Vergangene andere Veranstaltungen
SYMPOSIUM - Testing Women, Testing the Fetus 20th Anniversary Symposium
Keynote: Professor Rayna Rapp
Host: Dr Lucy Lowe (University of Edinburgh) and Professor Khiara M. Bridges (UC Berkeley)
7th – 8th November 2019
Edinburgh Centre for Medical Anthropology
University of Edinburgh
This year marks twenty years since the publication of Professor Rayna Rapp's seminal monograph Testing Women, Testing the Fetus: The Social Impact of Amniocentesis in America. This ethnography, an award-winning classic text of feminist and medical anthropology, has inspired a generation of scholars working on reproduction, disability, genetics, bioethics, and parenting. This monograph takes us to the complex intersection of intimate family relationships, cutting-edge medical technology, race, genetic counselling, and obstetric care, underscored by classic anthropological concerns with kinship and inheritance. Rapp's question, 'What does scientific literacy mean in a culture as deeply stratified as our own?' is perhaps even more pertinent in 2019 than it was in 1999.
Reproductive technologies have developed apace in the two decades since this ground-breaking ethnography was published, as transnational scientific communities continually produce new frontiers in reproductive science and genetic technology. This period of medical advancement has been fostered in shifting spaces of reproductive politics. Laws on access to contraceptives, abortion, and assisted reproductive technologies have remained the most visible, but by no means the entirety of reproductive politics, where we continue to witness 'the intersection of personal pain and national politics.' The theoretical challenges in Testing Women continue to be relevant. Where can we locate 'moral pioneers' in contemporary medical settings? How can we make ethnographic research speak to both anthropological and medical communities?
This symposium will draw together scholars inspired by Testing Women, Testing the Fetus to explore its continued theoretical contribution in present and future research. We invite abstracts (250 words max) that speak to the themes, theories, and methodological challenges presented by Professor Rapp's work. Please send them to email@example.com<mailto:firstname.lastname@example.org> and email@example.com<mailto:firstname.lastname@example.org> by 4th September 2019.
Dr Lucy Lowe
Director, Edinburgh Centre for Medical Anthropology
University of Edinburgh
15a George Square
WORKSHOP - Arts of Caring, Arts of Knowing. A workshop on Dementia and Knowledge Practices
- Prof. Janelle Taylor, Department of Anthropology, University of Washington
- Prof. Annette Leibing, Faculty of Nursing, University of Montreal
Dementia is often portrayed as the emblematic figure of morbid living in one’s later years, entailing “substantial human costs to countries, societies, families and individuals” (WHO, 2017). Despite many ongoing efforts to prevent, manage, and cure dementia through biomedical means, dementia remains as a condition that is to be endured and lived with/through. At the same time, we are observing the flourishing of different forms of knowledges about living with dementia and creative engagements with dementia that aim to improve what might be called “qualities of life” of people that are affected by dementia. The notion of quality of life is also constantly challenged, negotiated, and rethought in these knowledge practices. As such, dementia offers us generative opportunities to renew our attention to the ways we know, care, and live, thereby revitalizing critical, imaginative and creative engagements with people with dementia.
Whereas the dominant discourse considers dementia as an irreversible loss of personhood, people with dementia and their carers strive to seek new possibilities of living differently with dementia. Putting together rich empirical researches in dementia care, the workshop Arts of Caring, Arts of Knowing: Dementia and Knowledge Practices aims to explore the generative potentials of dementia that urge and inspire us to rethink, imagine, tweak, improvise our ways of knowing, caring, and living as well as our analytic concepts and methods in humanities and social sciences.
The two-day workshop challenges the prevalent imaginaries about dementia in particular and older age in general that are shaped in specific politico-economic and socio-cultural contexts, not least since these make it difficult for us to creatively imagine and engage with the life with/in dementia. We invite participants from diverse disciplines who are documenting and producing alternative discourses, practices, and imaginaries about dementia, and asking questions about what it means, is and takes to live a “good” life as humans. We hope the workshop to be a venue for conceptual, practical, and methodological innovations in dementia and dementia care research throughout the world.
