Apparently we were wrong. Our baby was sick. Her nuchal fold was measuring 15mm and there was a lot of fluid in her chest cavity around her heart. To make our long story shorter, we were told to wait for more answers and to come back at 15 weeks for a follow up ultrasound and possible amniocentesis test. November 30th we had a follow up scan. Again, the doctor came in and told us that things had gotten worse, much to our dismay. We (and so many others) had been praying so hard for the weeks leading up to the appointment with the hope the our God had performed a miracle for our sweet baby. Because the ultrasound looked worse the doctor advised us to do an amnio to find the exact issues we were facing. Again, to make this a little shorter, the results came back that our baby was a girl (woohoo!) and she had turner’s syndrome, meaning she was missing and entire X chromosome. We were told there was less than 1% chance that our baby would be born alive and that due to the severity of her disorder, her heart could stop beating at any time. She had already beat so many odds by making it past the first trimester and we were still praying for a huge miracle!













