Make the most out of life
Joseph Shore
I wrote a
partial autobiography named Good Dreams for many reasons, among them, to
encourage people who are born with deformities not to give up on their
dreams. I am such a person. I was
born with coarctation syndrome. Until recently, most people born with this
defect died young. This is a deformity of the heart and the blood vessels which
affects the circulation system, the immune system, and the functions of the
heart, lungs, and kidneys. When I was born, so long ago J, this condition was not even well
understood. The country doctor who delivered me did not have the instruments to
detect the condition. My childhood doctor in small-town Missouri, likewise
could only hear a heart murmur, but he wondered why little Joe-boy’s immune system didn’t work very well. He
tried giving me monthly injections of bicyllin to
boost my immune system. That seemed to keep me from getting sick as often. For
his next trick he gave my mother an enormous jar of tetracycline and said,
“Whenever he starts to get sick, give him a few of these.” That
helped a little bit, but soon I was immune to tetracycline and my teeth were
permanently yellowed. We look back at the primitive nature of medicine in the
early 1950’s and wonder how any of us survived.
I grew into
my childhood as a little boy with an undiagnosed, untreated birth defect. I was
just “different.” I could not do things that other boys could do. I
had ability in all sports which I played in sandlot. I was a good baseball
player. I could hit really far, field and throw well. I could even run fast if
it was just a short distance. I was good in basketball, had a good jump shot,
and could jump really well. What I couldn’t do was keep pace running up
and down the court. I was good in football, could throw the ball a long way and
could place kick the ball really well. Nevertheless, when I would try out for
any team at school, the doctor would get one listen to my heart and say,
“Sorry Joe, I just can’t let you play.”I grew up feeling sort
of like a leper. I couldn’t do anything that “normal” boys
could do. I wanted to play sports
so badly that I found ways to get around the doctor. I played intramural sports
and excelled. I took physical education in high school and excelled in all
areas except long-distance running. I was running the 60 yard dash one day and
the coach was watching. I ran it really fast and it caught his attention.
“Wow, Shore is really fast.” Then he let me run the 880 relay, and
I couldn’t keep up the pace for the longer distance. But that one little
bit of praise for my 60 yard dash meant so much to me. It made me feel almost
normal.
I had a very
kind coach in high school who noticed some of my frustrations, even if he
didn’t know what was physically wrong with me. He saw that I wanted to
play organized baseball but couldn’t because I had failed the physical.
He had been a professional baseball umpire after WWII and he still umpired area
baseball. He took me under his wing and gave me free instructions on how to be
an umpire. I worked at it with full diligence, like this was my chance to be
near the game and be “normal.”
He took me with him to umpire college ball when I was still a kid in
high school. Then he took me to the “big time,” to semi-pro
baseball. I was a good umpire and I loved being in control of the game I wanted
to play. My endurance was not a problem for the limited mobility required of an
umpire. It seemed like I had found a niche in sports. The next step was to go
to umpire school and get a placement in the minor leagues. That hope was
stopped however by my need for glasses. In those days umpires were not allowed
to wear contact lenses. If you didn’t have 20/20 vision uncorrected, you
could not be a professional umpire.
By the time
I was 19, my family doctor finally got around to telling my parents,
“There is something wrong with Joe-boy that I can’t understand. You
should take him down to the Houston Methodist Hospital and let Dr. Debakey
examine him.” So off we went. In 1967 heart surgery was still primitive
by today’s standards. But they found the coarctation in the aorta and
removed it. But even then the full details of coarctation syndrome were not
well understood. They sent me home without explaining what I could and could
not do and what I should expect my health to be like in the future. The reason
is that even Debakey didn’t know back then. In reality all they had done
was to fix the aorta. The stenotic aortic valve was
still left in place. They could not change the fact that in 19 years, the blood
vessels in the lower part of my body had grown small because of the
coarctation. They could not change the fact that in 19 years the condition had
made my lungs and kidneys weak. When we talk today about stem cell research, we
are envisioning a future when the developing fetus within the womb can be
scanned for genetic birth defects, and when found, those defects can be
eliminated during fetal development by the insertion of stem cells. We are
envisioning a future when nobody has to be born with birth defects. Today, had
I been born with coarctation syndrome, it would have been detected at birth and
surgery could have corrected it before its effects rampaged through childhood
growth. When modern doctors today hear my story they ask, “Why
didn’t they detect this at birth.” I answer, “Because in 1948 in
small-town Missouri there were no instruments to detect this at
birth.” They are always
amazed at this as if they cannot remember such an era.
