Bridges4Kids Review Panel |
In order to
accommodate the growing number of book and video review requests that
Bridges4Kids receives, we have formulated a panel of parents and
professionals to assist in the review process.
Click here for the first set of
reviews.
Click here for
the second set of reviews.
Click here for the
third set of reviews.
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Parenting
Kids with ADD/ADHD: Real Tools for Real Life
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Reviewed
By: Holly Carpenter
Review Date: February 28, 2005
Author: Dr. Al Winebarger,
Ph.D.
ISBN: 19755545-0-6
Price: $24.95
Description: Does your child have
ADD/ADHD? Could you use more parenting tools to help you with your
child? This book contains the “tried and true” tools used with
hundreds of parents in Dr. Al Winebarger's Attention Camp Programs
over the years. The tools in this book are "hands on" and should be
very helpful in your day-to-day lives. Written by
the founder of the Grand Haven and Wyoming Attention Camps,
psychologist Dr. Al Winebarger, this volume presents state-of-the-art
assessment and treatment information in useful and hands-on ways.
Most books tell parents WHAT to do, but fail to tell them HOW to use
the ideas. This book uses plain language, and teaches parents
how to use real-life tools to help their children as they struggle
with ADD/ADHD. (Spiral bound; 170 pages)
Holly's Review: This is an
amazingly insightful manual on how to raise your child with ADHD. Dr.
Al Winebarger touches on every aspect of helping your child in school
and at home. There is even a chapter on stress management for parents.
This is a wonderful book, as it does not stress medication. Like the
title says, it contains 'real tools for real life'. The ideas in the
book are based on a common sense approach
to learning, are not hard to follow, and will help everyone in
the family. Great book!
For More Information: Dr. Al
Winebarger is a Clinical Psychologist in Grand Rapids, Michigan. Learn
more about Dr. Winebarger at
www.westernbehavioral.com
or call 616-842-4772. |
Kids Law: A
Practical Guide to Juvenile Justice |
Reviewed
By: Jackie D. Igafo-Te'o
Review Date: March 15, 2005
Author: John W. Biggers
ISBN: 0-9647925-5-9
Price: $14.95
Description:
Written for kids, parents, teachers, counselors, social workers, youth
workers and anyone else involved in the lives of youth today, KIDS
LAW: A Practical Guide to Juvenile Justice is a down-to-earth and
invaluable guide to the many aspects of the Juvenile Justice system.
Through life story portraits, KIDS LAW deals with criminal law,
juvenile courts, dependency, adoption, marriage and divorce, property
and employment matters, and allows the reader to come face-to-face
with the evolving American law as it impacts kids either because of
their own actions or the actions of adults in their lives. (Paperback;
235 pages)
Jackie's Review: In the book
KIDS LAW, Attorney John W. Biggers combines
years of experience and a passion for
children to make a once difficult topic transform into an
easy-to-understand, enjoyable read. Biggers
explains everything from the crime to the arrest and from the trial to
incarceration. Includes a comprehensive glossary of terms.
I would recommend KIDS LAW to anyone
who is hoping to navigate the complexity of the Juvenile Justice
system. Intended for students and those who work with them,
KIDS LAW makes an
excellent addition to any school library, classroom, or in the home as
a study resource. A teacher's manual is also
available.
Crystal's
Review: The author succeeded at writing a textbook-style overview
of the juvenile justice system covering everything from how courts
assist juveniles who are not adequately cared for to how the justice
system handles youth who do not follow established laws. Besides
providing general information on juvenile justice, the author
argues--quite convincingly--that juvenile offenders must be treated as
children rather than as adults. He also focuses heavily on the idea
that individuals must work together to confront problems specific to
their communities in order to effectively protect juveniles and to
prevent them from falling into a pattern of criminal activity.
For More Information:
Attorney and Youth Advocate, John Biggers, has
worked closely with kids, parents and other adults in the Juvenile and
Adult Courts for over 30 years. To purchase the book, or for more
information, visit
www.kidslaw.com.
