Shyannes chance to SHINE

My daughter Shyanne was born July 10th, 2011 with a very rare genetic disease called Sly Syndrome. There are only about 40 in the world with her disease. THERE IS NO CURE! Shyanne is going through a cord blood transplant and will not get to go home until June 2012. She is in strict isolation and going through 10 days of chemo. She gets Busulfan for 5 days every 6 hours for 2 hours straight then she will start other forms of chemo that run for longer times and a bit stronger. Please help by donating & praying for our family the doctors and beautiful Shyanne.

Matthew 19:26 \'With God all things are possible\"