Heart surgery (sort of)

Emma's PDA, which normally closes after birth, never did. Therefore, in May of 2005 Emma had her first surgery to close it. They closed it with a surgical method called an intravascular coil. Basically, they enter through a vein and shoot this little coil into the heart and it ties up the hole. (now we just have to remember to tell x-ray technicians that "that metal thing in her heart" is supposed to be there...)

She wasn't too excited pre-surgery. She must have remembered the hospital...

Lock Down = Isolation

This has become our family ritual during the winter months of having to protect Emma by keeping her away from germs due to her extreme susceptibility to illness. We had to be especially careful the first winter after bringing her home from the hospital. It takes a long time for the body to fully recover from sepsis. We pretty much didn't leave the house from December to May. Jeff went to work and back, that's it.

Helmet Head (a new fashion accessory)

(Story in a nutshell) Emma developed torticollis which then lead to plagiocephaly and she had to have helmet therapy to help correct her "flat head." On a scale of 1-10, with 10 being the worst, Emma started at an 8 and the helmet corrected her to a 3. So, her head is still a little flat on one side (which is really only noticeable with pigtails), but we still love her. (of course!)

The first 28 days

Most parents prepare for the birth of their baby with the expectation that they will be bringing their healthy baby home from the hospital within a couple days. Emma has taught us, however, that we should always expect the unexpected. She came into this world in a whirlwind of sickness and complications. Within minutes, we knew of her initial diagnosis of Down syndrome, (a.k.a. Trisomy 21) which the doctor said would have to be confirmed still by a blood test. It was quite apparent, though, from her appearance that this diagnosis was true. She had several physical charecteristics of Down syndrome which the doctor explained to us: creases in the palm of the hands, low-set ears, slightly slanted eyes, and an unusually large gap on both feet between her large toe and the one next to it. Emma was struggling to breath from the beginning, and after working on her for a few minutes, the nurse allowed Lisa to hold Emma. It was a very brief moment, because Emma's breathing quickly got worse and became very labored. Little did Lisa know that she wouldn't get to hold Emma again for almost 2 weeks.

Emma in the nursery

She was taken to the nursery and assessed there by the doctor on call. Jeff went with her while Lisa was left all alone in an empty room wondering what was happening. Things happened very quickly that first hour as she went from being assessed in the nursery to being admitted into the NICU (neonatal intensive care unit). It was very difficult for us as parents to get thrust into a new world of medical terms and acronyms that we didn't understand and it all seemed so scary. A couple hours later, Jeff took Lisa via wheelchair up to the NICU to meet with the neonatologist. He discussed with us their intial assessment of Emma. She had an infection and was still struggling to breathe. He started discussing with us in more detail how many babies with Down syndrome are born with congenital heart defects, which in turn can cause pulmonary hypertension. They felt like this was the most likely cause of her breathing struggles. He went on to talk about the possibility of intubation if her breathing didn't improve. They also scheduled an echocardiogram for the next morning to look for heart defects, which meant a high probablity of open heart surgery... It was a rough night.... The next morning ("Black Thursday" as it became known) they had already intubated Emma during the night and the echocardiogram showed no defects (lucky girl!). The x-ray of her lungs, however was not so promising. She did, in fact, have pulmonary hypertension believed to be complicated by her abnormally shaped lungs. The doctor said her lungs looked like the Liberty Bell, which became her first nickname.

Thursday morning in the NICU

By Thursday afternoon, Emma's condition continued to decline. They explained that her infection had spread throughout her body by entering the bloodstream, also known as newborn sepsis. The regular ventilator wasn't enough to sustain her breathing, so they switched her to a high frequency oscillatory ventilator. Her blood pressure was dangerously low, admist other complications. This was the first time we were faced with the possiblility of losing our newborn baby. Nothing in the world can prepare you to face that reality...

We looked like crap and felt like it, too. (the smiles were very forced...)

That night, Emma took another turn for the worse. She was "maxed out," as they called it, on life support. They were giving her the max doses of her life-sustaining medications and her only option was ECMO, a heart/lung support machine. Basically, her body was shutting down and we made the decision to move forward towards ECMO, which meant a transfer to another hospital. The closest hospital with this capability was Primary Children's Medical Center, where she was taken by LifeFlight around 5:00 a.m. Friday morning. Emma arrived at PCMC in critical, but stable, condition (a shock to all of us). A fighter was born in Emma for the first time, as her condition slowly started improving after arriving. She was still very, very sick, but ECMO was put on the back burner. PCMC became our new "home away from home." Over the next couple days, Emma swelled up like a balloon and gained 3 pounds because they were constantly giving her IV fluids to sustain a stable blood pressure.

Her second nickname became "Sumo Baby," it was so sad!

The next 3 weeks consisted of ups, downs, and more ups and downs. It was a rollercoaster ride of strained emotions combined with gradual improvements in Emma's condition. We were dealt a crash course in NICU technology and terminology. We spent our first holiday in a hospital (Thanksgiving), and Lisa finally got to hold her baby (vent tubes and all) after 12 long days.

Lisa was in heaven!

Emma continued to get better and we did eventually get to bring her home. As long as this post has been, it doesn't do this experience justice. It was a bitter-sweet experience through it all.

Emma's coming home day. Notice the outfit barely fits that we had bought prior to her birth as a "coming home" outfit. This was about the only time she wore it...

SURPRISE!

Emma was born on November 3, 2004, at 10:18 p.m. She was 19" long and weighed 9 lbs 6 oz (a surprise to us, but not THE surprise). Labor and delivery were relatively smooth and quick compared to our first baby, and everything seemed to be going normal for the first couple minutes. At first glance, Lisa thought Emma's ear looked a little different, but didn't think much of it because babies come out looking funny anyway. Meanwhile, Jeff was oblivious and just content taking pictures like the one above of the nurses doing their initial cleaning in the delivery room. It seemed a little weird to Lisa that the nurse kept coming in and out of the room, each time bringing more nurses with her. After the second time of bringing in more nurses, Lisa started asking if everything was OK. The nurses response was that she just needed a little help with her breathing (her first APGAR was 7). But, after the nurse asked the doctor to come over, we really started to worry. They were all huddled around her and whispering (not a good sign). Next thing we knew, the doctor came over and sat down by us and gently broke the news to us that "we think your baby may have been born with Down syndrome." Oh, how our world changed so much in only a few minutes...