future inquiries regarding mental health in the communication discipline can be investigated. Scholars of health communication, mental health, psychology, history, and sociology will find this volume particularly useful.
Häftad, Engelska, 2020
550 kr
Skickas inom 10-15 vardagar
Diversity plays an important role in how people experience illness and healthcare as patients. Listening carefully to stories of how race, class, age, gender, sexuality, and disability can affect patient experience can be revealing and provide much needed change to health communication in the patienthood narrative. This book is a collection of vibrant and engaging essays by scholars of narrative methods in health communication. Each chapter takes readers into the fascinating world of patients who use stories from their personal lives to challenge us to rethink, reimagine, and reformulate what health communication means in practice. Each section of the book focuses on an important aspect of the theory and practice of the patienthood narrative. Part one explores the important ways that telling and sharing patient’s stories can lead to learning, empowerment, and advocacy. Part two explores several key forms of diversity and how they affect patienthood. Part three illustrates how personal, relational, and cultural aspects of identity intersect to shape the patient experience.
Inbunden, Engelska, 2019
1 085 kr
Skickas inom 10-15 vardagar
Narrative Journeys of Young Black Women with Eating Disorders: A Hidden Community among Us explores how the realities of three young black women who have experienced eating disorders since childhood were transformed, discussing the larger implications of disordered eating in underrepresented populations. People of all ethnic, gender, and socioeconomic backgrounds are susceptible to their grips, yet black women and children are experiencing eating disorders and suffering in silence due to shame and stigma. Due to barriers such as the conventional thought that eating disorders do not occur in the black community, they are often not acknowledged, discussed, or treated properly. Stephanie Hawthorne argues that these women’s lived experiences substantiate the need for culturally sensitive and inclusive prevention, intervention, and care when it comes to mental health, and offers recommendations to schools, clinicians, parents, and adolescents to accomplish this goal. Scholars of communication, mental health, race studies, education, and medicine will find this book particularly useful.
Häftad, Engelska, 2023
464 kr
Skickas inom 10-15 vardagar
Through vivid and engaging narrative accounts, written and collected by women, Women's Narratives of Health Disruption and Illness: Within and Across Their Life Stories explores how women experience the health disruptions and illnesses that span their lives. The collection examines how women’s broader and ongoing life stories impact and are impacted by health disruptions and illnesses. Organized into three parts, the chapters explore “Beginnings” in which health disruptions and illnesses impact early life, motherhood, and where early choices create the origins of health issues that impact later life; “Middles” which explores health experiences in and around middle age, or from the standpoint in middle-age looking back and forth; and “Endings” which explores narratives of ageing and end of life communication. Personal, revealing, and often beautiful, the women’s narratives featured in this book will invite the reader into the stories and lives of others, and toward the reflection, learning, and personal transformation that comes from truly connecting with the experiences of others. This book will be helpful for scholars of communication, health, women’s studies, family studies, and sociology.
Inbunden, Engelska, 2019
1 255 kr
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Social Support and Health in the Digital Age discusses how theinformation age has revolutionized nearly every facet of human communication—from the ways in which people purchase products to how they meet and fall in love. These exciting new communication technologies can both unite and divide us. People who are separated by great distances can now communicate with each other in real time, whereas parents often find themselves competing with smartphones and tablets for their children’s attention. This book explores the many ways that digital communication media, such as online forums, social networking sites, and mobile applications, enhance and constrain social support in health-related contexts. We already know a great deal about how the Internet has altered how people search for health information, but less about how people seek and receive social support in this new age of information, which is critical for maintaining our physical, mental, and emotional wellbeing.
