Recent scholarship has begun to acknowledge that the focus of Medieval and Early Modern Studies has long been on the elite, male, western European experience. New movements in academia are addressing this imbalance, acknowledging that women, ethnic minorities, and other marginalised groups contributed richly to the fabric of medieval and early modern life. Ceræ aims to join this shift in focus to the experiences of minority groups, marginalised peoples, and life in non-western territories with a conference session at IMC Leeds 2020.
Topics may include but are not limited to:
- Experiences of minority or marginalised groups
- Writings by minority or marginalised groups
- Literary depictions of minority or marginalised groups
- The effacement of minority or marginalised groups
- Experiences on the transition of a border or landscape
- The law of minority and marginalised groups
- Minority and marginalised cultures, beliefs, and celebrations
- Experiences of disability and physical and mental illness
Ceræ invites submissions encompassing all aspects of the late classical, medieval, and early modern world. There are no geographical restrictions. As an interdisciplinary journal, Ceræ encourages submissions across the fields of archaeology, art history, historical ecology, literature, linguistics, intellectual history, musicology, politics, social studies, and beyond.
Abstracts of 250 words should be sent to firstname.lastname@example.org by 1st September 2019.
Attendees are responsible for all fees and costs associated with attending the IMC, and for registering for the congress.
For further enquiries contact our Editor: email@example.com; or get in touch via Facebook (facebook.com/CeraeJournal) or Twitter (@CeraeJournal).
Gender & History is an international journal for research and writing on the history of femininity, masculinity and gender relations. This Call for Papers is aimed at scholars studying any country or region, and any temporal period, including the classical, medieval, early modern, modern, and contemporary periods.
This Special Issue will explore the gendered history of healing and caring from the perspective of the sick and suffering, and various types of healers and caregivers. It aims to move beyond institutional histories of biomedicine, canonical medical knowledge, and allopathic approaches to health. We seek to showcase research that reflects upon the gendered dynamics of palliative care and the formation of diverse communities and economies of health and healing. We recognize that historical reckonings of health and bodily knowledge in many locales have been dominated by sources maintained in state, colonial, and missionary archives, and by notions of medicine shaped in white settler institutions. In an effort to destabilize these reckonings and to uncover marginalized forms of knowledge and practice, we encourage research informed by diverse methodologies and an imaginative approach to source material.
In recent years, medical anthropologists have shed light on the complex and unequal co-production of biomedical knowledge and “traditional” forms of medicine while feminist sociologists have illuminated the gendered dynamics of caregiving and the devaluation of its everyday and emotional labor. How might historians engage these cross-disciplinary methods and insights to reconstruct more nuanced and more expansive histories of healing and caring? What happens to our gendered histories of illness and medicine when we de-naturalize biomedical formations and examine palliative care in addition to therapeutic treatment? How has gender shaped which forms of healing and caring are recognized and institutionalized, and how has such privileging changed over time?
We understand that historically a wide array of people have provided healing and caring including family members, shamans, spirit mediums, healers, Elders, herbalists, diviners, faith healers, and wise-women and men as well as midwives, nurses, aids, and doctors. Their practices have ranged from diagnosing illnesses, administering medicines, and performing procedures to offering spiritual and psychological counsel. They have also included forms of body work such as grooming, feeding, bathing, massage and manipulation, and handling the dead.
Papers are invited from established scholars as well as new, emerging, and unaffiliated scholars who consider a variety of historical moments and locations, or transnational and even global processes related to themes such as the following:
●Intersectional approaches that examine how social identities and inequalities rooted in gender,race, ethnicity, sexuality, class, religion, and nationality have long shaped people’s access tohealth resources and care and, in turn, given rise to disparate patterns and experiences of well-being and illness.
●Reconstruction of deep histories of gendered healing and caring, extending back well before thetwentieth century, that reveal how healing and caring practices have been central concerns forboth individuals and societies and how those concerns have often animated and reconfiguredcultural institutions, political ideologies, and economic relations and markets.
●Consideration of the connections and tensions between various modes of healing and palliation,and how those relations have informed the frequently gendered and racialized separation of“professional” and “modern” medicine from modes designated as “traditional,” “informal,”“alternative,” or “home-based.”
●Examination of how people have transmitted healing and caring epistemologies and practicesacross generations and geographic distances, including how women have sought to maintain orassert control over their health and how various archives have worked both to represent andobscure those efforts.
●Engagement with concepts from disability studies, queer theory, and crip theory to betterunderstand the history of illnesses and diseases that have often been both gendered andstigmatized such as depression, hysteria, reproductive maladies, infertility, and sexuallytransmitted infections.
Interested individuals are asked to submit 500-word abstracts, a brief biography (250 words), and a cv by 31 August 2019 at 5pm PDT for consideration. Abstracts will be reviewed by the guest editors and successful proponents will participate in a symposium at Vancouver Island University in British Columbia, Canada, on 8 May 2020. Papers must be submitted six weeks prior to the symposium. Papers should be 6000-8000 words in length. After the symposium, papers will go through the journal’s peer review system. As with any article, there is no guarantee of publication. The editors are in the process of applying for funding to defray the cost of the travel to the symposium for new, emerging, and unaffiliated scholars. Please send abstracts, biographies, and CVs by email to firstname.lastname@example.org or by mail to The Editors, Gender & History, Vancouver Island University, 900 Fifth Street, Nanaimo, BC V9R 5S5. The Special Issue will be edited by Drs. Kristin Burnett, Sara Ritchey, and Lynn M. Thomas.
