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Child Pain, Migraine, and Invisible Disability
Honeyman, Susan
Routledge / Hardcover / 2016-11-01 / 1138207861
Infant, Child & Adolescent / Disability Studies
price: $224.00 (may be subject to change)
208 pages
Not in stock - ships in one week.

In the twenty first century there is increasingly becoming a global recognition of pain relief as a basic human right. However, as Susan Honeyman argues in this original new take on child pain and invisible disability, such a belief has historically been driven by adult, ideological needs whereas the needs of children in pain have traditionally been marginalised or overlooked in comparison.


Examining migraines in children and the socially disabling effects that chronic pain can have, this book uses medical, political and cultural discourse to convey a sense of invisible disability in children with migraine and its subsequent oppression within hegemonic educational and medical policy. The book is supported by authentic migraineurs' experiences and first-hand interviews as well as testimonials from a range of historical, literary, and medical sources never combined in a child-centred context before. Representations of child pain within literature, art and popular culture are also pulled together in order to provide an interdisciplinary guide to those wanting to understand migraine in children and the identity politics of disability more fully.


Child Pain, Migraine and Invisible Disabilitywill appeal to scholars in childhood studies, children's rights, literary and visual culture, disability studies and medical humanities. It will also be of interest to anyone who has suffered from migraines or has cared for children affected by chronic pain.

Reviews

'The Western contemporary ethos confers innocence and nostalgia on childhood, a tendency that too often belittles, denies or oversimplifies the suffering that real children experience. Young sufferers from migraine are consummate examples of this dilemma, as Susan Honeyman documents well in Child Pain, Migraine and Invisible Disability. Health care providers, who generally ask children to report pain using a reductionist single answer on a pain scale, would do well to consider Honeyman’s complex, humane account (including first-person narratives).'—Cindy Dell Clark, Rutgers University, U.S.A

Table of Contents

List of Figures

Preface: a Note to Readers

Acknowledgements

Introduction

Migraine as Invisible Disability
A History of Pediatric Pain and the Politics of Pill Culture
Materia Medica
Testifying Against Trigemony
Visibility Machines and Pain Proxies
Conclusion

Afterword: Scars (a Migraine Diary)

Appendix

References

Index

About the Author

Susan E. Honeyman is Professor of English at University of Nebraska at Kearney, USA.


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