I
have pushed out four baby boys without the aid of medication. This was
painful and I don’t enjoy painful experiences even though I am told I
have a high tolerance for pain, whatever that means. Getting older only
increased my pain during pregnancy and childbirth. My back seemed to
hurt so much more and when I began pushing out my last boy, I didn’t
think he was ever going to come out (apparently the doctor didn’t
either as he was getting ready to give me an episiotomy). But I did
manage to push my baby out and he came to me, weighing in at 9 lbs. 3
oz.; two more pounds than his three older brothers.
With
my last boy I felt our family was complete and I was happy. But then I
had to deal with the other kind of childbirth “pain.” The pain of
sleepless nights, while trying to feed, clothe, bathe, launder and taxi
my family while I tried to maintain my “happy.” It was during this time
of motherhood management that I thought about introducing medication
into the equation. However, shortly after I made inquires about the
affects of Prozac on breast milk, things began looking up. My last baby
may have been difficult for me to push out but his larger tummy had the
ability to hold lots of milk which resulted in an infant that slept
through the night at three months. Sleep was the drug I needed most and
when I got a good dose, I was able to perform my role with greater ease
and happiness.
Unfortunately, after my last
pregnancy, my back
seemed to hurt constantly and I thought that I looked more crooked than
usual. I had scoliosis. I was diagnosed with scoliosis when I was 14.
I
dealt with its varying degrees of pain up until the point of my last
baby. Then I had discomfort every day. I did not like having scoliosis
as a teenager; not because I experienced any great amount of pain but
because of how it looked. I hated that I was skinny and the only curve
I had was a crooked spine.
Every three months I
would be
measured to see if my 20-degree curve had progressed. If it had, then
the dreaded “Milwaukee brace” would be prescribed to outfit my spine. I
feared every doctor’s visit, wondering if the outside metal rod would
be assigned to my back. I remember reading Judy Blume’s book, Deenie,
about a 14- year old girl who was going to be a model but had to
postpone her dream (or rather her mother’s dream) when it was
discovered she had scoliosis and had to wear the brace that went from
her neck to her hips.
“When Deenie sees the brace
for the
first time, she wants to scream, Forget it...I’m never wearing that
thing. Everyone will know. Everyone!”
And that is
how I felt.
I would never wear a brace and I faithfully did the exercises the
physical therapist gave me, every single night, no matter what was
going on. I’d go to my room and lie down on the hand-me-down, yellow,
shag carpet from my cousin, and time each exercise with a stop watch,
all the while praying to God, to please spare me from the ugly metal
rod.

I
chose the theatre as an escape
from my fears. On
stage I could forget about my scoliosis and become another character. I
could make people laugh, cry and think. I loved the theatre and I loved
performing. The theatre gave me a sense of purpose as well. I was able
to communicate the importance of “no place like home” by portraying
Dorothy Gale from Kansas as well as share the beauty of communication
through my portrayal of Helen Keller. I had high aspirations as I
entered college as a theatre major and my scoliosis wasn’t a problem
until my senior year.
In the fall of 1988 I did a play
called
Ourselves Alone. The show was about the Irish Republican Army and I was
given a leading role. But before rehearsals each night, I would visit
the chiropractor to try and obtain some relief from the pain that was
causing me such trouble on the upper left side of my back. The
chiropractor never seemed to help. I did travel the 100 miles from
school to the metro-area to see an orthopedic doctor and he gave me a
device so I could put my neck in traction. That wasn’t the solution
either and I used the “neck stretcher” just once.
By
Christmas time the pain had disappeared and didn’t plague me again
until a year later after I had graduated. I began doing what all actors
do while they wait to land a show; I waited tables. I would visit
chiropractors and I guess it would help some. Then I would have a
stretch of time where it would all seem fine, like I never had a
problem in the first place. This was a pattern that continued until I
couldn’t take the pain anymore.
After the birth of
my fourth
child, I saw a physical therapist who suggested I visit a pediatric/
orthopedic doctor. I made an appointment and saw a doctor who
specialized in teenage scoliosis. Looking at my spine on the x-ray, it
was startling to see how crooked my spine was and even more startling
was the discovery that my 20-degree curve had progressed to 40. At 18
years of age I had been relieved not to have my spine measured anymore
because I was done growing. But I guess my spine decided it wasn’t done
moving. Now at 36 years of age, I would have to have surgery to have
the metal rod inserted inside my back.
I actually
thought this
would be okay. No one would see the rod, I would be straighter and I
could have lots of medications to take away any and all pain.
“How
difficult could this be,” I thought? “I’ve delivered four babies
without drugs.”
The
doctor told me that he could see I was determined to go through with
this serious back surgery even though at 40-degrees it was still an
option. My husband agreed only because it looked like my curve might
still progress in the years to come. When it was finalized that
scoliosis surgery would be performed on my spine, I truly had no real
understanding of what was about to happen to me. But later I realized I
was about to enter a stage that would require me to perform a role that
would greatly impact and change my life.
When an
individual is
accustomed to performing many roles that go with her title of “mother,”
it is difficult for that individual to stop and take on a role that
requires a loss of control and a dependence on others. In others words,
it is difficult for a mother to have major surgery. She must understand
that for quite some time she will be unable to take care of herself and
her family.
I heard what the doctor and others
were saying but
I thought, “With my determination, faith, family and friends,
accompanied by serious pain killers, I would be different than other
mothers. Maybe a week or so I’d be useless but after that I’d be
performing again.”
Yes, this is what I believed.
But I was wrong.
