Veranstaltungen

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

12. Sep - 13. Sep 2019

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

Link zu dieser Veranstaltung

28. Jun 2019

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

Link zu dieser Veranstaltung

27. Jun - 28. Jun 2019

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

Programm

Poster

Kontakt

Cornelius Schubert - cornelius.schubert@uni-siegen.de
Ehler Voss - ehler.voss@uni-siegen.de

Link zu dieser Veranstaltung

25. Jun 2019

SYMPOSIUM - The Body and the Built Environment in the Long Nineteenth Century

Andere

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?

Please send abstracts of 250 words for 20-minute papers to: bodybuiltenvironment@gmail.com by 17 May 2019. For further details, visit: http://bodybuiltenvironment.wordpress.com

 

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.

 

Link zu dieser Veranstaltung

11. Jun - 13. Jun 2019

SYMPOSIUM - Making Medicine in Austere Times

 

Flyer

Link zu dieser Veranstaltung

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