About Team: Team Amelia
Our daughter was 5 days old when we were told she had PKU. Nobody in our lives had ever heard of this rare IEM. We would like to create awareness and help people understand what it is and how it has affected many lives. As a family, we participated in the Great Protein Challenge last year and were overwhelmed with the support we received from so many people. We are doing this in support of our little girl and the many other children and adults living with a rare IEM.