Professional Documents
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Etextbook 978 1598571943 Children With Disabilities by Mark Batshaw M D
Etextbook 978 1598571943 Children With Disabilities by Mark Batshaw M D
“An invaluable resource covering the range of disabilities and interventions used
to treat them.... This new version remains an indispensable classic in the field.”
Children with
—Fred R. Volkmar, M.D., Yale University School of Medicine and Yale New Haven Hospital
Disabilities
C
omprehensive, authoritative information from the most WHAT’S NEW
respected experts: For 30 years, that’s what Children ■ All-new chapters on diagno-
with Disabilities has given the thousands of students, sis, neuropsychological as-
faculty, and professionals who rely on it. Bringing together the sessment, “new” disabilities
faced by survivors of previ-
latest research and developments, this seventh edition is the de-
ously fatal disorders, and
finitive compendium of knowledge about the critical issues pro- complementary and alterna-
fessionals will encounter in their work with children and families. tive medicine
■ 30+ new contributors from
Covering developmental, clinical, family, education, and inter- diverse fields
vention issues, Children with Disabilities retains and strengthens ■ Expanded chapters on
the student-friendly features of previous editions. Readers will autism and ADHD
get concise and accessible chapters, a helpful glossary, chapter ■ New developments in
overviews, case studies that bring key concepts to life, extensive neuroscience, genetics,
cross-referencing to make information easy to find, and resource and imaging
lists for every topic. ■ Greater focus on interdisci-
plinary collaboration
An unparalleled text from the leading voices in the disability field, ■ Considerations from the
DSM-5
Children with Disabilities is the cornerstone resource profession-
■ Thoroughly updated
als will keep year after year to support their important work with
content in every chapter
children and families.
ABOUT THE EDITORS: Mark L. Batshaw, M.D., is the “Fight for Children” Chair of Academic Medicine and Chief Academic
Officer at the Children’s National Medical Center in Washington, D.C., and Professor and Chairman of Pediatrics and Associ-
ate Dean for Academic Affairs at The George Washington University School of Medicine and Health Sciences in Washington,
D.C. Nancy J. Roizen, M.D., is Director of the Division of Developmental-Behavioral Pediatrics and Psychology at University
Hospital’s Rainbow Babies and Children’s Hospital in Cleveland. Gaetano R. Lotrecchiano, Ed.D., Ph.D., is a former Leadership
Education in Neurodevelopmental Disabilities Program Director and is Assistant Professor of Clinical Research and Leadership
and of Pediatrics at The George Washington University School of Medicine and Health Sciences, Washington, D.C.
90000
Ocular Development
Development of Visual Skills
Common Disorders of the Eye in Children with Disabilities
Disorders of the Visual Cortex
Strabismus and Ocular Motility Disorders
Refractive Errors in Children
Vision Assessment
Blindness
12 The Brain and Nervous System
Amanda Yaun, Robert Keating, and Andrea Gropman . . . . . . . . . . . . . . . . . . . . . . . . . . . 189
The Brain and Spinal Cord
The Peripheral Nervous System
The Microscopic Architecture of the Brain
Techniques for Evaluating the Central Nervous System
13 Muscles, Bones, and Nerves
Peter B. Kang . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 213
Components of the Neuromuscular and Musculoskeletal Systems
Symptoms and Signs of Neuromuscular and Musculoskeletal Disorders
Laboratory Testing and Radiography
Disorders of the Neuromuscular System
Disorders of the Musculoskeletal System
Principles for the Management of Neuromuscular and Musculoskeletal Disorders
14 Patterns in Development and Disability
Louis Pellegrino . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 231
Defining Disability
Defining Development
Patterns in Development
Disturbances in Development
15 Diagnosing Developmental Disabilities
Scott M. Myers . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 243
Atypical Patterns of Development
Developmental Principles
Diagnostic Classification
The Diagnostic Process
16 Understanding and Using Neurocognitive Assessments
Lauren Kenworthy and Laura Gutermuth Anthony . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 267
The Purpose of Neuropsychological Assessment
A Model for Developmental Neuropsychological Assessment
Domains of Functioning Assessed in Neuropsychological Evaluations
