Another bit of excitement that we've been simultaneously looking forward to and fearing terribly were getting the results back from the genetic tests as well as the Ultra Screen visit to mom's office. We went for the genetic tests about four weeks ago, and they took about a gallon of blood from each of us. They tested us for genetic matches for a whole host of genetic disorders (Tay Sachs and a bunch of others I can't remember). We got the results a few days ago and we're completely mismatched for everything! That means anything wonky in my genes doesn't match anything wonky in Barry's genes, therefore we have nothing to worry about on that front. Another woo hoo!
Finally, we went for the Ultra Screen on April 14th. That's where they take even more blood from my poor, blood-let body and they do a sonogram of the baby, checking something called the nucal (sp?) fold. They looked at the thickness of the skin on the back of the neck and checked out some stuff in my blood. When they put all that information together, they can come up with a likelihood for Down Syndrome, along with several other abnormalities. We came back with a 1 in 10,00 chance of a problem! That's the highest number the doctors will give. Woo hoo number three!
This baby is one healthy little bean!
