Sophie Collier

Story updated 2/2/06

Sophie Collier of Indianapolis was born with a congenital heart defect called truncal arterisus that threatens her life every day. Along with the heart defect, she also developed an immune deficiency called DiGeorge Syndrome. The condition leaves her more susceptible to infection.

At just 18 days old, Sophie needed open heart surgery. After the long day her father Brian, who had kept family updated by e-mail, was finally able to send a message stating that, "Sophie is doing great!" Then he joked: "She has scared the heck out of us to the point where I think we'll keep her grounded until she's 23."

Sophie remained at Riley Hospital for three months, most of this time on a ventilator. As her family had hoped, she was released to go home by Easter, at which time her 3-year-old brother Drew met her for the first time.

"I cannot envision a group of doctors and nurses more caring, checking on us day and night," says her mother Katie. "They treated us like their own family, hugs and all."

Now at age 5, Sophie has met and exceeded the goals set for her long before anyone ever thought she would. Her zest for love and laughter is incredible. She appreciates everything. Her favorite color is pink and her brothers, ballerina videos and music keep her busy during the day.