We are a nonprofit organization dedicated to providing a WREX device to every child who needs one. Our organization was inspired by Emma, who was born with Arthrogryposis Multiplex Congenita (AMC), a rare disease which restricts normal movement. Without a WREX, Emma was not able to lift her arms to play, draw, or hug. We are committed to Emma and children like her, whose rare disease keeps them from being able to perform every day activities. Previous models of the WREX were too heavy and big for children as small as Emma. With the help of a mother’s relentless love,  the ingenuity of scientists, and an intricate 3D printer, Emma was the youngest child to  ever wear a WREX.