Monday, September 17, 2007

Screening Results & Dr. Fav

First, mea culpa. Not that anyone seems to be reading this thing, but I still can't get my act together when it comes to keeping up with this blogging thing. I've had some great ideas for posts, but somehow always get waylaid.

I’m still in PregnancyLand. Stick-It’s still sticking. All-day nausea has subsided somewhat, but I still have my moments. This morning I couldn’t get to work until 11:00 a.m. I almost passed out twice, something that never happens to me. DH made me take my BP. It was 80/48, at which point he said he didn’t want me behind the wheel; I agreed, because I felt like crap. So the next two hours was spent lying down, trying to drink and eat something to get my metabolism and BP up. Finally it went up to 90/58, and now I’m at work.

First trimester screening results from the practice I was referred to came back, and were great. I have gone from a 1/70 chance of having a child with Down’s Syndrome to a 1/1380 chance; the genetics counselor noted that that is the same risk a 20-year-old would face. Same level of risk (same as a 20-year-old) for Trisomy 13 or 18 – from a 1/137 risk to 1/2721.

Then she asks the question: to amnio or not to amnio? Mind you, the only amnio I’ve ever had was with Jimmy. I know it had nothing to do with his choking on his cord, and at least we knew of all the things that he didn’t die of, but I’m also a person who analyzes numbers. The question I raised at the screening appointment was the 1/200 risk of miscarriage that the amnio carries, which the older OB at my practice had confirmed the week before. The genetics counselor corrected that. Due to their review of the latest studies from NY, which apparently has a similar population to the New England area, this high-risk practice (out of Mass General Hospital) now says amnios have a 1/600 risk of miscarriage. Still, that’s twice the risk as have a child with Down’s, and four times the risk of having a child with Trisomy 13 or 18.

So we’re opting to not do the amnio. I had the APF drawn Friday for the neural tube defects, and have my Level II u/s next Monday.

More reassuring was finally seeing “my” doctor in my OB practice. Dr. Fav is just a great guy. There are four doctors in this practice, along with some midwives (who I’ve never seen). Dr. Lady is my second pick in the office. Then there’s Dr. Grandpa, a man that my mom, an OB/GYN nurse, worked with for a few years two decades ago, before he and his two partners split and she went with one of the other partners. He’s nice, but a little too old-fashioned at times for me. I had to see Dr. Grandpa for my first appointment at 10 weeks and then again at 12 weeks (he couldn’t hear the heartbeat at 10 weeks, and wanted to see me at 12). Then the last partner, Dr. A-Hole, is the one who let me bleed for 8 weeks after my miscarriage before my D&C. He’s the one that I informed the intake OB nurse I would not see with this pregnancy. Actually, I said I wouldn’t let him within 20 feet of me, and that I still had friends and family who thought I should have sued him for dragging out my second loss with their office.

Now, you may ask why I would return to the same practice. Because when I asked my RE if there were anyone in the area that he would recommend for someone who finally got pregnant with his practice, he recommended Dr. Fav. When I posed my issues with Dr. A-Hole, he just told me that any woman who’s gone down the IF path has to be her own advocate when she does get pregnant, because most OB/GYN offices don’t handle pregnancies after losses well. And Dr. RE is a man I had and have great confidence in who was at one of the better Boston hospitals when it comes to high-risk pregnancies.

Anyway, Dr. Fav was on for my 16-week appointment; I’ve also got my 20- and 24-week set up with him. He greeted me, and did all the regular checks. Heartbeat was fine, my BP was fine, and I’ve only gained 9 pounds to date (pretty good for a “big” girl – I’m 5’7.5” (that 0.5 inch is SOOOO important!) and now weigh in at 207.5 pounds. Then he asked how I was, how much stress I was under (my response was “quite a bit at work”), and his plans. He wants me scanned every 3 weeks to check for fetal growth, fluid levels, and placenta health. He also wants to see me every 2 weeks, and in between doesn’t care if I’m in the office for heartbeat checks every day if that’s what I want. He also mentioned that his and my anxiety levels would be going up dramatically from about Week 24 until this child is delivered healthy and is safe in my arms. Sounds good to me, and it’s comforting to feel like I have someone watching out for me and Stick-It.

So, the next step is the Level II u/s. Hopefully, Stick-It will cooperate and we’ll find out what we’re having.

2 comments:

Thalia said...

we're still reading sweetie. But through bloglines which means your stats probably drop as ppl don't come by until you post.

Glad to hear all is ok, in so many ways. Will be keeping it all crossed that it continues this way.

Trisomy 13 Life with Natalia ~ Transformed by Love said...

I'll be Praying for good health for you and your child.
Your blog popped up in my google alert for Trisomy 13, here is a support link those who embrace these lives. There is always hope.
http://www.livngwithtrisomy13.org
My daughter Natalia is now 7 yrs old and the JOY in my day. Many Blessings to your with your pregnancy,
ThereseAnn

You don't need to post this, its just for your info, unless you'd like to share the link...