As a passionate advocate for healthcare equity and patient-centered research, I am driven by a commitment to support communities and improve healthcare experiences for individuals with rare diseases and disabilities. Currently, I work as a Young Adult Patient Partner with RareKids-CAN, where I collaborate with researchers, healthcare professionals, and other advocates to create meaningful, patient-centered improvements in transitioning from pediatric to adult care. This role allows me to use my personal insights to enhance study design, ensure respectful and inclusive data collection, and contribute to clinical trials and research focused on the youth experience.Alongside this, I am the Secretary of the University of Toronto Accessibility Awareness Club, where I help build a welcoming community for students to discuss disability issues and support one another through organized events and initiatives. In my work as a Peer Educator with the Wellness Peer Program, I focus on substance awareness, leading workshops that educate on safer practices and health impacts, creating an open space for learning and support.As an intern at Scleroderma United, I am furthering my experience in healthcare advocacy by leading awareness and fundraising campaigns that strengthen my skills in advocacy, community engagement, and project management. These experiences reflect my dedication to raising awareness, supporting research, and implementing change for people living with rare and chronic conditions.Looking ahead, I’m exploring a path toward healthcare that combines my commitment to patient care with a strong interest in research. I’m eager to continue developing skills that bridge patient advocacy with meaningful, evidence-based advancements in healthcare.
