Introducing Jace John Nelson

We had our ultrasound last Wednesday. It was incredible to see the baby moving around and find out it's a boy! He was nice and cooperative while the technician took all his measurements, but once she was ready to get the picture shots, he put his arm over his head and fell asleep. When the tech tried waking him up (had me roll over, jiggled my tummy a lot, etc) he just curled up in a ball and rolled over with his back to us. I guess we have a good sleeper on our hands!

His heart and brain and limbs look like they're developing just fine. He size is right where it needs to be for how far along I am. But our doctor called the day after the ultrasound saying that when she took a look at it, they saw that he might have a small cleft lip/cleft palate, if one at all. So we're going back in for another ultrasound on October 5 to hopefully get a better look. She's thinking that a month of growth will help them see clearly if he has it or not. We're glad to hear that it isn't distinct enough or big enough for her to be conclusive at this time (from what I've read online, you can spot cleft lip as early as 16 weeks, and this ultrasound happened at 19 weeks). So we're hoping and praying that 1) if he has it, God might heal it before the next ultrasound or by time he's born, 2) he doesn't have it, or 3) if he does have it, we're praising God for medical advances and what they're able to do for this these days!

Cleft Lip/Cleft Palate is most common in boys, and 1 in 700 babies born in the US has it. So it's much more common than we thought it was. This in itself is a testimony to what a great job doctors are doing with it, in that you'd never realize how many people have had it.

If he does have it, we'll get set up with a team from Dornbechers up in Portland. Cleft lip is typically repaired when they are 10 weeks to 3 months old, and cleft palate repaired by 9 months old. So while it's so treatable, he could still have quite a first year of surgeries in store for him (and potentially many more surgeries ahead of him if it’s cleft palate).

All this made me REALLY want him to have a name already--to give him more of an identity. And I wanted his name to mean something, since he'll have so much to face at first. I started looking through names that meant things like strong, God heals, etc. Finally, we decided on "Jace" (which comes from Jason, but that won't be his name). Jace means healer, and on some websites, it also meant God is Sovereign. Both fit well we thought. Plus, Nolan loved that it's unique, since he likes names that he hasn't really heard before. So as of now, baby's name will be Jace John Nelson (Nolan’s middle name is John, it’s also his father and grandfather’s name).

We really have an incredible peace about the whole thing. I’m so thankful for a doctor who’s thorough and spotted this. From what I’ve read, not all doctor’s catch it. What a blessing to be able to know what we’re heading into and to be prepared for it! We're sad for the pain he could potentially face at such a young age, but at least he won't remember it as he gets older.

He'll be beautiful no matter what. And I'm just sure, if he does have cleft palate/lip, he'll be a much stronger person because of it.