Veranstaltungskalender
An dieser Stelle präsentieren wir ausgewählte Veranstaltungen aus dem interdisziplinären Arbeitsfeld Ethnologie und Medizin.
Wir freuen uns über Veranstaltungshinweise an events@agem.de
Vergangene Veranstaltungen
2019
WORKSHOP - Arts of Caring, Arts of Knowing. A workshop on Dementia and Knowledge Practices
Andere
Keynotes:
- 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 (jle@anthro.ku.dk) and Laura Louise Heinsen (llh@anthro.ku.dk) 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 - Living Politics. Remembering HIV/AIDS Activism Tomorrow
How are politics and life narratives in the fields of HIV/AIDS activism in Europe entangled?
The conference discusses the meaning, methods and importance of preserving histories of HIV/AIDS, and how these and other ongoing practices relate to current engagements with the epidemic. It brings together social science researchers, policy makers and representatives of NGOs and activist groups from the fields of HIV/AIDS, drug policy, LGBTQ rights, sex work, migration politics and prisons. The conference has been organised by the EUROPACH research team, which will present project outputs and concluding arguments about citizenship in Europe in relation to HIV/AIDS. Focus will be on Germany, Poland, Russia, Turkey, the UK and the European region. It will celebrate the opening of the exhibition “HiVstories” at the Schwules Museum, and the launch of the EUROPACH contribution to the European HIV/AIDS Archive, which includes over 100 oral history interviews.
Conference language: English with translation upon request.
For more information, visit: http://europach.phils.uj.edu.pl/project-outcomes/final-conference/
CONFERENCE - Caring for Elderly and Dependent People: Promoting Gender Equality and Social Justice
Andere
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: gendercare@urv.cat 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: gendercare@urv.cat
PODIUMSDISKUSSION - Heilungskooperationen: Was geschieht, wenn Ärzt*innen und Patient*innen aufeinandertreffen?
AGEM-Veranstaltung
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?
Es diskutieren
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
Veranstaltungsort
Haus der Siegerländer Wirtschaft
Spandauer Straße 25
57072 Siegen
Dokumente
Flyer
Kontakt
Cornelius Schubert - cornelius.schubert@uni-siegen.de
Ehler Voss - ehler.voss@uni-siegen.de
CONFERENCE – Preparing for Physicians. The ambivalences of empowerment
AGEM-Veranstaltung
Joint conference of the Collaborative Research Center 1187 Media of Cooperation and the Association for Anthropology and Medicine (AGEM)
Healing is a cooperative practice that involves multiple agents and requires negotiations of different needs and potentials. These negotiations are usually based on asymmetrical relations between healer and patient. Without specific expertise, skills, and knowledge of healing, there would be no need for consultation, and often patients are looking exactly for such an asymmetric relation to put themselves in the hands of an authority they can trust. Nevertheless, this asymmetry has often been criticized, especially in the realm of modern biomedicine and psychology, and especially in the context of chronic and rare diseases. Professional dominance (Freidson 1970) and a paternalistic imbalance in healer-patient relationships have thus led to an increasing claim for shared decision making and informed consent in order to empower the patient vis-à-vis her or his healer. The aim is to develop therapies and forms of interaction that explicitly seek to re-balance the relationship by taking into account the patients’ knowledge (as e.g. in many psychological therapies), or even trying to turn the asymmetric healer-patient relationship around and calling for full responsibility of patients themselves (e.g. in many esoteric therapies).
The Internet offers new possibilities for getting information and sharing experiences about the inefficacy or even harmfulness of popular and officially accepted therapies, on the one hand, and the efficacy of unknown and unconventional approaches, on the other, which may lead to distrust of professional or institutional authorities. Thus, patients can develop many strategies to carry out their own ideas and plans against a healer’s advice, if they disagree about the cause of the illness and the right course of treatment. Such strategies also may include simulating or neglecting specific symptoms to get a desired prescription, to avoid a specific treatment, or to get a temporary or permanent certificate of illness.
But empowerment is ambivalent. Patients are often torn between trust and suspicion, between the wish to be guided by experts and the wish to become an expert on their own, to give up or to keep responsibility for their health. Too much information can turn empowerment into confusion, and empowerment can also turn into manipulation, e.g. when pharmaceutical companies encourage patients to ask their healers for the drugs they sell (cf. Dumit 2012). Thus, empowerment is hardly straightforward. For instance, in which direction is empowerment oriented? Is it an extension of the patients’ biomedical knowledge? Or does it facilitate increasing demands from doctors, who are approached by patients who figure as consumers or customers? Does it include the right to remain a passive patient? Empowerment does not necessarily pit an autonomous patient against a dominant physician. This mélange opens up questions about the modes and means of empowerment. Who, beyond patients, has an interest in empowerment? Are Internet media engines of emancipation or sources of irritation?
After focusing on the healer’s perspectives and practices at the conference “Preparing for Patients. Learning the skills and values of healing encounters” in 2018, we now focus on the patient’s side and look for descriptions and analyses of their perspective and practices. We call for contributions that explore the ambivalences of empowerment both theoretically and empirically. We especially look for insights into the distributed nature of empowerment, the different constellations in which empowerment might be generated or reduced. Which resources are used to increase or to prevent the empowerment of patients, and which resources are used by the patients themselves? And what are the unanticipated consequences of empowerment?
Keynote: Prof. Nick Fox (University of Sheffield)
Conference language: English
Dokumente
Kontakt
Cornelius Schubert - cornelius.schubert@uni-siegen.de
Ehler Voss - ehler.voss@uni-siegen.de