In celebration of my charming nephew's first birthday, I've asked my sister, Jessica, to share Kade's story. So without further ado, here it is...
Kade Jameson Kerns.
My miracle.
My glimpse of God's goodness.
“He's perfect!”
Those were the words that tumbled from
my mouth moments after my son was vacuumed from my body. Yes, I said
vacuumed. That should have been the first red flag that my charming
little boy was going to be quite the adventure. After three days of
labor and not enough progress, I was finally taken in for a
C-section, but Kade was just not quite ready to face the world. Thank
God for vacuums.
He screamed louder than you could
imagine, and unfortunately, that scream has stuck with him since. I
remember the doctor saying he was an A++ baby or a 9/9 which is a
score they rate the babies after they are born. What that meant was
that he was as perfect as can be. These were the words I longed to
hear as I lay strapped to a bed after the C-section. After forty long
and miserable weeks, I was finally able to meet my precious miracle,
Kade.
Twelve hours after we were released
from the hospital, we noticed Kade felt warm and decided to take his
temperature. It read 100.7, which seemed a bit elevated from the
temperatures he had while at the hospital. We had a pediatrician
appointment the very next day so we debated whether we should just
wait until the appointment or take him in earlier. Brandon did not
want to wait. He insisted we call the pediatrician and ask even
though we were trying to persuade him to wait.
To this day, I am so grateful for
Brandon's anxiety over this matter. It turned out to be the biggest
blessing. Later we would find out that had we waited just one more
day, Kade would no longer be with us. Our pediatrician told us to
come in immediately. Because I was still recovering from my
C-section, my mom insisted on going with Brandon while I caught up on
my rest. I laid down and after two hours I woke up to find out my son
was being admitted back into the hospital. So many thoughts rushed
through my mind, but I don't think I came close to being prepared for
what was about to happen.
Meningitis and bacterial infection were
two things they suspected at first. They immediately sent out for
cultures and did a spinal tap. I remember the pain of knowing my son
was being pricked and prodded and I couldn't even hold him. I had
developed a fever of my own and was not allowed near my son or in the
maternity ward.
We were told they would need to keep
him in the NICU for at least two days. After two days, we were told
he would need another five days. After five days, it turned into
another twenty-one. In those first days, my son was put on four
antibiotics and received every test that was humanly possible to
take, yet they found nothing.
On August 10th, we received
unexpected and unwanted news. It was 11:30pm when my phone rang. Now,
for those of you who know me, you know I NEVER answer my phone. But
for some reason that night I did. It was the doctor calling to inform
me that my son had been digressing since Brandon had left earlier
that night. His heartbeat had reached three hundred and all of his
vitals were failing. They told me they had contacted Children's
Hospital and had assigned emergency transport. Kade now need a level
three NICU and that they were “scared he might not make it through
the night.”
When you go from hearing you baby is “a
perfect A++ baby” to “he may not last the night,” there is
something inside you that dies. It was as if my heart stopped beating
and my world completely stopped.
They went on to say that if Brandon
wanted to follow the paramedic, he could if he go to the hospital
quickly. I tried running out into the living room to tell everyone,
but words failed me. How could life take such a turn? What was even
wrong? How was he fine the week before? Was God's purpose just to
allow him a few days' visit on this earth? I had so many questions
racing through my mind and a barrage of emotions hitting me at once.
It is amazing how fast you can love
someone you barely even know. Kade had only been in my life for a
matter of days before I heard the words that he might be gone. But
somehow in that short time, I had come to love him more than I
thought possible. Kade Kerns was supposed to be number 56 on the
football field while I stood cheering from the bleachers. Mr. Kade
Kerns was supposed to be smart and talented and kind. He was supposed
to do big things for God and hopefully change the world. See, in my
mind, Kade needed more time on this earth. I was forced to face the
reality that God's plans may differ drastically from my own.
Kade was admitted to St. Elizabeth's in
Boston. He was at a level three NICU, which held the babies that had
lots of problems. After five days of not seeing my baby boy, they
finally allowed me in. I remember walking in and my heart breaking
for all of the families crowding around their sick babies. I cried
for them and felt sorry for them thinking they were worse off than my
own child. Little did I know that Kade was listed as the worst one in
the unit. I had no clue.
My baby had been placed in isolation.
It was a bright and cold room that frightened me. You had to scrub
in, wear gloves, and put on a sterile suit before ever stepping foot
into the room. My son lay naked on a small bed at the center of the
room. He was surrounded by wires, needles inserted into his hands and
feet, monitors hooked up, and what looked like a large fish bowl or
clear globe over his head for oxygen. At this point, he was so
dehydrated that his skin had started to peel. He went from being a
healthy looking baby to an ashen gray color. His veins were visible
through his thin skin. I fell to my knees and wept at the sight. That
was not my baby. This was not how it was supposed to be.
