Write 2 the Heart

                         Write 2 The Heart
                         January 13, 2005
         Welcome to your latest issue of Write 2 the Heart.


     Take a moment to browse our new bookstore at:
http://www.write2theheart.com/html/book_store.html
You will find wonderful books written, or include stories by many
of our talented writers. You will also find books that aide the
budding writer. I highly recommend “Sally Stuart’s Christian
Writers’ Guide,” and “2005 Writer’s Market.” Both are must haves
for all serious writers. They are great tools to find that perfect
market for your writing.

     Molly’s story is a tribute of her love for her sister. We also see
a mother filled with determination to see that her daughter receives
the best treatment while under the watchful eye of a loving family.   
 
                     We Will Never Fuss Again!
                           Molly Lemmons

     The rolling engine came to a screeching halt as the big train
came barreling into the Oklahoma City depot when I was five
years old. I was there to meet the train that was bringing home my
seven-year-old sister, Sally Ann.

     As I stood by Daddy who held my baby brother, Bob, in his
arms, we watched anxiously as Mother and Sally Ann got off the
train. I ran to grab her, and as we twirled around hugging, we both
squealed in happiness, "We will never fuss again!" My mind
flashed back to how we happened to be at the train station that late
October evening in 1942.

     We were in Crandall, Texas, a small town with a population of
only a few hundred folks, where we were visiting our grand-
parents.  
 
     It was a blistering hot summer that year, and both of us were
learning to ride her new bike, taking turns riding around our
grandparents' property. It was so terribly hot that Sally stopped
every few minutes to run in and grab a cold glass of water. I fussed
at her for "hogging" the bike and not giving me my turn! Sulking, I
plopped onto one of the gliders on the mammoth screened-in front
porch of Mama-Dear's house and I pouted with my lip stuck out as
I watched her ride on and on without "taking turns."

     "You'll be sorry!" I screamed. "I'm telling on you!"

     It wasn't long until Sally came back around and said she was
going in. "I don't feel so good."

     "Ha-ha, you shouldn't feel so good, because you haven't
shared!" And I stuck out my tongue!. She said nothing but silently
went into the house and lay down on the divan.

     Early the next morning, she awoke up with a fever of 105
degrees. Dr. Woods came out to the house and checked the little
girl, who by now could not walk, and her head was "frozen" at an
angle.

     Gravely and sadly, the doctor said as kindly as he could, "I'm
sorry but Sally Ann has Infantile Paralysis-commonly called,
Polio."

     A disease of the muscles, Polio was an especially crippling
malady, striking mostly children. I stood in the waiting room of
Scottish Rite Hospital in Dallas, and listened to Mother and Daddy
as they talked with the doctors.

     "If she is to respond to therapy, she must not be hindered by the
emotions of family around her. You will have to leave her with us
for a while. We will send for you when we feel it best."

     Believing Polio to be contagious, I watched sadly as they
wheeled her away and out of my sight into isolation. Tears
streamed down my face! How sad and how sorry I felt that I had
been so ugly to her that day.  Questions whirled in my mind:
Would she walk again? Would she die? I was terrified of losing
this sister of mine.

     Hearts heavy, we returned to Oklahoma City. Mother stayed
behind for a while where she could observe Sally through one-way
mirrors.

     And now here they were, and she was getting off the train! I
knew our reunion would be brief but we got to be together one
night before she had to check into Crippled Children's Hospital in
Oklahoma City.

     Once again, they jerked off her clothes, put on her hospital
gown and wheeled her away and out of sight. I recall so vividly
standing on the ground below her window four stories up and
waving at the tear streaked little face pressed against the window.

     Finally, Mother had enough! She marched up to the hospital to
check her out with the promise of giving the treatments to Sally
herself. The treatments consisted of hot packing. This involved
dipping wool rags into boiling water, running them through the
wringer and wrapping the aching little 7-year-old body in them.
The wraps were so hot that Sister cried. I had to run outside and go
down the street to keep from hearing her scream. The exercises
were even worse. Lifting her leg caused excruciating pain.

