
Carnival by the Sea
A Transplant Experience
While we were at Johns Hopkins I would often sit and think about how our
life resembled a traveling carnival. The type of carnival that sets up
for a few weeks or months, and than suddenly vanishes. We arrived one
day at the new carnival (hospital) excited
about the opportunities it could bring (a new life
for Christopher). However, we looked around at the scary rides
(chemotherapy and the transplant experience)
, the roller coaster (PICU), the
tilt a whirl (decisions having to be made)
and the spinning teacups (our emotions going round
and round) and knew there would be much tossing and turning on
our adventure. I took my baby's hand and together we walked into the
carnival. Eyes wide open and looking around. We always thought we
would be leaving with the best prize of all from the carnival, no more
Hurler's and Christopher's life!!!
We stepped on the rides, and off we went!!!! We constantly
alternated between the spinning teacups, tilt a whirl and roller
coaster. Some days it would be one ride, sometimes a combination of all
three rides. Along the way were the clowns, yes there really were
clowns! The Big Apple Circus ( a real circus like Ringling Brothers) has
a "medically trained clown care unit" that works at the hospital. We got
to know "Dr." Boots and his staff very well. They made their rounds in
the pediatric unit and knew Christopher loved bubbles. One day he
wouldn't stop crying and "Dr." Boots, with his big red nose and shoes
started blowing bubbles. Christopher laughed and laughed, you would have
thought he won the lottery.
We even tried a brand new game at the Carnival! Enzyme
Replacement Therapy (ERT) before transplant. It was a game no one had
tried before. Guess what? Christopher one the game! His prize from the
ERT game was a better airway (trachea), liver, and spleen!
In this carnival there was a house of horrors. The house of horrors can
best be described as the needles, chemo, and medications Christopher had
to endure. The house of horrors scared us all, and at times we all
cried. It truly was a horror.
We were introduced to new people at the carnival
(hospital), many who brought more smiles than tears. (Aren't
carnivals suppose to make things better)? There was even food
at the carnival! Nurse Becky became our angel who brought us food
every week, without Christopher going to the carnival we would never
have met her. Their were also many volunteers who came weekly to
cook meals for us at the Children's House.
We met other parents at the carnival whose kids were riding the same
"rides", and together we talked and formed a bond as our kids were on
the rides. We assured one another that it was just another turn or spin,
and everything would be OK. When the dizzying teacup ride was too much,
we let the other cry in our arms.
After that:
We got on the roller coaster... The PICU... We would be going up (
a good test result) and get to the top of the ride. We would want to
scream with joy at being so happy with such wonderful news.
After that:
As quickly we were up, we would crash down. Sometimes a big dip,
sometimes a small dip and up the hill again.
After that:
We would be staying on track for a while waiting to see if the next turn
in the ride was up or down.
After that:
We crashed, our ride went down hard and fast and we screeched to the end
of the ride. The lights went out on the ride. Everything was dark. The
prize was gone, we lost Christopher's life.
The
carnival suddenly in the snap of a finger disappeared. No more rides, no
more clowns, no more Hopkins friends.
Everything was dark, scary and gone. Joe and I
were in the roller coaster car and our precious baby wouldn't be leaving
the carnival with us. We brought him in with a twinkle in his eye and
the wind blew it out.
We were left with the sea (life) and
trying to figure out.
When we stand by the sea and look back at the sand where the carnival
was, it's gone. The rides, the roller coaster, all PHYSICALLY gone.
Our prize (Christopher's life) is
gone. We can't see it, we can't touch it. We worked SOOOO hard at the
Carnival. We don't understand where it all went. We only have the
painful memories of the carnival.
The only thing for us to do is to stick a toe in the sea
(life) and start
treading water. We are now riding the waves in the sea, looking
at where the carnival once was. The "waves" hit us when we least expect
it. The waves are grief, they come and go. Sometimes it is a big wave,
sometimes a little one.
Somedays:
We just paddle along
Somedays (most days):
Our friends or family are treading water helping us to figure out
everything
Somedays:
I just don't know
Somedays:
The waves suffocate us
Somedays:
I let myself lay on my back and look at the sky. I try not to look to
the sand where the carnival was. When I lie on my back and float I will
see a butterfly glide by in the sky and know it is Christopher. The
other day at the cemetery a white dove flew by. How many times does a
white dove fly by in a large metropolitan area that is 100 miles from
the ocean? Not much!
So......
I need to concentrate more on laying on my back, and floating along.
This way I will let myself see the butterflies that fly by. I still look
toward the sand and try to find the carnival and want answers as to
where everything went (what went wrong).
But, I will never, ever find them. Ever. The carnival has left.
The waves will always be there, forever, they
aren't going anywhere until I meet Christopher again in heaven.
Hopefully I can float along, and when the waves hit, just paddle through
the motions and come out on the other side. My tears will be added to
the waves, and that's OK. I love my boy.
I dedicate the carnival to (and the families of):
My angel Christopher, Katie, Dustin, Megan, Zoe,
Baby James, Baby Brady, Reesie Cup, Mighty Max, Andrew F., Aaron A.,
Cameron - My prayers would be to never put a child's name on this.
Some of us got off the carnival ride, and some of
us didn't. Our lives will never be the same after going through the
carnival, we are now all standing at the sea trying to readjust to life.