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Elyse's Website | 
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Elyse's Website The purpose of this site is to share our experience and let you know you are not alone. If you keep the faith, this ordeal will end before you know it. If you believe in God, have faith, if you don't believe in God, then have faith in the professionals who will help your baby!
A family webpage that celebrates the lives of the Smith children, Jake, Ryan and Shea as well as the experiences Ryan has had being born with TGA, a congenital heart defect that almost took his life as an infant.{;}
In about the 20th week of my pregnacy the Dr's discovered that the right side of my baby's heart was too small. When I heard those words my heart broke. Almost instantly I had a million questions. Will she live? What can you do to help her? Did I cause this somehow? After several more tests they told me that with 3 operations she could be fine. {;}
* Congenital Heart Disease Community * Personal websites about congenital heart{;}defects. Congenital Heart disease affects one in one hundred babies, it is the most common birth defect. Read our heart warming stories. Watch our children grow up. Most of our children are living and doing well, but many have lost their battle with CHD..
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