Showing posts with label Genre- Special Needs Kids. Show all posts
Showing posts with label Genre- Special Needs Kids. Show all posts

Sunday, October 27, 2013

Sun Shine Down: A Memoir by Gillian Marchenko

Tour Date: October 30th

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It is time for a FIRST Wild Card Tour book review! If you wish to join the FIRST blog alliance, just click the button. We are a group of reviewers who tour Christian books. A Wild Card post includes a brief bio of the author and a full chapter from each book toured. The reason it is called a FIRST Wild Card Tour is that you never know if the book will be fiction, non~fiction, for young, or for old...or for somewhere in between! Enjoy your free peek into the book!

You never know when I might play a wild card on you!



Today's Wild Card author is:


and the book:

T S Poetry Press (August 18, 2013)

***Special thanks to Gillian Marchenko for sending me a review copy.***

ABOUT THE AUTHOR:

Gillian Marchenko lives in Chicago with her husband Sergei and four daughters. Her writing has appeared in Literary Mama, MomSense Magazine, Chicago Parent, Thriving Family, Today’s Christian Woman, and Gifted for Leadership. A speaker, and active on Facebook, Twitter, and her website, Gillian says the world is full of people who seem to have it all together. She speaks for the rest of us.

Visit the author's website.

SHORT BOOK DESCRIPTION:

Sun Shine Down. A memoir.

What if?

What if you dreamed of having a beautiful child, and in your mind you saw the life you'd share with that child. First steps, little league (or ballet). Maybe the child would play piano or make you proud on the Honor Roll. There'd be eventual graduations, college, even marriage and grandchildren. You might dream it out that far. Or not. Every parent has hopes. No parents wish for pain—their own, or a child's.

Then you had a premature delivery in a foreign country. And the words swirling around you said a different kind of "what if." What if something was wrong? The dream was at risk—or so it seemed. Would you be ready for that? Could you make peace? Or would it take you down?

These are the questions author Gillian Marchenko faced as she woke up after an emergency C-section in Ukraine. Only her newborn child could answer them, in time. But first she had to find a way to hear more than the words "Down syndrome."



Product Details:
List Price: $15.00
Paperback: 136 pages
Publisher: T S Poetry Press (August 18, 2013)
Language: English
ISBN-10: 0989854205
ISBN-13: 978-0989854207


AND NOW...THE FIRST CHAPTER:

~ 1 ~



I woke up just before seven the morning of April 5, 2006, in a surgical recovery room in a hospital in Kiev, Ukraine. Sluggish, I scanned the room, unable to take in my surroundings. A thin white sheet covered my body. I shivered. A metal table housed a tiny television in the corner of the room. The bare walls were a pale shade of blue gray.

Did Sergei leave? Lifting my hand, I placed it on my breastbone and slid it toward my navel. My mid-section felt numb. Pushing down, it was as if I tapped another person’s toneless stomach. White gauze held my empty abdomen tight. I had been eight months pregnant.

Five hours earlier, I stood naked in a warm shower, my blond hair tucked into a flimsy paper cap. A delivery nurse crouched in front of my middle. “Krasata,” she hummed in Russian, smiling, telling me I was beautiful, while methodically shaving me.

I couldn’t see the nurse’s face over the bulge of my stomach. Her brown hair bobbed in and out of sight as she talked. I imagined her gold tooth sparkling as her mouth moved. In Russian, “krasata”  means beautiful as in, “you are a beauty.” My skin was now translucent, stretched to its limit. I looked like ET’s pregnant cousin, wide-eyed from fear, hair thinned.

“Tebye nada peesat?” the nurse asked as she cleaned off the razor. I nodded – yes, I have to pee, and then I squatted, awkward, as my bladder emptied. I hadn’t peed in front of someone since kindergarten, when I used to make my best friend, Carol Peruski, go to the bathroom with me. The yellow stream swirled around and around the shower floor before sliding down the drain. I wanted to be back home in Michigan, tucked away in an American hospital. I wanted to understand everything being said to me.

*

I had hugged my daughters goodbye that morning, expecting to return in a few hours. Elaina, five and a half years old, had a habit of patting my tummy hello and goodbye. Zoya, eighteen months younger, stood on her tiptoes and aligned her lips with my belly button for a kiss. They hurried our goodbye. They had big plans to make a fort underneath the dining room table with their beloved Ukrainian nanny, Lena.