Inbunden, Engelska, 2020
1 532 kr
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Even as life expectancies increase, increasing numbers of people are living with chronic illness and pain than ever before. Long-term self-management of chronic conditions involves negotiating the intersections of personal life choices, community and workplace structures, and family roles. Medical Humanism, Chronic Illness, and the Body in Pain: An Ecology of Wholeness proposes an ecological model of wholeness, which envisions wholeness in the dialogic engagement of the philosophical orientations of the biomedical and traditional medical systems. Vinita Agarwal proposes an integrative premise of being whole through revising the fundamental definitions of humanism, rethinking the self/body/environment, and thereby recognizing alternative ways of organizing knowledge and human experience as this model pushes the intersections of patient-centered care and sustainable health ethics. It is in the spaces of such intersections, Agarwal argues, that we accomplish healing as an integrative relationship of the individual with the multiple cultural logics underlying chronic conditions and the competing medical worldviews of our contemporary landscape. Scholars of communication, health, and medical humanities, along with practitioners working with patients who have chronic conditions, will find this book particularly useful.
Inbunden, Engelska, 2023
1 047 kr
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PCOS Discourses, Symbolic Impacts, and Feminist Rhetorical Disruptions of Institutional Hegemonies examines the power of hegemonic institutions and their impact on bodies, focusing on how women with Polycystic Ovarian Syndrome (PCOS) employ rhetorical strategies to resist and disrupt mass media and clinical discourses that seek to define them and their experiences. This monograph argues that through the enactment of bio-power (Foucault), digital and mass media have denied women with PCOS opportunities for autonomous subject formation, and, in turn, allowances for constructing their ontologies and epistemologies. However, by networking in participatory new media, McKinley posits, women with PCOS can reclaim their agency. To support this argument, McKinley rhetorically examines three PCOS artifacts—a television episode, an online popular culture forum, and an online health forum. This monograph bridges the personal and the academic and adds to and extends the work being done in the Rhetoric of Health and Medicine (RHM) on PCOS through the adoption of a unique theoretical lens (e.g., Lisa Melonçon’s performative phenomenology) and methodology (e.g., Norman K. Denzin’s Feminist Communitarian Model) and contributes to conversations surrounding femaleness, femininity, women’s health challenges, and advocacy, as located in RHM scholarship and related fields.
Inbunden, Engelska, 2023
1 047 kr
Skickas inom 10-15 vardagar
Numerous movies, YouTube videos, books, and public service announcements have begun to address people with narcolepsy, and this discourse has led to greater visibility and understanding about an often-misunderstood condition. In Narratives of Narcolepsy in Everyday Life: Exploring Intricacies of Identity, Sleepiness, and Place, Nicole Eugene draws on in-depth interviews, participant observation, and field notes to examine life with narcolepsy, witha particular focus on how certain socially-defined places play significant roles in determining the meaning of sleepiness, medication side effects, and other narcolepsy symptoms. Eugene also includes one autoethnographic essay that explores her own experiences with narcolepsy as a Black woman, refracted through the lens of the various places where sleepiness may arise. Throughout the book, an emphasis on making sense of narcolepsy by communicating with others with the condition demonstrates a peer-based approach to researching health communication and disabilities. Drawing on feminist disability studies, health communication, narrative inquiry, and autoethnography, this book is an example of interpretive qualitative communication research that renders the lives of vulnerable people with compassion and understanding.
Inbunden, Engelska, 2025
1 237 kr
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This edited volume offers an accessible avenue for improving health and well-being by demonstrating the power of narrative in advocating for yourself, your family, and your community. Leading scholars of health communication draw on a variety of perspectives, theories, and methodologies and incorporate their own personal experiences of narratives to demonstrate the compelling reasons why narratives should be studied and applied in a wide range of health contexts. Each chapter contains future directions for advancing research and applying narratives to encourage readers to explore what narratives for health mean for themselves and others.
