Thank the lord, finally some good news.
After all of this I am really wondering if it is better to know….or to not know. As an Accountant, I am a left-side brain thinker….my husband the landscaper right side. I need to know. I need to know how to prepare myself for the future. I make lists. I am organized, I can’t stand chaos or messiness. I like to think in terms of numbers and lists. Blake is very number conscious, but doesn’t make lists and takes things as they come.
At first I thought I would rather not know she had a heart defect until she is born. I think Dr. Shah told me about 30% of these cases are diagnosed before birth…..we are lucky! Now I think that is totally for selfish reasons, so I wouldn’t have to worry throughout this pregnancy. Now I realize it is so AWESOME that we do know. She will be born in the correct hospital and monitored right away once she is born. I don’t think there could be anything worse than delivering and having your baby being flown to Peoria.
Okay let me take a step back…..
Once we found out our baby girl had a heart defect I decided I wanted to learn more about the heart and how it worked so I looked her heart condition on the internet, BIG MISTAKE. When I typed in the “endocardial cushion defect” the next words that came up were downs syndrome……what? I didn’t know there was a correlation. I am not the type to research things to death….I would rather hear accurate info from my doctors rather than search online. So I called Blake and freaked him out….then I called Dr. Dameron. She reassured me that the baby had no signs of genetic issues, all of her measurements were normal (nose and spine width, not missing a thumb bone etc.). So I was fine after talking to her. Once we went to the Perinatologists he said not all babies have the abnormal genetic markers (missing thumb bones etc) and there is no way to know unless you get an amino done. The amino tests all the babies chromosomes to ensure nothing is abnormal.
So my instant reaction was let’s do it. He knew that would be my reaction as a left-brain person. I need to know. Blake on the other hand says, it doesn’t matter what the results are….it is what it is. He supported my decision to get it done. I almost backed out, but I decided to be brave and get it done. The (cardio) Dr. Shah and Dr. Leonardi thought it would be a good idea.
Now you might say….isn’t there a big risk for a miscarriage etc to happen? Well not really. The chances are 1 in 500…..the chances of having a baby with a heart defect is 1 in 100….and the chances of her having downs syndrome related to this heart defect are 1 in 3. This is how my brain works…..and I would say the odds are pretty good that nothing bad would happen that hasn’t happened already!
The amino wasn’t bad at all. I could feel it….it really wasn’t bad at all. I told Blake on a scale from 1 to 10…..it was a 1. They did stick a big needle through my belly to extract amino fluid…..this is the babies DNA. Blake watched it, he didn’t want to go in the room with me, but I needed him there. He said it was kinda cool actually.
So now I can breathe easy, the FINAL amino results came back NORMAL!!!!!!! THANK THE LORD! The only thing now is to pray her heart defect stays mild!

