Just received a report the doctors are trying to fix up all the tiny little leaks around where they placed the gortex and modified his aorta.
posted by The Petska Family @ 8/23/2006 04:11:00 PM
This blog was designed to share our son's journey - living with a congenital heart defect. Braden was born on August 17, 2006, and was diagnosed with HLHS two days later. After 2 open heart surgeries within three months of age, Braden thrived and marveled the doctors throughout his little life. On the late evening of March 16, 2009, Braden's heart went into a fatal arrhythmia. He earned his angel wings on March 17th. This blog now marks the journey of survival - living with the devastating loss of our hero, our son, our precious B.
2 Comments:
Yeah little Braden-
We know you could do it! We are so proud of you - and your mommy and daddy too!! I hope you can feel the kiss that comes to you from the Braden's! Justin and Jonah made pictures for you and cannot wait to give them to you!
Lots of love,
Ray, Melissa, Justin and Jonah
Our special candle has been burning brightly all day for Baby Braden and all of you at the hospital. The waiting is always the hardest part.
Post a Comment
<< Home