Inbunden, Engelska, 2023
1 047 kr
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A Culturally-Centered and Intersectional Approach to Reproductive Justice investigates and challenges assumptions and pre-existing notions regarding reproductive justice by grounding this work in a more inclusive and culturally informed context. Throughout history, contributors argue, reproductive justice movements have centered white, cisgendered, and non-disabled women in the West. Along with women in the Global South being underrepresented in scholarship, research tends to focus only on the abuses they have suffered, rather than delving deeper into issues of structures, barriers, or agency. Each chapter is written from an autoethnographic perspective to unpack the contributors’ challenges with achieving reproductive justice for themselves and their respective communities. Ultimately, this book asserts that when different facets of reproductive justice are presented in the form of narrative self-reflexivity, readers find a space to safely evaluate their positionality within the larger reproductive justice movement while simultaneously acknowledging the complexity of the movement itself. Scholars of communication, health, and women’s and gender studies will find this book of particular interest.
Inbunden, Engelska, 2024
1 363 kr
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In this book, Yuxia Qian and Rukhsana Ahmed explore health acculturation, which they argue is a complex, multidimensional communication process involving concerted efforts from migrants, health professionals, researchers, community members, policymakers, and the media, rather than a unidimensional process synonymous with assimilation. Qian and Ahmed examine individual migrant health acculturation experiences, community-based culturally-centered health interventions, and cross-cultural health promotion and campaigns. Ultimately, this book unpacks the complexity surrounding the health acculturation process through different theoretical frameworks and cross-cultural applications in a range of communication contexts, including the interpersonal, family, community, organizational, and media.
From Surviving to Metaviving
A New Rhetorical Formation in Metastatic Breast Cancer Patient Discourse
Inbunden, Engelska, 2025
971 kr
Skickas inom 10-15 vardagar
As treatments have advanced, metastatic breast cancer has become a disease that some women can live with for years, which has changed the language that women use to discuss living with this form of breast cancer as discussed in this book.Using the framework of Celeste Condit’s rhetorical formations, which includes uses of metaphors, topics, and values, among other rhetorical features, the author examines how language has shifted from one of war and survivor rhetoric to that of metavivor rhetoric, which includes metaphors of water and prison, among others. Another hallmark of this emerging rhetorical formation is existing in a state of liminality where the cancer neither progresses nor retreats, leading to women experiencing time differently. By examining how women discuss living with cancer in an online breast cancer support group, the author analyzes the language shifts taking place and argues that women have moved from the dominant war/survivor rhetorical formation to one grounded in metavivor rhetoric. Within this evolution comes an understanding of what it means to live with a chronic, yet ultimately, terminal, illness and an acknowledgment of the impact that their lives’ perceived time has on these language choices.
From Surviving to Metaviving
A New Rhetorical Formation in Metastatic Breast Cancer Patient Discourse
Häftad, Engelska, 2027
319 kr
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As treatments have advanced, metastatic breast cancer has become a disease that some women can live with for years, which has changed the language that women use to discuss living with this form of breast cancer as discussed in this book.Using the framework of Celeste Condit’s rhetorical formations, which includes uses of metaphors, topics, and values, among other rhetorical features, the author examines how language has shifted from one of war and survivor rhetoric to that of metavivor rhetoric, which includes metaphors of water and prison, among others. Another hallmark of this emerging rhetorical formation is existing in a state of liminality where the cancer neither progresses nor retreats, leading to women experiencing time differently. By examining how women discuss living with cancer in an online breast cancer support group, the author analyzes the language shifts taking place and argues that women have moved from the dominant war/survivor rhetorical formation to one grounded in metavivor rhetoric. Within this evolution comes an understanding of what it means to live with a chronic, yet ultimately, terminal, illness and an acknowledgment of the impact that their lives’ perceived time has on these language choices.
Inbunden, Engelska, 2020
1 185 kr
Skickas inom 10-15 vardagar
The Ethos of Black Motherhood in America: Only White Women Get Pregnant examines the ethos of Black and white mothers in America's racialized society. Kimberly C. Harper argues that the current Black maternal health crisis is not a new one, but an existing one rooted in the disregard for Black wombs dating back to America's history with chattel slavery. Examining the reproductive laws that controlled the reproductive experiences of black women, Harper provides a fresh insight into the “bad black mother” trope that Black feminist scholars have theorized and argues that the controlling images of black motherhood are a creation of the American nation-state. In addition to a discussion of black motherhood, Harper also explores the image of white motherhood as the center of the landscape of motherhood. Scholars of communication, gender studies, women’s studies, history, and race studies will find this book particularly useful.