Our “stalinka”—the historical apartment in Kiev where we’d been living for the last three years, since we’d moved from Chicago to Sergei’s native Ukraine to help start and grow churches—showed few signs of a baby coming. A pack of diapers and some second-hand clothes were piled in the corner. A stroller stood in the hallway by the front door next to a line of shoes. We needed more supplies: ointment and shampoo and bottles. Infant clothes needed laundering. There wasn’t a place for the baby to sleep.

After saying goodbye to the kids, I’d inhaled in an attempt to flatten my protruding belly, needing at least two buttons of my coat to fasten. Giving up, I grabbed a scarf hanging on a hook near the front door and looped it around my neck to keep the Ukrainian winter air at bay. There were three weeks left until my due date. A simple pregnancy check-up coaxed me out the door with a promise of some much-needed time with my husband.

We'd sat in the car a few minutes, waiting for the engine to warm and for the frost to break up on the windshield. I could see my breath. “Let’s swing by that American restaurant on the river after your appointment,” Sergei suggested.

 “You’re on!” I said. “And I know what I am going to order: Eggs Benedict. I am going to eat it all, too. It’s not like I can get any bigger than this, right?”

“You look beautiful,” Sergei said.

At the appointment, I lay on a long brown bed and watched the obstetrician measure my stomach with the kind of measuring tape my mother used to make our clothes when we were kids. The doctor measured once.

“Hmm.”

“Shto shto?” I asked in Russian. What? What do you see? Is something wrong?

Upon hearing my question, Sergei, who sat on the other side of the room, stood up and walked over to us.

“Shto takoye?” Is there a problem? Sergei asked.

“What? Oh no. Not a problem. I want to measure Gillian’s belly one more time.” The doctor positioned her right hand on the examination table next to my side and extended the tape across my abdomen. She hunched to ensure the right start and stop point on the tape and then held it out in front of her, stretching it wide.

“Your stomach hasn’t grown in two weeks.”

A sound like that of a police siren erupted inside my head, sending icy adrenaline shooting through me. Our baby wasn’t growing? Our baby wasn’t growing.

Sergei stood to the right of the doctor. He took hold of my hand and looked at me with that same steady gaze I'd noticed when we first met. When Sergei looked at a person, his eyes were unwavering, showing his confidence. At first that intimidated me but in our years together, it had become a great comfort. He heard what the doctor said and knew her words would worry me. He was with me and present, just as he had been for the last seven years.

The baby had measured small at checkups earlier in my pregnancy but the doctor had never been concerned about it. At one point the baby measured three weeks behind her due date in size and development. At that time, the doctor reassured me that I had nothing to worry about. “She is growing which is the main thing,” she'd said, winking. The doctor, jolly and round, acted like a female version of Kris Cringle. “There’s no problem. Either we miscalculated the due date or you have a petite little girl in there," she'd explained as she turned her attention to Elaina and Zoya who happened to be with us at that appointment. “Now, girls, are you excited about the baby? And how do you like living in Ukraine?”

“Sergei, please tell her we are concerned.” I'd wanted reassurance. To calm me, the doctor had ordered several ultrasounds and non-stress tests. Each time, the tests had shown the baby staying still. “Ona speet.” She’s sleeping, was all she’d say.

  Today she said, “Here’s what we are going to do, Gillian. We’re going to admit you to the hospital overnight. I suspect the baby needs extra vitamins and nutrients. That should get her back on track."

“Should we worry? Is it something else?” I glared at Sergei the way wives do when they want their husbands to telepathically understand they should jump in with questions and concerns of their own.

“No! Don’t worry!” the jolly doctor smiled at us.

Instead of heading off to breakfast as planned, we went directly to the hospital.  By noon I sat gowned in a room on the fourth floor. A nurse hooked a monitor to my belly to follow the baby’s heartbeats. I watched the squiggly green lines on the black screen dip low as my stomach tightened with each Braxton Hick's contraction. Something is wrong. I know it.

