Monroe artist is advocate for rare diseases awareness

Giusiana Prosser, a 22-year-old artist from Monroe, is using her platform as Ms. Wheelchair Northwest to advocate for rare disease awareness and community visibility. Her artistic journey began during her recovery from a major abdominal surgery in 2020, where she found solace in painting, expressing her emotions directly onto the canvas. As she prepares for the Ms. Wheelchair USA competition, Prosser is aware of the challenges that come with public exposure, especially given her health issues.

Her advocacy is rooted in personal experience; after years of being dismissed by medical professionals, she founded the Rare Living Foundation to support others facing similar struggles. This grassroots organization focuses on storytelling, education, and legislative advocacy for patients with rare diseases. Prosser’s art, characterized by loose brushstrokes and a cool palette, resonates deeply with viewers, often evoking tears and reflection. With initiatives like her float in the upcoming Easter Parade, she aims to further amplify the visibility of rare diseases. Ultimately, Prosser's work seeks to foster a sense of belonging and hope among those who feel isolated by their conditions.