In February we found out that we are having another boy! We are very excited to even up our numbers. At the ultrasound they thought something might be wrong with his heart, so they scheduled us to get a fetal echocardiogram at Primary Children's hospital, we had that visit the first week in March. We found out there, that our baby has hypoplastic left heart syndrome, or HLHS, which basically means that the left side of his heart is underdeveloped, so it's kind of like he has a half of a heart. They can do a series of 3 operations to make it so the right side of the heart takes care of the left side's duties. The first operation will be 3-5 days after he is born, and the second is at 4-6 months, and the third is around 3 years old. They told us that he has a 60% chance of survival to age 5.
Obviously this news came as a bit of a shock, we are feeling overwhelmed of course, but we are hopeful for the best possible outcome. We also have felt so much love and support from our families, that we know we won't have to go through this alone, which is a huge blessing. We are just planning on taking things one day at a time, and putting our faith in God that whatever happens will be the best for our family.
If you know of anyone that has had a baby with HLHS, please let me know, I would love to talk to some other people that have gone through this.
This blog will probably turn into more of an update on the baby's status, so that I won't have to tell a million people the same thing over and over. We appreciate everyone's concern and prayers for our family, I never thought that I would have a trial like this in my life. Feel free to check back, we have another appointment the 8th of April for another fetal echocardiogram at Primary Children's.
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