We were assigned a new doctor, tall and tan with a wide smile. His fuzzy, brown hair was gone in the back of his head. He wore glasses. He looked the part of the new Ukrainian, the guy who achieved success somehow during economic instability. The first two buttons of his crisp white shirt were open revealing a heavy chain that shimmered around his neck. Two huge, gold rings covered his knuckles. He was excited to have an American patient because he was learning English.

He introduced himself to Sergei first, in Russian, and shook hands with him. Then he peeked at me. “Hello, there. I see you having a baby? That’s great. I…um…ugh… I am happy to be of assisting of you today here in Ukraine. I am fond of America. And, um…, I am tried to work on my English.”

The new doctor continued to sputter and pause as he talked to me, searching for the right words to say in English. I would answer him in Russian, to let him know I could, and then wait for him to find his next English word.

I had studied Russian with a private tutor three times a week, two to three hours a session, for three and a half years. The day I met Tatiana Nikolayevna, my Russian teacher, I was nervous. She was a mountain of a woman with bleached blond hair. Her high cheekbones and pointed nose gave her a diplomatic air. She walked with a limp, suggesting she'd suffered a hip dislocation at some point in her life. One moment she’d give me an icy glare, then seconds later an approving smile would spread across her face.

For years I'd trudged along, immersing myself in basic conversation, memorization and grammar study. I cried at some point in every session. Tatiana was firm, but kind. In the beginning, I likened Russian to a blurry photograph. I knew something was there, but I could not make out the picture. It was humiliating and exhausting to try to speak a foreign language. Then one day the picture started to come into focus. I heard actual words, sentences, and eventually full conversations. I became an avid eavesdropper. My time deaf and mute in Ukraine came to an end. I had survived basic Russian language acquisition.

*

Outwardly I kept my cool at the hospital. But inside, I yelled at everyone who walked through the door. Check me and go away! Let me lie here and worry in peace. I’m not in the mood to teach English as a second language.

After meeting the new doctor and helping me settle into the room, Sergei left the hospital to go home and check on Elaina and Zoya, and arrange the rest of the day's schedule. About an hour after he left, I realized I would need a few things to stay overnight. I called him on the cell but got voicemail. “Hi, it’s me. Hope the kids are okay. Listen, since I’m going to be here for the night, can you grab a few things for me while you’re home? I need a change of clothes, my contact case, and maybe a book to read. Thanks. Love you.” After I hung up, I lay back on the hospital bed and focused on the clock on the opposite wall. There was nothing to do but wait. My hands were shaking.

Sergei got back to the hospital around four o’clock. Occasionally, the English-learning doctor came in, checked the monitor, and listened to my stomach with a stethoscope. Sergei asked questions. “How’s the baby doing? Do we know if the glucose and extra vitamins are helping yet?” We discovered that one phrase the doctor knew well in both English and Russian was “wait and see.” He would not outright answer our questions. “Wait and see,” he’d say, already turning to leave.

By nine o’clock, our American colleagues started to call. Julie, the mother hen of our ex-pat group, called first. Her husband James was our team leader, and they had been living in Ukraine for over ten years.

“I hope you don’t mind, but I called Lydia to tell her about you and the baby.” Lydia was another American working with us. Before moving to Ukraine, she was a postnatal nurse at Children’s Memorial Hospital in Chicago.

“That’s fine, Julie,” I muttered, my frustration breaking through. I wasn’t mad at Julie. I was mad that I was stuck in the hospital. I was mad that we were told over and over again to wait and see.

Julie continued, “And we are coming to the hospital. Once our sitter gets here, James and I will pick up Lydia and we’ll be on our way.”

As soon as I hung up, the phone rang again. Lydia’s voice, strong but soft, filled my ear with questions and greetings.

The threat of tears tightened my throat and I could only manage a whisper,  “The baby hasn’t grown at all since the last visit to the doctor two weeks ago. I have an IV in right now, and I’m receiving glucose and other vitamins. The doctor says this will help bulk the baby up and get her back on track.” Sergei sat in the corner of the hospital room, pretending to be interested in a newspaper he'd picked up in the hospital lobby.

“Whenever I feel a contraction, the green squiggly line on the monitor drops low,” I said. I expected a response from Lydia. Instead, silence. For a second, I wondered if the phone lost its connection.

