When My Daughter Was Diagnosed With a CHD
It all started when we went for our 12 week nuchal translucency scan, where they measure the fluid behind the neck. The doctor came into the room and we could feel the discomfort. He said our baby’s fluid behind the neck was measuring double the norm. This was a red flag for either Down syndrome or a congenital heart defect (CHD). He sent me to get blood work the same day. Ten long days later, I got the results that our baby tested negative for Down syndrome and the other genetic stuff they tested for, and we found out she was a girl! We were so excited and thought we were in the clear since we have no history of CHDs on either side of our family.
Fast forward eight weeks when we went for our 20 week anatomy scan. When the doctor came in, we got that same feeling. She said, “All organs look good, except her heart. Unfortunately, she has a heart defect which puts you in that 1 percent.” It was one of the worst days of our lives. My world shattered as I tried to process these foreign words: “congenital heart defect.” They weren’t quite sure how severe her defect was at that point and we were referred to a high risk OB and then a pediatric cardiologist.
When we saw the pediatric cardiologist, he broke the news that she does indeed have a complex heart defect which is very rare. Once again, my heart sank to the floor after hearing this news. Emersynn has congenitally corrected transposition of the great arteries (ccTGA or l-tga), a large ventricular septal defect (VSD), pulmonary stenosis (PS) and dextrocardia. Out of the one percent who end up with a heart defect, 0.5 to 1 percent end up with ccTGA. That is how rare the defect is. Only 5,000 to 10,000 people in the US have this condition. After leaving the cardiologist that day, my husband and I looked at each other in the car and looked back down at the paper that had a drawing of our baby’s heart. We were so confused and wondered if we would ever be able to understand the anatomy of our little one’s heart. Overwhelmed was an understatement.
We live in Fort Myers, and, unfortunately, the hospitals around here are not equipped to deliver babies with severe heart defects. We were given the choice to deliver in Miami or Tampa. Although Emersynn’s ped cardiologist (who is exceptional) is in Tampa, we decided to deliver in the Miami area at Memorial Regional Hospital (connected to Joe DiMaggio Children’s Hospital). This decision was made through countless hours of research after finding out about her heart condition (this is how I essentially coped with the news). During our research, we came across a Facebook page for a boy who has the same defect. I reached out to his mother who led me to a private Facebook group for Emersynn’s particular defect. Only immediate family or the person affected is allowed to join this group. It turned out to be an extraordinary group that helped us tremendously! We found out, through this group, that a top surgeon for Emersynn’s defect was mentoring at Joe DiMaggio Children’s Hospital, and was there about once per month. This made us feel comfortable, as her defect is so rare and there are only a handful of surgeons who are successful in doing the major surgery that she will eventually need in the future.
We were told throughout the pregnancy that Emersynn would need a shunt within a week of birth, as they thought she wouldn’t get enough blood to her lungs. She would then need a major surgery called the double switch down the road. I ended up delivering on November 22, 2016 and she was a big baby, which defied odds. They watched her closely in CICU for three days as her PDA closed. Once it was closed, they monitored her saturation. She proved to be miraculous and was sent home on day four with no surgery and thriving.
Emersynn just turned 1 year old and has not had any surgery thus far. She is defying all odds and doing amazing. She is growing well and hitting all of her milestones on or before she is supposed to. This little girl amazes us more and more every day. She is such an inspiration to everyone around her and is a strong little warrior. Emersynn will need a major open-heart surgery in the next few years. The doctors say her body will tell us when it’s time. This is a very risky surgery and hard to put her through when she is currently doing so well. We know she will eventually need this surgery to continue to thrive and give her the best life. Some days, I hardly think about her heart defect, and other days it totally consumes me. It’s something I wouldn’t wish on anyone. However, we wouldn’t change Emersynn for the world. We believe we were chosen to be this sweet girl’s parents, and we are handling the challenge. Through this experience, we have learned to take it one day at a time.
We want to hear your story. Become a Mighty contributor here.
Banner image via getty: mmpile