A Heart Transplant Survivor Story
Memoir
Date Published: December 12, 2023
Publisher: Acorn Publishing
Read An Excerpt Below
About the Author
A heart transplant survivor, Dr. Darla Calvet won a gold medal for ballroom dance in the 2022 Transplant Games of America. Currently, she serves as the vice president of the board of directors for the Southern California Transplant Games of America team. She is also the CEO of Blue Tiger, Inc., a strategic planning consultancy. A doctor of education, Calvet holds degrees from Claremont Graduate University, San Diego State University, and the University of California, Berkeley. She lives in San Diego, California, with her husband Pat and their French bulldog Quinn, and she is the proud mom of two adult daughters, Claire and Annie.
Contact Links
Purchase Links
Barnes and Noble: Barnes and Noble
Excerpt from "My Life in Stitches"
My fears that something was seriously wrong were confirmed as we checked into the musty, overcrowded emergency room. I showed the admitting clerk my elephantine ankles, and she immediately bumped me to the head of the line. I was out of breath and wheezed repeatedly. I thanked her on my way to the exam room and gasped, “I can’t breathe.” She looked me straight in the eye and responded, “You have a heart
virus. I can already tell.” She was correct in her diagnosis.
After being quickly assessed in the triage area, the silver- haired, haggard-looking physician on duty looked at my vital signs and ankles. He frowned. “It looks like you are in heart failure. They are going to transport you to the regular hospital for tests and admittance.” Before I could plead with him for more information, he was gone. I noticed that the man in the bed next to me began urinating in a bedpan. I wanted to scream but shut my eyes instead. I prayed to God that this was some kind of horrible dream, and I would wake up in my normal life. I was only thirty-nine years old.
A half hour passed, and two young male paramedics loaded me up on a sitting gurney. It was bright yellow and black and reminded me of a giant bumblebee robot transformer. Although I must have looked monstrous with my slicked-back hair and sweating forehead, they were kind to me and tried to be reassuring. “Okay miss, we will be transporting you over to the main hospital now,” said one of them as he lifted up the giant gurney.
The half-mile trip between the emergency room and the main hospital was a ridiculous exercise in logistics. It took them twenty minutes to get me loaded and buckled in, then five minutes to drive over to the main building and another twenty to unload me. They placed me in a temporary patient holding room on the main floor of the hospital, where I encountered a pudgy, peroxided nurse.
My husband Pat had gone home to leave the kids with some trusted neighbors while I waited for more treatment. I sat alone in the holding room in a despondent state. After hours of sitting alone considering my bleak diagnosis, a tall, older priest with a shock of white hair entered the room, smiling. I took one look at him and whispered, “Oh my God. Are you here to administer the Last Rites?”
In a predictable Irish brogue, he took my hand and replied, “No, child. I am just here to see if you are hungry. I know you have been here a while. I brought you a bit of something.” He pulled his hand from his shirt pocket and produced a tiny peanut butter sandwich, neatly wrapped in plastic. I had been at the hospital for over eighteen hours and had been given nothing but water and intravenous fluid. “Oh, thank you, Father,” I said with relief. “Yes, I am a bit hungry, and I would love that.” We both shared a good laugh before he gave me a standard blessing and continued his rounds. I was going to need it.
The first lesson I learned as a heart
transplant patient is that a sense of humor is vital on the road to recovery.
You cannot survive without it.
EXACTLY SIXTY-TWO DAYS after I had fainted in the Scripps Green hospital room, I woke up in complete darkness. My heart raced. I had no idea where I was or what happened to me since I passed out on the day I was admitted. I was unable to see without my contacts or glasses and tried to speak but could not emit a sound. For those first few moments, I thought perhaps maybe I was in some kind of purgatory and that this was my eternal bus stop. I felt a distinct heaviness as I tried to move my legs. I reached down around my abdomen and detected the LVAD unit, with a drive line going through my abdomen and its two large lithium batteries attached to my body. The LVAD surgery had occurred. But when, why, and how had it happened? I sat in darkness, vainly searching for the remote control and the button to call the night shift nurse.
