Tuesday, May 06, 2008

Ultrasound and Perinatal Visit

It was good to "see" Nathaniel again on the ultrasound. Mel loved seeing him for the first time. We could see his little feet and hands moving. At one point he was lifting his head up and down like he was nodding and opening and closing his mouth. It was so cute. Mel said it looked like he was kissing the inside of my belly.

The doctor did a quick 3D picture of Nathaniel for us. I can't stop looking at it. He's so beautiful.

(The shadowing on top is because Nathaniel started moving around and this was the best image the doctor could get.)



Aside from all our excitement of seeing our baby, we didn't receive news that was any more reassuring than before. In addition to Nathaniel's small chest cavity, the doctor is also concerned because his spine and front ribs have not hardened like they should have by now. Basically they are soft like cartilage still. They should appear bright white on the ultrasound, but look more pale gray.
There are three skeletal dysplasia conditions the doctor believes Nathaniel could have. Thanataphoric Dysplasia, Achondrogenesis, and Osteogenesis Imperfecta. Based on the ossification problem, the doctor is leaning toward Achondrogenesis. Unfortunately, all three are not compatible with life.

We are being realistic about the prognosis, but we are also trying to stay hopeful. Please help us continue to pray for Nathaniel and God's plan for his life.

5 comments:

Anonymous said...

He's beautiful, Andrea. I will continue to pray for you all.

Kim said...

Andrea,
Argh! Doctors! Remember in Cat and my situation they could not even diagnos simple achon! I was told TD as well. Insofar as the chest cavity-what they need to do is do a measurement and plug it into the measurement chart based upon fetal measurement. When they did that my son's chest was in the 66th percentile. His chest was smaller at birth than an average babies and still is slightly smaller. That comes with the territory!
I hate that these doctors are just guessing. More often than not they are wrong, just covering themselves. Feel free to also go to yahoo groups or google Parents of Little People 2 which is a forum of all parents of kids with skeletal dysplasias.

Anonymous said...

Our family is praying for you....that is one good looking babe you are carryin'!!!

IrishMommy said...

Yeah-another sunshine of hope! Nathaniel we are praying for you and your family!

Undomestic said...

Love the picture!