October 9, 2014
22qdeletion syndrome, Developmental System, Family Stories, velocardiofacial syndrome
6 Comments
In May of 2013, we were asked if we wanted to review the file of a little girl with a repaired Congenital Heart Defect, Tetralogy of Fallot (TOF). We had been waiting several months and were so ready for THE phone call. When our doctor reviewed the file, she told us about Velo Cardio Facial …Read More
February 6, 2009
22qdeletion syndrome, Developmental System, Family Stories, velocardiofacial syndrome
1 Comments
By Anonymous, mother to Gui Ai from China with DiGeorge syndrome I want to share our family’s journey of adoption. I hope in doing this it will encourage others to consider children with unknowns and more involved special needs. When we received the referral for our daughter we knew she had a repaired heart condition …Read More
