Our doctor's office had sent us over to the Maternal Fetal Specialists office to perform a sequential screening. A sequential screening is a two-part test that screens for fetal Down syndrome, trisomy 18 and open neural tube defects. On September 7th they basically they drew my blood to send off for several lab tests and then we'd have to go back for an ultrasound so they could take measurements of the baby's limbs and organs. Once they'd taken my blood, we'd gotten test results a few days later saying everything appeared normal. We only had a 1 in 5,600 chance our baby could have Down Syndrome - this number sounded scary to me, but nurse assured me it was normal. There were other tests ran too, but this number was burned into to my memory.
We were back again on September 16th to have the second part of the screening. My husband and I had already been irritated by sitting in the waiting room for an hour and now the ultrasound was taking forever too. Of course I was in love watching our little girl on the small screen in that dark room, but this was not helping my PTO available at work (hence shortening my PTO available for maternity leave). The nurse got through with measurements and gave us a few pictures she'd printed for us and stated the doctor would be in shortly to go over everything. Everything seemed routine and normal as she smiled and exited our room.
After a few minutes the doctor came in and sat down next to us. She stated that the baby's neck was not measuring thick enough and that they wanted to give us the opportunity to run more tests. I was confused and felt a lump swelling in my throat. The doctor said this marker made our odds 10% of what they previously thought for Down Syndrome. We were now 1 in 560 - gulp. She told us that an amniocentesis procedure could determine 100% if we were about to face the toughest road ahead. She explained the procedure and the risks involved. They'd stick a needle through my stomach and remove a small amount of amniotic fluid, which contains fetal tissues, extracted from the amniotic sac surrounding the baby and the fetal DNA would be examined for genetic abnormalities. The risks mentioned were serious complications resulting in miscarriage and other possible complications included preterm labor and delivery, respiratory distress, postural deformities, fetal trauma and alloimmunisation of the mother. She said most patients say they go through the procedure for a few reasons: pregnancy termination is still an option and peace of mind/acceptance of results. She left us to discuss this option and for us to decide if we wanted to proceed or to leave it as an unknown until the baby's arrival.
I've never been so scared in my entire life. I felt like I'd just went over the biggest drop on Six Flag's Goliath roller coaster - my stomach had butterflies and I thought I might throw up. I would never forgive myself if we go through with the procedure and something happens to the baby, but on the other hand would I be able to forget until her delivery or would I be a train wreck until she's here and we know for sure. So many 'what if' thoughts were running through my head in those short minutes we were alone. When the doctor came back in it seemed like it was the best idea for us, in order to move forward, that we have the amniocentesis performed. As I lay there while they prepped me, I felt our baby's first movements (exactly 13 weeks on Sept. 16th). It was still a happy pregnancy memory and even though I'd been crying I remember feeling amazed that there is a baby doing somersaults inside of me. The amniocentesis didn't hurt that bad since they'd numbed me up, but while my eyes were closed I heard the pop of the needle going through my belly. Ewwy!
The results took two weeks to test the baby's DNA. The waiting game was the hardest part to handle. I really didn't want to talk to anyone about it...not co-workers, friends nor family. I spent a lot of the next two weeks crying. It was a self reflection for me as well. It made me wonder how things would turn out if I had a baby with a genetic abnormality and how I would react if I in fact got that news. Would my life or marriage ever be the same? Matt told me 'don't worry until we have something to worry about'. And still I cried. He told me a few days later that I was making it hard for him to stay strong, and I started to feel guilty that he was right. He was being the rock for our growing family and I was clinging to him for every ounce of hope. I tried to keep my concerns to myself until we got some news since I was really turning into a Debbie Downer. Plus, the stress I was going through was probably not healthy for the baby either. It was hard to keep a smile on at work and outside the house. It was hard to keep my faith.
The days passed slowly, but finally we got a voicemail from the Specialists office. My heart was racing. We would finally know, without a doubt. I closed my office door and dialed as quickly as my fingers would move. The nurse's voice sounded like an angel when she said the results are normal. They also confirmed with her DNA that the baby was a girl and that our pink nursery was a safe decision. I called my husband and my mom to spread the wonderful news. The boulder I'd been carrying on my shoulders for 14 days had now disappeared. I thought to myself I need to try and enjoy being pregnant and nothing else matters, but that our little girl is healthy. It was an amazing feeling and a relief to everyone who knew. However, it really made me wake up and appreciate the battles some families can face. I follow a blog about one of these families journey's because it helped me cope during my toughest times throughout this period of my pregnancy: http://www.kellehampton.com/p/about.html
Having pregnancy hormones already made me think of my deceased grandmother often. We definitely had an angel watching over us - love and miss you Grandma!
![]() |
| May you always have an Angel to watch over you |



