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More...Inspirational Readings

All these stories and poems have been an inspiration to our family...please enjoy them!

"Snowflakes and fingerprints--
you'll always find--
Each one is different, one of a kind.
And just like a snowflake
This, too, is true,
No one else is exactly like you!"
Author Unknown

Welcome to Holland
by Emily Perl Kingsley 

I am often asked to describe the experience of raising a child with a disability-to try to help people who have not shared that unique experience to understand it, to imagine how it would feel. It's like this.....

When you're going to have a baby, it's like planning a fabulous vacation trip-to Italy.You buy a bunch of guide books and make your wonderful plans. the Coliseum. The Michelangelo David. The Gondolas in Venice. You may learn some handy phrases in Italian. It's all very exiting.

After months of eager anticipation, the day finally arrives. You pack your bags and off you go. Several hours later, the plane lands. The stewardess comes in and says, "Welcome to Holland"

"Holland?!?" you say. "What do you mean Holland?? I signed up for Italy! I'm supposed to be in Italy. All my life I've dreamed of going to Italy."

But there's been a change in flight plan. They've landed in Holland and there you must stay.

The important thing is that they hav'nt taken you to a horrible, disgusting, filthy place, full of pestilence, famine and disease. It's just a different place.

So you must go out and buy new guide books. And you must learn a whole new language. And you will meet a whole new group of people you would never have met.

It's just a different place. It's slower-paced than Italy, less flashy than Italy. But after you've been there for a while and you catch your breath, you look around....and you begin to notice that Holland has windmills...and Holland has tulips. Holland even has Rembrandts.

But everyone you know is busy coming and going from Italy... and they're all bragging about what a wonderful time they had there. And for the rest of you life, you will say "Yes, that's where I was supposed to go. That's what I had planned."

And the pain of that will never, ever, ever, ever go away... because the loss of that dream is a very very significant loss.

But... If you spend your life mourning the fact that you did'nt get to Italy, you may never be free to enjoy the very special, the very lovely things....about Holland.

 

HOLLAND SCHMOLLAND

written by Laura Kreuger Crawford ~ whose son has autism ~ essay discusses her feelings on her trip to "Holland"

"When I read that, my son was almost three, completely non-verbal and was hitting me over a hundred times a day. While I appreciated the intention of the story, I couldn't help but think, Are they kidding? We are not in some peaceful countryside dotted with windmills. We are in a country under siege -- dodging bombs, trying to board overloaded helicopters, bribing officials -- all the while thinking, What happened to our
beautiful life?

That was 5 years ago. My son is now 8 and though we have come to accept that he will always have autism, we no longer feel like citizens of a battle torn nation. WITH the help of countless dedicated therapists and teachers, biological interventions, and an enormously supportive family, my son has become a fun-loving, affectionate boy with many endearing qualities and skills. In the process we've created, well, our own country, with its own unique traditions and customs.

It's not a war zone, but it s still not Holland. Let's call it Schmolland. In Schmolland, it is perfectly customary to lick walls, rub cold pieces of metal across your mouth and line up all your toys end to end. You can show affection by giving a "pointy chin." A "pointy chin " is when you act like you are going to hug someone and just when you are really close, you jam your chin into the other persons shoulder. For the person giving the "pointy chin" this feels really good, for the receiver not so much, but you get used to it.

For citizens of Schmolland, it is quite normal to repeatlines from videos to express emotion. If you are sad, you can look downcast and say "Oh Pongo." When mad or anxious, you might shout, "Snow can't stop me!" or "Duchess, kittens, come on!" Sometimes, "And now our feature presentation" says it all.

In Schmolland, there's not a lot to do, so our citizens find amusement wherever they can. Bouncing on the couch for hours, methodically pulling feathers out of down pillows, and laughing hysterically in bed at 4:00am, are all traditional Schmutch pastimes.