     Finally, because Mother so faithfully fulfilled the responsibility
of the heart-rending therapy, Sally recovered without having to
wear the leg brace for which she had been fitted, and the only
outward sign that she had polio was that one leg was shorter and
smaller than the other.

     There were changes from inside the little girl, however. At
school, she wasn't chosen for the planned recess games of choosing
up relay teams, so she just stayed in from recess and read. Studying
the Bible became her first priority and for all of her suffering, good
things did come out of it. She developed depth of character and
faithfulness of heart, preparing her to fulfill her strong desire to be
a missionary.

     While as children, we didn't always keep our promise to "never
fuss again," we did, however, always remember why we said it that
day so many, many years ago. That sister, today is my dearest
friend.

  
Molly Lemmons
mollyloubelle @ cox.net


     This is an excerpt from my book, "Kind of Heart," a
compilation of columns I wrote for newspapers. I am retired from
the Mustang Public Schools, and have become a professional
storyteller, "Miss MollyLouBelle with Tales to Tell,"
www.storyteller.net/tellers/mlemmons.  I am a member of
Territory Tellers, and the National Storytelling Network. My
stories have been published in “Chicken Soup for the Mother's
Soul,” “The Christian Chronicle,” “The Christian Journal,” “Ideals
Magazine,” and “Christian Woman.”  In April 2005, Wings ePress
will release my second book, “The Passing of Paradise,” an
inspirational romance. I live in Mustang, Oklahoma with my
husband of forty-eight years and my seven cats!  We have two
grown children and two grandchildren.

     You are encouraged to write to the authors to let them know
what you think of their story. Have a comment on today's story?
Send it to: moderator @ write2theheart.com


     Write 2 the Heart now has an affiliate program with Cognigen.
They have several long distance plans to chose from. I personally
use the PowerNet Global 4.5¢ Per Minute Plan. I love having my
own toll free number without the monthly fee; I only pay for actual
calls. My family can call home whenever they are out of town. I
have used it more times than I care to remember over the last three
years in emergency situations.

   Cognigen has more than just great long distance rates; they have
calling cards, internet access, web hosting services and much more.
You can check out all of their telecommunication products and
services at http://ld.net/?cbspeir.  Looking for an affiliate program?
You will be surprised at all the products and services you will have
access to.




                     Military Prayer Reminder
    
     As you read over this list of names, please take a moment to
pray for these young people and their families:
 
Chris Speir                   
Tim Speir                     
Alan                              
Todd Holland
Graham
William
Julie Sagel
Jessie
Marshal Thompson
Jason
Eric Hernandez
Kristin Danielson
Ryan
Larry Miele
Daniel
Amy
John
Joanne
Gary Boardwine
Josh
Hadassah
Chanz Wackerly
Robert Henderson
David Habighurst
Tonia
Melissa Bair
Matthew Nutter
 
     Please continue to pray for our country, our leaders, and
our troops at this time. If you have loved ones in the military,
or who are being called to go overseas, send their names
(first and last or first only) to be included in our prayer
reminder.


                           Cheryl’s Corner

     Last year, David’s gout acted up for months. It kept getting
worse and worse until he thought he had a broke foot. He was
having a very hard time getting around and the pain was
excruciating. Finally he broke down, went to the doctor, and came
home with a new diet and medication. Every time David goes to
the doctor, it seems he comes home with a different diet. Of course
none of these diets allow the same thing.

     After cross-referencing all these diets, I have discovered the
only thing he can have is water and some vegetables. At my wits
end, I asked him which diet he would like to follow today.

     “You decide, you can either kill me quick or kill me slow.”  

     There’s nothing like a serving of high pressure. 

God bless,
Cheryl


Copyright © 2005, Write 2 the Heart
Nothing may be reproduced or published without
the written permission of the individual author or
copyright owner. All rights belong to the authors.