Haemophilia in Aotearoa New Zealand provides a richly detailed analysis of the experience of the bleeding disorder of haemophilia based on long-term ethnographic research.
Haemophilia in Aotearoa New Zealand provides a richly detailed analysis of the experience of the bleeding disorder of haemophilia based on long-term ethnographic research.Hinweis: Dieser Artikel kann nur an eine deutsche Lieferadresse ausgeliefert werden.
Julie Park is Professor Emerita of Anthropology at the University of Auckland, New Zealand. Kathryn M. Scott works in social research and advocacy. She is an Honorary Research Fellow in Anthropology at the University of Auckland, New Zealand. Deon York works in the health sector. He is currently President of the Haemophilia Foundation of New Zealand (HFNZ) and on the Board of Directors of the World Federation of Hemophilia (WFH). Michael Carnahan has worked in health services management and is former President of the Haemophilia Foundation of New Zealand (HFNZ).
Inhaltsangabe
Chapter 1 A bleeding nuisance in Aotearoa New Zealand Chapter 2 'Pretty normal really' Chapter 3 Blood and sacrifice: sex, gender, and haemophilia Chapter 4 New networks and technologies of care: different haemophilias Chapter 5 The shadow on our lives: hepatitis C in the haemophilia community Chapter 6 Joint action: asserting rights, inclusion, and equity through voluntary association Chapter 7 Conclusions
Chapter 1 A bleeding nuisance in Aotearoa New Zealand Chapter 2 'Pretty normal really' Chapter 3 Blood and sacrifice: sex, gender, and haemophilia Chapter 4 New networks and technologies of care: different haemophilias Chapter 5 The shadow on our lives: hepatitis C in the haemophilia community Chapter 6 Joint action: asserting rights, inclusion, and equity through voluntary association Chapter 7 Conclusions
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