Ensuring that Assessment Informs Management
Appendix A Glossary
Arlene Gendron . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 719
Appendix B Syndromes and Inborn Errors of Metabolism
Kara L. Simpson . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 757
Appendix C Commonly Used Medications
Michelle L. Bestic . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 803
Appendix D Childhood Disabilities Resources, Services, and Organizations . . . . . . . . . . 819
Index . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 843
About the Online
Companion Materials
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Please visit www.brookespublishing.com/batshaw to access
• Customizable PowerPoint presentations for every chapter, totaling over 450 slides
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• Extension activities for class use, group projects, and homework to help students apply the
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• Extended case studies to enrich discussions of how concepts are interconnected
• Sample syllabi from various fields to help you determine what chapters and sequence best
suits the needs of your course
• Resource listings with functional links for easy access
xiii
About the Editors
Mark L. Batshaw, M.D., is the “Fight for Nancy J. Roizen, M.D., is Director of the
Children” Chair of Academic Medicine and Division of Developmental-Behavioral Pedi-
Chief Academic Officer at the Children’s atrics and Psychology at University Hospi-
National Medical Center (CNMC) in Wash- tal’s Rainbow Babies and Children’s Hospital
ington, D.C., and Professor and Chairman of in Cleveland. She is certified in neurodevel-
Pediatrics and Associate Dean for Academic opmental disabilities and in developmental
Affairs at The George Washington Univer- behavioral pediatrics.
sity School of Medicine and Health Sciences Dr. Roizen received her B.S. and M.D.
in Washington, D.C. degrees from Tufts University. After com-
Dr. Batshaw is a board-certified neuro- pleting an internship in pediatrics at Mas-
developmental pediatrician who has treated sachusetts General Hospital, she did a
children with developmental disabilities for residency in pediatrics at The Johns Hop-
more than 35 years. In 2006, Dr. Batshaw kins Hospital. Her fellowships were in neu-
received both the Capute Award for notable rodevelopmental disabilities at the Kennedy
contributions to the field of children with Krieger Institute and in developmental and
disabilities by the American Academy of behavioral pediatrics at University of Califor-
Pediatrics and the Distinguished Research nia, San Francisco. She then was a staff phy-
Award from The Arc. sician at the Child Development Center at
Before moving to Washington in 1998, Oakland Children’s Hospital for 8 years, fol-
he was Physician-in-Chief of Children’s Sea- lowed by 16 years as Chief of the Section of
shore House, the child development and Developmental Pediatrics at the University
rehabilitation institute of The Children’s of Chicago. Then, at SUNY Upstate Medi-
Hospital of Philadelphia. Dr. Batshaw is a cal University, she was Vice Chair of Pediat-
graduate of the University of Pennsylvania rics, Professor of Pediatrics, and Chief of the
and of the University of Chicago Pritzker Division of Neurosciences for 4 years. Next
School of Medicine. Following pediatric res- stop was the Cleveland Clinic, where she
idency at the Hospital for Sick Children in was the Chief of the Department of Develop-
Toronto, he completed a fellowship in devel- mental Pediatrics and Physiatry for 2 years.
opmental pediatrics at the Kennedy Krieger Dr. Roizen has published more than 100
Institute at The Johns Hopkins Medical articles, chapters, and reviews on her clinical
Institutions. and research interests in Down syndrome and
Dr. Batshaw continues to pursue his hearing loss, and on collaborations in con-
research on innovative treatments for inborn genital toxoplasmosis and velocardiofacial
errors of metabolism, including gene ther- syndrome. She lives in Shaker Heights, Ohio,
apy. He has published more than 150 articles, with her husband. They have a daughter who
chapters, and reviews on his research inter- is working on a postdoctorate fellowship in
ests and on the medical aspects of the care organic chemistry at Stanford University and
of children with disabilities. Dr. Batshaw was a son who is a fellow in pediatric endocrinol-
the founding editor-in-chief (1995–2001) of ogy at Children’s Hospital of Philadelphia.
the journal Mental Retardation and Develop-
mental Disabilities Research Reviews.
