Do you follow the Different Dream for My Child blog by Jolene Philo? It is a wonderful special needs resource. Now comes the book. And I have one to share in a Giveaway!
Ms. Philo is kindly allowing Rileys-Smile to give away a copy of this invaluable resource. I am so excited and ask that each parent/caregiver/family member of a child with disabilities to please enter my giveaway.
Excerpt
Entry: Different Dream Parenting Book Giveaway
Please enter the comments below and share your name and your preferred contact information. You may also use the email button instead to the right of the page under "Stacie's & John's Links." Should you be willing, I would love to hear a little about the child in your life along with your entry. Multiple entries are welcome with additional comments. Giveaway entries will be accepted through November 30th. The winner will be determined by a drawing.... perhaps Riley will rummage around a hat for us to make the choice, I'll ask him.
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
Entry: Different Dream Parenting Book Giveaway
Please enter the comments below and share your name and your preferred contact information. You may also use the email button instead to the right of the page under "Stacie's & John's Links." Should you be willing, I would love to hear a little about the child in your life along with your entry. Multiple entries are welcome with additional comments. Giveaway entries will be accepted through November 30th. The winner will be determined by a drawing.... perhaps Riley will rummage around a hat for us to make the choice, I'll ask him.
The book is available at 10% off the retail price:
4 comments:
hi sounds fab! you already know about me and my beautiful Tilly with Smith Magenis Syndrome.
you can contact me via my blog. sending love and hugs to you!xxxx
Hey just to let you know im a new follower via hop hoping you will follow us back at http://www.beckvalleybooks.blogspot.com thks in advance xx
Hi, I am not only a parent of a special needs son but also a widow. I am doing this all alone and appreciate any advice or resources. Looking forward to reading more about what you do. I already like the right hand column with resources like "Parents Reaching Out" and "Special Mom Preneurs".
Sharyn
You're Amazing, Keep up the good work...
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