We seek papers that engage with the following questions, but not limited to:
- Everyday experiments in dementia care both in informal and formal care settings
- Production and circulation of caregiver knowledge on dementia care
- Relationships between biomedical knowledge and caregiver knowledge on dementia
- Mattering of “quality of life” of people with dementia and their carers in different contexts
- Historical changes in dementia-related policies and their ethical and political implications
- Innovative and creative engagements with dementia
If you are interested, please submit an abstract (250 words max.) including 3-5 keywords and a paper title to Jieun Lee (email@example.com) and Laura Louise Heinsen (firstname.lastname@example.org) by May 1, 2019. Due to space limitations, selected participants will be notified by mid-May, 2019. Participants will be asked to submit a short paper by the end of August, which will then be circulated among participants and discussed during the workshop. The workshop will take place in September 19-20, 2019 in Copenhagen.
The workshop is a part of the ERC funded project “The Vitality of Disease – Quality of Life in the Making” (https://vital.ku.dk/).
CONFERENCE - Caring for Elderly and Dependent People: Promoting Gender Equality and Social Justice
Social care for dependent people and the elderly is one of the major challenges currently facing our societies. According to demographic estimations, European countries will experience an increase in their elderly population in the near decades. On one hand, the increased longevity represents an historical triumph; however, on the other it brings with it the responsibility to even greater levels of care. Moreover, chronic diseases and functional diversity will also call for help and social support.
The starting point of the conference is the urgent need to democratize care to enable societies to take on more and larger responsibilities on a sustainable basis. Care is still disproportionally provided by the family and women, as the progressive and increasing role of men in childcare is not matched by a similar level of involvement in the care of dependent people and the elderly. Ways to enabling men to enter elderly and dependent care is an urgent yet under studied issue.
The purpose of this conference is to acknowledge the current challenge of democratising care at many different levels of the care organisation. Participants will reflect on the current distribution of care work from an intersectional perspective and in different contexts like families, labour market (private for profit or not for profit, and public organisations) and in communities; as well as in global care chains. Democratising care involves socializing care responsibilities, sharing care work between men and women, recognizing care and its centrality for life sustainability, dignifying and consolidating its professionalization, and taking into account the rights and demands of the people who are giving and receiving care. Special emphasis will be placed on emerging ways of redistributing care among men and women, care recognition (caring masculinities, public involvement, communitarian initiatives, labour dignification, among others). The main purpose is to identify key elements for promoting gender justice and social justice in care.
We invite contributions that reflect on these topics and analyse new data from different contexts and situations in which dependent people and the elderly are cared for. The conference values (cross-) regional, national, and transnational perspectives.
The conference will be held in September 12th and 13th at Rovira i Virgili University (Tarragona, Spain). The official languages of the conference are Spanish and English. Further information on symposia and conferences will be updated in the following weeks. The organization of the conference does not cover travel and accommodation expenses.
DEADLINE FOR SENDING ABSTRACTS: APRIL 30th, 2019
Abstracts, in English or Spanish, of a maximum of 500 words should include: title, name and affiliation of author/s, academic position and e-mail. They should also contain: selected thematic area, objectives, methodology, main lines of analysis and main sources, as well as 5 keywords.
Abstracts should be sent before April 30th to: email@example.com The list of accepted proposals will be published on 5th of June 2019. The registration period (40€) will open on 6th of June 2019.
For any additional information, please contact with the conference administrator: firstname.lastname@example.org
PODIUMSDISKUSSION - Heilungskooperationen: Was geschieht, wenn Ärzt*innen und Patient*innen aufeinandertreffen?
Ausgangspunkt dieser Podiumsdiskussion ist die Beobachtung, dass es bei dem Aufeinandertreffen von Ärzt*innen und Patient*innen immer wieder zu einem gegenseitigen Befremden kommt. Standardisierungsverfahren wie die Leitmedizin und die Evidenzbasierte Medizin, welche für Transparenz, Effizienz, Rechtssicherheit und Qualitätssicherung sorgen sollen, führen dazu, individuelles Erfahrungswissen sowohl von Ärzt*innen als auch von Patient*innen zu vernachlässigen. Besonders in Fällen, in denen sich Symptome einer eindeutigen Diagnose und chronische Erkrankungen einer Heilung entziehen, beklagen Patient*innen, dass sie zu wenig Gehör finden und ihnen ihr eigenes Erfahrungswissen abgesprochen wird. Mit der Verbreitung des Internets haben die Möglichkeiten, sich selbst über Krankheiten, ihre Ursachen und Therapiemöglichkeiten zu informieren, neue Formen angenommen und dabei neue Interaktionen und Herausforderungen in der Arzt-Patient-Beziehung mit sich gebracht.