Dr. Batshaw lives in Washington, D.C. Gaetano R. Lotrecchiano, Ed.D., Ph.D., is
He and his wife Karen have three children a former Leadership Education in Neurode-
and six grandchildren. velopmental Disabilities Program Director
xiv
About the Editors xv
and is presently Academic Director of Trans- of Education for the Khalifa Bin Zayed al
lational Science Programs as Assistant Pro- Nehyan Foundation initiative to create a
fessor of Clinical Research and Leadership sustainable rehabilitation center and profes-
and of Pediatrics at The George Washington sional education in the Eastern United Arab
University School of Medicine and Health Emirates. Dr. Lotrecchiano focuses on pro-
Sciences, Washington, D.C. fessional development through his dedication
Dr. Lotrecchiano received a Ph.D. in to those who care for children with special
ethnomusicology in 2005 from the Univer- needs. As a result, his scholarly interests have
sity of Maryland and an Ed.D. in human and focused on complexity leadership, transdisci-
organizational learning in 2012 from The plinarity team science, and blended-learning
George Washington University Graduate models in professional development, which
School of Education and Human Devel- he feels are key aspects of contemporary pro-
opment. He is a member of the Center fessional health care. Recently recognized as
for Neuroscience Research at Children’s a Morton A. Bender Teaching Scholar, Dr.
National Medical Center and the Center for Lotrecchiano has dedicated his entire career
the Study of Learning at The George Wash- to excellence in teaching and instruction. His
ington University. He has served in a number recent published material is in the Interna-
of positions administering disabilities and tional Journal of Transdisciplinary Research and
rare disease programs throughout his career, VINE: The Journal of Information and Knowl-
including the Intellectual and Developmen- edge Management Systems and Integral Leader-
tal Disabilities Research Center (IDDRC), ship Review. Dr. Lotrecchiano and his partner
the Rare Diseases Clinical Research Center Paul live in Beltsville, Maryland, with a his-
(RCDRC), and the Child Health Research toric home in Snow Hill, in the lower Del-
Center (CHRC). Presently, he is the Director marva Peninsula.
Contributors
Kruti Acharya, M.D. Michael J. Bina, Ed.D.
Assistant Professor of Pediatrics and President
Medicine The Maryland School for the Blind
University of Chicago 3501 Taylor Avenue
950 East 61st Street, SSC Suite 207 Baltimore, MD 21236
Chicago, IL 60637
Pamela Buethe, Ph.D.
George Acs, D.M.D, M.P.H Director of Audiology
ACS Consulting and Publishing Children’s National Medical Center
7120 Chilton Court Children’s Hearing and Speech Center
Clarksville, MD 21029 111 Michigan Avenue, NW
Washington, D.C. 20010
Laura Gutermuth Anthony, Ph.D.
Assistant Professor Philippa H. Campbell, Ph.D.
The George Washington University School Professor
of Medicine and Health Sciences Thomas Jefferson University
Children’s National Medical Center 6th Floor Edison, Suite 663
111 Michigan Avenue, NW 130 South 9th Street
Washington, D.C. 20010 Philadelphia, PA 19107
xvi
Contributors xvii
xxii
Preface
One of the first questions asked about a resource, parents, grandparents, siblings, and
subsequent edition of a textbook is “What’s other family members and friends have used
new?” The challenge of determining what to the book. They have found useful informa-
revise, what to add, and, in some cases, what tion on the medical and rehabilitative aspects
to delete is always significant in preparing a of care for the child with developmental dis-
new edition in a field changing as rapidly as abilities.
developmental disabilities. Since the publi-
cation of the sixth edition in 2007, advances FEATURES FOR THE READER
in the fields of neuroscience and genetics We have been told that the strengths of previ-
have greatly enhanced our understanding of ous editions of this book have been the acces-
the brain and inheritance. This brings forth sible writing style, the clear illustrations, and
opportunities for treatments previously not the up-to-date information and references.
thought possible for children with devel- We have dedicated our efforts to retaining
opmental disabilities. The human genome these strengths. Some of the features you will
has been mapped and the brain probed by find include the following:
functional imaging techniques. The need to • Teaching goals—Each chapter begins with
examine and explain this increased knowl- learning objectives to orient you to the
edge and its significance for children with content of that particular chapter.