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Autism:
Heartfelt Thoughts from Mothers |
Reviewed
By: Jackie D. Igafo-Te'o
Review Date: March 17, 2005
Author: Judy Lynne
ISBN: 1-883175-08-9
Price: $16.00
Description: In Autism:
Heartfelt Thoughts from Mothers, nearly 100 mothers from all
over the United States and moms from Finland, Australia, Belgium,
Canada and The Netherlands, share their honest, most heartfelt
thoughts regarding what it is really like to raise a child with
autism.
(Paperback;
214 pages)
Jackie's Review: Autism:
Heartfelt Thoughts from Mothers is a beautiful compilation of personal
stories from mothers of children with autism. The stories contain
words of wisdom, details of challenges that each mother has faced,
ways they feel that they have been blessed, and resources that they
found useful during their journey. Readers will gain insight into the
world of Autism, as experienced first-hand
by moms from around the world. There are stories in this book that
will make you laugh and cry...there is
something for everyone. The raw human emotion is a refreshing
alternative to the drab textbook versions of what
parents might expect during their child's lifespan.
Individuality, uniqueness and compassion
prevail in this book that proves that one size does NOT fit all.
As I neared the end of the book, I arrived at
a page dedicated to Ryan Long, who
unexpectedly passed away. I was overcome with emotion while reading
the words penned by his
mother on the first anniversary of his passing. As the parent
of a child with autism, it is a life changing moment when you realize
that you're not alone, and that there are others out there who dream,
laugh, grieve, and cry...just like you do.
Cammy's
Review: I really enjoyed reading this book and seeing the
photos of mothers with their child. Each were special and unique and
each mother showed unbelievable strength, courage and determination in
raising their child. I felt like I got to know each child personally,
just through the astounding love and devotion these mothers have for
their children. I commend these mothers to the fullest extent for
having such positive attitudes and hope for the future. After reading
this book, I became more grateful for my life and everyone in it.
These mothers face far more challenges than I ever have and yet they
have a positive outlook and are grateful for being the ones chosen to
raise and care for their child with autism. I also learned that there
are many forms and degrees of severity of autism. Reading this book
helped me understand autism and the effects it has on the whole
family. I recommend reading this book to open your eyes about autism
and to read about the awesome dedication that these mothers have for
their children. It truly is a "heartfelt" book.
For More Information:
Judy Lynne is the proud mother of a 21-year-old
daughter with Autism. She is a dedicated
parent advocate and
former President of her state's Autism Society. |
Sanity
Savers |
Reviewed
By: Andrea A. Miller
Review Date: March 21, 2005
Author: Sharon MacDonald
ISBN: 0-87659-236-1
Price: $14.95
Description: From clean-up
solutions to storage ideas to inventive cost-cutting strategies, and
everything in between, this book will truly help you keep your sanity
in the classroom! Use the creative suggestions to help children
resolve conflicts and solve problems, to deal with interruptions in
the classroom, and to utilize your small space effectively. Sanity
Savers helps solve everyday problems, giving you more time to teach
and enjoy the children in your classroom.
(Paperback; 160 pages)
Andrea's Review: “Sanity Savers” by
Sharon McDonald contains a potpourri of ideas for making teaching
easier and more fun for teachers and students alike! It is chock full
of suggestions for everything from smoothing out transition times to
removing tempera paint from clothing. This book would be particularly
beneficial for new teachers. It provides some basic information
(introducing centers one at a time at the beginning of the year) along
with some suggestions even seasoned teachers might not have thought of
(using a chalk line to prevent ants from intruding on a picnic). Many
of the ideas in the book can be adapted to a home setting as well! The
author’s 28 years of teaching experience provides readers with a
wealth of useable information for making classrooms more effective and
enjoyable!
