SLIIT International Conference on Advancements in Science and Humanities [SICASH]
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SLIIT International Conference on Advancements in Science and Humanities is organized by the Faculty of Humanities and Sciences of the Sri Lanka Institute of Information Technology (SLIIT), the annual research multi-conference of the faculty.
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Publication Open Access Is epilepsy solely a medical condition? A Review of “Fit Thamai” (2019), a Sri Lankan Autobiographical Short Film Representing Epilepsy(Department of Linguistics, Faculty of Humanities and Sciences, SLIIT, 2025-10-10) Dissanayake, A.KThis study explores the representation of epilepsy in Channa Bawantha’s autobiographical Sri Lankan short film titled Fit Thamai: Channa’s Untold True Story (2019). Employing content analysis and a discussion of the medical, personal tragedy and social models of disability, the study highlights the importance of well-roundedrepresentations of epilepsy in the attempt to challenge misinformation and stigma that surrounds epilepsy. The strengths identified in this short film are both its autobiographical narration and its emphasis on the importance of people with epilepsy sharing their epilepsy experiences with each other, as this creates friendship and camaraderie among people with epilepsy. Also, the short film shows different reactions to epilepsy as well as different treatment approaches towards epilepsy in Sri Lanka. Furthermore, it creatively contributes a uniquely Sri Lankan meaning to the word ‘fit’ (a word used interchangeably with seizures) alongside the range of other meanings conveyed via this word. However, the short film also posits people with epilepsy as ‘sick’ persons, or as patients, and equates epilepsy to a personal tragedy. It also treats epilepsy as exclusively medical in nature and ignores the socio-cultural factors in Sri Lanka which lead to the stigmatisation and misinformation surrounding epilepsy. Furthermore, the short film seems to unwittingly generalise Bawantha’s experience with epilepsy treatment as well as his symptoms to the wider population of Sri Lankanswith epilepsy. Therefore, this paper emphasises the need for representations of epilepsy in Sri Lanka which are backed by more in-depth understanding, reflection and analysis of epilepsy lived experiences.Publication Open Access Queer Identi ti es in The Seven Moons of Maali Almeida by Karunati laka (2022) and The Song of Achilles by Miller (2011): A Comparati ve Analysis from a South Asian Perspecti ve(Faculty of Humanities and Sciences, SLIIT, 2024-12-04) Rodrigo, D; Jayamanna, TThis research study att empts to present a comparati ve analysis of the queer identi ti es portrayed in The Seven Moons of Maali Almeida by Shehan Karunati laka (2022) and The Song of Achilles by Madeline Miller (2011) from a South Asian perspecti ve to examine how cultural, historical, and socio-politi cal aspects of their geographical setti ngs infl uence such identi ti es in both novels and to identi fy the narrati ve techniques and characterizati ons used in them to portray their queer relati onships. Moreover, the central questi ons that guide this study are: 1) how queer do the identi ti es depicted through their main characters appear to be; and 2) and what similariti es and diff erences emerge in the portrayal of their queer relati onships. In order to achieve these objecti ves a qualitati ve research approach is adopted where the data is collected by subjecti ng the respecti ve novels to a thorough criti cal reading and extracti ng the relevant evidence from their narrati ve using criti cal discourse analysis. The data is analyzed using techniques developed from queer theory, semioti cs, and criti cal discourse analysis. Finally, this research att empts to reveal from a South Asian perspecti ve the author’s expectati on for the queer identi ti es portrayed in the two relevant while illuminati ng on the fact they appeal for inclusive society.Publication Open Access An Analysis of the Representation of Epilepsy in Pramod Rathnayake’s Short Film Natta (2019)(Faculty of Humanities and Sciences, SLIIT, 2023-11-01) Dissanayake, A.KThis study explores the representation of epilepsy in the Sri Lankan short film Natta (2019) by Pramod Rathnayake. Epilepsy is a neurological disease that may lead to unconsciousness. Epilepsy is also a disability. A disability is distinguished from an illness in that the former is understood as created due to socio-cultural factors that could lead to marginalization of individuals with certain medical conditions. Although the condition of epilepsy has been understood and analyzed from a medical perspective, the human experience of epilepsy has not received much attention, especially in Sri Lanka. In this context, the short film Natta fulfills the role of portraying the dayto- day experiences of an individual with epilepsy named Samantha, from the first-person point of view. The film visually represents some symptoms of epilepsy and sheds light on how superstitious beliefs and misinformation about this condition hinder Samantha from successfully medically controlling his epilepsy. The impact of epilepsy on an individual’s employment opportunities and ability to drive a vehicle too are highlighted in the short film. While these are the strengths of the short film, Natta equates the epilepsy condition in a person to something inherently wrong or lacking in a person. Also, the film ignores the social stigmatization of epilepsy patients and indirectly blames people with epilepsy for marginalizing themselves. Finally, through the portrayal of the character of Sugandika, Samantha’s wife, the short film fails to acknowledge the role that family members or informal caregivers play in the process of looking after patients with epilepsy. Therefore, based on this content analysis of Pramod Rathnayake’s short film, it could be concluded that similar short films would be helpful in giving voice to the daily, personal experiences of people with epilepsy. However, such representations should not avoid blaming patients with epilepsy for their condition and social isolation but should be understanding and inclusive of the social pressure and stigmatization encountered by people with epilepsy.