disabilities has necessitated an increase in the
depth and breadth of the subjects covered in • Situational examples—Most chapters include
the book. Yet, while the book is now more one or more stories, or case studies, to help
expansive and has several new chapters, we bring alive the conditions and issues dis-
have worked hard to ensure that it retains its cussed in the chapter.
clarity and cohesion. Its mission continues • Key terms—As medical terms are intro-
to be to provide the individual working with duced in the text, they appear in boldface
and caring for children with disabilities the type at their first use; definitions for these
necessary background to understand differ- terms appear in the Glossary (Appendix A).
ent disabilities and their treatments, thereby • Illustrations and tables—More than 200
enabling affected children to reach their full drawings, photographs, x rays, imaging
potential. scans, and tables reinforce the points of
the text and provide ways for you to more
THE AUDIENCE
easily understand and remember the
Since it was originally published, Children material you are reading.
with Disabilities has been used by students in
a wide range of disciplines as a medical text- • Summary—Each chapter closes with a
book addressing the impact of disabilities on final section that reviews its key elements
child development and function. It has also and provides you with an abstract of the
served as a professional reference for special covered material.
educators, general educators, physical thera- • References—The reference list accompa-
pists, occupational therapists, speech-lan- nying each chapter can be thought of as
guage pathologists, psychologists, child-life more than just a list of the literature cited
specialists, social workers, nurses, physicians, in the chapter. These citations include
advocates, and others who provide care for review articles, reports of study find-
children with disabilities. Finally, as a family ings, research discoveries, and other key
xxiii
xxiv Preface
references that can help you find addi- development, the birth process, and prema-
tional information. turity are explained. The next section of the
• Appendixes—In addition to the Glossary, book, The Developing Child, covers environ-
there are three other helpful appendi- mental causes of developmental disabilities
ces 1) Syndromes and Inborn Errors of and examines the various organ systems—how
Metabolism, a mini-reference of pertinent they develop and work and what can go wrong.
information on inherited disorders causing Nutrition, vision, hearing, language, patterns
developmental disabilities; 2) Commonly of development, and the brain and muscu-
Used Medications, to describe indica- loskeletal systems are discussed in individual
tions and side effects of medications often chapters. As its title implies, the third section,
prescribed for children with disabilities; Developmental Disabilities, provides compre-
and 3) Childhood Disabilities Resources, hensive descriptions of various developmental
Services, and Organizations, a directory disabilities and genetic syndromes causing dis-
of a wide range of national organizations, abilities and includes chapters on intellectual
federal agencies, information sources, self- disability, Down syndrome, inborn errors of
advocacy and accessibility programs, and metabolism, psychiatric disorders in develop-
support groups that can provide assistance mental disabilities, autism spectrum disorders,
to families and professionals. attention-deficit/hyperactivity disorder, spe-
cific learning disabilities, cerebral palsy, neu-
CONTENT ral tube defects, epilepsy, and traumatic brain
In developing this seventh edition, we have injury. The final section, Interventions, Fami-
aimed for a balance between consistency with lies, and Outcomes, contains chapters that
the text that many of you have come to know focus on various interventions, including early
so well in its previous editions and innovation intervention and special education services,
in exploring the new topics that demand our feeding, dental care, behavioral assessment
attention. All chapters have been substan- and support, assistive technology, and physi-
tially revised and many have been rewritten cal and occupational therapy. This section also
to include an expanded focus on psychoso- concentrates on the ethical, legal, emotional,
cial, rehabilitative, and educational inter- and transition-to-adulthood issues that are
ventions as well as to provide information common to most families of children with dis-
discovered through educational, medical, abilities and to professionals who work with
and scientific advances since 2007. In addi- them. The book closes with a discussion of the
tion, four new chapters have been added to prospects for providing health care in the 21st
address the following topics: 1) the new face century.
