|
|
Books > Health, Home & Family > Family & health > Advice on parenting > Child care & upbringing > General
 |
Moving Day
(Hardcover)
Dionna L Hayden; Dionna L Hayden; Foreword by Marcus L. Arrington
|
R637
Discovery Miles 6 370
|
Ships in 10 - 15 working days
|
|
|
Research shows that 'normal' infant sleep is not what most experts
claim it to be. In fact, many of today's sleep 'problems' with
young babies and children predominantly occur in the developed
world. In Why Your Baby's Sleep Matters, renowned gentle parenting
expert Sarah Ockwell-Smith demonstrates how nurturing babies at
night helps their brain development, and covers the topics every
parent of a new baby will need to know about, including naps, SIDS,
night weaning, coping with your own exhaustion - and even dealing
with advice and criticism from others.
 |
The Silver Dozen
(Hardcover)
Marquett Brewster; Illustrated by Caruso Anya
|
R544
R509
Discovery Miles 5 090
Save R35 (6%)
|
Ships in 18 - 22 working days
|
|
|
ABOUT THE BOOK: It seemed nothing Tracy did for her son would
work-testing, counseling, medication, therapy-and violent meltdowns
were a daily occurrence. She agonized over What is next? What is to
become of my beautiful son? Tracy's struggles were long and hard,
but with a mother's determination, a supportive family, and God's
love and intervention, she found strength, endurance, and
unexpected open doors. To the Land of the Lost is a mom's gripping,
true story account of the trials faced while parenting a child who
has Asperger's syndrome. The story is gut wrenching and
heartbreaking, while at the same time loving, uplifting,
encouraging, and inspirational. To the Land of the Lost is a must
read for any parent, caregiver, teacher, or friend of someone
living with an autism spectrum disorder. **** ABOUT THE AUTHOR:
Tracy M. Maguire lives in Dublin, Ireland, with her three children:
Graham, Sophie, and James. Her eldest son, Graham, now almost 19
years old, has Asperger's syndrome. Tracy is passionate about
encouraging parents who are raising a child with Asperger's and
giving them hope in what can often feel like a hopeless situation.
This book exposes the skyrocketing rate of antipsychotic drug
prescriptions for children, identifies grave dangers when
children's mental health care is driven by market forces, describes
effective therapeutic care for children typically prescribed
antipsychotics, and explains how to navigate a drug-fueled mental
health system. Since 2001, there has been a dramatic increase in
the use of antipsychotics to treat children for an ever-expanding
list of symptoms. The prescription rate for toddlers, preschoolers,
and middle-class children has doubled, while the prescribing rate
for low-income children covered by Medicaid has quadrupled. In a
majority of cases, these drugs are neither FDA-approved nor
justified by research for the children's conditions. This book
examines the reasons behind the explosion of antipsychotic drug
prescriptions for children, spotlighting the historical and
cultural factors as well as the role of the pharmaceutical industry
in this trend; and discusses the ethical and legal responsibilities
and ramifications for non-MDs-psychologists in particular-who work
with children treated with antipsychotics. Contributors explain how
the pharmaceutical industry has inserted itself into every step of
medical education, rendering objectivity in the scientific
understanding, use, and approvals of such drugs impossible. The
text describes the relentless marketing behind the drug sales, even
going as far as to provide coloring and picture books for children
related to the drug at issue. Valuable information about legal
recourse that families and therapists can take when their children
or patients have been harmed by antipsychotic drugs and alternative
approaches to working with children with emotional and behavioral
challenges is also provided. A chapter on effective parenting
coauthored by a leading parenting expert, Laura Berk Contributions
by noted medical journalist Robert Whitaker, author of Anatomy of
an Epidemic Information on legal issues by Harvard-educated lawyer
Jim Gottstein Insights from former pharmaceutical industry insider,
Gwen Olsen An examination of community approaches to children's
mental health care by internationally known psychologist Stuart
Shanker
I have been blessed to share Cori's journey through life. I have
also discovered that life isn't short of resources; it is about the
opportunities that we have been given. I have found that life
begins at the end of your comfort zone, and doing things that used
to be "outside the box" challenges the opinions of one's
single-minded beliefs. You would think that by surviving with
limitations, you're grounded or destined to only live life within
your abilities and not beyond. Do not allow your restrictions to be
an excuse to ground you. Do not accept that you can only live a
certain life. Cori has taught me to think of a life without
boundaries. Allow the sunshine to bring warmth upon your face and
smile at those who are inexperienced or misguided to the fact that
you are significant-challenged, but just as important. Being
impaired and nonverbal does not define your life. It's the life
that was given; this is who you are, and this is who we remain. We
hope that you will perceive our journey as encouragement and
inspiration, to live outside the box with no boundaries and to have
faith in yourself and be certain of change. I feel that life just
falls into place, since real life's destiny is not of our own
choosing. The true measure of a person's strength is how we
continue to exist when that moment does arrive. This is our journey
we share with you to learn there are no limits to the life of
experience a cerebral palsy child can have.
Mika is a nine-year-old girl that sees the world differently than
anyone else. Even though she is going through what every girl may
one-day face, fighting with her best friend and feeling like an
outcast, she is not like every other girl. Her mother, Ava and
brother, Javi stand by her side while Mika struggles endlessly to
feel normal, when instead she must embrace her uniqueness. Children
with Down syndrome, like Mika, are angels that help us see the
world with our hearts, instead of our eyes.
|
|