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| Welcome to Phillip’s Home Page. Our son Phillip
was born on August 9,1996. Phillip was born with a very serious congenital heart defect
called Hypoplastic Left Heart Syndrome (HLHS). He has been through three open heart
surgeries and several other procedurs. We have written this web page to share our
experience with others who may have a child with a Congenital Heart Defect. We hope that
by doing this we can help other parents who have a child with a CHD. The road has not been
an easy one. As you read Phillip’s story you will see that there have been many bumps
in the road along the way. The road may be rough, but the rewards are great. |
Disclaimer
| I have written this page to share my experiences with
other people who have similar experiences. I am not a doctor, and I am not in a medical
profession. This page should in no way be a substitute for professional medical care or
attention by a qualified practitioner, nor should it be inferred as such. ALWAYS
check with your doctor if you have any questions or concerns about a condition. |
We would gladly correspond with any parents with
similar situations.
So feel free to e-mail us.
Thanks for visiting Phillip's Heartpage
 Please
E-Mail me with any comments
 visitors since 6/20/98.
Created: 6/20/97, Last Updated:
January 2002
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