Personal Narrative: Spinocerebellar Ataxia

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Stumbling over nothing, my father falls flat onto the ground. Unsurprised, a hint of annoyance pricks at my mind. I stand with an exasperated sigh and help him up. Just another day. I hate my compulsive anger, but I am not angry with him. I’m angry at this disease that is slowly destroying my father and taking him away from me.
My father has Spinocerebellar Ataxia, a neurodegenerative disease that affects a person's speech and balance; a rare and incurable condition that runs throughout the family. My days consist of enduring the sounds of his everyday struggles: continuous coughing as he chokes on his saliva, irregular shuffling of his feet, and his slurred words. On his worst days, he only mumbles, where his thoughts are incomprehensible
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I won’t be able to communicate with the ones I love or participate in my favorite physical activities. I want to live my days to the fullest before my mentality can disintegrate. I witness his perseverance: exercising daily, attending speech and physical therapy, and routinely taking his medication. This has made me persevere through my own struggles, even if there might not have a significant impact. Most of all, my father has a significant impact on how diligently I work academically. If I fail to succeed, then all that he sacrificed becomes a waste. All my dad has to live for now is to witness my accomplishments. So, whenever I lose motivation or going through academic struggles, I remember I’m determined to make him proud and prove that his life is not as useless as he believes it is, and I am grateful for all he has done and return the same love and compassion he gives me.
It’s hard to live with the fact that there’s little I can do for my father to improve his conditions, so these circumstances influenced me to become a neurologist. There is a possibility I will find a cure, but if not, I hope to advance research findings and help other families affected by someone with a mental

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