Sophie Stewart

Sophie gets ready to go on her holidays thanks to Cash for Kids.

Published 15th Feb 2013

Sophie was born in Nov 2007 with a congenital heart disease called Hypoplastic Left Heart Syndrome. She was given only hours to live unless she had emergency surgery carried out on her tiny heart, she then had to be hospitalised for most of her first year. After this, she still has to have daily hospital visits and regular updates and yet another surgery when she turns three.

The Cash for Kids grant will give Sophie and her family the chance to go on an unforgetable holiday to Disneyland to recapture lost memories of Sophie's first years of life. Her family has struggled during the difficult times and are thankful that their beautiful daughter is still here today.

!Sophie Stewart

!Sophie Stewart

!Sophie Stewart