Beruflich Dokumente
Kultur Dokumente
Thomas Cody
Ms. Jizi
UWRITE 1103-006
18 February 2018
In the eighteen short years that I have been alive my journey has been filled with many
ups and downs, but it is how you overcome the challenges that come your way that determine
who you are as a person. One of the challenges that has played a large role in my life was the
second time my lungs collapsed in 2016. This forty-day journey has shaped me as an individual
On May 16, 2016 I began to feel a sharp pain and it began to feel like a giant was
standing on my chest. I finished the remaining two hours of the school day and proceeded to go
to the Emergency Room with my Dad shortly after. After a short wait I was moved into the back
to get the first round of many chest x-rays. The images came back showing that I had a bilateral
pneumothorax which meant that both of my lungs had fully collapsed. The doctor asked, “How
are you walking around right know?” and explained that with the severity of my condition I
should be practically unconscious. They immediately rushed me into surgery and placed one
chest tube into my right lung and one chest tube into my right lung. I woke up and to my
surprise I had two garden hose resembling tubes attaching me to continuous suction supplied
through the wall of room 4E26. I was monitored for forty-eight hours before the surgeons
decided that it was time to take further steps to heal the air leaks.
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The next morning, I was woken up around 6:00 am to get a dose of x-ray radiation and
once the images were cleared I was taken on this long bumpy journey. The transport nurse
came up and we embarked on a trip that seemed to never end. As I was rolled to the Operating
Room it felt like everyone that you passed in the hallway was looking at you like it was going to
be the last time that they would ever see you, so they made sure to stare and wonder what I
was going in for. The pre-op process was long and full of IV placements and administration of
drugs. As I began to fade out of consciousness everyone wished me luck and they wheeled me
into the cold sanitary environment. Placed awkwardly on a metal table the surgeons began the
necessary torture to allow me to breathe again. After about thirty-six hours I regained
consciousness and was alerted with the news that the surgeons were not able to find the air
leak in my right lung and had to switch from an orthoscopic surgery to a thoracotomy where
they simply cut open my side and filled my lung cavity with water to search for air leaks, like
tactics used to find air leaks in bike tires. This process put my body through too much for that
day, so they just kept me unconscious over night and went in to cut off the top section of the
left lung and place a row of titanium staples across the apex of the lung the following day. As I
woke up in the ICU my breathing tube was removed, and I was told that the day was Friday and
that the surgery did not go exactly as planned. This was shocking because I went into the
supposedly four-hour procedure on Wednesday morning. They informed me that my left lung
procedure went textbook and should be healing however they still did not find the location of
the air leak in my right lung. This left everyone dazed, confused and unsure of the next course
of action.
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The equipment utilized to indicate whether or not I still had an air leak was a chest tube
attached to wall suction that is fed through this water box and if there were bubbles in the box
than air was still leaking out. After the failed thoracotomy the doctors kept coming in everyday,
checking to see if I had bubbles and would shake their heads and say, “I guess we’ll just have to
wait another day.” This process was demoralizing because at that point I was about twenty
days into my visit and being caged up that long isn’t good for anybody. To wake up every
morning hopeful only to be told that the only thing that you want in that moment is just out of
Another few days passed, and the doctors decided that my chronic leak was not going to
heal itself like it does in most patients, so they flew out a bronchial valve to be placed the
following morning. This one-way valve would be placed in the leaking bronchi and prevent air
from entering that lobe of the lung. This will allow the air flow to stop and give the lung wall a
chance to seal and heal. I was wheeled down the eternal hallway for another time and it is
obvious that you have been to the Operating room too many times when people start to
recognize you. I was unconscious for about three hours before I woke up and was told that the
valve could not be placed because they couldn’t determine which bronchi was attached to the
leaking lobe. At this point I had accepted the reality that I would never heal, and I needed a
After recovering for two days the doctors proposed an idea that they had never tried for
patients with a spontaneous pneumothorax, a blood patch. This was typically used to stop
bleeding in different organs such as the heart and was not typically used on lungs. The idea was
a last hope opportunity because I was so far outside the normalities of this condition. The
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average hospital stay is six days, the average procedures needed is two and the doctors are
very rarely not able to find the location of the leaking air. It was a long shot, but I agreed to the
Blood Patch procedure and hoped for the best. The next morning, I was rolled down to a room
in the ICU and shortly after my surgeon and a team of nurses came into the room and began
going through the procedure. Without administering any pain medicine, the surgeon stitched
tightly around the chest tube in my side checking to see if the hole in my side was simply not
sealed, however that was not the case, so he began the blood patch. My surgeon called for a
big bore needle and the nurse turned the corner with a syringe the size of a coffee stirrer. After
trying to find a vein in my bicep four times because all my other veins had already been used
the finally hit the vein and extracted two large containers of blood from my body. They then
tilted my bed so that I was laying upside down at a forty-five-degree angle with my head facing
the ground and reinserted all my blood back into my lung cavity hoping that the blood would
coagulate and clot over the leakage site. I stayed in this position for about four hours and it was
the most emotionally draining four hours of my life because if this didn’t work there was no
plan F.
The miracle had occurred. I woke up the next morning with no bubbles and the
surgeons monitored me for another day before finally releasing me back into the real world. My
chest tubes were pulled, one of my nurses sang to me and I was sent out in a parade of bubbles
down the hallway because I had been a patient for so long. After forty grueling days in that
place I was finally able to feel freedom again and walk around without being tethered to
suction. This procedure was truly a miracle for me because since my procedure the doctors
have tried the blood patch on lungs six times and it only worked on one of the other patients. I
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have learned many things about patience throughout this experience that I have implemented
into my everyday life as I continue to grow and encourage others who may be going through
Date: 2/19/18
1. Velcro Words/Phrases
Lungs Collapsed
“Eighteen Short Years”
“Like a giant was standing on my chest”
“A dose of x-ray radiation”
“Necessary torture”
Demoralizing
“Eternal hallway”
“Forty grueling days”
2. Feelings
Shocked
Sad
Sorry
Hopeful
Amazed
Relieved
Touched
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3. Questions
Did he contact his parents right away after feeling the chest pains? If not, why?
Did he ever feel like those would be his last moments?
Even though the last surgery was a success, have any other problems with his lungs occurred
after?
How did he stay so patient?
How did his parents / family feel?
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