Hi, I'm Christina. Wife, pet momma, and new momma to twin boys. I've been told time and time again that I should blog about our twin adventures.... so here we go!!
I'd like to use this first post to give you some background on how we got to the place we are in today and hopefully give some insight into the reasons for some of our madness. This is going to be a long one, so I apologize in advance.
From the moment my husband, Chase, and I discovered we were expecting twins, our lives have been turned upside down, sideways and every direction in between. Things were pretty smooth sailing throughout all of the first trimester. I spent my days working, resting and planning for babies. At our 19 week ultrasound we found out that we were going to be the proud parents of little boys- we were so ecstatic! I went into instant nesting mode and began registering, decorating , picking out names , etc.
At 21 weeks, our OB referred us to a maternal fetal specialist (Dr. Smith) for a routine exam since pregnancies of multiples are considered high risk. We were pretty excited because we knew that they used 3-D ultrasound technology and up to this point everything had looked pretty normal. Come the day of the appointment, we were all smiles and laughs throughout the ultrasound and had a million questions lined up for the doctor when she came in. Right way, we fired off some ridiculous question like "So doc, can we tell whether or not our boys are identical?". We quickly knew something was wrong when she took a breath and said "We'll get to that. We have a lot to discuss today". Over the next 30 minutes she unfolded our twins' story. She told us that our twins had a complication called Twin to Twin Transfusion Syndrome (TTTS). In layman's terms, it occurs when identical twins share a single placenta's resources unevenly. Our larger twin (twin A) was getting most of the blood supply and had an abundance of amniotic fluid. Our smaller twin (twin B) had little to no visible amniotic fluid. The suggested treatment was laser ablation surgery to attempt to create two separate environments for the babies. Success rate for the surgery was about 75% and we were told that without intervention we had 0% chance of delivering two healthy babies. The leading place for the surgery in the Midwest was the Texas Fetal Center in Houston. Within an hour we had a caravan of 7 people headed to Houston with us to try to save our baby boys.
The next few days in Houston were a living nightmare for Chase and I. TTTS has 5 stages of progression based on symptoms. We were considered stage II. We were told that twin B was the "donor" and was in a small sling-like amniotic sack with very little fluid. We were told that eventually, without enough amniotic fluid and blood supply, his body would start trying to conserve resources for his heart and brain so his less important organs would begin shutting down. Twin A had an abundance of fluid which was also dangerous because all of the pressure could send him into congestive heart failure. Again, we were given heart breaking statistics. We were told that there was less than 10% chance that we would have two living babies without medical intervention. Even if they did live without intervention, they would almost certainly have severe birth defects. If we did go into surgery, there was a chance of the placenta detaching sending me into labor or rupturing the amniotic sacks. That chance was increased, because my placenta was anterior, which is opposite of 90% of the surgeries that they performed. Instead of going in through the front, they would have to use a scope to guide them through my back. At 21 weeks there wasn't much chance for survival if we had to deliver immediately because it isn't until 24 weeks that a fetus is considered to be at the age of viability. We were introduced to terms like: poly & ogli hydroamnios, genetic disorders, and selective reduction. On top of the really scary stuff, we also found out that twin B had a small hole in his heart and an enlarged kidney. Twin A had choroid plexus cysts on his brain. All of these things sounded really scary, but were told that most of them alone were not cause for alarm because they normally resolved themselves. However, together they could indicate a genetic syndrome like any one of the Trisomies. They wouldn't operate until they ruled genetic disorders out so they drew lots of labs and we were sent back to the hotel for a few days to wait it out. Desperate for something to do, I asked the doctor how I could help. He recommended that I lay on my side as much as possible to increase blood flow and eat Greek yogurt at least 3 times per day. Studies had shown that the increased levels of protein from Greek Yogurt or protein drinks increased blood flow in some TTTS cases.
That night, in our hotel bed, Chase and I decided that we should designate the names that we had picked just in case the worse happened. Twin A would now be called "Aedan" and twin B would be called "Conor".
All in all, we spent two weeks in Houston. I started taking bump pictures and planning again because I knew that God had a perfect plan for us, and I just couldn't believe that it was going to be one that didn't include our boys. At first, we were waiting on lab results and the "inevitable" progression into the next phases of TTTS. The doctor told us that in rare cases, mild TTTS, resolved itself. He had never seen it happen in a stage II that looked like ours. But then, we saw something wonderful begin to happen... each day that we went in for our ultrasound, things looked BETTER. When we were diagnosed with TTTS, there was no visible fluid around Conor and 13cm around Aedan. By the end of the two weeks, we had over 2cm around Conor and 11-12cm around Aedan. We weren't out of the woods yet, but the doctors were scratching their heads and couldn't justify surgery without evidence that this was going to progress. We went home to be monitored twice a week without undergoing surgery. We could still operate up to the 26 week mark if things progressed to stage II or higher.
