ACCEPTANCE COMES SLOWLY By Jonnie Sue Gillum Willis
My sister, Jonnie, who I always think of as the Angel of Fourche Valley, tells in her own words of the struggle to save her life when Polio hits.
" My parents, and my two older
brothers and I lived with my Grandma Gillum until I was four and a half years
old. From the start, I was the family weaklin'. They tell me that Grandma
rocked me in her lap as long as she could hold me. Then I sat beside her as
long as there was space. I remember rocking so hard in my own chair that I
turned over. This girl might have been sickly, but determination led her to
pick up the chair and ride it to many big towns which were foreign to my
country environment.
It seems that I had tonsulitis very often.
The doctor never considered me
well.enough to remove my tonsils, until I was grown. Because of my weaknesses,
I had to take many medications. Many months of my fifth grade year were spent
in bed. I had some problem with my heart, and the doctor advised complete bed
rest. Santa Clause Brought my gifts to my bedside table that year.
Because of my frailty, Mom insisted that I wear long handles and long stockings
to school. My first grade picture reveals my rebellion. The stockings are
rolled down and the long handles are rolled up.
Several months of my first grade year I
had to stay home battling bronchitis and tonsulitis. By that time, I was so
caught up in the magic of reading, writing, and arithmetic that I kept up with
my school work at home. School was such a joy.
As I reached those pre-teen years, I felt
it necessary to play as rough as my brothers and sisters. We would ride
homemade carts with blinding speed down hills, played in the creek, built
playhouses around trees, played ball, rode bushes to the ground, swung on
grapevines, and climbed every tree in our yard.
From a very young age, I struggled to get
a squeaking sound from our worn-out pump organ. Then one day, I succeeded. That
was it! I wanted to play the piano. Of course that was out of the question. We
couldn't afford to buy a piano, and there was no piano teacher available in our
small rural town of Wing. That didn't keep me from dreaming. I walked around
playing the notes with my fingers in the air. One day I found an advertisement
for music lessons by correspondence. I begged and pleaded and continued to play
in the air until my Dad finally found an old piano that he could afford. Then
he agreed to order 12 of the 96 lesson correspondence course. After he saw how
faithfully I practiced, how hard I worked, he ordered the remaining lessons.I
could picture myself as a famous musician, music teacher, or at least a church
pianist. (This was a major, major concession for Dad, coming at about the
time the sharecroppers notes were being paid off, many years after the Depression had ended - for others.)
In January of 1946, I accepted Christ as
my Savior. I was on top of the world. I just knew I'd outgrown the health
problems and live happily ever after. Ours was a very busy life, and I always
enjoyed my part in our many jobs to be done. When a new brother, Pat, arrived I
learned to help with the cooking, housework, food preservation, gardening, etc.
I continued to make time for those all-important piano lessons for one year.
That's when my world came tumbling down.
The pain in my neck began on a hot, dry
August day in 1946 when I was 13. My right arm was weak. Mom insisted that I
rest while she, Jan, and Barbara continued to carry water from the creek,
bringing it up the hill to water the flowers. (Mom always kept a variety of
pretty flowers around the house, and always made time to care for them.) I
insisted on carrying a bucket after they got it in the yard. I never realized
that this would be the last thing my right arm and hand would ever do.
The next day, I was in bed, in pain, with
total paralysis in this arm and hand. My entire body grew weaker as I lay in
bed for three days. The country doctor had never seen a case, but he suspected
polio.(That country doctor was uncle Arthur) My parents hired a neighbor
to take us to a doctor in Russellville. In a short time, he headed us to the
University Hospital in Little Rock.After the painful spinal tap, my diagnosis
of polio was confirmed. My memory left me after I was rolled through a door
with a sign which read, "Isolation Ward - No Admittance." I was put
to bed, unconscious, on a Saturday afternoon.
By Tuesday morning, the doctor felt sure
that I'd never survive, so he allowed Mom to put on a mask, a gown, and gloves
to visit me. Evidently this was the turning point, because I remember the tears
flowing as I opened my eyes and saw her. I couldn't talk because of a tube
through my nose to my stomach. Also, my entire body except my head was in an
iron lung. I can still hear the laborous sound as it forced my lungs to
breathe. Since I am a very modest person, I still remember the embarassment as
the doctor came to check on me daily, housed in this respirator for a week, no
gown or covering was placed over my naked body. The pain in my neck had
intensified because of the rubber collar surrounding it. I still have a scar from
the irritation of that collar.
Gradually, I learned to breathe without
help. Then I was placed on a firm bed with no pillow. My left hand, eyes and
mouth were all that moved above my waist. Both arms were tied above my head at
night. Later, I learned this was to help my lungs expand.
Two weeks after the initial attack, I was
moved to Children's hospital. There was my Dad outside that isolation ward. He
had spent many hours there the past two weeks. Tears of joy flowed from my eyes
as he rode in the ambulance across town with me. During all this time to save
my life, no brush or comb had ever touched my hair. It was matted, tangled, and
dirty. I felt like a mess, but I was alive! As soon as they had me in bed one
nurse shampooed and brushed my hair. After a bath I began to feel much better.
Now the real workout began. The heat packs
felt good to my sore, stiff muscles. Slowly, the physical therapy began to
loosen my limbs. Strength gradually returned, and I couldn't wait to be on my feet
again. I can still see the frightened shock on the nurse's face the first day I
put one foot against the side of my bed and raised myself up. She was afraid I
would fall flat on my face, but I didn't! From that day on, I began to
experiment to see what I could do. Many days, planning creative ways to do
simple daily tasks was half the challenge. There was no time to say "I
can't". The act of sitting up in a wheelchair one afternoon was one of the
hardest tasks I ever accomplished. I gradually relearned to walk, feed myself,
and to write in manuscript with my left hand
(before polio, I was right handed.) Soon I was able to help other girls,
and I felt like the most blessed girl in the ward.
After three months I was fitted with brace
around my body which held my right arm out and up. "Oh please, don't make
me wear this out in public," were my thoughts as the nurse strapped it on.
The Barnum and Bailey Circus had come to Little Rock and the nurse was taking
some of us. "You might as well wear this and start getting used to the
public," she said as we left the hospital. After I began to enjoy my first
circus, I soon forgot how I looked.
Just before Thanksgiving the doctor said I
could go home. My dreams of going home and starting to school in the 8th grade
had kept me going all those sleepless nights in the hospital. Dad came on the
bus to get me. Normally the bus didn't come by our house. However, the driver
made an exception and took us to our driveway. Seeing my home again and my
family running to meet us brought tears of joy. I was a survivor, and I was
home!"
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