Wir haben Ärzt*innen, Patientenvertreter*innen und Sozial- und Kulturwissenschaftler*innen eingeladen, die Ambivalenzen von Heilungskooperationen gemeinsam zu diskutieren. Wir fragen nach den möglichen Gründen für das diagnostizierte Befremden zwischen Ärzt*innen und Patient*innen und nach den Möglichkeiten einer Verbesserung dieser Situation: In welchen Bereichen wird die Mehrdeutigkeit des medizinischen Wissens zum Problem in der Arzt-Patient-Beziehung? Was vermissen Patient*innen an Ärzt*innen und umgekehrt? Was sind die Vor- und Nachteile informierter Patient*innen? Sollte sich, etwa in der Ausbildung von Mediziner*innen, etwas ändern? Wenn ja, was wäre wünschenswert und was ist realistisch?
Charles Christian Adarkwah - Vertretungsprofessor für Versorgungsforschung, Universität Siegen
Lutz Bergemann - Mitarbeiter der Geschäftsstelle des Klinischen Ethikkomitees, Universitätsklinikum Erlangen
Nicole Ernstmann - Leiterin der Forschungsstelle für Gesundheits-kommunikation und Versorgungsforschung, Universitätsklinikum Bonn
Claudia Liebram - Journalistin und Mitbegründerin und -betreiberin des Patientenforums psoriasis-netz.de, Berlin
Birgit Rabanus - Vorsitzende der MS-Selbsthilfegruppe Siegen e.V. und Vorsitzende des Beirats der Menschen mit Behinderung, Siegen
Nadia Schwirtzek - Fachanwältin für Medizinrecht, Gründerin und Geschäftsführerin der premedicare GmbH, Berlin, Zertifizierter Compliance Officer (SHB)
Regina Weinert - Behindertenbeauftragte der Stadt Siegen
Organisation und Moderation
Cornelius Schubert - SFB Medien der Kooperation, Universität Siegen
Ehler Voss - SFB Medien der Kooperation, Universität Siegen
Haus der Siegerländer Wirtschaft
Spandauer Straße 25
Cornelius Schubert - email@example.com
Ehler Voss - firstname.lastname@example.org
SYMPOSIUM - The Body and the Built Environment in the Long Nineteenth Century
The period between 1750 and 1918 is widely acknowledged to have been one of dramatic societal and cultural change, not least in terms of people’s experience of the spaces in which they lived. The unparalleled urbanisation that took place over the course of the long nineteenth century necessitated new ways of existing in increasingly built up environments. The move to such locations demanded new habits, routines, and modes of movement, all of which had a discernible impact on the body. As Elizabeth Grosz points out, ‘through exercise and habitual patterns of movement, through negotiating its environment whether this be rural or urban […] [that] the body is more or less marked, constituted as appropriate, or, as the case may be, an inappropriate body for its cultural requirements’ (1994). Where, for example, the navigation of uneven rural terrain would have strengthened certain muscles, the negotiation of flat, urban streets produced a markedly different body. Beyond the purely muscular level, the countless cultural elements of the nineteenth century city also impacted in numerous ways upon the embodied subject.
This one-day interdisciplinary symposium invites papers that explore how the shifting relationship between the body and the built environment was interrogated in literature and culture of the long nineteenth century. The symposium aims to stimulate academic discussion on a range of topics relating to embodiment and architectural space in the period ranging from 1750-1920. As such, we welcome papers from those working in the fields of Literature, History, Medical Humanities, Geography, Architecture, Philosophy, Film and Media, Psychology, Modern Languages, Gender/Women’s Studies, Law, and Politics.
Paper topics might include, but are not limited to, considerations of: questions of ownership and access; health; urban planning; agoraphobia and other spatially related disorders; sensory perception; the diseased body; policing, surveillance, and public order/disorder; sanitation and pollution; and phenomenological approaches to the body and space.
Potential research questions might include:
- In what ways did the built environment either encourage or preclude access to certain kinds of bodies in the long nineteenth century?
- How was the relationship between the embodied subject and architectural space interrogated in literature and culture of the period?
- What impact did scientific and medical advances in the understanding of the human body have on the construction and/or organisation of the built environment?
This event is supported by the Centre for Nineteenth Century Studies, and is presented in association with the Institute for Medical Humanities at Durham University.