I feel horrible that i have not posted in so very long. It has been a whirlwind of a year. A very worrisome year. When I posted my last entry, we still did not know if our rainbow was a boy or a girl. We had no clue if she was going to make it. What happened 2 months later was very scary.
On the year anniversary ofour angel Mason’s birth, I was admitted for the pregnancy with our rainbow because of the resistance in the cord. They wanted to administer the Steroid shots for her lungs and then I could go home. They had previously decided against them, so when he admitted me, it scared me. Plus I was put in a a labor and delivery room on the day of his birth a year later. I was an emotional mess. The midwife wanted me to take some tiny pills to calm me down. they were homeopathic, but I did not want to risk anything. I was 25 weeks along. I still had a long way to go. They told me I would be there two days.

After two days, the doctor did a doppler ultrasound and noticed that my amniotic fluid had increased. So he sat us down and told us that he was admitting me for the duration of the pregnancy. I couldn’t believe what I was hearing. I had to stay in the hospital for 15 weeks? Yes I wanted my baby, but two days in that hospital was driving me nuts. The german way of eating is horrible for Americans. No TV in English. Nurses did not speak English. It was torture. But I did it. For 5 weeks.
At an ultrasound, as the doctor looked at the resistance in the cord I noticed some excessive coiling in the cord. I asked him if he could go back and measure how many coils were in the cord. There was 3 in 7.5cm. That is 2 per 5cm. Too many. It is part of the reason Mason died. So needless to say, I freaked. I was 30 weeks…same gestation he died. Everything was looking bad at this point. Blood flow to placenta, cord resistance, brain profusion…all of it was going down hill. it was just a matter of time before he delivered her, until we saw the twisting of the cord. He wanted to go two more weeks, but I couldn’t wait. I could not chance it. My emotions got the best of me. My nerves were shot. I could not lose this precious baby.
The doctor got word that I was pretty much losing my mind, so he came and talked to me. He told me because of my emotional state and the baby’s cord that he was going to schedule a C-section in 2 days time. However, he wanted a chance to go home and research the cord accident that Mason had died of and was presenting in this baby.
The next morning he came in while I was having a NST or CTG as they call it here. He told me, “Mrs. B, We will be taking the baby tomorrow morning. You are correct and this baby needs to be delivered.” I was terrified. I had been researching premature birth. I had researched statistics of babies born at 30 weeks when Mason died. I knew the risk. I knew the numbers. So we did it.
At 8:40am on April 30, 2014, our precious Paxton Hazel was born. She weighed 3lbs 4oz. She was 15 inches long. I had to wait a couple of hours to go see her, but my husband went to see her while I was in recovery. He brought me back a photo. She was so red, so tiny, so beautiful. I was finally moved to my room and I was ready to go see my baby. The midwife told me I had to wait until the next day because I needed to recover from the csection. Had this woman lost her damn mind? I was going to go see my baby. There was no one that could stop me. I could understand if the baby was in danger, but my husband could go see her….so I knew she was okay. So my husband had to take the Midwife out of the room and explain to her that she was going to have to let me go, that I would not give up until I saw our little girl. So they got me a wheelchair and I painfully made my way into it. I was in tremendous pain, but I had to see her. Seeing her was worth any amount of pain I might suffer doing so.
I was instantly brought to tears when I saw her. She was so tiny. So fragile. She had all these lines and tubes. She had a CPAP on. The breath was knocked out of me. This was the first days of many that would be spent sitting next to her little incubator praying.


Her first couple of weeks she spent on the high side of NICU, she flew through all the things she needed to to go down to the next level. She was breathing on her own, she was doing well. The doctor called Paxton, her “Nerd”. This baby was doing so well. Then they moved her down to the next level. That’s when things got rough. Paxtons heart rate and oxygen levels kept dropping. She could not remember to breathe. She had to be stimulated so very often. They finally decided to do an EEG to check for issue with the brain. She had spikes, as they called it. There is not much NICU lingo I know because of the language barrier here in Germany, so forgive my small NICU vocabulary. I can only explain the way it was explained to me. Okay, so they found spikes in the brain waves. They determined she was having Neonatal Seizures. So they put her on Anti-seizure meds. After a week or so, it was not helping. They finally decided it was time to put her back on the CPAP. Maybe it was Apnea of prematurity? After three days of CPAP, she finally remembered to breathe. She only needed a little oxygen to keep her oxygen up. Many more days were spent in that part of NICU.
Around June 14th, she was moved to the regular Peds Nursery. This was our last step before home. I couldn’t wait, but I was so scared. The day they asked me if I was ready for her to come home I asked them, “Are you sure?”. Most NICU parents can’t wait for that day. Me? I was trying to have them keep her longer. She was 39 weeks Gestation when she came home on July 2nd. It was an amazing day. I was able to walk out of a hospital with a baby in my arms….like I should have the previous year. God watched over us and our little girl. We had so many prayers being said for us. So many thoughts, so many good vibes. It was amazing.

There has been little issues along the way. Paxton failed her hearing test upon release. She failed them a second and third time a month later. So we worried about her being deaf. It turned out she only needed time or she was ignoring us. She hears fine now. She also has an issue with Hypertonia. Too much muscle tone. So we have therapy twice a week and I do her exercises at home. There is a lot of work with it and a lot of work ahead of us. Paxton also has a cataract in her eye that I noticed before discharge. It was so tiny, that even the eye doctor missed it, until I pointed it out. It has gradually grown larger, but it is only in one eye and it is still small enough so that she can see around it. We dilate her eye daily to help. We are trying to avoid surgery while she is this young, because it is just too much on a little baby. Then there is the problem with her kidney that was noticed before birth. They told us she had Hydronephrosis, swelling of the kidney, but now it may be a number of things. She is till too little for an MRI the doc says, so we are waiting. He said it could be a cyst or hydronephrosis. He also said it could be a third kidney. We don’t want to do anything until there are issues. She needs to wait for anything that will require he being put under. So it is a waiting game.
She is beautifully amazing. She has healed our hearts so much. I could go on forever about this little fighter, but I must close because she is a demanding little booger.
