Now that I have completed my posts about the bishops in my
life, I can return to the chaotic ramblings of my history. As you may have
noticed by now, I do not do to well in sequentially presenting events in my
life. That is why I chose to use this blog. I feel this blogging medium is a
forum that is open to the chronological as well as the immediate posts.
To that end, I am now including a post about an experience I
had with a young, sick boy named Tanner Larsen. First, let me provide you some background.
David and Tricia Larsen moved into our ward about five years
ago. They had been living in California and doing well in their jobs and in
their relationship with each other but were deeply discouraged because they
were unable to have children. After years of trying, they finally decided to
adopt and were blessed with an infant girl whom they named Brinley.
In the few years after their adoption, in-vitro technology
improved and the Larsen’s connected with a lab that had a high rate of success
in live-birth babies. They went through the program and were able to create
dozens of viable embryos. To increase the chances of at least one live birth,
the doctors implanted three embryos. All three embryos seemed to flourish.
When the Larsen’s arrived in the ward Tricia was pregnant with
triplets. Soon after they arrived, one of the three embryos lost viability. But
they knew the risks and were still pleased at the prospect of having twins.
Then came the bad news.
With an extremely low percentage of embryos grown in this
lab there is a chance of chromosomal anomalies that would likely result in the
death of the baby just before or soon after birth. If the child survived the first
few months, it would suffer serious birth defects including blindness,
deafness, and severe learning disabilities.
While the doctors were closely monitoring the development of
the babies, they detected that one or both of them had this rare anomaly. David
and Tricia were devastated. They had waited so long to be able to have children
and had come so far. Yet within days the lost a fetus and then heard the news
that neither of the remaining twins may survive.
I don’t think there is anyway life can prepare you for this.
There is no manual to help you through the roller coaster of these types of emotions.
But Dave and Tricia adapted quickly and prepared themselves from the worst
while hoping for the best.
In early December Tricia gave birth to twin boys, Tyler and
Tanner. They both survived birth and, when we arrived on the scene, they both
looked like very healthy and normal babies. But, as the months progressed, it became
obvious that Tanner had serious issues.
There is not space on this blog to explain the 35 major
surgeries or the numerous life-threatening illnesses poor Tanner endured. His
head is so scarred and misshapen from all the different brain surgeries. But
somehow he survived. He learned to walk. He learned to talk, well, he learned three
words, “Hi”, “Bye”, and “Go”. His progress, though painful to watch, was a
miracle to behold.
Recently, Tanner was diagnosed with a serve seizure issue.
He would have hundreds of seizure a day which made his life and his parent’s
life impossible. The doctors decided the only course of action was to perform a
corpus colostomy where they split the hemispheres of his brain. This required
yet another major brain surgery for the poor little boy.
As was usual, the ward pitched in to care for Brinley and
Tyler while Dave a Tricia stayed with Tanner and to stay with Tanner when Dave
and Tricia needed to attend to things at home. Karen and I took a shift at
Primary Children’s to sit with Tanner for three hours. This was extremely hard
for me. But it was even more difficult for Tanner.
This poor boy had tubes all over his body. They had a tight
gauze hood on his head to keep him from pulling out his shunt. To make matters
worse we had to keep his head below a line on an IV pole so that his brain
fluid could drain properly. I will be honest, that was the longest three hours
of my life.
He finally came home from the hospital and the family
prepared to move to New Hampshire where Dave had found a job. While Dave was
gone Tanner developed a fever and began vomiting repeatedly. Tricia was afraid
that yet another infection had grown in Tanner’s body and that it would result once
again surgery to repair his brain shunt. Not only would this negatively impact
their plans to move, it would be yet another brain surgery for Tanner.
As I was called to be their home teacher, I was alerted to
this most recent emergency. Because I was already in the Salt Lake Valley, I arranged
to meet Tricia and Tanner at Primary Children’s’ ER. Following is an e-mail I
wrote about this experience.
I
wanted to share with you a rare positive experience I had with Tanner Larsen. I
do this not to sound heroic, for I am not at all a hero, but simply to provide
each of you a glimpse of the miracle of this small boy that I have not had up
to this point.
I
have felt uneasy about being around Tanner as a result of a long-standing fear
I have had to associate with the disabled that still plagues me to this day. I
have been envious of Bonnie and Martin's first experience at Primary Children's
when they had an enjoyable time tending Tanner. When Karen and I went it was a
less than positive experience. Perhaps it was my fault. I went to our shift
very apprehensive so I may have muddied the waters some when I arrived.
