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Parker

Truncus Arteriosus I, repaired at birth


Parker with Dad and Mom

Parker

Greetings, Our little man, Parker, was born May 9, 1997 in Richmond, Virginia. Upon his CHD diagnosis the day after his birth, Parker was airlifted to Children's Mercy Hospital in Kansas City, Missouri.

Our cardiologist in Virginia truly believed the surgeon at this hospital was the best one for Parker. His name is Dr. Gary Lofland, and he was the best! Ironically I am from that area originally so we were fortunate to have a lot of family support while we were there. We will always be indebted to Dr. Lofland and his staff as well as the Ronald McDonald room volunteers and supporters in the hospital. As well, we will always be deeply indebted to my brother, Greg, for "making it all happen". He came to Virginia when he got the news about Parker and took over dealing with all of the red tape that it takes to get a sick child and his "crazed" parents to a hospital for a life saving surgery. My Mother, Judy, was also on the first plane to Virginia when she heard the news and was a wonderful compassionate supporter. And thank God for my sister Cathleen who met us at the airport in KC with a suitcase full of clothes for me. Somehow she just knew that I would not have been able to think to pack and she saved me! And to my Dad who said "dear God, I will take care of the birds (he was outside feeding the birds when he heard the news) while you take care of Parker. And God did just that.

After Parker's surgery we were fortunate enough to be able to recuperate at my parents house in Lawrence. Having Parker's "Ganna and Papa" sole support was incredible. We would never have made it with out them. Parker is a thriving 6 year old now and we count every day as a blessing and love every minute that we have with him. We wish all of you health and happiness.

— Diane and Peter, Parker's Parents (Wichita, Kansas)


This article was last updated on December 7, 2003
Photo updated March 10, 2006

  • Born:  May 9, 1997
  • Diagnosis:  Truncus Arteriosus I, Supraventricular Tachycardia (SVC), Pulmonary Stenosis
  • Treatment:  Repair at age 4 days. Will modify conduit as Parker grows.


 

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Disclaimer: Our members' stories represent their own perception of their experiences, and the medical information contained within has not been reviewed for accuracy prior to publication. Stories are presented for informational purposes only, and should not be substituted for professional advice. Always consult your (child's) physicians with your questions and concerns.
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