When I went
to college I didn’t really know what I wanted to do since sports was out
of the question. My grandfather, Vernon Shore, had been a well-known Baptist
preacher during the depression and afterwards. I felt pressured to move into
his shoes, not knowing just exactly where my
shoes were at the time. I graduated from high school in 1966 and headed to
Southwest Baptist University the next year.
I still had
music in my life. Even though I had given up on voice lessons, I had been
accepted into the choir. I was happy but a bit timid because there were a lot
of music majors in it with "real" talent. To make matters more
intimidating, the director, Dr. Cowan, was a star. He had sung with the famous
Robert Shaw Chorale. He let us hear his rich, bass-baritone voice from time to
time and we were all convinced that only Ted Harris had a better voice in all
of Missouri. Ted Harris was a Professor of Voice who had sung with Jerome Hines
of the Metropolitan Opera. Mr. Harris commanded respect and more than a little
awe. The year that I arrived at SBU, Mr. Harris was preparing a role in Jerome
Hines' sacred opera on the life of Jesus called I Am The Way, which was going to be
performed in
A lot of
good things happened at SBU. One of them was that I was elected to Who’s
Who in
Southern
Baptist Theological Seminary in
The campus
was Southern beauty itself, situated in rolling,
The
fundamentalists within the denomination were fearful of all that Southern
Seminary stood for. They distrusted modern scholarship. They wanted the old
time religion where everyone knew his place! And they wanted every modern
professor and student OUT of the denomination. As much as anything, the war was
about political power.
The one
student who always competed with me for top grade was an interesting fellow
named Lynn Fann.
Some might have called
I grew more
and more empty inside in seminary. I wanted desperately to be a minister but I
felt very much out of place, like I didn’t really belong there. It was
1972 and while I was at my most desperate I cried out to God for help. I actually
heard an inner Voice say to me, "Your sermons can be your characters on
stage. The stage can be your pulpit. The audience can be your congregation. Now
go put feet to your faith." I
had absolutely no reason to believe this Voice. Baptists do not hear voices.
Maybe Pentecostals do but not Baptists! I had taken no voice lessons. Nobody
heard any special singing talent in me of this magnitude. Remember my only
teacher in university, Nathan MacAllister, had even
refused to teach me because I was so untalented. I had no reason to think that I could
ever get on a professional stage and sing Grand Opera. It sounded like a stupid
idea! But at some level deep inside of me I must have believed it. I wondered
why I had never really felt a “call” to the ministry. But this
experience definitely fit the description of a “call” to sing
opera. Eventually, after fighting seminary another semester, I left, got an
apartment across the street and a job in a pizza restaurant. When I wasn't
working I was listening to opera. One day in 1973 I opened my mouth to see if I
could make a sound like one of those guys on the records and out came the
essential sound that I have today. A couple of weeks later a friend heard me
singing as he came for a visit and
said, "Wow, you've got quite a voice. You ought to enter the Metropolitan
Opera Auditions." I didn't
know what they were but I said. "Ok." I sent off and got an entrance
form. The first level of the competition was in
People from
Tulsa Opera were there and offered me beginning roles with their company as
well as a scholarship to
One of the
judges was from The Santa Fe Opera which was also hearing singers audition for
Apprentice Artists. Later I discovered that ten thousand singers across
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The next year, 1975 I was one of the ten winners of the Met National
Auditions and the following year I won The WGN Auditions. I was off to a
flying start. I had no intention of telling anyone that I had heart disease.