June
16, 2003, I lay on a stretcher. I watched the anesthesiologist prepare
me for my scoliosis surgery. I was to have four rods, screws and hooks
installed. A nurse-person was taping wire electrode things to my legs
because of course; there is always the possibility of being paralyzed
when dealing with this type of back surgery.
When
the
anesthesiologist man said, “I understand you have four little boys at
home,” all I could do was nod and start crying. I looked up at my
husband to see tears running down his face as well.
I
then said to the man, “I’m scared.”
He assured me,
“Well, I’m going to give you something right now that will calm you
down.”
And
that is the last thing I heard until I woke up nine hours later with a
tube up my nose leading down into my stomach and heard a nurse saying,
“It’s over Debbie.”
I didn’t open my eyes and I
couldn’t talk,
but I started to motion with my index finger, pointing to my stomach,
hoping the nurse understood I was about to throw up. That is when the
pain hit. The doctor had made a 13- inch cut to install the hardware I
needed, and that area felt to me like a third-degree burn with knives
poking into my flesh. I tried not to pass out as I vomited nothing.
I
soon realized that no amount of morphine or any other drug was going to
allow me to escape this painful experience. I was in intensive care for
two days and then moved to the recovery area where I would deal with a
bladder infection, a bacterial stomach infection, and constipation. On
day three, I would get my period. I guess when it rains it pours.
I
must note that the surgery itself went beautifully. The real drama was
spent in the week after the surgery, with me trying to function well
enough so I could leave the hospital. It was so hard to eat because I
had such stomach cramps. Despite several suppositories up my rear, I
never did have a bowel movement before leaving the hospital. When I did
leave, I was anemic and weighed 98 pounds. The only thing I managed to
consume were cans of Boost energy drinks (beverages I will never touch
again).
I was scared to go home. I missed my boys
and I hadn’t
seen them in ten days, and I knew I wasn’t going to be able to take
care of them because I couldn’t take care of myself. I was angry too.
Not at God or the doctors, but at myself for putting so much hope and
pride in my own abilities and strengths. None of the medications worked
for me, they only made me nauseous. And that made me mad. The pain was
almost unbearable to me. Valium, it turned out, was not the answer to
my physical or emotional pain. The answer was...acceptance. I needed to
accept my own weaknesses and reach out and receive the help from the
many friends and family members who were there for me. Most
importantly, I needed to let go of the expectations I had of myself and
others for not doing things the way I thought they should be done. I
needed to “let go.” But that was a really difficult thing for me to do
when I was so used to “doing” and performing.
Three
weeks into
my recovery, my dear friend from high school, Shannon, arrived from
Minneapolis to visit me. She lay on the bathroom floor with me and
stroked my hair after I had thrown up once again and spoke words of
comfort and reassurance.
I cried out, tears
streaming down my
face, “What if I never get better? What if I never can eat again, have
a bowel movement, and what if the pain never really goes away?”
I
was so scared and I hurt. But eventually I did get better; the pain
lessened and my attitude improved. I believe much of that relief came
from me just letting go and enjoying what I had. I became really
thankful for the things I had been given. I now had the time to truly
stop and smell the flowers. I stopped focusing on my fears but instead
focused on the love I had; the love of my family, my friends and
especially the love from God. Every day my boys would gently crawl up
on my bed and play games with me, something I rarely seemed to have
time for before the surgery. It was our sweet and special time. I heard
their stories and their adventures and rarely did I hear their
tattling...and that was sweet.
After three months
I could not
believe how great I felt physically. The pronounced hump on the left
side of my back was gone and I discovered I had grown an inch in
height. But not only did I have relief from my pain and the way I
looked, I had also grown emotionally and spiritually. One morning, as I
was opening the freezer to see if there were any more fruit smoothies
leftover from when my mother had been at my home caretaking, I noticed
the Bible verse magnet that read, “In quietness and in confidence shall
be your strength.” And I realized that that was the true key to my
recovery. When I was still and quiet, focusing on the blessings in my
life, I was at peace.
I also began to have a
confidence that
there was hope because I began to have a confidence in who I was and
what I had to offer my family. I became a better listener and a better
receiver. I also received confidence from my hope in God. My faith gave
me strength. In accepting who I was I got better at accepting others
for who they were. I’m a bit of a” neat nut” and I’ve always had the
philosophy, “there is a place for everything and everything has a
place.” My mom, without whose help I couldn’t have survived, doesn’t
follow this rule the same way I do. Her style is a little more
bohemian, so I would become frustrated when the house and laundry
weren’t done my way.
As I began to heal however, I saw the beauty
of who my mother really was. I saw that we each had our own unique
style and
my way wasn’t better it
was just
different.
There is a difference between pride and confidence in
oneself and I had been more proud than confident. That attitude changed
during my recovery process.
I
am not only thankful for a surgery that corrected my spine from a
40-degree curve to a 17-degree one, but I’m also thankful for the work
done on me as a person.
I guess it’s true, “What
doesn’t kill
you only makes you stronger.” I’m now stronger and feeling really good
about life. Of course, I’m only human, and I have days and times where
I’m frustrated with my family and with irritating or disappointing
circumstances, but I deal with them from a healthier perspective. I
appreciate the simple pleasures in life, like being able to have a
regular and normal bowel movement. But most of all, I appreciate the
beautiful family I have, my supportive and caring friends, and a loving
God who gives me strength and confidence. Who would have thought that”
being performed on” would end up providing me with lessons and tools so
I could go on and give a more true and genuine performance myself?
Six
months after my surgery someone asked me, “Having experienced what you
did, are you glad you went through with the surgery?”
My
answer was, “Yes, most definitely, yes.”