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What's To Come...



I knew I was pregnant the moment I conceived. Call it a woman’s intuition or a case of mother-knows-best, but I knew. As the weeks went on and I could finally take a pregnancy test and receive reliable results, Brian and I stared at the giant plus sign and I said, “I told you so.” As things progressed, I also knew I was having another boy. Friends and family members would wink and say, “oooh, what if it’s a girl this time?” And I would smile and nod and join in the what-ifs, but I always knew deep down that Atticus would be getting a little brother. And when our doctor confirmed this at 16 weeks, I just shrugged at my own intuitive nature.

So when I got the news today about our son, I was shocked that I didn’t already know….

It all started at our 20-week ultrasound. It’s supposed to be a fun glimpse at the life growing inside, a check of basic anatomy, and a reassurance that all is well. For most moms it is. Our doctor found that our little guy had slightly dilated kidneys, but she wasn’t worried about it too much. Even so, she sent us off for a level II ultrasound the following week, just to make sure that it wasn’t anything serious.

Brian offered to come with me, but I took my doctor’s reassuring words to heart and told him I’d be in and out in no time at all. He had just started a new job and couldn’t realistically make every single appointment. I did a little research into what dilated kidneys could mean, and learned that it could be anything from a temporary fluid build-up that corrects itself before birth, to a marker for Down syndrome. As I was lying on the table with the unbearably cold ultrasound jelly smeared over my abdomen, it became clear to me that the ultrasound tech was looking for other signs of Down syndrome. She measured the heart, the level of fluid behind the neck, the length of the arms and legs, and the shape of the pinky finger. She said very little as she worked, then told me the doctor would be in soon to talk with me. It turns out that in addition to the dilated kidneys, the baby also had an echogenic intracardiac focus. This is a calcification on the heart muscle that usually, like the kidneys, clears up on its own and isn’t a cause for alarm. But it’s also another marker for Down syndrome, and coupled with the kidneys, was therefore a cause for concern.


A genetic counselor came to talk with me and rattled off a number of statistics and testing options, ending with a recommendation that I have a DNA test that can definitively say whether the baby suffers from a chromosomal abnormality. She stressed that there was still less than a 1% chance that anything would be wrong and the test was merely a tool to give me peace of mind. The results would take two weeks and she’d call me when they came in.

Enter the longest two weeks of my life. I must have googled every variation of the words “soft markers for Down syndrome” a thousand times. Sometimes the results made me feel better, more often they sent me into a tailspin of worry. In these two weeks, I learned that my friend Susan was in the ICU after a horrendous car accident and every member of our family had a terrible bout with the stomach flu. It was a dark time.

I finally got a call from the doctor and I rushed to the phone, expecting results. Turned out my sample was somehow insufficient and we needed to redraw blood and begin the waiting process all over again. I tried to keep my mind off the waiting. I read, played music, absorbed myself in work, all to avoid thinking about this test and its results. People I confided in told me to remain calm; that everything happens for a reason. Since I’ve never believed much in the idea of destiny, their well-intentioned words did little to comfort me. And then I got a call today that will forever change my life.

Our second child has Down syndrome. 

The news was mind-shatteringly, heart-wrenchingly painful. I managed to cycle through a wide series of emotions in the matter of minutes. I grieved for the "normal" child I expected. I cursed whatever higher power would place this on our shoulders. I stared dumbfounded at the wall thinking that if I remained still long enough, the room would stop spinning.

We were suddenly faced with a multitude of choices. According to recent statistics, 85% of prenatal Trisomy 21 diagnoses end in termination of the pregnancy. It crossed my mind for a moment, and should I have received this news at 12 weeks into my pregnancy, it would have been a viable choice. I can’t judge women who take this path when faced with such severe news, even when they are as far along as I am. The emotional, financial, and physical implications of raising a child with Down syndrome are mind-boggling. But for us, at 23 weeks along, this wasn’t a choice we could make. Our baby is no longer a clump of cells. I’d been feeling him roll and tumble in my stomach for weeks. We gave him a name. We gave him an identity. Termination was not an option for us.

Apparently there are waiting lists for infants with Down syndrome so the option of placing him up for adoption seems a legitimate choice. Despite all I said above regarding the true “life-likeness” of this child, he’s still an abstract idea. He’s no one I’ve met yet, and our bond has not developed. Somehow having this diagnosis now instead of after birth actually makes it harder for these reasons. I only had attachments to what this child could become, and I expected him to become something very different than he might ever be. That’s not to say that he won’t be amazing, but raising a child with Down syndrome poses a new set of limitations. I will likely never see him graduate from college. He probably won’t marry or have kids of his own. He will be either fully or partially dependent on us his entire life. And since the life-expectancy of an individual with Trisomy 21 is only 55-60 years old, I very well may outlive my son.  These are harsh realities, especially for parents already daunted by the task of raising a two-year-old in a new city, working new jobs, and starting new lives. We've been isolated and lonely for months now, and this news just makes us feel completely lost.

Nevertheless, I don’t think I can let someone else raise my child. I know that even if I did decide to give him up for adoption, I wouldn’t be able to bring myself to let him go when the time came. And despite my surprise at this new challenge when my intuition into every other aspect of this pregnancy seemed so strong, I do know for certain that I will love him no matter what when he arrives. And that’s worth holding on to.

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