“Gillian, I will be there in a half hour. The next time your doctor comes in the room, you need to demand an emergency c-section. I don’t want to scare you, but in the States your baby would have already been delivered. She is not doing well. She’s in trouble. Listen to me; you have to talk to your doctor.” I tightened my grip on the phone. Sergei stood up, came over and sat down on my bed. “What’s wrong?” he mouthed. I shook my head and turned to the window.

“Okay, Lydia. We’ll tell him.” I hung up the phone and started to cry. Sergei leaned in and took me in his arms.

“Lydia said it sounds like the baby is in extreme distress. She said we need to demand a c-section.”

Always pragmatic, Sergei wondered out loud, “How can we know she is right? She isn’t even here. The doctor said the baby needs some extra help.” I moved out of Sergei’s arms so I could look him in the eye.
 “Lydia said if we were in the States, the baby would have already been delivered.” I felt a sob rise and my body began shaking. “Sergei, please find the doctor.”

My husband agreed and went to get the doctor. I was alone. I knew it. I’d known for weeks that something was wrong. I should have spoken up more. Oh God, please let the baby live. I want to go home. I did not trust the doctors in this hospital. I wanted my mother. A few minutes later, Sergei came back to the room with the English-learning doctor who had his usual broad smile.

“Umm, your husband said that you are worried that the baby be born?”

“Yes. I have an American friend who is a nurse. I talked to her on the phone and she said that with the baby’s heart beat dropping so low, I would have already had a caesarean section if we were in the States. I’m worried. We need to talk about delivering the baby.”

I stared at this man who was dressed in white pants and a white, button-down shirt with a lazy stethoscope draped around his neck. He was a doctor. I wasn't sure of the schooling process in Ukraine, but in America he would have completed close to a decade of education in order to qualify for this job. Shouldn’t he know? Didn’t he know?

“The baby is stabilizing with the IV. It hasn’t been enough time. I think we should wait and see. She needs more time.” The doctor glanced from my face and Sergei’s to see if his words registered. Sergei spouted back in Russian.

They talked a few more minutes and then the doctor smiled at both of us and left. The clock next to my hospital bed read eleven o’clock at night. The baby had been receiving fluids since noon. I studied the monitor next to my head. The baby’s heart rate still dropped once in a while.

“He doesn’t know what he’s doing!” I snapped at Sergei.

“I know this is hard, but he’s a doctor. He’s your doctor. We should listen to him. And I’m not saying this lightly. That’s my baby too in there. I’m worried. But Lydia isn’t here and the doctor is, and I think we should listen to him.”

Julie, James and Lydia arrived within the hour. They were upbeat, commenting on the nice hospital room, cracking jokes and squinting at me through the room’s bright lights. All three tried to act like it was the most natural thing in the world to hang out in a Ukrainian hospital room at midnight. I loved them for it.

A nurse located the English-learning doctor. When he came into the room, Lydia stepped forward and introduced herself. She went on to tell him what she told me on the phone. As she spoke, she kept taking steps closer to him. Soon, she stood right in front of his face. The doctor no longer smiled. “Doctor, this baby needs a cesarean section right away!” James and Julie hung back on the other side of the room. Sergei got up from the bed and stood next to Lydia.

“We are going to wait and see if the IV helps,” the doctor declared. Lydia persisted, eyeing my husband for language assistance and nodding incessantly as her words poured in a mixture of English and Russian. Her stern face and tone of voice pleaded with the doctor to take action.

I could tell by the projection of her voice that Lydia meant business. Here was one of my people, not only a colleague and a friend, but an American medical professional weighing in on the fate of my child.

After hearing more from Lydia, Sergei took her side. “We need to see if anything else is going on with the baby. My wife is frightened. We don’t want to wait and see anymore.” Sergei squared his deep blue eyes on the doctor.

“All right. I guess we can take a closer look at the baby through an ultrasound.”

“Spaseebo,” Sergei said. Thank you. “Spaseebo,” Julie, James, and Lydia all chimed in.

“Nyezashto,” the doctor replied. Don’t mention it. His expression was blank when he left the room.

