Skip to main content

Press Release

Page 1

23-year-old Ballroom Dancer with Brain Malformation Defies Odds and Launches Foundation to Support Individuals with Rare Neurological Disorders

Chicago, IL, September 5, 2024 — Sabrina Blair Schoenberg, a national champion ballroom dancer and multiple Fred Astaire Dance Studios (FADS) world titleholder, is proud to announce the launch of the Sabrina Schoenberg RES Foundation. This foundation is dedicated to raising awareness and providing support for individuals diagnosed with Rhombencephalosynapsis (RES) and Gomez Lopez Hernandez Syndrome (GLHS), rare neurological disorders that aHect balance, coordination, vision, and many other functions. Sabrina was born with a rare brain malformation that has left her without a part of her cerebellum—the part of the brain that controls balance, movement, vision and various sensory and cognitive functions. As her doctors explained when she was young, Sabrina has "no autopilot." Unlike most people who can perform basic functions like walking, talking, and eating with little conscious thought, Sabrina must focus all her energy to accomplish even the simplest of tasks. "Every action I take, whether it's walking down the street or tying my shoes, requires 100% of my focus," she explains. "It’s a daily struggle, but I refuse to let it define me." Overcoming Challenges Through Dance and Dedication Sabrina’s journey has been marked by constant challenges, from undergoing numerous brain scans and medical treatments to navigating a world that often doesn’t see or understand her invisible disabilities. She experiences daily symptoms such as low vision, tics, involuntary head movements, diHiculties with social cues, learning disabilities, and balance issues. Yet, she has defied expectations and found solace and empowerment in the world of ballroom dance.


Turn static files into dynamic content formats.

Create a flipbook
Press Release by Sabrina Schoenberg - Issuu