May 28th
Sunday, May 28th, 2006We will be meeting with the chief of the heart transplant program at Children’s Hospital this Wednesday, May 31st.
This is the journey through our daughter’s Congenital Heart Defect and eventual heart transplant. When you “decide” to go down the transplant route as it is called there are certain things you find out after you sign on the dotted line.
We will be meeting with the chief of the heart transplant program at Children’s Hospital this Wednesday, May 31st.
Our cardiologist called this evening (finally) and let us know what the team at Children’s had decided. He met with approximately 10 cardiologists, the chief of transplant surgery, several surgeons and some electrophysiologists. They all agreed she needs a pacemaker because her heart rhythm is not regular. The surgeons were very nervous about attempting any […]
We went to University of Washington Hospital today to do an ultrasound, an echo and to meet with the perinatology and neonatology specialists. Here is a rundown of what they found. Her size is okay and her amniotic fluid level is fine. The small amount of fluid around her heart hasn’t changed […]