of developmental disabilities (long-term out-
comes of previously fatal disorders), 2) novel THE AUTHORS AND EDITORS
therapies and treatment efficacy (alternative Nancy J. Roizen joined me as an editor for
medicine), 3) understanding and using neu- the sixth edition of the text. Like me, she is
rocognitive assessment, and 4) diagnosing a a neurodevelomental pediatrician. Gaetano
child with developmental disabilities. They R. Lotrecchiano, an educator for interdisci-
focus on recently gained knowledge that is plinary training in developmental disabili-
transforming our understanding of the causes ties, joined as an editor on this edition. We
of developmental disabilities. have chosen physicians, psychologists, social
The chapters are grouped into sections workers, therapists, and other health care
and have been organized to help guide read- professionals who are experts in the areas
ers through the breadth of content. The book they write about as authors of Children with
starts with a section titled As Life Begins, Disabilities. Many are colleagues from Chil-
which addresses what happens before, dur- dren’s National Medical Center in Wash-
ing, or shortly after birth to cause a child to ington, D.C. Each chapter in the book has
be at increased risk to manifest a developmen- undergone editing at Paul H. Brookes Pub-
tal disability. The concepts and consequences lishing Co. to ensure consistency in style and
of genetics, embryology, infections and fetal accessibility of content. Once the initial drafts
Preface xxv
were completed, each chapter was sent for interventions, thus emphasizing the capa-
peer review by major clinical and academic bilities rather than the impairments of
leaders in the field and was revised according individuals with intellectual disability.
to their input. • “Typical” and “normal”—Recognizing
diversity and the fact that no one type
A FEW NOTES ABOUT of person or lifestyle is inherently “nor-
TERMINOLOGY AND STYLE mal,” we have chosen to refer to the gen-
As is the case with any book of this scope, the eral population of children as “typical” or
editor or author faces decisions about the use “typically developing,” meaning that they
of particular words or the presentation style follow the natural continuum of develop-
of information. We would like to share with ment.
you some of the decisions we have made for • Person-first language—We have tried to
this book. preserve the dignity and personhood of
• Categories of intellectual disability—This all individuals with disabilities by consis-
book uses the American Psychiatric Asso- tently using person-first language, speak-
ciation’s categories according to the term ing, for example, of “a child with autism,”
mental retardation (i.e., mild, moderate, instead of “an autistic child.” In this way,
severe, profound) when discussing medi- we are able to emphasize the person, not
cal diagnosis and treatment and uses the define him or her by the condition.
categories that the American Association As you read this seventh edition of Chil-
on Intellectual and Developmental Dis- dren with Disabilities, we hope you will find
abilities (formerly the American Associa- that the text continues to address the fre-
tion on Mental Retardation) established quently asked question “Why this child?”
in 1992 (i.e., requiring limited, inter- and to provide the medical background you
mittent, extensive, or pervasive support) need to care for children with developmental
when discussing educational and other disabilities.
Acknowledgments
We would like to thank our colleagues at Paul Seth Canion, Charles J. Conlon, Philip W.
H. Brookes Publishing Co. for their great Davidson, Carolyn Drews-Botsch, Ann-
help. Steve Plocher served as Associate Editor Christine Duhaime, Diana M. Escolar, Sara
for the text and Johanna Cantler as Acquisi- Helen Evans, Erynn S. Gordon, Karl F.
tions Editor, and both provided developmen- Gumpper, Michael J. Guralnick, William
tal oversight of the project; Danica Crittenden H.J. Haffner, Mark L. Helpin, Janet S. Isaacs,
assisted with the review process. A book such Dorothy O. Jones, Annie Kennedy, Carol
as Children with Disabilities is best understood A. Knightly, Alan E. Kohrt , Lisa A. Kurtz,
with illustrations that help to explain medical Mary F. Lazar, Sheryl J. Menacker, Gretchen
concepts. An expert medical illustrator is cru- A. Meyer, Linda J. Michaud, Gary J. Myers,
cial in this effort. Lynn Reynolds has contrib- Man Wai Ng, Jeffrey P. Rabin, Mark Reber,
uted to this endeavor in both past editions and Howard M. Rosenberg, Andrew J. Satin,
with new additions in this volume. We deeply Tomas Jose Silber, Harvey S. Singer, Annie
acknowledge her important contribution. G. Steinberg, Ana Carolina Tesi Rocha, Cyn-
We also gratefully acknowledge Arlene Gen- thia J. Tifft, Laura L. Tosi, Kenneth E. Tow-
dron, who helped organize the project as well bin, Symme Wilson Trachtenberg, Mendel
as contributed to the book’s appendixes. We Tuchman, Kim Van Naarden Braun, Shari L.