For More Information: Sharon
MacDonald has been training teachers for over fifteen years throughout
the United States. She trains on a variety of early childhood topics,
based on years of classroom experience. With a Masters in Education,
Sharon has taught ages ranging from three-year-olds to adults, and has
taught an inclusion program for children with disabilities. For more
information or the purchase the book, visit
www.gryphonhouse.com.
|
Alex: The
Fathering of a Preemie |
Reviewed
by: Amie Stid, Early On Service Coordinator
Review Date: March 28, 2005
Author: Jeff Stimpson
ISBN: 0-89733-528-7
Price: $23.50
Description: Stimpson traces the life of his child from birth
to kindergarten: four wings in two hospitals; coming home with a
roomful of medical gear and round-the-clock drugs and nursing; the
gains and downturns of home therapy through Early Intervention;
finding and prospering in a special-needs preschool; a diagnosis of
autism; and the ongoing battle to give Alex a fair shot a childhood,
and at life. (Hardcover, 270 pages)
Amie’s Review: This book is a “must read” for all who work with
families of preemies or special needs children. No matter how much we
care about our families, or how much experience we have with working
with special needs children, we can’t fully understand the journey
these parents take. Reading this book is the closest I’ve come to
beginning to understand what kind of an emotional roller-coaster ride
these families go through. This father’s candid story about dealing
with his son’s health, doctors, hospitals, insurance companies, home
visiting nurses, therapists, early intervention teachers, family,
friends and strangers was a humbling experience for me. Stimpson uses
a diary format that reads very quickly. Although the subject matter is
heavy, he shares the highs and lows with honesty and humor. To see
this child through the eyes of his parents and his early intervention
team at the same time was a valuable reminder to me about the kind of
service person I want to be. We have the utmost respect for all of the
families on our caseloads, but it is difficult to keep in mind that
they all have their own individual stories. Because we like to help,
we offer lots of “shoulds” and “musts” and wonder why families don’t
always follow through. This is a wonderful reminder about how and why
parents pick the battles that they do.
For More Information: To order,
call 1-800-621-2736, and mention code "ALEXFLYER" for a 20% discount.
For further information about the book or author, please
contact Ann Avouris at
publicity@academychicago.com or
1-800-248-READ (7323).
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Eating Gluten-Free With Emily: A Story For Children With Celiac
Disease |
Reviewed
by: Penny Ray & Mikalea (Age 7)
Review Date: April 11, 2005
Authors: Bonnie J. Kruszka, Richard S. Cihlar (Illustrator)
ISBN: 1890627623
Price: $14.95
Description: With its lighthearted, colorful illustrations,
this book helps children see that having celiac disease is not so
scary after all. Emily acknowledges that having celiac disease is
sometimes tough, but talking about her feelings with her mom always
makes her feel better. She knows that celiac disease is only part of
who she is—-she also likes to jump rope, paint, tell jokes, and pick
flowers! This book’s positive message will be a huge boost to children
with celiac disease, especially those who have been recently
diagnosed. For children ages 4-8. (Hard cover; 32 pages; 2004)
Penny’s Review: Eating Gluten-Free with Emily is a
children's book that not only explains a gluten-free diet, but also
details Emily's digestive symptoms and the route from doctor to blood
draw to scope to get the diagnosis. The illustrations are colorful and
cute. The story, which is told from Emily's perspective, explains
celiac disease in a way that children understand, and gives examples
of what foods contain gluten and which ones do not. Emily also
explains how she deals with real-life situations, like camp and
birthday parties. My favorite line in the book comes from Emily and
her mom when they question restaurant staff: "We say, 'We are gluten
detectives. Answer the questions, please.'" This book has been helpful
to my family in two ways. My five year old daughter is autistic, and
has been on a gluten free/casein free diet for four years, and it has
given her twin brother and older sister a perspective of what a
special diet is like for their sister. Additionally, my elder daughter
is about to see a pediatric gastroenterologist, to rule out (or in?)
celiac disease. This book has given us a wonderful opportunity to talk
about the process of going to the doctor and making dietary changes.
Seven year old Mikalea tells me she thinks this book is good because
it shows that Emily is just a regular kid who needs to eat special
food.
Ordering Information:
To order, visit
Amazon.com and enter "Eating
Gluten-Free With Emily: A Story For Children With Celiac Disease" into the search box or click on
the link provided here: (http://www.amazon.com/exec/obidos/tg/detail/-/1890627623/qid=1113500904/sr=8-1/ref=sr_8_xs_ap_i1_xgl14/102-0494800-1895321?v=glance&s=books&n=507846).
|
Love, Jean: Inspiration for Families Living with Dysfunction of
Sensory Integration |
Reviewed
by: Jackie D. Igafo-Te'o
Review Date: April 23, 2005
Authors: A. Jean Ayres, Philip R. Erwin, and Zoe Mailloux
ISBN: 0-9725098-1-X
Price: $15.95
Description: Captured in correspondence written by sensory
integration pioneer A. Jean Ayres to her nephew Philip Erwin, Love,
Jean provides hope, insight, and inspiration to parents of children
who have been diagnosed with dysfunction of sensory integration.