We continued to count down to 24 weeks. We knew if we could make it that far, our boys would have a chance. Right at 24 weeks I started having contractions and was sent to labor and delivery. They gave me the evil, evil "bag-o-mag" that helped control the contractions. NICU nurses came to visit us to give us the statistics for survival and prepare us for what a 24 week delivery would be like. They told us that chance of survival doubled at 27 weeks and chances or a sever birth defect decreased as well. After 4 days, my contractions were completely gone and the doctor was alright with me returning home. We went back home with a new goal of 27 weeks.
Chase ran out of things to do :) |
The days turned into weeks and everything seemed to be looking good. Our 27 week goal passed and we set a new 30 week goal. June 3rd marked our 30
week milestone. This was HUGE, it meant that our boys had a 98% chance of survival and there was almost no chance of birth defects. That was pretty good compared to the 50% chance of survival that we were facing at 24 weeks! We had our regular twice a week ultrasound and things generally looked good. They said that my placenta was "looking old", which basically just meant that there were spots that had calcified. They also wanted to watch Conor because he looked border-line anemic. June 4th started like any other day. I logged into work remotely, took my morning meds and was waiting to eat breakfast when the nurse came in to monitor the boys. After about an hour she came back and said that Conor's heart rate wasn't rising and falling like the would like to see. The nurses wheeled me over to our doctor's office so that they could look in via ultrasound. Nothing looked too suspicious, but my doctor was out doing rounds so they wanted to talk to her before they let me eat or drink anything just in case. I started contracting a little because I was so nervous and wasn't allowed to eat or drink while I waited. My doctor couldn't come to my room right away because she was delivering at another hospital that day, so she asked the nurses to check to see if I had dilated anymore. The nurse pulled back a glove full of blood when she checked. She told me that I was dilated to 5cm and she felt the sack with her fingers. YIKES!!
Around 6 o'clock that night my phone rang, it was Dr. Smith. "Hey Christina, how are you? Are you ready to deliver some babies tonight?". A lump settled in my throat.... was I ready? Were the babies ready? The nurses immediately started prepping me for a C-Section. Everything was such a whirlwind. I remember seeing my dad, being wheeled into the O.R., talking to the Anesthesiologist, seeing Dr. Smith, and holding Chase's hand. Again, all I could do was pray for my baby boys as they operated. I felt a little pressure when they cut me open, then lots of tugging. A few minutes later they opened the curtain so that I could see our first baby being delivered. It was the longest minute of my life. I held my breath when I saw him lifted from my body. He was so tiny and still. Then, I heard the most beautiful sound I had ever heard- my precious Aedan screamed! "Thank God! He's breathing!" I burst into tears, looked at Chase, and said "He's crying!". They carried him out of my sight and began delivering Conor. He came out screaming!!! At that moment, nothing else in the world mattered to me. We had gotten both babies here! An hour or so later, the doctors came to deliver the good news that both boys were stable. They were 10 weeks early, so they would do some growing in the NICU, but they were likely to be just fine.
Aedan Ryan 3lb 11oz |
Conor William 3lb 3oz |
Our NICU stay lasted 9 weeks (63 days). It was one of the most difficult times in our lives so far, but each day was a gift from God and we made the most of it as best we could. I'm not going to reminisce about every detail of the time we spent there, but I will talk about it briefly (as brief as possible).
Conor 2 days old |
Aedan 2 days old |
Storybook time! |
Wearing our shades with Conor |
Aedan snoozing |
My first time holding Aedan |
We were at the hospital almost every waking hour, and when we weren't, we were calling to see how they were doing. They were too young to know how to eat, so I just pumped furiously and took the milk to the hospital so that they could tube feed it to them. The nurses became our saviors. They cared for our boys when we couldn't or didn't know how to care for them.
The pacifier swallowed Conor |
We finally got to hold both boys in the same room! |
The newborn hats looked huge |
Tandem kangaroo holding |
We brought them home one week before their due date on apnea monitors, but that was the only piece of equipment that our strong little guys came home with. A couple months later we found out that the enlarged kidney that Conor had on the ultrasounds has 0% function. by the grace of God his other kidney is fine, so he is able to live a normal, healthy life. They've been going steady ever since they came home and we have two happy, healthy 10 month old boys home with us today. That is the short version of how we got our boys home with us. Now it's on the the fun stuff!!! :)
You are one of the most amazing families I have had the pleasure of working with! You absolutely bless my heart! You are precious, and I love you all, dearly.
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