J. W. von Schliefen

 

 




For Helping To Fight The War Against Birth Defects Given on
3/26/99, by CHERUBS- The Association of Congenital
Diaphragmatic Hernia Research, Advocacy, and Support.

My Story........

I was born on Sept. 17, 1996  with a congenital diaphragmatic hernia (CDH). There is a long explanation, w/ a lot of details about exactly what that is. But, in short, that means that before I was born, a hole was in my diaphragm, which allowed my stomach & intestines to fill the space in which my lungs were supposed to develop. Since lungs develop later than digestive tract organs (because you don't need them until you have been born) there was very little space in which they could develop. Well shortly after I was born, I had to be put on a machine called E.C.M.O. (Extra Corporeal Membrane Oxygenation) This is basically a heart/lung machine. It took my blood & pumped it through an artificial lung & then pumped it back into me. Four days later, the world's best doctors did surgery to repair my hernia. I spent A LOT more time in NICU at the hospital. My body had to learn how to breathe, & how to move food through my intestines, since they had been re-configured during the surgery. Despite all the yucky things the doctors & nurses did to me, I was a happy baby. (and because of all those yucky things, I'm still here to be a happy baby!)

Anyway I would like to say thanks to all the doctors & nurses who helped me out, but especially I would like to thank all the people out there who prayed for me, and all the Angels who watched over me. Everyone says that I'm a "miracle" baby.......well I think so too, and I am so glad that so many people care about me.

Thank You All!

 

Links:

More detailed explanation of CDH


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