We’ve all heard it before.
Maybe it was in preschool or your lab partner muttered it in high school
Anatomy class. We’ve all heard it
before.
The toe bone
connected to the heel bone,
The heel bone connected to the foot bone,
The foot bone connected to the leg bone,
The leg bone connected to the knee bone,
The knee bone connected to the thigh bone,
The thigh bone connected to the back bone,
The back bone connected to the neck bone,
The neck bone connected to the head bone.
The heel bone connected to the foot bone,
The foot bone connected to the leg bone,
The leg bone connected to the knee bone,
The knee bone connected to the thigh bone,
The thigh bone connected to the back bone,
The back bone connected to the neck bone,
The neck bone connected to the head bone.
Yes, I knew how it worked.
Or so I thought.
At 20 weeks pregnant for the second time, I went in for a
normal ultrasound. This would be the day
we would find out if we were having another boy or a daughter. We were amazed to see the active little
person inside and were thrilled to hear it was another boy. I just knew it. This pregnancy I was not afraid to ask all
sorts of questions. Can you see anything
at the back of the neck at this point that might indicate Downs Syndrome? Can you tell how big he is already? The little guy kept squirming around as she
answered my questions and checked for some of the other more common signs of
Downs Syndrome. We spent 45 minutes, and
we were amazed by how adorable his little feet were, and how he seemed to be
giving us a thumbs up in the 4-D shot.
The technician even measured his femur to see how big the little boy we
would shortly name Henry was. He
measured 10 days bigger than his gestational age, and I remember thinking I was
glad I would have a c-section so his size would not matter.
We left the ultrasound room and met with one of the doctors
in my OB’s practice, as was the norm.
She told us that the technician had found an echogenic foci in his
heart. This was a mild marker of Downs
Syndrome, and no other markers were found.
My husband and I realized then why the tech had spent so much time, and
why she had shown us all these other signs were not evident. We were given a referral to see a specialist
to find out more or get more specific odds that our son would actually have
Downs Syndrome.
That was a Friday afternoon, and I spent the weekend
agonizing over what this meant. I was
less worried about Downs Syndrome. I had
once had a student in my class with Downs, and though I knew it was not always
easy, I knew I had the strength to handle it.
No, I was worried about his heart.
Could this mean he would have heart problems? How would we know? On Monday I called and talked to my regular
OB, and she assured me it most likely meant nothing, possibly a heart murmur.
Reassured I decided not to proceed with meeting with a
specialist. My understanding is that the
doctor could not say for sure if my son had Downs Syndrome without risky tests
I was not willing to take. Though I
would wonder for the next 19 weeks, I knew I would love my little guy no matter
what.
So, fast forward to birth day, May 15, 2009. We left early in the morning, after kissing
our older son, to be at the hospital at 8.
I admit, a tiny piece of me was apprehensive about finding out that
Henry had Downs Syndrome, mostly because I wasn’t sure how you shared that kind
of news. What would I say? Mostly, though, I couldn’t wait to meet and
see the baby who had been hiccupping inside of me for months.
Around 10 the c-section began. The first surprise was to discover that Henry
was breech. Due to the scheduled
c-section, my doctor had not done the typical exams to see if I was dilating or
what position the baby was in, so we had not known. Oh, my, I had been patting his head up by my
ribs thinking it was his butt! Shortly
after that I heard the most incredible sound – my son’s cry. My husband assured me that he looked as
perfect as he sounded.
The nurse who was in charge of checking him out and weighing
him, soon became nervous, according to my husband. He remembers that whispering soon began. He could tell something must not be right,
but could not see what it was. The nurse
carried my 6 pound, 14 ounce baby over to me and held him up. She said that his left leg was not
right. She wondered aloud if the skin
was somehow stuck in a way that did not allow him to stretch out his left
leg. The nurse also pointed out that his
head tilted to the left. I did not see
anything wrong. His right leg was also
bent, and no new born can hold their head up when upright. No, I could only see the miracle who had just
joined our family. The nurse said that
they would have to take him to find out what was wrong. Okay was all I could say.
With my belly still open, I lay there looking at my husband
wondering what was going on. Henry
stayed in the OR until after the second Apgar score was taken at five
minutes. I would later learn his Apgar
was 9, a perfectly healthy little guy.
Then I got one last look at my now bundled baby, a chance to admire how
adorable his nose was, and then he was whisked away to the nursery, my husband
at his side. Left alone in a room full
of doctors and nurses, my OB talked about what she was doing, and how she was
glad my ovaries looked good. I don’t
recall any comments about what might be wrong with my newborn.
Soon, I was returned to my room, where my father and sister
awaited. After greeting them, it became apparent
that they had no idea where Henry was. I
told them what I knew, and they both went down to the nursery to be with my
husband and newborn. My sister returned
to quickly give an update and to be with me.
The pediatric nurse came in shortly thereafter and told me what they
knew so far. They had done some x-rays
and think he has no femur in his left leg.
Later x-rays would show he also had no fibula in that same leg. Wait a minute, the song says that the foot
bone is connected to the leg bone, the leg bone is connected to the knee bone,
and the knee bone is connected to the thigh bone. How does he have a beautiful foot without a
thigh bone? I had never heard of such a
thing.
After 2 hours of x-rays and testing (they could find nothing
else to worry about), Henry finally returned to my room. We were quickly moved into our official
hospital stay room, but the adventure was just beginning. Henry had been gone long enough that his blood
sugar had dropped, and my first attempt at nursing did not alleviate this. I had to give him a supplemental bottle for
him to drink one ounce. For the next
nearly 24 hours, nurses had to prick his heel and take his blood sugar before
and/or after every feeding to make sure he was okay. Luckily, his blood sugar went to normal and
stayed there.
