The non-profit, National Organization for Rare Disorders, giving the award to Villarreal said she is a shining example of rare disease youth advocacy and leadership.SAN ANTONIO — Abigail Villarreal is described as little, but mighty with a big voice. The teenager all her life has battled with something most of us take for granted.
"I am excited," she said."I am also nervous. I am scared. I just feel very grateful. Everything is falling into piece. It's just amazing." Villarreal has a rare genetic disorder that she has been living with her whole life. Soon after she was born, doctors gave her mom the diagnosis.She essentially has to watch what she eats and be extremely careful.
The teenager has to take medicine. However, through her years in school, she was bullied. Villarreal being courageous has turned that pain into a purpose.