So far he was only on oxygen. The first time I held him I cried and cried. She was given a Smith Lemli Opitz Syndrome Prenatal Diagnosis as an initial likelihood and possibility. “All my life I had dreamed of becoming a mother. However, all studies on survival rates show that there is a high mortality rate for children with Trisomy 18 before or shortly after birth. The doctors informed me that he would never leave the hospital and most likely die by the end of the week; they also said he would be on all kinds of machines to keep him alive. There is no cure. My little boy that I had dreamed of and had worked so hard for was going to die and there was nothing anyone could do. All Rights Reserved. I went back home and waited impatiently for the results for the amnio, which usually took around 10 days. Every baby is unique. I went to bed that night wondering if I would ever see my baby or if he would die that night.”, “The next day was so much better than the day before, because I got to see my precious baby boy. Had nuchal scanning results came back with 1:49 chance of having Edwards Syndrome. He wanted to perform another amnio because he would like to deliver early. “We got to take him home 3 days later and he was perfect when we left the hospital, he had an EKG on his heart and it said he had a VSD. Sadly, most babies with Edwards' syndrome will … Edwards' syndrome, also known as trisomy 18, is a rare but serious condition. I don’t look at their faults and what might be different about them because I know what it is like to have a child who is different. Trisomy 18 is also known as Edwards’s syndrome which is marked by the presence of one extra chromosome 18. No one would tell me what was wrong with my son and I was getting upset because I could tell by the way everyone was acting that something was wrong.”, “When we got back to my room a pediatrician came in and informed me that my son had Trisomy 18. That is all the motivation I need to be a better person. The extra copy of chromosome 18 is already present at the time of fertilization and results from random errors in cell division. If you think this page contains objectionable content, please inform the site administrator and include the link to the page in question. I remember when they pulled Bryce out, he was not breathing so they had to rub him a lot and then I heard him cry. So my doctor rushed in and asked me what I thought about an emergency C-section. This means that there is no hard and fast rule about what Trisomy 18 will mean for a specific child. Just as children with Down syndrome can range from mildly to severely affected, the same is true for children with Trisomy 18. This is when only parts of chromosome 18 are diagnosed as abnormal. “I was devastated now because I could not believe that my baby could have Down syndrome and they explained to us about Down’s, Trisomy 18 and Trisomy 13. Bryce was in the NICU, on only oxygen.”, “That night was hard because I wanted to see him but I could not. During the amnio, they performed an ultrasound and found that Bryce also had a short femur bone which is a marker for Down syndrome. All Rights Reserved. Common Problems associated with Trisomy 18 can include: To read more about the general characteristics of Trisomy 18 for impacted children, you may find the following review articles helpful. According to the United States National Library of Medicine, individuals with Trisomy 13 often have heart defects, brain or spinal cord abnormalities, very small or poorly developed eyes, extra fingers or toes, a cleft lip or palate, and weak muscle tone.. 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