Interspersed with Dr. Ayres's letters are Erwin's poignant and
sometimes gut-wrenching stories about what it felt like before,
during, and after his aunt diagnosed his condition, and renowned
sensory integration therapist and researcher Zoe Mailloux's insights
into sensory integration from a therapist's perspective. The result is
a book that gently unfolds for parents of children with sensory
processing issues what sensory integration is and how their children
and they should be filled with hope that help is on the way. (paperback;
150 pages; 2004)
Jackie’s Review: This book, written by A. Jean Ayres, is a
must-have for those living or working with children who have sensory
processing issues. This compilation of years of letters and stories
between A. Jean and her nephew, Philip Erwin, is heartfelt, uplifting,
and inspiring. Love, Jean contains insight that is sure to help
parents avoid common pitfalls and misunderstandings associated with
the treatment of sensory integration dysfunction.
Ordering Information:
To order, visit
http://www.crestport.com/lovejean.html and click on "order" at the
top of the page.
About the Authors: A.
JEAN AYRES, PhD, OTR - About 50 years ago, A. Jean Ayres, working
as an occupational therapist with neurologically disabled children and
adults, began to realize that the weak muscles and poorly coordinated
hands and legs of these clients were not always their most severe
handicaps. Her approach with these children differed from that of
other professionals, for she believed that the best answers would be
found in a better understanding of how the brain processes sensations
- from not only the eyes and ears but other parts of the body as well.
She is credited with founding the field of sensory integration. Dr.
Ayres earned advanced degrees from the University of Southern
California and undertook post-doctoral work at the Brain Research
Institute at the University of California at Los Angeles. She was on
the faculty of the University of Southern California for over 20
years. She is the author of Sensory Integration and the Child, Sensory
Integration and Learning Disorders, and the Sensory Integration Praxis
Tests. PHILIP R. ERWIN - Mr. Erwin received his bachelor's
degree in Philosophy from the University of Oregon and certification
from the Einstein School of Medicine's Institute of Emergency Medicine
and the International Yacht Restoration School. Prior to advancing his
career as a writer and shipwright, he taught wooden boat restoration
at the International Yacht Restoration School and served as a
paramedic and emergency medical technician in New York, Connecticut,
California, and Oregon. ZOE MAILLOUX, MA, OTR, FAOTA - Ms.
Mailloux is nationally and internationally recognized within the
profession of occupational therapy in the area of sensory integration
theory and practice. She is currently the Director of Administration
at Pediatric Therapy Network, a non-profit children's therapy center
serving over 1000 children and their families. She was a research
assistant to Dr. A. Jean Ayres from 1978 to 1984 and was involved in
many clinical and research projects with Dr. Ayres. In addition, she
has published numerous journal articles and textbook chapters on these
topics. Ms. Mailloux was the chairperson of the Sensory Integration
Special Interest Section of the American Occupational Therapy
Association from 1993 to 1996 and was named a fellow of this
organization in 1993.
|
Planning for the Future: Providing a
Meaningful Life for a Child with a Disability After Your Death |
Reviewed By: Jackie D. Igafo-Te'o
Review Date:
September 24, 2005
Authors: Mark L. Russell, Arnold E. Grant
Price: $56.67 Amazon.com; $89.95 Retail
ISBN: 0912891203
Description:
The completely
revised and greatly expanded 5th edition of Planning for the Future: Providing a
Meaningful Life for a Child with a Disability After Your Death
discusses all the steps that parents should take to assure a secure
and happy life for their disabled son or daughter. (Paperback, 642
pages)
Jackie's Review: Reviewing “Planning for the Future” was a real
educational experience. I have never seen so much information
in one place about future planning for a child with a disability. The
first section blew me away - the second and third – same thing. From
cover to cover I was constantly learning something new. After
finishing the remaining pages in this whopper of a book (which is 642
pages in length), I am happy to report that this was an extremely
fruitful investment of my time. I now have the knowledge that I need
to move forward in planning for my own child’s future. I plan to
consult its content for many years to come. The authors cover
everything from the differences in housing options to applying for SSI
to caregiver options to community living to managing finances to
specifying your child's joys so that they may continue after your
death (even down to writing a letter which specifies that your child
likes to bowl or go to the movies). Great care was taken to ensure
that caregivers could understand the intended message. The lesson was
never overshadowed by meaningless 15-letter words or trendy phrases.
