Team Kaser Grand Slam Gender Reveal

Thursday, July 20 was the big day my appointment was at 4:30pm. My mom, sister, Theodore, and of course Brian came with me. In our package, I added a stuffed animal that could have the baby’s heartbeat recorded, so I could listen to it whenever I wanted and I figured it would be a fabulous gift to Theodore from his baby brother or sister. The appointment went fine except baby was not moving much. Baby Kaser was lying very low in my pelvis and seemed to be sleeping on the placenta. The ultrasound tech took a few images and then left and asked me to get up and walk around to see if we could get the baby to move to get some better images. After jumping up and down, walking around, laying down, standing up, baby was not moving more. The tech took a few more images and scheduled me for a recheck August 24 to get some better 3D/4D images of the baby since he/she would not move away from my placenta. Finally, the tech identified the gender and then we went home. Later with close family I threw a baseball to Brian and he busted open a ball of pink powder. Our baby was a GIRL!!! We were so excited and I thought it was a "she" all along.

Comments

Pulmonary Atresia with Ventricular Septal Defect (VSD)

To everyone that has prayed for Oscar. Please keep praying. Today at his fetal echo cardiogram we found out he has Pulmonary Atresia with Ventricular Septal Defect (VSD). What this means is that there normally is a pulmonic valve that opens and allows blood to exit the heart through the right ventricle. Oscar's pulmonary atresia valve is permanently sealed or absent. Along with that, the main pulmonary artery is very small about 1/4 of the size it should be and it is much smaller than the Aorta. Oscar also has fluid surrounding his entire heart which was not there on the August 1 ultrasound. His heart function is okay, but it is not good. During the 2 hour fetal echocardigram there were also signs of fetal arrhythmia of Oscar's heart rate dropping lower and more quickly then it should. Going forward we need your prayers for our son's heart. We believe in a God that heals and does miracles. We don't know if Oscar being born alive is going to be that miracle we are gi...

3 years

3 years today since Oscar left us and went to Heaven. I can't help, but replay his last days in my mind and vividly recall certain details. For any parent with a sick child whether that child was an infant, child, teenager, or adult those last days, hours, and minutes are such a blessing to have, but still so painful when you allow yourself to really remember them. You look back and you can't help, but wonder if you made the right decisions, did you push them too hard, why didn't you see how sick they really were. Those are things that after 3 years I still wonder and I am sure always will. To someone that hasn't lived through their child dying you are probably thinking that doesn't seem healthy, but for us that have lived through this I beg to differ that I think it is completely normal. You see as a parent you always want to do what is best for your child to make sure they are happy, healthy, and feel loved. My child is not here to think about those things prese...

Meeting some of Estella's Team

Brian and I headed for the MFM office Tuesday, August 1. Our appointment was at 10:45am and we got called back around 11:00am. Our ultrasound technician was wonderful. She was so kind and it turned out she lived in the same town we did. It was a long ultrasound and one where questions were asked, but answers were not able to be given. Estella was moving a lot during the first half of the ultrasound which was fun to see and good to hear her heartbeat (155 bpm). Throughout the ultrasound the technician had to leave from time to time to talk to the doctor and to see what remaining images he wanted. About 12:30pm the ultrasound was finally completed and into the room came the maternal fetal medicine specialist doctor and genetic counselor. The doctor told Brian and me that our baby had some significant birth defects: a bilateral cleft lip with possible palate involvement, a VSD heart defect, and Dandy Walker Malformation that affects the cerebellum in the brain. I sat on the ultrasou...

Oscar's Odyssey/Stella's Story

Search This Blog