*

Twenty minutes later I concentrated on Sergei’s face, as a coiled cord smeared icy liquid over my midsection. Doctors and nurses huddled around the ultrasound screen, whispering to one another in Russian. The technician tapped on my stretched skin, seeking the baby's beating heart beneath it. As my abdomen tightened again, the small huddle of Ukrainian professionals all gasped at the monitor.

“Sergei, ask them what they see.”

Sergei cleared his throat. “Izveneete pozshalusta. Shto takoye?” Excuse me, please. What is wrong? Our doctor turned around from the group and faced us. Oh no, here we go. Sergei took my hand in his.

“The baby’s heart beat goes too low with the contractions. We need to do a caesarean section right away.”

*

Back in my room, shaved and ready for surgery, I perched on the end of the high hospital bed and studied the imperfections on the tan walls. Sergei had gone downstairs to sign papers to allow the surgery. James, Julie and Lydia had gone to search for the nearest waiting room. All of a sudden I felt the need to take everything in. I wanted to remember every detail. A well-polished wooden desk with a matching chair stood against the wall in front of me. Cream-colored curtains with deep pleats framed the window. My stocking feet dangled above the alabaster tile floor. They seemed disconnected from my body.

I thought about Elaina and Zoya sleeping in their Estonian-made bunk beds back at the apartment. Sergei and I searched all over Kiev before purchasing the pale, hardwood beds. Thick cotton blankets were probably tucked up under the girls’ chins. I imagined their Babushka, Sergei’s mother, asleep in the next room, ready to provide a drink of water or a trip to the toilet. I wished I had kissed them goodnight.

I heard footsteps in the hall. The doctor stuck his head through the doorway. “Gotova?” No time for English now.

I nodded—ready.

Tuesday, January 3, 2012

Different Dream Parenting AND A Different Dream for My Child by Jolene Philo


Tour Date: Jan. 6th

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It is time for a FIRST Wild Card Tour book review! If you wish to join the FIRST blog alliance, just click the button. We are a group of reviewers who tour Christian books. A Wild Card post includes a brief bio of the author and a full chapter from each book toured. The reason it is called a FIRST Wild Card Tour is that you never know if the book will be fiction, non~fiction, for young, or for old...or for somewhere in between! Enjoy your free peek into the book!

You never know when I might play a wild card on you!



Today's Wild Card author is:


and the book:

Discovery House Publishers (November 1, 2011)

Discovery House Publishers (August 1, 2009)

***Special thanks to Susan Otis, Creative Resources, Inc. for sending me a review copy.***

ABOUT THE AUTHOR:

Jolene Philo has been a teacher for 25 years and has published numerous articles on parenting a special needs child and preparing children for a hospital stay. She is the author of Different Dream Parenting and Different Dream Parenting: A Practical Guide to Raising a Child with Special Needs and a regular contributor to a regional monthly women’s magazine, has spoken to MOPS groups, and is a commentator for Iowa Public Radio’s “Iowa Voices.” She and her husband have two children and live in Boone, Iowa.


Visit the author's website.

SHORT BOOK DESCRIPTIONS:



Different Dream Parenting: Parents of a special needs child will benefit by Jolene Philo's handbook of resources, inspiration and tested wisdom. Practical strategies and spiritual reflections are balanced with resources for aid and information. From becoming an effective advocate for your child, dealing with hospitalization, to family concerns and long-term care, Philo presents wisdom from voices of experience. Hope-giving help, resources and direction are clearly provided for parents of a child with a medical condition, behavioral or educational concerns.


  • Product Details for Different Dream Parenting:

  • List Price: $12.99
  • Paperback: 336 pages
  • Publisher: Discovery House Publishers (November 1, 2011)
  • Language: English
  • ISBN-10: 1572934670
  • ISBN-13: 978-1572934672




A Different Dream for My Child: Hope and encouragement for the parents and caregivers of critically ill children comes in an inspirational devotional package. Jolene Philo shares personal accounts from her own experiences with a seriously ill newborn son. Interwoven are the stories of how other parents have found peace and hope, how they have dealt with hospitalization, private pain, grief, guilt and loneliness, and even the death of a child. Targeted scripture, simple prayers and questions for reflection provide a valuable spirit





Product Details for A Different Dream for My Child:

List Price: $10.99

  • Paperback: 272 pages
  • Publisher: Discovery House Publishers (August 1, 2009)
  • Language: English
  • ISBN-10: 1572933070
  • ISBN-13: 978-1572933071


AND NOW...Excerpts from both books:

 Different Dream Parenting Excerpt: 



I Didn’t Sign Up for This, God!