Yesterday
I went to the ER to sit with Tricia and Tanner. I have had a habit of going to
the hospital to visit ward members but for the most part I do not look forward
to such visits. Unlike President Monson, who is at his best visiting the sick,
I tend to visit having an exit strategy for I never know if my visit is a help
or a hindrance. This is exactly how I felt driving up to Primary Children's
yesterday. It is one thing to volunteer to go that is easy. It is an entirely
different matter to actually be there having no idea what to do to help.
When
I arrived, Tanner and Tricia were sitting in the lobby. This is a most
depressing lobby as it is filled with children in varying degrees of sickness.
Many were throwing up. Some were semi-unconscious. Most were looking scared or
just lethargic. No one wanted to be there, but who really ever wants to be in
the ER?
Then
there was Tanner....
He
was dressed in a blue T-shirt and green scrub pants. He looked neither
lethargic nor scared and he was totally conscious. Tricia had to hold tightly
to one of his arms to keep him from roaming around. He was yelling his usual Hi
and Bye to all who would listen – not even caring if anyone listened. Tricia
looked exhausted and concerned about the possibility of having to admit Tanner
and trying to determine how that would impact their pending move. The stress
Tricia bears on a daily bases is, to me, unfathomable.
I
sat next to her as we chatted. Again, I was struggling to find any positive
thing I could contribute, but I noticed that what she needed most was adult conversation.
Talking to Tanner for any amount of time can be a challenge. After chatting for
a while, I took the risk to pick up Tanner to see if he would respond to me. As
soon I a picked he up he completely relaxed and his anxious demeanor
evaporated.
Tricia
explained that he reacts better to men and showed me her arms that are scarred
from Tanner's constant pinching. I was wearing long sleeves so I was confident
Tanner would be less than successful at pinching my arms. I carried him for
about 10 minutes around the ER trying to get him to look at the paintings or to
touch the colorful wall, anything to keep him distracted.
Seeing
an opportunity, Tricia's asked if she could run out to her car to get
something. Tanner was still calm and I figured I could handle her absence, so
she left. About a minute after she left, the charge nurse called Tanner's name
and said his room was ready. Now I had a bit of a dilemma. I did not want to
lose that room to another sick child. But I was neither parent nor guardian. I
was just a guy holding a sick child. I tried to explain my case to the nurse
and she simply said: "Follow me!" So I followed her.
Now
I am in room 12 of the ER with Tanner and I have no idea how to let Tricia know
where I was or how long she would be gone. Tanner was not concerned at all. So,
I took this alone time to see if I could communicate with him. Each time he
said hi, I would say bye. Whenever he said bye, I would say hi. Then he would
make the biggest grin and laugh. We did this for 20 minutes and each time he
laughed as though it was the first time we played the game. This basic level of
communicating would become key later on.
After
about five minutes in room 12, I stepped out into the hallway with Tanner and
saw Tricia looking in the window of the door. She returned from the car just
minutes after I was called back to the room and sat there for a while figuring
that I was taking Tanner for a walk. As the minutes went by, she got concerned
and deiced to look for me. Evidently the nurses did not tell her that we were
in room 12. But, she found us.
We
are in room 12 for about two hours with nurses and doctors coming in and out.
They explained that they need to draw blood and insert an IV. I had a feeling
this was not going to be a pleasant experience for Tanner as I knew it would
not be for me. Finally the nurses came in with their implements of torture and
it took them 15 minutes to prepare the hypos and medicine destined for Tanner.
It seems the medical profession is really in no rush.
Tricia
mentioned that she hated having to restrain him as Tanner tends to associate
pain with her. This may be why he pinches her and bangs her with this
head—especially in hospitals. So, since I won't have a long-term relationship
with Tanner, me being the bad guy seemed a fair trade. When the nurses were
ready to work on Tanner, Tricia left the room to make some calls. Now I was in
charge of keeping this poor boy still as they injected the IV and drew his
blood.
Tanner's
demeanor changed has we restrained him. I could tell he was scared. His eyes
welled up with tears and he looked at me and said, in a very timid voice,
"hi." I looked at him and said "bye." With this he gave me
a big toothy grin and we played the Hi/Bye game for the 15 minutes it took to
draw the blood and clean the IV tube. He never cried. He never screamed. He
never resisted against my restraint. We just laughed together.
That
was my one positive Tanner experience. He will likely never remember this
event. But that doesn't matter. For the first time since I have known Tanner,
and Karen and I were at the hospital the day he was born, I finally had a
chance to feel like a contributor. I made him laugh so that he could forget the
pain. That was enough.
I
still envy those who have contributed positively far more than I have. But I
will forever cherish that night in the ER playing the Hi/Bye game with Tanner.
Just read this again and was very touched by it! He still loves to play the hi/bye game! Thank you for being such a wonderful home teacher when we needed it most! Tanner is doing remarkably well. He is still a daily challenge, but his doctors and therapists in Boston are amazed at his progress.
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