CHIN: Information and resources for Families, Adults and Professionals

CHIN Community Portrait Gallery

 Name   Diagnosis   Treatment   Birthdate   Updates 
Community

Resources

Links

About

Home

What's New

Contact

Search
 

Connor Andrew

ASD, VSD, IAA, Sub-aortic membrane , dextrocardia


Connor (April 2002)

Connor was born at 42 weeks. C-section after 22 hrs of labor. He looked perfectly normal to us. Within 8 hrs they heard a murmur and transferred him to the Montreal Children's Hospital.

At 12 days he underwent open heart surgery to close the ASD and VSD and repair his interrupted aortic arch. The dextrocardia remained the same. It was an 8 hour operation and all went well. He was in the hospital for roughly 8 weeks.

Connor came home on a few medications (Lasix and phenobarbital). He was weaned off them in the weeks to come.

He had his last open heart in May 2001 for a sub-aortic membrane. It was removed successfully but there is the chance that it may grow back.

We had our cardiology appointment in August and all looked and sounded well, so we are free for another year.

We cannot say for sure but they figure because of a lack of oxygen during Connor's operation, Connor is intellectually delayed by roughly 2yrs. He is constantly making great progress. At the present moment he is at a school for the disabled, but with most probability he will be going to a regular school next year for grade one. He has done 2 yrs of pre-k and presently is in Kindergarten.

— Stacey and Andrew, Connor's Parents (Montreal, Quebec)


This article was last updated on October 28, 2002

  • Born:  July 4, 1996
  • Diagnosis:  Ventricular Septal Defect (VSD), Atrial Septal Defect (ASD), Dextrocardia, Interrupted Aortic Arch (IAA), sub-aortic membrane
  • Treatment:  Open heart surgery at 12 days to repair the ASD, VSD, IAA (1996). Open heart surgery at 4.5 yrs to repair the sub-aortic membrane (May 2001)


 

To comment on a portrait or send a message to the author, please email portraits@tchin.org.
Be sure to identify the portrait so we can properly direct your message.

Portraits are a benefit of membership in the Congenital Heart Information Network.
Click here to find out how you can become a member!


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.
Become a Member

 Community Resources Links About