I’ve always been the quiet type; the back-of-the-room and good grades and small-group-of-friends type. But I have a voice and passion, and for those who will listen, I have quite the story to tell. My life truly began on April 13, 2010, in a busy orphanage in Shenzhen City, Guangdong Province, People’s Republic of China. It’s a sad beginning, but one that has only made me stronger. Unlike many others, I was fortunate enough to be brought into an American family, and given everything, including treatment for a heavy burden. I live life with a rare genetic blood disorder known as Beta Thalassemia Major, which qualifies as a disability under article 107.05 of the Social Security Administration's bluebook; a physical disability severely affecting stamina and growth. Often referred to as an “invisible disability”, it shapes my life in ways many might never understand, requiring blood transfusions every three weeks, and nightly infusions five days a week. My condition demands meticulous attention—blood transfusions, nightly infusions, and countless hospital visits—but it has also granted me a unique perspective on life. I understand the value of time, the importance of compassion, and the power of perseverance. One of the most powerful ways I have found to cope with my condition is through writing. Sharing my story, my experiences, and my thoughts on living with Beta Thalassemia Major has been both cathartic and empowering. I write about the strength found in vulnerability, the light in the darkness, and the unspoken solidarity that unites us all. Writing allows me to process my emotions, to reflect on my journey, and to inspire others to find their own strength. For my excellence in writing, I was awarded the Laban Carrick Hill Junior Writers Award by the Essex High School English department. I believe everything happens for a reason, and I find truth in that idea. Despite its challenges, my experience with Thalassemia has become a source of inspiration. In October 2020, while receiving a routine blood transfusion at the University of Vermont Medical Center, the hospital was hit by a massive ransomware attack. Seeing the chaos made me realize how vulnerable healthcare systems are, especially for people like me who need them for life-saving treatments. This experience sparked my interest in cybersecurity and digital forensics, driving me to defend the critical infrastructure so many rely on. I want to protect those who cannot protect themselves. In navigating the complexities of Beta Thalassemia Major, I have often felt like a soldier in my own quiet battle. Each day presents a choice: to succumb to the weight of my challenges or to rise above them. My journey mirrors the tenacity displayed by John Sherman, whose unwavering spirit in the face of Multiple Sclerosis and cancer inspired those around him. Like him, I refuse to be defined by my limitations. I continue to pursue my passions—whether it’s through writing or my interest in cybersecurity—because I believe that every challenge has the potential to be a stepping stone. In moments of pain, I draw strength from the love and support of my family, echoing John’s commitment to his community. This scholarship not only represents a means to further my education but also symbolizes hope—a hope that reminds me of the power in resilience and the importance of using my voice for those who cannot speak for themselves. Especially as my same-age brother and I both pursue higher education, our family faces a significant financial burden. This scholarship is crucial for my finances and my future. Thank you for listening to my story, and I deeply appreciate your consideration.