I write this post not to be negative, or show how naive I was during the last two months of my life, and first two months of my baby's life. I write this post, because I still find myself in somewhat denial (if that is the right term..?) I don't understand how a completely healthy pregnancy ALL 38.5 weeks can take a turn for the worst in an instant. I have heard a couple times that it was because he was born at 38.5 weeks, and that his lungs weren't developed. That is false. His lungs were fine, in that sense. Believe me, once I got to PCMC that was one of the first questions that I asked. I asked if the fact that he was born at 38.5 weeks was the cause of this, and if his lungs were under-developed, they were not.
I always run through my head what I told my Doctor at almost every appointment after 20 weeks.. "just another boring day at the Doctor's office, nothing eventful to report here" and his reply would always be, "we like uneventful here." I always wonder, and think in my head if my "excitement" for an uneventful pregnancy lead Ryker to have this happen to him. Seriously, I know what you are thinking.. But that is what I think, ALL THE TIME. My pregnancy was so good to me. Besides being and feeling huge which is to be expected, I didn't have any symtoms. Maybe the ocassional indigestion. But I threw up ~maybe~ 3 or 4 times, never got swollen, didn't have high blood pressure (it actually improved) no gestational diabetes, even my headaches went away.
I just don't understand how such a healthy and happy pregnancy can change in an instant. No one will ever know what it is like, the feeling that has been consuming me, unless you have been there.
While in the NICU I met a whole bunch of parents, with babies that have different needs, different conditions, different prognosis, etc. I met parents that weren't as careful as they should be when they were pregnant. Sadly resulting in their baby needing NICU care. I also met parents that were just as or even more careful than I was that were also in the NICU. Doing everything right, and never forgetting to take a prenatal vitamin, avoiding certain foods, and drinks and still having a sick baby. I even stopped taking my anti-depressant, before I even took a pregnancy test. I wanted a healthy baby, and I wouldn't have wanted something that I did affect their quality of life.
The hardest thing that I kept hearing from almost every nurse while we were there was how sick my baby was. I mean, I knew he was sick but I hated hearing those words. Here comes the naive part of me. Okay, I'm not so sure if it was the naive part of me, or if it was the comfort from the priesthood blessings that I received. But I would hear
negativenot so positive comments from multiple people; Doctors, NNP's, nurses, & family members. I know they were just preparing us for the worst, but I honestly wouldn't listen. Again, here's my naive self.. I knew or had a feeling that everything was going to be ok. Looking back now, it kills me to look at his pictures. Thank goodness for medications that can sedate. Thank goodness that the wonderful people that took care of him could control his pain. He is honestly the strongest person I have ever EVER known, and he calls me his Mommy.
Since being home, I have had the strength to learn about PPHN {Persistant Pulmonary Hypertension Newborn} I am in complete shock. It is honestly amazing the things the medical field can do, and amazing that he is alive.
*Persistent pulmonary hypertension of the newborn (PPHN) occurs when a newborn's circulation system does not adapt to breathing outside the womb. While a fetus is in the womb, it gets its oxygen from its mother's placenta through the umbilical cords, so the lungs need little blood supply. There is high blood pressure in the lungs, so blood in the pulmonary artery is sent away from the lungs to the other organs through a fetal blood vessel, called the ductus arteriosus.
When a baby is born and takes its first breaths, the blood pressure in their lungs falls and there is an increased blood flow to the lungs, where oxygen and carbon dioxide are exchanged. The blood is then returned to the heart and pumped back out to the body. The ductus arteriosus constricts and permanently closes in the first day of life. However, in babies with PPHN, the pressure in the lungs remains high and the ductus arterious remains open, allowing blood to be directed away from the lungs.
PPHN is a rare, but life-threatening condition. It occurs most often in full-term or post-term babies who have had a difficult birth, or conditions such as infection or birth asphyxia, in which a baby receives an inadequate amount of oxygen during delivery.
*information taken from http://www.persistent-pulmonary-hypertension-newborn.com/Persistent-Pulmonary-Hypertension.html
Baby Ryker is doing extrememly well. We have been home for 3 weeks now. He is still on oxygen at night, and at nap time. But, he is on the lowest setting on his oxygen tanks. We are extremely thankful for all of the prayers that have been offered in his behalf. We are extremely thankful for the people that have donated financially to Ryker to help out with medical bills, and other financial obligations that were thrown our way while in the hospital. We are extremely thankful for all of the family members that have taken time out of their lives to help us and be with us, especially helping care for Dax. We are thankful for people that donate blood. Ryker didn't have to have many transfusions, but he did need some. We are thankful for the medical team at PCMC. We are thankful for their knowledge.