Have you ever had one of those dreams where you can’t move? The car is racing toward the edge of a cliff and you can’t lift your foot to press the brake pedal. An attacker is breaking down the door to your house and you can’t raise your arm to dial 911. Your child is about to run in front of a truck and you can’t open your mouth to scream.

My bad dream became a reality in 1982. My husband and I stood beside our son’s isolette in the neonatal intensive care unit. An IV needle pierced Allen’s tiny arm, and angry red scars crisscrossed his chest. One end of his feeding tube hung on a pole beside his IV bag. The other end rose from the soft skin of his tummy. Pain etched his wide forehead and tugged at the corners of his perfect rosebud mouth.

More than anything, I wanted to reach out and take his hurt away. But I was trapped in a bad dream. Immobilized. Inadequate. Helpless. Though God had assigned me to love and care for this beautiful child, I could do nothing to minimize his pain. My thoughts were an inward scream. This isn’t what I signed up to do, God! I don’t want to be a helpless onlooker. I want to parent my child. How can I care for him? What can I do?

As the parent of a child with special needs, you’ve probably experienced the same sense of helplessness. Whether your child is critically or chronically ill, mentally or physically impaired, develop- mentally or behaviorally challenged, you want to do something. You want to ease your child’s pain, but you don’t know how. You want to help your child realize his or her full potential, but you don’t know where to begin. You want to ask God about your child’s suffering, but you don’t want to be condemned for questioning His wisdom. You want to believe God is with you, but you don’t know how to find Him.

You’re stuck in a bad dream. You can’t move. You can’t speak. You want someone to shake you awake and tell you everything will be okay. Instead, you wake up and must become the parent you never expected to be. You doubt that you’re up to the task. You’re worried about your child’s future. And you’re wondering, Does anyone understand what I’m experiencing?

The answer is yes, many parents understand your situation. In the United States,
•        10–15 percent of newborns, or 431,000 annually, spend time in neonatal intensive care according to the March of Dimes.
•        12 percent of children between ages 1 and 17 had medical conditions serious enough to require hospitalization between 2004 and 2006, the most recent years for which statistics are available at the Centers for Disease Control and Prevention.
•        13.6 percent of students between ages 6 and 21 were enrolled in some kind of special needs program according to the National Center for Educational Statistics. That’s 706,000 of our country’s school-aged children.

Lots of kids mean lots of parents, dads and moms who are valuable sources of information and advice. In this book, dozens of them share with you the wisdom they gained while parenting kids with special needs.

Support can also come from the surprising number of professionals who work with families of kids with special needs. These professionals—and the resources they’ve created—are available at hospitals, medical facilities, government agencies, private organizations, businesses, schools, churches, and more.

This book brings you advice from professionals around the country and provides information about national organizations and resources. It also gives tips about where to start searching for state and local resources. More often than not, your problem won’t be a lack of resources, but a lack of awareness of them or inability to access them.

Different Dream Parenting contains six sections: Diagnosis, Hospital Life, Juggling Two Worlds, Long-Term Care Conditions, Losing a Child, and Raising a Survivor. Each section is divided into four chapters. Three chapters address practical issues. The last chapter in each section addresses spiritual concerns.

Parents of kids with special needs often wrestle with prickly spiritual questions. I sure did. Sometimes I still do. So do all the parents interviewed in this book, and most of the professionals, too. Every day, we continue to ask questions about our kids’ lives and futures. Gradually, we learn more about how to trust God’s timing and wait for His answers.

As you read this book, please ask your faith questions. Read about how parents and professionals learned to ask questions, wait, and listen. Consider the answers they have discerned and their suggestions about how to find comfort and courage in God’s Word. When you are ready, try out their ideas about how to pray and use Scripture to hear God’s answers to your hard questions. The thirty-day prayer guides in appendix A are designed to help you engage in conversation with Him.

