Hello my friends, 
It has been a long time since I have posted here.  My chd baby is now 14, and will head to high school in a couple of weeks.  She has her limitations, but we are so grateful to have her here today.  She got a good check up at the heart doctor a week ago, and they would like to do a 3 d mri on her.  They need to check if it is safe for her since she was coiled when she was a baby.  Stay tuned for more info on my dear Abby.  Until then, here is a link about stem cells and how doctors are using them for babies with chd.  

http://abclocal.go.com/kabc/story?section=news%2Fhealth%2Fyour_health&id=9179106