Tuesday, February 21, 2006

 

"What It Means to Be The Parent of a Child with a Heart Defect"

Thanks to Jamie from CHD Families KC for posting this in the yahoo group.
This is a link about what it it is like to have a child with a CHD. You can order posters and books about CHD kids and Parents at the website.

We are still in the hospital. Sophia has started Digoxin. We will hopefully be home soon.
-Michael
Comments:
Thanks for posting this info.

Boy do I wish that the internet was around 33 years ago, when my mom was going through this with me. I was born with TOF and everytime I read your site I am more amazed at my mother's strength back then.

Thanks for sharing your story.

Susie from Minnesota
 
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