But even with prayer guides and Scripture to guide you, I know how hard it can be to trust the God who is allowing your child to suffer. So I won’t condemn you for asking prickly questions. Instead, I’ll encourage you, cry with you, and support you when your faith grows weak. When you can’t hang on a minute longer, I’ll hold you close until your strength and your faith return.

I hope this book helps you break out of your bad dream, wake up, and move forward with joy and confidence. I pray that the stories of parents and professionals in this book will give you hope and strength.

Most of all, I hope you discover the truth God has revealed to me and many other parents. Raising a child with special needs isn’t a bad dream. It’s just a different dream. And surprisingly, a different dream can be the best dream of all.

Taken from Different Dream Parenting, © 2011 by Jolene Philo. Used by permission of Discovery House Publishers, Box 3566, Grand Rapids,  MI 49501.  All rights reserved




A Different Dream for My Child Excerpt:


Children Are a Gift from the Lord, Period

Don’t you see that children are God’s best gift?
The fruit of the womb his generous legacy?
Psalm 127:3

From the moment Hiram and I learned of Allen’s condition, we knew he had a good chance of living a relatively normal life. And though his first five years were hospital
heavy, that prognosis proved true. He did well in school and participated in extra-curricular activities. Now an adult, he’s out on his own.

Not every child’s future is so rosy. Many parents of kids who survive an initial health crisis know their lives, and their children’s lives, will be quite different from what they once expected. If your child is one of those kids, you will grapple with the same issue Bruce and Peggy faced when their second child was a baby.

Their daughter Lacey, born in 1984, has the mental ability of a four or five–month–old infant. Her mental and physical disabilities weren’t immediately obvious to her doctor or her parents, though by the time her daughter was three months old, Peggy knew something was wrong.

Throughout the first year of Lacey’s life, her limitations became more noticeable. Her parents’ lives changed when they decided to keep Lacey in their home as long as they could. They understand that other parents who place severely disabled children in a care facility have made the right choice in their personal situation. “It’s not like one’s right and one’s wrong,” Peggy says.

“You have to do what God gives you peace about,” Bruce adds. The decision to care for Lacey in their home gave them peace. To accommodate their new lifestyle, Bruce changed employers. “I used to have a job where I traveled and was gone all the time. We knew when Lacey was a year old that I was going to have to be home a lot more.”

Early on, many well-meaning people acted like Lacey was a burden her family had to bear, especially for Peggy, whose life revolved around caring for their daughter. Once in a while, Peggy viewed her daughter in the same way. She began to question God. “Children are meant to be a gift from the Lord, not a burden, aren’t they? So why is Lacey a burden?”

Deep down, Peggy knew something was wrong with her thinking. One day she sensed God telling her to think about what the Bible says about kids: Children are a gift from the Lord. The light bulb went on, and she understood that the verse wasn’t just about the “perfect children,” the darling, whole and healthy, look-at-me children. “He doesn’t put any clause or condition on this statement. It’s just plain, ‘Children are a gift from the Lord.’”

In that moment, Peggy realized she’d been asking the wrong question. The question wasn’t whether Lacey was a gift or a burden. God said children are always a gift. Instead, He showed her the right questions to ask: How are you going to take care of this gift? How are you going to show the world that Lacey is a gift from the Lord? Those questions changed Peggy’s outlook about caring for her daughter. Every day, she tells herself, “I better act like this is a gift.” Over the years, she’s discovered that when she acts like her daughter is a gift, she thinks of her as a gift.

After more than two decades of caring for her daughter, Peggy wants to pass on this piece of advice to parents of special needs kids: No matter what your child’s level of need is — able to lead a normal life, in need of total care, or somewhere in between — you treat your child as a gift, you’ll think of your child as a gift. “This child is a gift from the Lord, period,” Peggy says. “Start with that foundation and move on from there.”

Father, forgive me for viewing my child as a burden. Teach me to act like my child is a gift, even during difficult times, so I will think of this child as a gift. Help those around me see my child is a gift, too.

Do I consider my child a gift from God? Do I treat my child like a gift? How do I show other people that my child is a gift?
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Taken from A Different Dream for My Child, © 2009 by Jolene Philo. Used by permission of Discovery House Publishers, Box 3566, Grand Rapids MI 4950l. All rights reserved.