The morning arrived and I was so nervous! We headed to primary children's we had a hour and half or longer ultra sound just focused on her heart! They took me and zach to a little little room where 2 cardiologists, an nurse consultant, and a social worker came in! There was tissue boxes everywhere! I looked at zach with fear in my eyes wondering what on earth were they going to tell us! They first started off explaining how the normal heart works I had to stop them and say ok first tell me if she is going to be able to live.. They said yes! This was a huge relief and I said ok now continue! They began to tell us that she has a congenial heart defect called Double Outlet Right Ventricle (DORV) that she will need open heart surgery to fix it! I am so thankful that it is fixable but open heart surgery!!! I about died! They went on saying that 1 in 100 babies has a heart defect but 1% of those has what she has! It is very rare!! I know even though her heart needs fixing she is going to have the biggest heart out there!!
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