I know it’s been so long since I updated this blog. I’m sorry about that.
As the title states, we are still here. As in, me, Wonderboy, and Flea are still around in this world. It’s been a bit of a slog sometimes, what with morning sickness and my undeniable need to sleeeeeeeep so much. But I am in my fourth month with this pregnancy, and all appears to be going well.
We’ve had our share of ups and downs, though. It’s taken me a while to process the big “scare” we had about three weeks ago. In the part of the world where I live, women over a certain age are forced offered the opportunity to undergo Integrated Prenatal Screening (IPS). I opted for the screening, simply because I wanted to be certain that we had missed the big scary things in this screening test (namely, trisomy 18). We didn’t care about Dow.n’s Synd.rome or Spin.a Bi.fida – WB and I had discussed these as very real possibilities, and we both knew that we would manage as a family to get through any challenges these two situations would throw at us (note: we know it’s a challenge to have a child with these two life-changing situations, but we also know how we feel about people with differences… that they are the colour in the world, 9 times out of 10).
The IPS is a set of tests – 1 blood test + 1 u/s on one day, followed by another blood test on a specific future date. No problem, ran the tests. The ultrasound showed excellent nuchal translucency (showing less probability of SB). The blood tests were also done with no trouble at all.
The Tuesday after I submit to the second blood test, I get a phone call at home (whilst I was en route to work). It is my GP, saying that they want to talk to me right away. It kind of freaked out my WB, so he left me a message at work. When I get to work, I have two messages waiting for me – one from WB, one from the GP. All I can think is “Oh shit… what’s wrong with the IPS??”. I call the GP’s office, where they insist on my attending their office TODAY to talk about the IPS results. Bugger. I’m panicking now. I take an appointment, call WB and proceed to melt down in my office.
So… we get to the GP’s office, and everyone is doom and gloom. Nobody smiles. Nobody talks to us. They just pull our chart sans questions. We wait a few minutes until the sad-faced nurse calls us back. The GP comes in and, after the perfunctory “how are you?”s, gets down to business. The IPS showed a 1 in 70 chance of having a child with Dow.ns. Normally for a woman my age the odds are 1 in 150.
Oh.
We digest that. We calculate that in our heads (a 1.42% chance of having a child with Dow.ns – greater than 97% chance of having a “normal” child). Okay.
The doctor then proceeds to go through the various options, and the reason to pursue amnio. We already knew that we didn’t want to risk amnio’s equally small but very real possibility of causing a m/c. The doctor proceeds to carp on about the challenges of raising a “Dow.ns child”, how it will take a toll on our marriage/finances/career (duh! having a child does that too…). She brings up the spectre of ter.min.ation. More than once.
Now my GP is a smart cookie. She’s been through the whole IF game with me. She knows how much this baby is wanted. And she mentions termination… yikes.
We get home from this appointment, only to receive a call from the High Risk Unit (the place where I will give birth). They were just checking in to see if I had the results (yes), and to reassure us that it was our choice as to how to proceed. The thing they did offer was genetic counselling, to help us decide what to do, and how we wanted to proceed (also to figure out what kind of support might be out there in the case that our child did have Down.s). Overall, the tone was so much better, so much more positive, so very gentle… I am in love with the HRU doctors. We made the appointment for genetic counselling for the end of the week.
Fast forward to the following Friday. We are in the genetic counsellors office. We give her our position (8 years of IF, 3 m/c, IUI x2, and no amnio). She is incredibly respectful and supportive. She then proceeds to go over the test in detail.
We go through the basic demographic information. WB suddenly asks “Well, Tally’s weight isn’t on this form… would that make a difference to our results?” The counsellor considers this, asks for my weight and gets the results recalculated.
Everything stays the same, except…
The chance of having a child with Down.s changes – to 1 in 2,100. Wow. it’s amazing what extra weight can do to your odds…
That was the big scare. Since then we have heard Flea’s heartbeat (152 bpm almost two weeks ago). My belly has suddenly expanded. My hips hurt when I sleep on my sides. I am waiting until the 21 week anatomy scan before I get too terribly excited (I know, I know… I should be excited now. But I don’t know how!! Call it “survivor’s guilt”, if you like… I think it might be that kind of thing happening to me. Another post for another day). We will be finding out the Flea’s sex. I don’t know if we’ll broadcast it, though…
Anyway, that’s the latest episode in the soap opera that has been my TTC life. Hopefully next time you tune in, I’ll have something truly upbeat (without the drama drama drama). 🙂