Sophia's favorite sleeping position is to sleep with her little arms above her head. If we try and bundle her up and she cannot move her arms she gets SO MAD.
Friday, July 30, 2010
Sleepy Baby
Sophia's favorite sleeping position is to sleep with her little arms above her head. If we try and bundle her up and she cannot move her arms she gets SO MAD.
Tuesday, July 27, 2010
Friday, July 23, 2010
Saturday, July 17, 2010
Sophia Grace is here!
After about 14 hours of labor, on July 8th 2010 at 2:07pm our beautiful baby girl Sophia Grace made her way into the world. She weighed 6 pounds 13 ounces and was 20 inches long. When she came out Sophia was a tiny bit blue so the NICU nurses took her into the hall to take a better look but she pinked up very quickly and was breathing fine on her own. I got to hold her for a couple minutes but then she was admitted to the NICU where her daddy kept a very close eye on her and stayed with her for all of her tests. The Cardiologist did an echocardiogram shortly after Sophia's birth and the diagnosis was exactly what we had anticipated. Sophia's pulmonary valve still looks great for a baby with TOF and her oxygen saturation is at 100 percent for now. Sophia did so well that on Friday night after one full day and night in the NICU she was released to my room. Kyle stayed up all night just watching her. He is already such a good dad! On Saturday afternoon we brought Sophia home and things are going really well. She already sleeps great during the night and she only cries when she is hungry or getting her clothes changed. We love our little girl so much! She is truly an angel.
Monday, June 7, 2010
What is TOF?
With Sophia's due date rapidly approaching I decided that I should update everyone on how she is doing and what is expected in the months to come. At our last doctors appointment, May 25th, we had an ultrasound done that showed Sophia is growing beautifuly and has already reached the five pound mark! The doctor said she will probably be between seven and eight pounds which is GREAT! Each time we get to see her Kyle and I become more anxious to meet our little girl. As of right now Sophia's heart is looking really good for a baby that has TOF, her pulmonary artery is only the slightest bit narrow so our cardiologist thinks we will probably be able to wait until Sophia is about four months old to do her surgery which is great, because she will be much stronger by then. We will have another fetal echo done to observe Sophia's heart next week, so please continue to pray for us. If everything goes as planned Sophia will only have to stay in the NICU for a couple of days and then we will be able to bring her home, we will be seeing Sophia's cardiologist biweekly to keep a close eye on her condition and we will see how everything plays out and hopefully she will not need surgery before her fourth month. I am posting a picture along with the definition of Tetralogy of Fallot below so everyone can get an understanding of her condition. Thank you so much for all of your prayers and support!
What Is It?Tetralogy of Fallot occurs in about 5 out of every 10,000 babies. There is no known reason for this. It just happens. Tetralogy of Fallot has four key features.
Large Ventricular Septal Defect (VSD) - A VSD is a hole in the part of the septum that separates the ventricles—the lower chambers of the heart. The hole allows oxygen‑rich blood to flow from the left ventricle into the right ventricle instead of flowing into the aorta, the main artery leading out to the body.
Pulmonary Stenosis - This is a narrowing of the pulmonary valve and the passageway through which blood flows from the right ventricle to the pulmonary arteries. Normally, oxygen-poor blood from the right ventricle flows through the pulmonary valve into the pulmonary arteries and out to the lungs to pick up oxygen. In pulmonary stenosis, the heart has to work harder than normal to pump blood, and not enough blood can get to the lungs.
Right Ventricular Hypertrophy - This is when the right ventricle thickens because the heart has to pump harder than it should to move blood through the narrowed pulmonary valve.
Overriding Aorta - This is a defect in the location of the aorta. In a healthy heart, the aorta is attached to the left ventricle, allowing only oxygen-rich blood to go to the body. In tetralogy of Fallot, the aorta is between the left and right ventricles, directly over the VSD. As a result, oxygen‑poor blood from the right ventricle can flow directly into the aorta instead of into the pulmonary artery to the lungs.Together, these four defects mean that not enough blood is able to reach the lungs to get oxygen, and oxygen-poor blood flows out to the body. So TOF does not mean the heart is failing, it really means the child is suffocating. Babies and children with Tetralogy of Fallot have episodes of cyanosis (si-a-NO-sis), which is a bluish tint to the skin, lips, and fingernails. Cyanosis occurs because the oxygen level in the blood is below normal. Babies and children can also have what are called TET spells or blue spells when their oxygen levels get too low and the child may quit breathing. Ever heard of a "blue baby" if so, this is what they were referring to. For this reason, the child must not get too upset, crying can easily bring on a tet spell. Tetralogy of Fallot must be repaired with open-heart surgery, either soon after birth or later in infancy.
Complete Repair -To do a complete repair, the surgeon closes the ventricular septal defect with a patch and opens the right ventricular outflow tract by removing some thickened muscle below the pulmonary valve, repairing or removing the pulmonary valve and enlarging the peripheral pulmonary arteries that go to both lungs. Sometimes a tube is placed between the right ventricle and the pulmonary artery.
What Is It?Tetralogy of Fallot occurs in about 5 out of every 10,000 babies. There is no known reason for this. It just happens. Tetralogy of Fallot has four key features.
Large Ventricular Septal Defect (VSD) - A VSD is a hole in the part of the septum that separates the ventricles—the lower chambers of the heart. The hole allows oxygen‑rich blood to flow from the left ventricle into the right ventricle instead of flowing into the aorta, the main artery leading out to the body.
Pulmonary Stenosis - This is a narrowing of the pulmonary valve and the passageway through which blood flows from the right ventricle to the pulmonary arteries. Normally, oxygen-poor blood from the right ventricle flows through the pulmonary valve into the pulmonary arteries and out to the lungs to pick up oxygen. In pulmonary stenosis, the heart has to work harder than normal to pump blood, and not enough blood can get to the lungs.
Right Ventricular Hypertrophy - This is when the right ventricle thickens because the heart has to pump harder than it should to move blood through the narrowed pulmonary valve.
Overriding Aorta - This is a defect in the location of the aorta. In a healthy heart, the aorta is attached to the left ventricle, allowing only oxygen-rich blood to go to the body. In tetralogy of Fallot, the aorta is between the left and right ventricles, directly over the VSD. As a result, oxygen‑poor blood from the right ventricle can flow directly into the aorta instead of into the pulmonary artery to the lungs.Together, these four defects mean that not enough blood is able to reach the lungs to get oxygen, and oxygen-poor blood flows out to the body. So TOF does not mean the heart is failing, it really means the child is suffocating. Babies and children with Tetralogy of Fallot have episodes of cyanosis (si-a-NO-sis), which is a bluish tint to the skin, lips, and fingernails. Cyanosis occurs because the oxygen level in the blood is below normal. Babies and children can also have what are called TET spells or blue spells when their oxygen levels get too low and the child may quit breathing. Ever heard of a "blue baby" if so, this is what they were referring to. For this reason, the child must not get too upset, crying can easily bring on a tet spell. Tetralogy of Fallot must be repaired with open-heart surgery, either soon after birth or later in infancy.
Complete Repair -To do a complete repair, the surgeon closes the ventricular septal defect with a patch and opens the right ventricular outflow tract by removing some thickened muscle below the pulmonary valve, repairing or removing the pulmonary valve and enlarging the peripheral pulmonary arteries that go to both lungs. Sometimes a tube is placed between the right ventricle and the pulmonary artery.
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