When you are competing with thousands of good singers, the last thing you
want to announce is some major heart problem you have. I didn't want to give
the business an excuse to get rid of me. So I tried to put on an act that
nothing was wrong with me and I was as strong as an ox. My voice was as
strong as any Verdi baritone of my day. But my heart and lungs were weak. I
would be in the middle of rehearsals for heavy roles like "Rigoletto" and my body would just break down from
the stress. I would have to lay out of rehearsals
for a few days and come back in. But I can honestly say that I always came
through in performance, and out of over 300 reviews there may be only two or
three that are not just glowing--like your manager wrote them himself. But I
pushed myself relentlessly to be able to perform in this high environment. If
you look at all the Rigolettos I did, all the big
roles like Macbeth, Telramund, Amonasro,
Boris Godounov, Barnaba, Scarpia, I literally had to draw on my will in order to
command my body so that I could do the role. The great basso, Martti Talvela, had heart
disease and he dropped dead at his daughter's wedding. A diseased heart and
lungs are not well suited to opera. This is what I had to overcome each
performance, without anyone knowing about it. I was determined to make as much out
of my singing life as I could. I
sang the greatest roles for baritone in the best opera houses in the United
States, among them, Rigoletto, Germont, Amonasro, Renato, and Falstaff, among the Verdi roles,
as well as for Alfio, Tonio,
Scarpia, Barnaba, Telramund, Boris, Pizarro, and Salieri.
I achieved my dream of moving an audience with great singing and acting and
shared the stage with some of the greatest singers of my day: Jerome Hines,
James McCracken, Lucine Amara,
Carlo Cossutta, Ezio Flagello, Gilda Cruz-Romo,
Frances Yeend, Lucia Evangelista, Sherrill Milnes, Paul Plishka, and many
others. Some people complained that I was difficult to work with. My
combination of heroic vocalism and fragile health was confusing. Perhaps I
erred in not telling the truth about my heart from the beginning, but I was
afraid they would not cast me in the big roles if they knew. Instead I got a
reputation of being difficult to work with---which I am not really. I really
pushed my heart and body hard in some roles, Telramund,
Barnaba, et al, and finally it all caught up to me.
In 1994 I had to have another heart surgery. I recovered from that one
quickly and was back on the stage in three months. Then in 2006 my artificial
heart valve cracked and I began drowning in my own blood. It took the
Canadian medical system almost a year to give me a new surgery. By that time
my lungs were damaged. Now my heart is too weak to sing and my lungs hold
enough air for about four tones. Singing, my art, my greatest joy, my
calling, I can do no more. But I made the most of my life. My sadness now is
a part of the joy then. That's the deal. If in 1974 when I debuted in opera,
a psychic had told me that I could play it safe with my voice and sing less
demanding roles and have a longer career, or sing the greatest roles in opera
and wear my heart out early, I would not change a thing. I would still sing Rigoletto, Macbeth, Amonasro, Renato, Falstaff, Boris, Pizarro, Telramund,
with a mind possessed of a dream to unite legitimate acting with world-class
vocalism. Of course I am sad now that I can no longer sing, but the sadness
now is a part of the high times then. That's the deal. For all of you who were born with a birth defect: I know how it feels to be different. I
know how easily one can feel like a prisoner inside your defective body. My
message to you is this: Whatever limitation you have been given in life, make
the most of your life. Don’t let anyone define for you what you can do
or can’t do. YOU make the call. There is something you can do with your
life even with the limitations you have been given. When you find that
something, give it all you’ve got. Don’t hold back. Play the game
as hard as you can. Life is too short to hold back. Go for it on fourth down.
Don’t punt. Swing away for the fence. Don’t slap at the ball.
Shoot that three point jump shot. Don’t pass for the lay-up. Go for
that knock out. Don’t win on points. Sing with all your might and with
all your heart and soul, and be grateful for the chance to live and make the
most out of your life. That’s what I have learned this life-time. |