He moved right after Cole's surgery in March 2003, I think he may have moved around 2004.
HE IS GREAT!!!
If you meet him, tell him a family from UVA mentioned him, he is so nice!!!
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He moved right after Cole's surgery in March 2003, I think he may have moved around 2004.
HE IS GREAT!!!
If you meet him, tell him a family from UVA mentioned him, he is so nice!!!
Tara on another note, I see you are from Ohio, GO BUCKEYES!
cdh found at birth. 28 days NICU. Vent 7 days. Repair at 3 days. No ECMO. NG Tube 28 days http://i319.photobucket.com/albums/m...don/0004-1.jpg
Primary Children's Medical Center in Salt Lake City, Utah, has ECMO and a fantastic ECMO staff. To this day, we still keep in contact with Ian's primary nurse from the NICU. The doctors and nurses are amazing at PCMC and continue to be. Ian actually likes going to his checkups!
Tracy - mom to Ian, LCDH diagnosed at birth, 4/3/04. Ian was born at 36 weeks, spent 53 1/2 days in NICU, 7 days on ECMO, surgery was on day 5, 29 days on a vent, 23 days was an oscillating vent, 546 days on oxygen. Inguinal right and left hernias and undescended left testicle surgeries were done on day 48. Currently has heart related medical issues and exercise induced asthma, but is one happy, happy boy!! Also mom to Cole - 13, Shane - 9, and Toby - 4. CHERUBS Parent Advisory Board Member and Co-Chair, Volunteer Co-Coordinator, and Wyoming State Representative.
email: tmeats@cherubs-cdh.org
Children's Hospital of Birmingham, Alabama has ECMO
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