I felt a weird combination of
relief and confusion. I could decipher from the blurry digits on the clock that it was about 4:00 a.m. I had no
idea what day, month, or year it was. I knew from the LVAD installation that
some time must have passed, but how much? I must have woken up during a
skeletal night shift with very few nurses in
the hospital unit. I swung my head as far around as I could, only to see the
outlines and lights of seventeen machines in the room, all helping to keep me
alive. I immediately started to panic. I seemed to be more machine than human
with all of the leads and tubes running in and out of my body. I was also
intubated and unable to speak, which was terrifying. I could discern from the
many machines attached to me that I was also in the Cardiac Intensive Care
Unit, known as the CICU. This was where the gravely ill cardiac patients were
sent by their teams.
“Stay calm,” I told myself.
Someone had to be around . . . somewhere. The heavy blackout curtains were
drawn around my glass cube room, making me feel claustrophobic. After a long
wait, the curtains were flung open by Patricia, my morning nurse, who was starting
her shift. She smiled sweetly, saying, “Oh, good. You are awake. We have been
waiting for you to wake up.” I was confused and had no idea how I had arrived
at my current state in the hospital bed. At that time, the CICU was located in
the basement of the Scripps Green Hospital Facility, next to the morgue. It was
not exactly a cheery place. I heard some orderlies joking to each other that it
was “death’s waiting room.”
Realizing that I could not
speak, Patricia took my hand and spoke softly, “You are okay. You have been in
a medically induced coma for over two months. During that time, we needed to
perform emergency open heart surgery and save your life by installing the LVAD, which
you have probably noticed is attached to your body.” I shuddered and pulled the
sheets up around my neck. God only knew how close I had come to death. I was
about to find out.
While I was very grateful and
relieved to be alive, I thought of my family. How had my husband coped during
my absence with our two young adult girls? How had they dealt with this
horrible situation? My eldest, Claire, was a high school senior. My youngest,
Annie, was now a high school freshman. It made me sad to think about missing
the important events that were going on in their young lives.
My next thought was my job.
What had happened to it? Had someone finally disclosed how sick I had been
while continuing to work? It gave me pause to consider that this had happened
during my absence. I did not know that my husband had requested a one-year
leave of absence after I fainted at the hospital. I was grateful he did this on
my behalf. During my last days at my job, my ego kept me from seeking support
even as I struggled to walk a few hundred feet from the parking lot to the
elevator up to my office.
A few moments later, Nurse
Patricia returned with my “breakfast.” It was a peach
colored
container of liquid protein that looked like cement. I watched in awe as she
said, “Down the hatch” and poured it into my feeding tube. “Can you taste
anything?” she asked. I shook my head “no.” The only sensation I felt was the
cold sludge making its way down the feeding tube in the back of my throat. I
had lost quite a bit of weight during my two-month nap. Thirty-four pounds to
be exact. My body, which had always been very muscular, was now atrophied and
weak.
The LVAD was the third device
to be surgically placed into my body after the AICD defibrillator and pacemaker. It cost over a
million dollars to install. Now, my job of learning to live with it began.
There would be no swimming in the near future. The eight pounds of life-saving
state-of-the-art medical equipment that was now part of my body would require
ongoing care. I had no idea at that time the battles that had taken place to
get the LVAD device installed. I would have certainly died without it.
The next lesson I learned as
a transplant patient is: Your medical
team must fight to save your life.
Even with your insurance company. You do not have
the luxury of time on your side.
No comments:
Post a Comment
Hateful and Unrelated Comments Will Be Deleted. Anonymous comments are invalid to enter into giveaways.
If you see any spam comments, please notify me. My email is on the "About Me" page. Thanks much.