I'm talking about testing for birth defects.
At my last OB-GYN appointment, Aaron and I were presented with the choice of pursuing birth defect testing. The first blood draw has to be between 10 weeks and 13 weeks and 6 days. The second blood draw has to be between 15 and 20 weeks of pregnancy. The two blood test results are then combined and we are given our baby's risk assessments for down syndrome, trisomy 18, neural tube defects (such as spina bifida), etc.
With Ella, we were also given the choice to pursue testing, and we opted not to. We had no worries whatsoever.
And, really, this time around I don't have any worries.
But, at the same time, I sure would love to do the testing and have everything come back fine.
But, what if it didn't? Aaron and I would not consider aborting our baby. No way, no how! Our doctor said it's good to know in advance to mentally prepare ourselves, rather than waiting the day of our baby's birth to find out something is "off."
Even though I agree with that idea, I am a firm believer that this baby is a gift from God. He is entrusting us to be this child's parents. Be it a boy or a girl, mentally healthy or not, it is the child God intended for us to raise in this family. I don't need to mentally prepare myself for that.
Plus, the statistics are very low.
According to March of Dimes, the following statistics hold:
- At age 25, the risk of having a baby with Down syndrome is 1 in 1,250.
- At age 30, the risk is 1 in 1,000.
- At age 35, the risk is 1 in 400.
- At age 40, the risk is 1 in 100.
- At age 45, the risk is 1 in 30.
I'm 27 years old.
Trisomy 18 is a harder pill to swallow. Children born with Trisomy 18 suffer severe mental retardation, heart defects and other health problems. They usually die early on: 30% by 1 month of age, 50% by 2 months of age and 90% die by 12 months of age. Sad, huh?
But, it is still not my place to "terminate" a life. Only God can give life and take life away.
My OB-GYN was such a strong advocate for testing - it made me second guess myself! He told me based on this ultrasound, he does not see any red flags, but that he always tells his patients to test. Well, we'll see if this patient decides to! :)
And, if you recall, I had some testing done before my IVF cycle, and it was determined that I am a carrier for cystic fibrosis. That came as quite a shock! Aaron did preliminary testing, and thank God, he is NOT a carrier.
However, because insurance wouldn't cover the more extensive testing and we were already forking out thousands of dollars for infertility treatment, we chose not to pursue the more extensive testing. Our doctor told us that given that I'm a carrier and Aaron's preliminary testing was fine but further testing wasn't done, we have a 1 in 500 chance of having a kid with cystic fibrosis.
Yet some more numbers to worry about.
I refuse to live in fear for the next six months, though. There are always scary statistics to throw at vulnerable people, especially pregnant women. Heck, each of us carry a statistic over our heads every time we get in our car.
So, even though our minds aren't completely made up on birth defect testing, writing this post helped me see where I really stand. Thank you for listening. :)






