An Identity Crisis for Sickle Cell Disease in Brazil Öffentlichkeit
Creary, Melissa Shawn (2016)
Abstract
The concept of race and its contribution to health disparities has garnered global attention and has planted itself firmly in medical, public health, and scientific discourse. The current debate over the epidemiology of health disparities reflects long-standing disagreement about the meaning of the concept of race in science. The interpretation of this concept cannot be separated from the epistemology of its creators. This is especially the case in the interpretation of race and admixture in sickle cell disease (SCD), particularly in Brazil. SCD is often ascribed to African ancestry, but it is a marker for ancestry in a geographic location where malaria is or was prevalent. Despite this, the cultural malleability of biology and the subsequent definition of racial disparity allows for SCD to be produced in different ways. This dissertation is based on eighteen months of collective ethnographic fieldwork data gathered primarily in Brasília, Rio de Janeiro, and Salvador, Brazil between 2011 and 2014. It examines how patients, non-governmental organizations, and the Brazilian government, at state and federal levels, have contributed to the discourse of sickle cell disease (SCD) as a "black" disease, despite a prevailing cultural ideology of racial mixture. This multi-level identity crisis is in constant contestation of competing racial frameworks at the micro, meso, and macro level. I explore how the multiple constructions of SCD in Brazil demonstrate the cultural malleability of biology via political processes of sickle cell disease (SCD)-based social policy. I examine the experiences of those who draw upon both the sickle gene and African heritage to make competing claims upon the State as well as legitimize their belonging to a social group. Ultimately, I argue that SCD represents a deep entanglement of biology and culture as shown through Brazilian actors who attempt to gain access to fuller participation in society through what I call biocultural citizenship--a flexible mode of enacting belonging that varies depending on skin color, social class, recognition of African lineage and other identifiers. This analysis provides lessons relevant to both Brazil and the US on how future policy can be designed. Specifically, I examine how policy developed around specific population groups can be measured against policy framed in relation to a specific disease.
Table of Contents
Preface--The Assignation of Blackness
Introduction
Positionality and Limitations
Organization of the Dissertation
Chapter One--The Contemporary Trajectory of Historical Quandaries
Part I: Background
Part II: Research Sites
Part III: Research Data and Methods
Part IV: Methodology
Part V: Analysis
Chapter Two-- Contestations of Citizenship and the Cultural Malleability of Biology
Mutual Inclusion: Policy Making for Sickle Cell Disease in Brazil
Part I: Sickle Cell Disease, Race, and Nation
Historical Constructions of Race and Nation in Brazil
Classification and Brazilian Conceptions of Race
Genetics, Race, Identity Politics, and Bounded Justice
Sickle Cell Disease
The Construction of Sickle Cell Disease
Situated Knowledges
Part II: Negotiating Citizenship
Aspirational Citizenship
Biological Citizenship and Sickle Cell Disease
Cultural Citizenship: Diasporic Membership in Hegemonic Spaces
Biocultural Citizenship
Chapter Three-- Color, Class, and Claims: Narratives of Biocultural Citizenship
Characteristics of the Sample
The Narrators
Structural Boundaries
Negotiation
Authenticity
Place
Conclusion
Chapter Four-- Bicultural Competence and Policy Formation:
A Story of Elite Engagement
Repression and Liberation
Capital Building and Investment
Race Gets a Promotion
Growing Pains
Bicultural Competency
An Unstable Seat at the Table
A Social and Political Convergence
Chapter Five--Conclusion: Strategies in Belonging
About this Dissertation
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