Häftad, Engelska, 2022
506 kr
Skickas inom 10-15 vardagar
The Ethos of Black Motherhood in America: Only White Women Get Pregnant examines the ethos of Black and white mothers in America's racialized society. Kimberly C. Harper argues that the current Black maternal health crisis is not a new one, but an existing one rooted in the disregard for Black wombs dating back to America's history with chattel slavery. Examining the reproductive laws that controlled the reproductive experiences of black women, Harper provides a fresh insight into the “bad black mother” trope that Black feminist scholars have theorized and argues that the controlling images of black motherhood are a creation of the American nation-state. In addition to a discussion of black motherhood, Harper also explores the image of white motherhood as the center of the landscape of motherhood. Scholars of communication, gender studies, women’s studies, history, and race studies will find this book particularly useful.
Inbunden, Engelska, 2021
1 510 kr
Skickas inom 10-15 vardagar
Mental Health among Higher Education Faculty, Administrators, and Graduate Studentsaddresses how many academics who experience mental distress or mental illness are afraid to speak out because of cultural stigma and fears of career repercussions. Many academics’ reluctance to publicly disclose their struggles complicates attempts to understand their experiences through research or popular media, or to develop targeted mental health resources and institutional policies. This volume builds on the existing studies in this greatly under-researched area of mental health among faculty, administrators, and graduate students in higher education. The chapters’ research findings will help institutions communicate about mental health in culturally-competent and person-centered ways; create work environments conducive to mental well-being; and support their academic employees who have mental health challenges. This book argues that discussions of health and wellness, equity, workload expectations and productivity, and campus diversity must also cover chronic illness and disability, which include mental health and mental illness.
Häftad, Engelska, 2023
492 kr
Skickas inom 10-15 vardagar
Mental Health among Higher Education Faculty, Administrators, and Graduate Studentsaddresses how many academics who experience mental distress or mental illness are afraid to speak out because of cultural stigma and fears of career repercussions. Many academics’ reluctance to publicly disclose their struggles complicates attempts to understand their experiences through research or popular media, or to develop targeted mental health resources and institutional policies. This volume builds on the existing studies in this greatly under-researched area of mental health among faculty, administrators, and graduate students in higher education. The chapters’ research findings will help institutions communicate about mental health in culturally-competent and person-centered ways; create work environments conducive to mental well-being; and support their academic employees who have mental health challenges. This book argues that discussions of health and wellness, equity, workload expectations and productivity, and campus diversity must also cover chronic illness and disability, which include mental health and mental illness.
From Surviving to Metaviving
A New Rhetorical Formation in Metastatic Breast Cancer Patient Discourse
E-bok
Engelska, 20251 052 kr
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As treatments have advanced, metastatic breast cancer has become a disease that some women can live with for years, which has changed the language that women use to discuss living with this form of breast cancer as discussed in this book.Using the framework of Celeste Condit's rhetorical formations, which includes uses of metaphors, topics, and values, among other rhetorical features, the author examines how language has shifted from one of war and survivor rhetoric to that of metavivor rhetoric, which includes metaphors of water and prison, among others. Another hallmark of this emerging rhetorical formation is existing in a state of liminality where the cancer neither progresses nor retreats, leading to women experiencing time differently. By examining how women discuss living with cancer in an online breast cancer support group, the author analyzes the language shifts taking place and argues that women have moved from the dominant war/survivor rhetorical formation to one grounded in metavivor rhetoric. Within this evolution comes an understanding of what it means to live with a chronic, yet ultimately, terminal, illness and an acknowledgment of the impact that their lives' perceived time has on these language choices.