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Hi my name is Kim Hancock and I was born Hi my name is Kim Hancock and I was born{;} with T.G.A.(transposition of the great{;} arteries) I had open heart surgery when i{;} was born and many after that, the final one{;} I had was when I was 2 years old. I go for{;} check up every year in Toronto, Ontario at{;} the Toronto General Hospital. I was told{;} that I had rhythm problem at one of my{;} yearly check ups. Its went away by the{;} next check up, and has been fine since, I{;} am now 20 years old and gave birth to a{;} Healthy Baby Girl on October 22, 1998.
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. {;}
Millie was in the hospital for 9 days, she got released yesterday. She was at Children's{;} Hospital and Medical Center in Seattle. I spent the entire week staying with her. It feels{;} good to be home. Our Christmas lights are still up and I have not put away my Christmas{;} presents yet. The three weeks since Millie was born have been a blur! First the 3 day labor{;} then getting released from the hospital when I was too sore to take care of just myself. Then{;} the bout with Jaundice, then Christmas when I was too sore to leave the house. Then the power{;} went out for 4 days. Then Millie quit eating right so we took her to the pediatrition and she{;} was diagnosed with Congestive Heart Failure. Then the ambulance ride to Mary Bridge{;} hospital. Then another ambulance ride to Childrens hospital. Then heart surgery and a 6 day{;} stay in Seattle. Now I have to give her digitalis and other medicines twice a day and she is{;} going to have open heart surgery as soon as she is big and strong enough.
* 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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