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i was only a child when my life took a sharp turn. at around five or six years old, i started noticing odd changes in my body that i didn’t understand. the day i landed in the hospital was the day the word “diabetes” entered my life, even though i didn’t know what it meant.
i overheard my father telling my mother about my diagnosis, but all i could follow was that a few injections would make me feel better. i didn’t realize these injections would become a part of my daily routine for the rest of my life. the simplicity with which my condition was explained to me was a shield, protecting me from the gravity of what living with type 1 diabetes (t1d) would truly entail.
as i grew older, the impact of t1d on my daily life became more apparent. living with this condition is a rollercoaster — some days are good, others are a battle. in the early years, i grappled with feelings of negativity and depression. the constant question of “why me?” weighed heavily on my mind, and the sense of guilt associated with my condition isolated me from others.
i felt alienated, like an outsider in my own life. but i was determined not to let this condition define me. over time, i took mental control of my situation, transforming every roadblock into a new direction or a message from life.
living with t1d has made me resilient, and i take pride in the strength it has forged within me over the past three decades. it has also deepened my understanding of the importance of empathy. i’ve learned to give people the benefit of the doubt because i know firsthand how limiting assumptions can be.
this empathetic approach has been welcomed by my community and enriched my interactions with others. however, i recognize that awareness and understanding of chronic conditions like t1d are still lacking in many cultural communities. people often disregard issues that don’t affect them personally, and misconceptions about t1d are rampant.