The hard part about living in our country is dealing with people from other countries. We try to assimilate ourselves and mimic their customs, but we aren't always successful. It's perfectly understandable that an 8-year-old boy from Schmolland would steal a train from a toddler at the Thomas the Tank Engine Train Table at Barnes and Noble. But this is clearly not understandable or acceptable in other countries, and so we must drag our 8 year old out of the store kicking and screaming while all the customers look on with stark, pitying stares. But we ignore these looks and focus on the exit sign because we are a proud people.

Where we live, it is not surprising when an 8-year-old boy reaches for the fleshy part of a woman's upper torso and says, Do we touch boodoo? We simply say, "No we don't touch boodoo" and go on about our business.

It's a bit more startling in other countries, however, and can cause all sorts of cross-cultural misunderstandings.

And, though most foreigners can get a drop of water on their pants and still carry on, this is intolerable to certain citizens in Schmolland who insist that the pants must come off no matter where they are, regardless of whether another pair of pants are present.

Other families who are affected by autism are familiar and comforting to us, yet are still separate entities. Together we make up a federation of countries, kind of like Scandinavia. Like a person from Denmark talking with a person from Norway, (or in our case someone from Schmenmark talking with someone from Schmorway), we share enough similarities in our language and customs to understand each other, but conversations
inevitably highlight the diversity of our traditions. Oh your child is a runner? Mine won t go to the bathroom without asking permission. "My child eats paper. Yesterday he ate a whole video box." "My daughter only eats 4 foods, all of them white." "My son wants to blow on everyone." "My son can't stand to hear the word no. We can't use any negatives at all in our house." "We finally had to lock up the VCR because my son was obsessed with the rewind button."

There is one thing we all agree on: we are a growing population. 10 years ago, 1 in 10,000 children had autism. Today the rate is approximately 1 in 250. Something is dreadfully wrong. Though the causes of the increase are still being hotly debated, a
number of parents and professionals believe genetic pre-disposition has collided with too many environment insults -- toxins, chemicals, antibiotics, and vaccines -- to create immunological chaos in the nervous systems of developing children. One medical journalist speculated that these children are like the proverbial canary in the coal mine here to alert us to the growing dangers in our environment. While this is certainly not a view shared by all in the autism community, it feels true to me.

I hope that researchers discover the magic bullet we all so desperately crave. And I will never stop investigating new treatments and therapies that might help my son. But more and more my priorities are shifting from what could be to what is. I look around at this country my family has created, with all its unique customs, and it feels like home. For us, any time spent "nation-building" is time well spent."

BEFORE I GO TO SLEEP
by SALLY MEYER
 
Dear Mommy, don't you cry now and Daddy don't you weep.
I want to whisper in your ear before I go to sleep.
I know that when I came here I seemed perfect in every way.
and you were so proud Daddy when you held me on that day.
And Mommy when you kissed me and wrapped me up so tight,
I felt as if I belonged here, and everything was right.
 
When things got really scary and I began to slip away
I saw your face dear Mommy as you knelt by me to pray.
And Daddy, I always notice when you wipe away a tear,
or watch the other little boys as they run and laugh and cheer.
I may not be able to tell you how much I love you so,
or even show you how I feel and what I really know.
 
But when you hold me Mommy at night when all is still
I hear your dear heart beating and I know that all is well.
And Daddy when you take me to the park to run and play
I know that you still love though the words I cannot say.
So Daddy don't you cry now and Mommy don't you weep,
I want to tell you something before I go to sleep.
 
I may be sort of different, and you may not understand.
I know that I am not that child that you and Daddy planned.
But I love you both so very much and I know you love me too
and one day when this life is done you will feel my love for you.
I know the future is unknown and you will always have to be
the one's that love and listen and take good care of me.
 
The road we walk is rough sometimes and you cry a lot of tears,
but one day we will turn and laugh as we look back o'er the years.
So Mommy don't you cry now, and Daddy please don't weep...
I want to say,
I LOVE YOU!
before I go to sleep.
 
