Embodying Tourette’s Syndrome in Young Adult Literature

The article foregrounds two protagonists with Tourette Syndrome (TS) from contemporary Young Adult (YA) novels written by authors with TS. Grounded in the interdisciplinary field of cultural disability studies in education (CDSE), each protagonist is analyzed for (1) physical manifestations of TS (external depiction), (2) emotional reactions about having TS (internal depiction), and (3) the response of parents and family members, friends, acquaintances, and strangers (societal depiction). Both main characters navigate a world in which they are viewed as abnormal, frequently working through internalized feelings of freakery as they struggle to become more self-accepting during their adolescent years. Such depictions “engage with disability as an isolating, hurtful, and joyful experience” (Bolt 11), allowing for the complexities, tensions, contradictions, and general messiness of embodying TS. These depictions suggest that the authors seek to provide readers with an empathetic understanding of TS, while allowing the simultaneous contemplation of ways in which the embodiment of TS informs us about our culture.

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Publication Details

Journal
Journal of Literary & Cultural Disability Studies
Published
2024-10-25
DOI
https://doi.org/10.3828/jlcds.2024.38
Citations
1
Primary Topic
Obsessive-Compulsive Spectrum Disorders
Type
article
Field-Weighted Citation Impact
0.64
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article

Embodying Tourette’s Syndrome in Young Adult Literature

Melissa Schieble, David J. Connor
1 citations
Journal of Literary & Cultural Disability Studies
Obsessive-Compulsive Spectrum Disorders
0.64
article

Embodying Tourette’s Syndrome in Young Adult Literature

Melissa Schieble, David J. Connor
article en
1 citations

Abstract

The article foregrounds two protagonists with Tourette Syndrome (TS) from contemporary Young Adult (YA) novels written by authors with TS. Grounded in the interdisciplinary field of cultural disability studies in education (CDSE), each protagonist is analyzed for (1) physical manifestations of TS (external depiction), (2) emotional reactions about having TS (internal depiction), and (3) the response of parents and family members, friends, acquaintances, and strangers (societal depiction). Both main characters navigate a world in which they are viewed as abnormal, frequently working through internalized feelings of freakery as they struggle to become more self-accepting during their adolescent years. Such depictions “engage with disability as an isolating, hurtful, and joyful experience” (Bolt 11), allowing for the complexities, tensions, contradictions, and general messiness of embodying TS. These depictions suggest that the authors seek to provide readers with an empathetic understanding of TS, while allowing the simultaneous contemplation of ways in which the embodiment of TS informs us about our culture.

Journal of Literary & Cultural Disability StudiesVol. 18(4)
City University of New York (US), Hunter College (US)
Openalex Percentile: Top 27%
Obsessive-Compulsive Spectrum Disorders
0.64
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