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Curating and/or suffering: On palliative care and museums

Published online by Cambridge University Press:  23 March 2023

Jan Gresil Kahambing*
Affiliation:
Department of Philosophy and Religious Studies, University of Macau, Macao, SAR China
*
Author for correspondence: Jan Gresil Kahambing, Department of Philosophy and Religious Studies, University of Macau, Taipa, Macao 999078, SAR China. Email: yc07706@umac.mo
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Abstract

Type
Letter to the Editor
Copyright
© The Author(s), 2023. Published by Cambridge University Press.

In this journal, there are crucial references to museums in connection to palliative care. Museum art re-enables the ability to return to childlike amazement, to be astonished, to “still paint the last portrait of our patients’ lives” (Julião et al. Reference Julião, Najún and Bragança2021, 381) – that is, to project the possibilities of curating oneself in the midst of suffering or illness (hence, curating and/or suffering). Here, illness should not become an ethical hindrance for reexpression but a viable phenomenological method to uncover deeper existential – or return to ontological (Kahambing Reference Kahambing2022a) – meanings. This article thus attempts to expose more clearly such curation possibilities in order to provide explicit grounds for the nexus between palliative care and museums.

In reviewing the museum-related ideas in this journal, what lies at the core of curating amidst suffering is the question of meaning. Museums, according to meaning-centered group psychotherapy, forge the connection to the beautiful (Fraguell et al. Reference Fraguell, Limonero and Gil2018). Moreover, museums are part of the immersive experiences to get the community better in rural palliative care (Pesut et al. Reference Pesut, Robinson and Bottorff2014). Some patients find meaning in returning to museums as an “unfinished business,” curating the end of their lives in co-constructing meanings with it: that is, curation hinged on the idea that “our responsibility as human beings is to live life to its fullest potential, to construct a life of meaning, identity, direction, growth, connection, purpose, and fulfillment” (Masterson-Duva et al. Reference Masterson-Duva, Haugen and Werth2020, 641).

Furthermore, this is also extended to those who accompany and support the patients: their families and loved ones. As a form of participation in the experience of bereavement support, parents who lost their children from illnesses like cancer also become curators when they keep tangible stuff linking memories to their children. One parent, for instance, says: “I still have a little museum [with my child’s belongings] in my house” (Berrett-Abebe et al. Reference Berrett-Abebe, Levin-Russman and Gioiella2017, 354). This can further be applied not just to humans but even to pets.

Museum-based education has “great promise as a pedagogic strategy to improve metacognition, tolerance of uncertainty, appreciation of multiple perspectives, and teamwork among hospice and palliative care professionals” (Zarrabi et al. Reference Zarrabi, Morrison and Reville2020, 1510). The Michael C. Carlos Museum on the Emory University Campus, for example, facilitates a course on the “art of palliation” as a “novel, interprofessional museum-based” approach that seeks to address perception, attention, empathy, communication, implicit bias, and resiliency – putting a premium on the latter – in mitigating suffering for patients with serious illness. In the V&A museum at Dundee, the palliative care patients themselves work like curators in that they conceptualize and redesign a communal space.

But concerning those who have an encounter with death or those who had seen death in their communities within an experience of tragedy, curating becomes an act of preventive medicine carefully treading the sensitive nature of personal suffering. While survivor-curators themselves acknowledge the intergenerational necessity of portraying resiliency amidst tragedy in their museums, there is also the sense in which “survivor-visitors,” so to speak, have complex histories with different personal accounts of trauma (Kahambing Reference Kahambing2022b).

Recently, “breaking death-denying taboos and promoting occasions for awareness and reflection about death has been argued to have beneficial effects” (Lindqvist and Tishelman Reference Lindqvist and Tishelman2015, 7). It seems then that relationship between curating and suffering is more vivid as “curating and dying,” which showcases not art in objects but involving oneself in the art, referencing the manual Ars Moriendi (The Art of Dying) written probably by a Dominican friar (Espi Forcén and Espi Forcén Reference Espi Forcén and Espi Forcén2016). For curator O’Neill (Reference O’Neill2012, 69), this explores the ways in which curation can act as “the primary cultural work of creating meaning in the face of human mortality.”

The term “curator” comes from the Latin cura, which means to “take care.” An important shift that curators can then ask is not “what do curators take care of?” but, as Harrison et al. (Reference Harrison, Bergqvist, Kemp, Harrison, Bergqvist and Kemp2016, 3) ask, “to whom are curators responsible?” It can be clarified here that this does not only point to bosses, sponsors, or philanthropists, but to people – especially to the people who need the museum most. In short, to those who are in touch with the sense of loss, suffering, and death: those who need care.

Acknowledgments

The author would like to thank Prof. Victoria S. Harrison and Teng Wai “Nicole” Lao for the interesting discussions on museums, photography, and death. Similarly, he is grateful to the instructors of the Museum Teaching Strategies at the Museum of Modern Art.

Conflict of interest

None declared.

References

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