About My Campaign
My daughter was 5 days old when we were told she had PKU. Nobody in our lives had ever heard of this rare IEM. I 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. I am doing this in support of my little girl and the many other children and adults living with a rare IEM.