Yesterday was a big day for us! But before I get into all the details, how about a couple of new images?

The little one in profile, about 12 and a half weeks.

Perfect little hand and strong jaw.
I started off the day meeting a midwife at the house, part of my process of checking out local midwives and seeing if there’s one whom I’d like to care for me and help us deliver our baby at home. I’ll write more about that process when it’s all finished.
Then I went over to UCSF for the big “genetic counseling and nuchal translucency ultrasound” visit, which is supposed to take place anytime between 11 and 14 weeks gestation. I’d already submitted blood samples so they could test the chances that our baby has either Trisomy 21 (Down Syndrome), Trisomy 13 or 18. So this visit was to measure the thickness of the fluid at the back of the baby’s neck and to combine that measurement with my bloodwork to determine our chances (again, it’s not absolute; it’s probability) that our baby has one of these chromosomal defects. Because I’m 35 I’m considered “higher risk” for these things — as we age so do our eggs, making them more prone to having flaws and then copying those flaws in gestation. Going by just my age, my chances of Down Syndrome was given as 1 in 246, and the chances of one of the others was 1 in 444. Less than 1%, but still high enough that the risk of them happening is comparable to the risk of miscarriage with CVS or amniocentesis (about 1 in 200-300), so they start arguing that it’s worth it to go ahead and do the riskier procedures to be sure the baby is healthy, unless the screen shows that things are very likely just fine.
I came in and talked to the counselor, who asked me questions about my and Devin’s genetic and ethnic backgrounds, and the genetic histories in our families. Then I went in and had the ultrasound, which lasted ages and I got to see the baby for close to half an hour.
When the scan started, the baby was wiggling a little bit but mostly holding still enough that the technician got lots of good images she could use to see the baby’s organs as well as measure the back of the neck (a perfect 1.8mm). We started off with a sight of the baby’s brain — including both little hemispheres — and then the body, legs, feet. The baby seemed to grow more active, stretching its legs and pushing its head against the opposite wall of my uterus, which the technician called “stretching out.” Then at some point the baby stretched its legs out fully and started kicking and springing against one side of the womb, which from the position of the sonogram wand looked like it was jumping up and down! From there the baby generally wiggled and waved its arms, put its hands to its face a few times, and so on. It was a delight to watch — I think I could have watched all day.
Everything looked good — we could count the correct number of fingers, legs, arms, heads, etc. We could see the jaw and stomach clearly, as well as the strong and perfectly curved spine, and the little heart beating (she even turned on the sound so I could hear it whooshing away, 146 beats per minute). She finished up and printed a bunch of pictures for me, including some of the 3D ones (which didn’t come out that well — by that point the baby was jumping and wiggling a whole lot). Then another doctor came in with a resident-in-training and was going to show her how the machine works and try to do some more measurements, but the baby wouldn’t cooperate for him at all and kept moving all over the place. Hee hee. Oh, and its total length is about 4 and a half inches. The technician gave me another due date — which they estimate by the size of the fetus — as March 2. “What did they say last time?” she said. “March 2,” I said. “If you get two that are exact like that, I’d say go with it!” she said.
I cleaned all the gel off myself and went back to the waiting room, after which the counselor called me back into her office. Even before I sat down she said, “You got the best results you possibly could have.” She showed me a print-out that goes by my bloodwork, the NT measurement, our genetic history, my age and so on. Risk of Down Syndrome was reduced to 1 in 4,116; risk of Trisomy 13 or 18 reduced to 1 in 8,861. These are akin to what they’d be if I were 19 or 20. There’s always a small chance of false negatives — the screen is 90% accurate — but the odds are definitely in our favor. She did recommend I also take a screening for cystic fibrosis to see if I am a carrier, so I had another blood test in the afternoon and will hopefully get results in a week or so. And then, in mid-September, there’s another blood screen that checks for the chances of neural-tube defects such as anencephaly. But, I am much, much relieved; the combination of seeing that our little one is developing well physically and is very active and bouncy, and learning the results of the screen, have put me greatly at ease.
And, I’m sure, will put all of you at ease as well. :) Now all I can think about is the little one boinging up and down in there. That’s going to hurt in about 12 weeks, isn’t it?
– Beth