Our next issue was getting Henry all cleaned up. Normally, the newborn is bathed in the LDR
room I had previously occupied. However,
Henry was not there long enough before they moved us to prepare that room for
another mother. So the nurse had to be
convinced that she needed to do it, and she had to find all the equipment from
the other wing. The room we would spend
the next two days was newly renovated, so it was beautiful and comfortable but
did not have everything stocked yet.
Over the next few hours, we would be visited by the
pediatrician, the pediatric nurse, two physical therapists, and even my OB
returned to check on us herself. She
came to see what we knew, how we were handling it, and to apologize for not
having discovered it before Henry was born.
I simply responded, how could she have known. We had seen two beautiful feet, so who would
have thought two of the bones in between would be missing? Besides, he had been moving so much, we had
just assumed he was kicking his leg up out of the way in the one ultrasound
picture we had of the butt and right leg.
It had never crossed my mind that it could be anything different.
In between all these visits, I sent a quick text message to
a co-worker to spread the news that Henry had arrived. I gave no details. If I had been worried about how to tell people
my son had had Downs Syndrome (the doctors assured us he did not) which is so
much more common, how did I tell them about such a rare physical birth
defect? My father had stepped out of the
room between visitors and called family and told them the news. The family who did come to visit that day
were not surprised and responded wonderfully to the miracle that Henry still
was.
Back to all the visitors.
The pediatrician of course came in to tell me in person what she found
and to reassure me all else was well.
She scheduled appointments for Henry with a genetics specialist and
orthopedic specialist at Cincinnati Children’s Hospital to help us get more
answers. You see, she could not give a
name to his birth defect, for it was a first for her as well. The pediatric nurse came in frequently that
day to answer questions. She even spent
time discussing the x-rays with the technician so she could better explain what
they showed to us. She made sure we had
multiple copies to give to doctors and to keep.
She even discussed with us whether or not we thought it was causing him
any pain.
The two physical therapists came in together and were there
to discuss his leaning neck. They were
not there to address his leg at all. We
learned the neck issue is called torticollis, and it is relatively common among
newborns, especially those that are breech.
We would learn months later that Henry’s torticollis was more likely
related to his leg birth defect. We were
given some advice and some exercises to try.
Unfortunately, they gave me a list of what to do if his head was tilted
in the other direction. Lucky for them,
it was the least of my worries at the time.
One of the special visitors was my mother-in-law with my
older son. We, as a family, got to
experience that wonderful moment when brothers meet. It was all that I had hoped, and Henry’s leg
didn’t play a part. It was quite
possibly the most “normal” moment we had all day.
Sometime around midnight, when all my family had gone
(except my husband who rarely left mine or Henry’s side), the specialists had
stopped coming in, and I was peacefully holding my new miracle (he had the
longest fingers I had ever seen!), I finally had to figure out how to tell the
rest of the world (or at least the part of it that was waiting to hear about my
new baby) about the surprise birth defect.
So how do you share news like this with friends and co-workers? We were so blessed that Henry’s birth defect
was life affecting and not life threatening, but most of the time you just
heard how big the baby was and that mother and baby were doing fine. I personally had not experienced a precedent
on how to spread the news.
After some thought, I attached a picture of a typically
swaddled sleeping newborn (though Henry was cuter than most!), titled the
message “Isn’t he adorable!”, and typed the following:
Henry
Joseph Horton made his great arrival Friday, May 15 at 10:36 a.m., weighing in
at 6 lbs and 14 oz (not quite as big as I thought!) and 20 in.
He has a sweet personality! Though he isn't afraid to let us know when he isn't so happy.
Henry is perfectly healthy, but he was born with a serious birth defect. He is missing the femur bone and fibula bone in his left leg. We just ask for a special prayer as we await meetings with specialists to help us better understand this unexpected reality.
He has a sweet personality! Though he isn't afraid to let us know when he isn't so happy.
Henry is perfectly healthy, but he was born with a serious birth defect. He is missing the femur bone and fibula bone in his left leg. We just ask for a special prayer as we await meetings with specialists to help us better understand this unexpected reality.
It wasn’t more than a minute after
I sent the message that I wished I had changed the word “reality” to
“blessing”. “Reality” gave it a more
negative spin, and though I was like every mother who just wanted her new baby
to be perfect, I did not feel negatively about it. Just overwhelmed. Surprised.
Amazed. It was early on a
Saturday morning, so most would not get the message until Monday, which was
fine. A few people did read it on
Saturday and sent messages of congratulations and prayers. Our blessings continued.
Day 2 of Henry’s life was a little calmer, but was still
full of visitors. I chalk this up to
being a Saturday when not as many doctors are around. Another pediatrician who was on call at the
hospital checked him out, saying that he looked healthy. I had a long list of questions
to get answers to, and she didn’t help either.
Henry also suffered the agony of a circumcision, which left
a bruise that had me scared a few days later.
I hadn’t really been a nervous mommy with my first son, but to some
level, that had completely changed.
Especially in those first few days, I kept waiting for the other shoe to
drop. What else was wrong? What had we not yet discovered? Could there be something more serious,
something life threatening, we had yet to detect? I even began to picture Henry years out as a
20-something looking for love. I prayed
that he would be able to find someone to love him, someone who could disregard
the leg as just some bones and see how truly wonderful he was.
More family came and properly oohed and aahed. We came home the next day.
Go Henry! :-D
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