Hi!
Well Bill and I had our genetic screening and counseling today. Since I am 35 years old (0r 36 when the baby is due) my doctor requires us to go to this appt and talk about family history etc. Everything in our history doesn't indicate any problems. We did apt for the 1st trimester screen test (although I start 2nd trimester today WOOHOO).
This test is non-avasive and will give us odds (in about a week) of us having a baby with 3 chromosomal problems. There are more than that but this shows the 3 major ones. The odds will come back as 1:300 or some form of that. It won't make a bit of difference to us however we thought if the odds were high, then at least we could educate ourselves more about the difference disorders.
The test consists of an ultrasound and blood work. They look for certain proteins in the blood combined with measurements from the baby. They measure the baby's nec area and the normal range is 1-3mm. As the area gets bigger, that could indicate a problem. Our baby's measured 1mm. So we are in the very NORMAL range on that. So that is a great sign. Now we just wait for the blood work. However the doctor (this is a perinatal doctor, a specialist, not our reg. doc) said that everything looks wonderful.
We got to see our sweet baby today. I saw a sweet face, body, arms and legs. The baby had her (I think it is a girl, however too early to see any boy/girly parts yet) hands up against her mouth at one point. And what was SO wonderful was seeing the heart beat. That was so great!!
Anyway, here is a pic of our sweet baby. I did label the parts since some of you may not have any idea of what you are looking at. HAha!!
Have a great week!
