In her own words... Before my Lupus diagnosis, I attempted to rationalize the pain I was enduring and overlooked my symptoms because they weren't visibly apparent. Despite being vocal about my issues and seeking help, it felt like a wild goose chase as I navigated from one doctor to another, only to be told that my health was in the clear, despite my palpable sense of my body failing me. It wasn't until I was rushed to the ER at the age of 19 that I received a life-altering diagnosis of Lupus, later discovering its significant impact on my kidneys, leading to severe Lupus Nephritis. This unexpected journey immersed me in a world of unfamiliar terminology, experiences, and information. 

Along this path, I faced not only medical challenges but also social obstacles arising from a widespread lack of understanding about Lupus. In response, I have dedicated myself to not only comprehending my own illness but also educating others and gradually dispelling the stigmas, stereotypes, and misconceptions surrounding Lupus and chronic illnesses.

 A prevalent misconception that accompanied my journey is the belief that my goals should be limited due to the constraints of my illness. I challenged this idea while participating in Miss Texas, advocating for Lupus awareness under the mantra "My ambitions will not be limited by my conditions." This mission continues into the present year as I prepare to compete again in Miss Texas 2024, with the support of the Lone Star Chapter from Lupus Foundation of America. Together, we aim to amplify awareness, providing Lupus patients with improved prospects for receiving proper medical and social treatment.