Over and over again, the authors stressed how important it is to get
input from the person with the disability and to tell the people who
you expect to care for your child about your decisions, which may
involve them. Readers are prodded to write a "letter of intent" and
to revise it each year so that it's always current and changes with
the needs of the child. The book is expensive (when compared to the
average novel or hobby book) but if you're looking into this topic, I
would highly recommend making this purchase before consulting
an attorney or hiring someone blindly. After all, planning for the
future of a child with a disability is no simple work of fiction.
Happy reading!
For More
Information:
This book can be
ordered by calling 1-800-247-6553
(credit card only). You can also visit Amazon.com at
http://www.amazon.com/exec/obidos/tg/detail/-/0912891203/qid=1125945610/sr=8-1/ref=pd_bbs_1/002-4446099-0620033?v=glance&s=books&n=507846
for more information or to purchase this book.
About the Authors:
L.
Mark Russell,
who has an older brother dual diagnosed with a mild intellectual
disability and mental illness, has concentrated his law practice for
over fifteen years on estate planning for families who have a child
with a disability, advising hundreds of families. He is a nationally
recognized conference speaker, regularly speaking to national, state,
and local disability organizations across the country, including
seminars for Public Television. Arnold E. Grant is a partner in
the Chicago office of McGuireWoods LLP, a nationally recognized law
firm with more than 700 attorneys. Mr. Grant has been named a member
of the leading lawyer network, which is a peer selected listing of the
top 5% of the lawyers in the state of Illinois. Mr Grant is a former
adjunct professor of law at Chicago-Kent College of Law and a former
chairman of the Corporate Tax Division of the Chicago Bar Association. |
Special Needs Trust
Administration Manual: A Guide for Trustees |
Reviewed By: Jackie D. Igafo-Te'o
Review Date: January 24,
2006
Authors: Barbara D Jackins, Richard S. Blank, Peter M Macy, Ken
W. Shulman, Harriet H. Onello
Price: $15.95 Amazon.com
ISBN: 0595331068
Description:
The Special Needs Trust Administration Manual is an
invaluable guide for anyone who is managing a Special Needs Trust for
a person with disabilities. In clear and
easy to understand language, the authors explain how a trustee can use
trust funds to meet the financial needs of a person with disabilities
while complying with the complex rules of government benefit programs. (Paperback,
143
pages)
Jackie's Review: I found this manual to be
of great benefit in future planning for my child with Autism.
The authors cover many important topics,
including public benefit programs (SSI, SSDI, Medicare, Medicaid),
taxes and trusts, how to arrange payment for housing, recreation,
transportation, and medical costs. Great care was taken to ensure
that readers understand the intended message.
Knowing what to expect
and how to handle the important issues discussed in this book will
make you more prepared to face tomorrow with your loved one. I
recommend this book to anyone who wants to know more about special
needs trust administration. I
would strongly recommend making this purchase before
hiring an attorney.
Its affordable price makes it an easy, yet important, purchase
decision that will give you the vital background and operations
information that you will need throughout this process.
For More
Information:
Order online through Amazon.com at
http://www.amazon.com/gp/product/0595331068/ref=pd_bxgy_img_b/104-1143751-2051165?%5Fencoding=UTF8.
About the Authors:
Barbara D. Jackins,
Richard S. Blank, Peter M. Macy, Harriet H. Onello, and Ken W. Shulman
are all Massachusetts attorneys. Their individual practices, which are
located in the Greater Boston area, focus on estate planning, Medicaid
planning, public benefits, and trust administration. They are all
experienced speakers and writers on disability related topics. |
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