 
 

THE SPECIAL MOTHER
BY ERMA BOMBECK
 
Most women become mothers by accident, some by choice, a few by social pressures and a couple by habit.
 
This year nearly 100,000 women will become mothers of handicapped children.  Did you ever wonder how mothers of handicapped children are chosen?
 
Somehow I visualize God hovering over earth selecting his instruments for propagation with great care and deliberation. As he observes, he instructs his angels to make notes in a giant ledger.
 
"Armstrong, Beth; son. Patron Saint...give her Gerard.  He's used to profanity."
 
"Forrest, Marjorie; daughter. Patron Saint, Cecelia."
 
"Rutledge, Carrie; twins. Patron Saint, Matthew."
 
Finally he passes a name to an angel and smiles, "Give her a handicapped child."
 
The angel is curious. "Why this one God?  She's so Happy."
 
"Exactly," smiles God, "Could I give a handicapped child to a mother who does not know laughter?  That would be cruel."
 
"But has she patience?" asks the angel.
 
"I don't want her to have too much patience or she will drown in a sea of self-pity and despair.  Once the shock and resentment wears off, she'll handle it."
 
"I watched her today.  She has the feeling of self and independence that is so rare and so necessary in a mother.  You see, the child I'm going to give her has her own world.  She has to make her live in her world and that's not going to be easy."
 
"But, Lord, I don't think she even believes in you." God smiles, "No matter, I can fix that.  This one is perfect - she has just enough selfishness." The angel gasps - "selfishness? is that a virtue?"
 
God nods. "If she can't separate herself from the child occasionally, she'll never survive.  Yes, here is a woman whom I will bless with a child less than perfect.  She doesn't realize it yet, but she is to be envied.  She will never take for granted a 'spoken word'". She will never consider a "step" ordinary.  When her child says 'momma' for the first time, she will be present at a miracle, and will know it"
 
"I will permit her to see clearly the things I see...ignorance, cruelty, prejudice...and allow her to rise above them.  She will never be alone.  I will be at her side every minute of every day of her life, because she is doing my work as surely as if she is here by My side".
 
"And what about her Patron Saint?" asks the angel, his pen poised in mid-air.
 
God smiles, "A mirror will suffice."
 
 
 
I am Every Child
(Written by Bill Roberts ~ My professor who had inspired me)
 
You have chosen to be a part of my life,
To teach me for a year
I may not be what you expected,
But you have nothing to fear.
 
Show me that you care.
Teach me how to cope,
So that in spite of my difficulties
I may always have hope.
 
I didn't choose to be this way,
Nor did my parents know
That like every other child,
I was not destined to grow.
 
I live with my impairments,
Each and every day.
I rely on teachers like you,
To guide me along the way.
 
Please look for my strengths,
The way that I learn best,
And together we will meet,
The challenge of any test.
 
If you don't think of me as different,
With special wants and needs,
You'll find a capable learner,
Just wanting to succeed.
 
Don't see me with my label,
Sometimes severe and sometimes mild.
Please see me as a student,
For I am every child.
 
