I always thought that nightmares had one thing going for them. You
woke up. Safe.
With the reassuring reality of daylight, you sigh with relief and
snuggle deeper into the blankets while your heartbeat slows to normal.
This is the way nightmares are supposed to progress: first the nightmare,
then the waking, and finally the comfortable feeling that the really
b-a-d things happen to you only in dreams.
At least that's the way nightmares happened
with me until the day 20 years ago when I woke up in the recovery
room at Duke University Medical Center, to see my husband, George,
bending over me. I had asked him to tell me the truth as soon as
I opened my eyes. I couldn't bear having to look to see if all of
me was still there, if my "twin
peaks" were still familiarly in place. To see if I was still "whole." George
said, "I love you," and then said, "It was malignant." I
remember lying on that gurney, flinging my head back and forth on the
pillow and screaming, "No!" with all the strength that the
waning anesthesia allowed. And I remember thinking, this is a nightmare
-and I am awake!
What I had was breast cancer, and it changed my life. Suddenly and
completely. Irretrievably and forever. I was not safe. Not anymore.
Never again.
As I lay in my hospital room that day, only dimly
aware of the numbing flurry of activity around me, I watched with despair
as my lifelong sense of security just floated out the window. Here,
in addition to the cancer and the mastectomy, was the nightmare that
would never fade: no more security - ever. At first, fear colored every
aspect of my life, including my language: with the increasing anxiety,
even my sentences became jerky and choppy.
Friends and family surrounded me on that Friday, bringing me hugs
and prayers and flowers, and, best of all, themselves. It was wonderfully
distracting.
But then Friday night came (as Friday nights
always do) and everybody went home. There I was, all by myself. As
all of us ultimately are. I lay there in the little white hospital
room, in the little white hospital bed, staring up at the little
white hospital ceiling...having just swallowed a little white hospital
pill that was not working! And my mind drifted back to my unusual
parents. My college professor father and my teacher mother never
chose the well-worn paths. Every time I had a problem, faced a crisis,
or ran into the various and sundry brick walls that are always a
part of growing up, one or the other of them would exclaim: "Isn't that fascinating! I wonder how many ways
you can deal with this?" And off we would go, exploring possibilities
and turning problems into adventures.
Thus, with the terror of a life-threatening and body-altering disease,
began the fascination of how to deal with it. Of how to face this new
challenge. I started hesitantly to confront my new self and the new
view that others would have of me.
My doctor during this time at Duke was, without
question, the most unapproachable man I had ever met. He looked like
a Russian czar, massive and dramatic, with a lion's mane of flowing
white hair. Everywhere he went, a worshipful, white-coated entourage
trotted behind, notebooks in hand, writing down every word he uttered.
I would have sworn that even the plants in my room stood straighter
when he strode in! He was brusque, all business, always in a hurry.
My stomach-turning panic was that this man, in charge of my health
- my life - scared me to tears. In an abnormal situation, with a desperate
need for a reassuring hand on my shaking shoulder and I was totally
intimidated by this imposing, intimidating doctor. I began thinking
about what I could do to get him to see me as an individual and not
just a number on a hospital room door, somehow sensing that such a
bond might enhance my chances of recovery.
(How fascinating - what are my options?) I got permission
to leave the hospital with George, and we went to a T-shirt shop where
I spent $7.99 having a T-shirt made for him: a dark green one with
big white letters across the front that said: ONE OF AMERICA'S 10 BEST
BREAST MEN.
I almost didn't give it to him. The whole
thing was beginning to feel so silly. But, after all, I had spent
$7.99 and didn't want to throw money away. You can only begin to
imagine the lump-in-the-throat nervousness with which I presented
this so-silly shirt to Duke's most not-silly surgeon. He took one
look at it, laughed, and said with quiet astonishment, "You...did
this...for me?"
And one more time it hit me: We are all alike in
that, whatever our role, whatever our profession, whatever our lot
in life - all of us are looking for someone to make us feel important.
That T-shirt made my brilliant, world-renowned surgeon feel important.
Imagine that!
The honest facing of reality and the effort
to deal with it creatively started affecting other areas of my life.
My family relationships became closer and more open. Two weeks after
the mastectomy, my ten-year-old son and several of his friends burst
into the kitchen. They looked at me searchingly, and son Joe blurted
out, "Are you wearing your
artificial breast today?" "No" - I laughed - "I
left it in the bedroom." And off they went outside to play. My
visiting mother asked, "Are you sure you want your son and his
friends discussing your breast?" "He's having to face the
fact that he might lose his mother," I responded. "If he
needs to take me to school for show-and-tell in order to deal with
this, I'll go. Now, there," I said to her, remembering all the
times she had said it to me, "is a fascinating idea!"
Marvelous things began to happen. I entered upon a speaking career,
which has plunged me into the business community and into the fields
of medicine, education, technology, insurance, sales, travel, finance,
and government. Fortune 500 companies fill my client list. My presentations
are not about cancer, just because of cancer. (Fascinating! I wonder
how many ways there are to deal with each day's celebration of new
possibilities, with each day's new and unique audience, with each day's
wonder at what lies ahead.) Rejoice in your own willingness to step
out and you'll see new doors opening for you where once there were
only blank walls.
Having had cancer has freed me forever from
what I call the Scarlett O'Hara syndrome of: "I can make a new
friend...tomorrow. I can make an impact...tomorrow. I can write a
book...tomorrow...I can start a new business...tomorrow. I can take
more risks...tomorrow." I've
had a smack-in-the-face realization that there may not be three score
and ten cards in my deck. Because I am not guaranteed a tomorrow,
my life has taken a unique and enriching direction. Today.
Isn't that...fascinating? I'd always thought that
life was about building security. And then a great teacher - cancer
- taught me that this is not what life is all about at all. It taught
me that nightmares can become springboards.
How much difference does it make to step outside
the bounds of the expected and the ordinary? Five years after finishing
the prescribed therapy, I read in the paper that the "doctor
from Duke" was
coming to Charlotte to do a symposium on breast cancer. As I stepped
into the back of the auditorium to hear him speak, he saw me and called
out "Emory! Emory Austin!" Five years later, five thousand
patients later, he remembered me. "My goodness," I thought
- this truly is fascinating."
[And so, dear reader, because I've had cancer, I no longer have any
security that is based on guarantees of time. Wherever you are, just
raise your hand if you believe you have any more of that kind of security
than I do. All of us want to live. All of us want to believe that a
dream can come true. Each of us can make at least one dream come true.
And doing that might set a brave new pattern! If you want to do what
you were put here to do, it's essential to get on with it today.]
Sometimes we face monsters who have names - disease,
fear, age, job security, financial hurdles, addictions, cruelty. Conquering
these monsters will depend (to some extent) on the patterns we have
developed for ourselves in the past and continue to develop today.
Celebrate patterns that will bless you!
- Emory Austin