Kade was fully dependent on oxygen as
his lungs were filled with fluid and he had developed severe
pneumonia. He was now on five antibiotics, which made his eyes roll
in every direction. The nurses had to start taking blood from his
head because they had run out of places on his tiny body. They
confirmed our worst fears. Our child was very sick. It wasn't what we
wanted to hear. On a positive note, they had finally narrowed it down
and believed to have figured out what was wrong with him.
Herpes Simplex Virus, referred to as
HSV type 1. What I began to learn was there were different types of
herpes. People tend to automatically think of genital herpes because
it is the most commonly known form. However, this was not what Kade
had. Kade had tested positive to HSV type 1 which is the virus that
shows up in the form of cold sores. It took me awhile to understand
this. We sat at a conference table for hours each day with twenty
different doctors to have them explain to me how a cold sore almost
killed my son. What happened is someone, within his first few days of
life had HSV1 and gave it to Kade by either holding him closely or
kissing him.
Apparently, ninety-five percent of
Americans have HSV1 even if they have never had a cold sore in their
life. Most of the time it is passed to you by your mother. You can
have HSV1 and never know. The odd thing is I tested negative and
therefore did not pass on the virus to Kade nor did I pass on any
antibodies to fight it which means I am one of the five percent.
However, at this point, Kade had passed it on to me.
If you have HSV1, you could be
spreading the virus without knowing it. A cold sore is a sign of what
they term “shedding” or spreading of the virus. Someone who
worked with or visited Kade was shedding and through contact passed
it on to him. Because I did not have it initially, he did not possess
the antibodies to fight it off.
Because a baby's immune system is a
clean slate, a virus takes advantage and goes about ruining the body
as fast as it can. A baby's body can come in contact with any type of
virus at an early age and it will attack the main organs first. It
will attack the liver, lungs, heart, brain and then move onto the
eyes, ears, and so on. Sure enough, that is was happened. Kade's
heart was no longer beating regularly. His liver count had
skyrocketed and was shutting down. His lungs were filling with fluid
and extremely weak. And his third spinal tap showed that the virus
had moved to his spinal chord and brain.
We were told at this point that if our
son lived there was no guarantee concerning what kind of life he
would lead. It was explained to us that out of the babies that had
come in contact with this particular virus fifty percent of them died
within the first few days. Twenty-five percent were completely brain
dead and lived in a vegetative state. The remaining twenty-five
percent would suffer from neurological defects such as seizures and
abnormal development.
At this point, I didn't know how I should pray. I just remember praying “not
my will, but Yours be done.” I humbled myself and pushed my desires aside and asked God what He desired. If God wanted to miraculously heal him, I would praise Him. But if Kade's purpose was just to live for two weeks or live a life in a brain dead state, I would still praise Him.
Brandon and I sat back and watched God
show up in a big way. For the twenty-one days he spent in St.
Elizabeth's, we watched God heal each individual organ in his body.
The nurses said they saw things they had never seen before in their
careers. They took pictures of Kade and told us he would be in the
medical books. They had never seen a baby this young pull through
something like this. It was such a rare story, but to them it also
had a rare ending.
Kade somehow left NICU with
instructions to have physical therapy three times a week, antibiotics
three times a day for a year, weekly blood test for six months, and
bi-monthly for the following six months. He was to have appointments
with neurologists and cardiologists. To date, Kade had yet to fulfill
any of these instructions because he has surpassed everything they
expected. We still have to
examine his development but so far Kade is the smartest baby I know
(although, I may be biased).
See, God's plan was not to take him
early, but to use Kade to show me and Brandon many things. Never
before had we ever been brought to our knees in such desperation. We had never known
loss until this. We had both lost our jobs and were homeless during
that time. We learned total dependence on God. We learned what real
worship and prayer was like. We learned how
to love on those who are hurting as we were surrounded by many
hurting families with their sick babies. We learned that God uses
things to bring Him glory even if it doesn't make sense to us.
Now every time I look into Kade's big
blue eyes, I thank God. Every time I think things can't be worse, I
remember it isn't that bad. Every time I want to complain, I remember
to be grateful. And every time I want to doubt God's goodness, I am
reminded of His unending love.
Hauntingly beautiful, Jessica, and a true testament to the Glory that is God. I prayed, but never knew what was happening. Thanks for sharing this intimate glimpse into the true meaning of "Thy will, not mine, be done." Much love to all of you -- Debi(Robinson)Spivack
ReplyDeleteTo God be the glory. So much more to this story but thank you for sharing as much as you did. I got to take this journey with you and I am privileged to have witnessed this miracle of God's healing and the miracle of strength you and Brandon have exhibited through this past year. love you guys
ReplyDeleteKade's beautiful story will help so many, only God knows where it will be used. Thanks Jess for this today! Thank you God for showing us what prayer and faith can do. Love you guys!!
ReplyDeleteGod has special plans for this little boys life story. Thank you for sharing your prayer life with us, how powerful prayer is. Waiting on Him may be the hardest thing ever....but praising Him for staying by our side and loving us thru the storms. What a testimony...sending lots of love.
ReplyDelete