Special Issue Timeline Abstracts to SI editors — 31 August 2019 Papers circulated to symposium participants — 15 March 2020 Symposium at Vancouver Island University (Nanaimo, British Columbia) — 8 May 2020Full submissions to SI editors (papers submitted on ScholarOne) for peer review — 31 August, 2020 Revised submissions (and any image permissions) to SI editors — 31 May 2021 Publication — October 2021
The year 2018 marks the centennial of the 1918 Influenza Pandemic, one of the deadliest outbreaks of disease in recorded history. To acknowledge the social impact of illness on humanity, the History Department at Seton Hall University will host a two-day symposium on disease and wellness in historical perspective. Some of the questions we seek to investigate over the course of this symposium are as follows: How have notions of illness and wellness changed over time? In what ways have medical progress and discovery been shaped by wars and natural disasters? How did regimes of hygiene fashion social hierarchies or imperial policy? What have been the social, political, and economic consequences of the diseased body and/or mind in various societies? How do civilizations conceptualize disease and miracles within faith practices? How do public health and issues of social justice intersect?
Some additional topics for research papers include the following:
- Medicine, war, and natural disasters
- Medical progress, discovery, and vaccines
- Colonial diseases and medicines
- Traditional practices and practitioners
- Professionalization of medicine
- Cultural representations of health care
- Saints, shamans, and spiritual dimensions of health
- Gender dynamics of health
- Disease and persecution
- Drugs and addiction
- Trauma and mental health
The symposium will be held on Thursday and Friday, 7-8 February. A keynote address by Alan Kraut, Professor of History at the American University, will open the symposium on Thursday, 7 February. The second day of the symposium will consist of panels and a roundtable discussion. The symposium will be held at the South Orange, New Jersey campus of Seton Hall University, about a half hour outside of New York City.
We welcome proposals from scholars from all fields interested in the historical implications of disease and wellness including history, literary studies, anthropology, and religion, from the ancient to modern period. Advanced graduate students, early career scholars, and senior researchers are encouraged to apply. Please send a single document containing 1) a title and an abstract of up to 250 words and 2) a short (one-paragraph) biography, to email@example.com by Monday, 19 November, 2018.
Seton Hall will provide two-nights of accommodations for all invited participants coming from outside the New York City/Northern New Jersey area, as well as meals for all invited panelists. Travel funding may also be available on a case-by-case basis.
Please feel free to contact Anne Giblin Gedacht at firstname.lastname@example.org, or Golbarg Rekabtalaei at email@example.com, with any questions. For more information about History at Seton Hall, please visit our website, https://www.shu.edu/history/.
Keynote speakers: David Lederer, Maynooth University; Donna Trembinski, St. Francis Xavier University; David Turner, Swansea University
In recent decades, dis/ability history has become an important field in its own right, standing at the crossroads of the social history of medicine, the history of minorities and the history of everyday life. Conceptions of and attitudes to physical and mental wellbeing and to difference are and have always been key elements in any human society, while the lived experience of dis/ability has varied across societies and time periods, but also depending on the person’s socioeconomic status, age, gender, and the nature of the impairment. Experiences of disability, whether personal or communal, have long continuities in the past, but they have also changed dramatically with the development of medical science and institutionalized care.
This conference aims to concentrate on the experiences of those with physical or mental impairments and chronic illnesses, with special reference to the period between the late Middle Ages and the mid-twentieth century. We understand dis/ability in a broad sense, covering a wide range of physical, mental and intellectual impairments and chronic illnesses. How, then, were various dis/abilities lived and experienced, how did communities shape these experiences, and what similarities and changes can we detect over the course of time? An important viewpoint is also that of methodology: how can a modern scholar approach the experience of those living in the past?
We thus invite papers that explore the ways in which ‘disabilities’ have been lived and experienced, in all stages of life, and by people of different social status and background. The conference aims to promote dialogue between disability historians across national and chronological borders and we welcome papers presenting new research and work in progress.
Possible topics include, but are not limited to:
- How to approach the experience of dis/ability (sources, methodology)?
- Different categories of dis/ability experience, or what counts as experience of disability?
- How have society, religion and practices of care and cure defined the experience of disability?
- Lived religion and dis/ability
- Medicalization, institutionalization and everyday life
- The impact of gender, age and social status on the experience of dis/ability
- Lived welfare and everyday experiences of people with disabilities, e.g. living at home, in a workhouse or mental institution, the impact of various welfare systems.
To submit a proposal, please send title and abstract of 200 words, with your contact information and affiliation by February 15, 2019, at https://www.lyyti.in/disabilityexperience2019_callforpapers
Conference website: https://events.uta.fi/disabilityexperience2019/
Participation is free of charge, and includes lunches and coffees for speakers.
The conference is organized by the Academy of Finland Centre of Excellence in the History of Experiences (HEX, https://research.uta.fi/hex/) at the University of Tampere and the group “Lived Religion” and has received funding from The Jenny and Antti Wihuri Foundation (https://wihurinrahasto.fi/?lang=en) and HEX. For more information, please write to the organizers (firstname.lastname@example.org and email@example.com)