I remember asking my doctor about a certain test that they do during the actual sonogram (they take a sample of your blood and look for fluid on the neck of the baby during the sonogram). I had one done with both Ella and Hunter, but so far I hadn't had one with this new doctor. He told me that it was pretty expensive and that he doesn't automatically offer it because most women don't want to pay the extra money. He also told me that this certain test checks for birth defects and really only aids in helping the woman decide if she wants to keep the pregnancy. I hadn't realized that this was the main purpose for doing this test and I immediately said that it wouldn't matter because I wouldn't have an abortion if I found out the baby had a birth defect.
This was a moment that I remember very clearly and it comes to my mind as a tender mercy. To know that no matter what, I wouldn't have changed the outcome, to have complete clarity in those times of heartache and mourning, that I could not have done anything different and that I would not have done anything different even if I did have the choice.
3 comments:
Aww that is a great story. It is so true though, regardless of the test, we wouldn't change anything because these little spirits are perfect and bless our lives tremendously!!! I LOVE YOU LILS!!!
PS I never got any sweet profile shots of Eke either. He always hid his face. But his man parts.... ohh no shame there!!!
We got to have one last look at Olivia around the 38 week mark of my pregnancy. My doctor couldn't feel her very well and so ordered the ultrasound to see if she was head down. She was, so yay for that. As for the test...we did the triple screen early on in the pregnancy only because my doctor recommended it. I failed it. It came back high risk for Down Syndrome. We had a level II ultrasound when I was 22 weeks and Olivia showed no soft markers for any problems at all. I wouldn't have made any other choice other than to have her either, but I'm glad my husband I never even had to have that discussion. I'm actually glad I got to have those blissful nine months, (and two years, really, since we didn't get O's diagnosis until she was older) just because it gave us time to get to know her without the extra baggage the syndrome can bring.
I love this series, by the way. Thank you for sharing your memories with us.
I never did any tests with Olivia...and it wouldn't have changed a thing! I enjoy these memories too!
Post a Comment