[Last modified: December, 7 2024 02:48 PM]
When I began researching “The Untold Gynecological Diseases,” I focused on how women’s illness narratives reveal disempowerment within the medical and patriarchal systems. Initially, I planned to use qualitative methods, like ethnographic observations and in-depth interviews, to explore these narratives from patients and healthcare providers.
As my studies progressed, I encountered several methodological challenges and realizations. For example, being an Asian woman and a cultural outsider in my field, I faced difficulties gaining the trust of my interview subjects, which could potentially skew the authenticity and depth of the narratives collected. This realization pushed me to think about alternative methods, like employing cultural intermediaries or extending my fieldwork to build trust.
Furthermore, my understanding of the role of illness narratives expanded. I learned they do more than reveal instances of disempowerment; they actively contest and disrupt the prevailing medical discourse. This insight led me to rethink how I approached these narratives—not merely as stories to be collected but as powerful tools for advocacy and change.
Most importantly, my methodological thinking shifted towards a more intersectional approach. Acknowledging my own marginal status helped me recognize the intricate layers of gender and racial inequalities affecting the medical experiences of non-Western women. This has sharpened my focus on not only documenting narratives but also understanding how these women navigate and are shaped by their cultural, social, and medical contexts.
In conclusion, this module has not only refined my research methods but also deepened my appreciation of the complex dynamics at play in the narratives I seek to understand and amplify. This has fundamentally changed how I view and approach my research, making it a more inclusive and critically engaged project.