PDA

View Full Version : Hi,


Chrissie
11-12-2009, 11:20 AM
Hi everyone! There is a new little heart family the Stewarts; she hasn't had the time to join the group, but their little guy Teagan was born with a rare case of HLHS. He wasn't pre-diagnosed so this is all new to them. He was able to come home but is now back at PCMC due to NEC. Has anyone ever heard of this or had experiences with it she wanted me to ask? His heart function is fantastic so the cards are a little confused what caused it. He will be there for a little more than a week to figure things out. His mom Amanda said she would love to meet and talk with anyone who has time. He is in O pod room 3088. Please let me know if anyone else has dealt with NEC. They are such a nice family and are a little overwhelmed with this "new heart world" Thanks for all your help! You guys are amazing!
Chrissie

Chrissie
11-12-2009, 11:21 AM
Opps I forgot to post their blog, http://teaganstewart.blogspot.com