 
Thoughts of a Mom
by Maureen K Higgens
 
Many of you I have never even met face to face, but I've searched you out every day. I've looked for you on the Internet, on playgrounds and in grocery stores. I've become an expert at identifying you. You are well-worn. You are stronger than you ever wanted to be. Your words ring experience, experience you culled with your very heart and soul. You are compassionate beyond the expectations of this world. You are my "sisters." Yes, you and I, my friend, are sisters in a sorority. A very elite sorority. We are special. Just like any other sorority, we were chosen to be members. Some of us were invited to join immediately, some not for months or even years. Some of us even tried to refuse membership, but to no avail. We were initiated in neurologist's offices and NICU units, in obstetrician's offices, in emergency rooms, and during ultrasounds. We were initiated with somber telephone calls, consultations, evaluations, blood tests, x-rays, MRI films, and heart surgeries. All of us have one thing in common. One day things were fine. We were pregnant, or we had just given birth, or we were nursing our newborn, or we were playing with our toddler. Yes, one minute everything was fine. Then, whether it happened in an instant, as it often does, or over the course of a few weeks or months, our entire lives changed. something wasn't quite right. Then we found ourselves mothers of children with special needs. We are united, we sisters, regardless of the diversity of our children's special needs. Some of our children undergo chemotherapy. Some need respirators and ventilators. Some are unable to talk, some are unable to walk. Some eat through feeding tubes. Some live in a different world. We do not discriminate against those mothers whose children's needs are not as "special" as our child's. We have mutual respect and empathy for all the women who walk in our shoes. We are knowledgeable. We have educated ourselves with whatever materials we could find. We know "the" specialists in the field. We know "the" neurologists, "the" hospitals, "the" wonder drugs, "the" treatments. We know "the" tests that need to be done, we know "the" degenerative and progressive diseases and we hold our breath while our children are tested for them. Without formal education, we could become board certified in neurology, endocrinology, and psychiatry. We have taken on our insurance companies and school boards to get what our children need to survive, and to flourish. We have prevailed upon the State to include augmentative communication devices in special education classes and mainstream schools for our children with cerebral palsy. We have labored to prove to insurance companies the medical necessity of gait trainers and other adaptive equipment for our children with spinal cord defects. We have sued municipalities to have our children properly classified so they could receive education and evaluation commensurate with their diagnosis. We have learned to deal with the rest of the world, even if that means walking away from it. We have tolerated scorn in supermarkets during "tantrums" and gritted our teeth while discipline was advocated by the person behind us on line. We have tolerated inane suggestions and home remedies from well-meaning strangers. We have tolerated mothers of children without special needs complaining about chicken pox and ear infections. We have learned that many of our closest friends can't understand what it's like to be in our sorority, and don't even want to try. We have our own personal copies of Emily Perl Kingsley's "A Trip To Holland" and Erma Bombeck's "The Special Mother." We keep them by our bedside and read and reread them during our toughest hours. We have coped with holidays. We have found ways to get our physically handicapped children to the neighbors' front doors on Halloween, and we have found ways to help our deaf children form the words,"trick or treat." We have accepted that our children with sensory dysfunction will never wear velvet or lace on Christmas. We have painted a canvas of lights and a blazing Yule log with our words for our blind children. We have pureed turkey on Thanksgiving. We have bought white chocolate bunnies for Easter. And all the while, we have tried to create a festive atmosphere for the rest of our family. We've gotten up every morning since our journey began wondering how we'd make it through another day, and gone to bed every evening not sure how we did it. We've mourned the fact that we never got to relax and sip red wine in Italy. We've mourned the fact that our trip to Holland has required much more baggage than we ever imagined when we first visited the travel agent. And we've mourned because we left for the airport without most of the things we needed for the trip. But we, sisters, we keep the faith always. We never stop believing. Our love for our special children and our belief in all that they will achieve in life knows no bounds. We dream of them scoring touchdowns and extra points and home runs. We visualize them running sprints and marathons. We dream of them planting vegetable seeds, riding horses, and chopping down trees. We hear their angelic voices singing Christmas carols. We see their palettes smeared with watercolors, and their fingers flying over ivory keys in a concert hall. We are amazed at the grace of their pirouettes. We never, never stop believing in all they will accomplish as they pass through this world. But in the meantime, my sisters, the most important thing we do, is hold tight to their little hands as together, we special mothers and our special children, reach for the stars.
 

 
 
 

"Sometimes we are asked to wait.
But this we know~
God's never late!"
Author Unknown
 
"The Lord is good to those who put their hope in him.
He is good to those who look to him for help.
It is good to wait quietly for the Lord to save."
Lamentations 3:25-26

"I praise you because you made me in an amazing
and wonderful way."
Psalm 139:14