thank previous contributors whose work on Wade, Steven L. Weinstein, and Marshalyn
the sixth edition laid an excellent foundation Yeargin-Allsopp. Finally, many of our col-
for this text: Terry Adirim, Karen Batshaw, leagues reviewed and edited the manuscript
Michael Batshaw, Michael J. Bell, Nathan for content and accuracy, and we would like
J. Blum, Jill E. Brown, W. Bryan Burnette, to acknowledge their efforts.
xxvi
Why me?
Why me?
Why do I have to do so much more than others?
Why am I so forgetful?
Why am I so hyperactive?
And why can’t I spell?
Why me? O’why me?
Andrew Batshaw
1989
xxvii
In applying to colleges during my senior year of high school, I found that
most had as an essay topic, “Tell us something about yourself.” I decided to
write about my ADHD and learning disability as it is a big part of who I am.
I wrote “I have found that while a disability inherently leaves you with a
weakness, adapting to that disability can provide rewards. I feel that from
coping with my disability, I have gained pride, determination, and a
strength that will be with me all of my life.” I guess Vassar College agreed;
they admitted me.
When it came time for high school graduation, we had a problem. My sister
was graduating from the University of Chicago on the same day that I gradu-
ated from high school in Philadelphia. The only solution was for one parent
to attend my graduation while the other one was with my sister in Chicago.
The decision as to who would go to which graduation was easy. My mother
insisted that she attend my graduation because it was a product of her hard
work as well as my own. I remember she said to me that day, “When I think
of the boy who cried himself to sleep because he could not remember how to
spell the word ‘who,’ it makes me so happy to see you now.”
My parents expressed themselves in different ways about my leaving for
college. My mother and I found ourselves getting into many arguments over
simple things (the old severing of the umbilical cord; I am the baby of the
family). My father, however, made sure to remind me to start my stimulant
medication 2 weeks before classes began!
The first semester I took four courses: Poetry, Linear Algebra, Computer Sci-
ence, and Music Theory. As the semester continued, I developed an increas-
ing interest in computer science, until finally I decided to become a computer
science major. I was very flattered, however, when during a meeting with my
English professor, she asked if I planned to be an English major. To think that
someone who could not read until the end of second grade would become a
member of the Vassar English department seemed almost unbelievable. Well,
I might have been proud but not that proud. I stuck with computer science.
On the whole, I would say that my freshman year was a good one. I learned a
great deal, both inside and outside of classes, about myself and others. What
will I do after college? What will I end up doing with my life? These are
questions that continually run through my mind. I have no clear answers,
but there is one thing of which I am sure: My disability will not keep me
from doing anything. I will not let it.
AndrewBatshaw
Andrew Batshaw
June 1996
1996
xxviii
As a college graduate, I find that my ADHD and learning disabilities are much
less of an issue; however, that was not the case during my early college years.
In my second year of college, I took a year-long introductory German class
that fulfilled my language requirement. Forgetting that languages don’t come
easily to me, I chose the intensive German class that met an extra day a week
and moved faster than the regular class. I watched my exam grades slowly slide
into the C range during the first semester and decided to switch to the regular
class for the rest of the year. While this was happening, some medical
warnings were issued concerning the stimulant medication I was taking,
so I decided to discontinue its use.
In the new German class, we had exams every other week, so I received regu-
lar feedback on how I was doing. Unfortunately, it was not positive feedback.
After receiving an F on the first quiz, I decided that I needed to work harder in
the class. I started studying more and was less than relieved when on my next
exam my grade rose to a D! Again, I studied even more and still received a
D on the test that followed. At this point, I began to doubt myself. I felt like
I was doing everything I could, and still I wasn’t improving. I said to myself,
“I know you have always told yourself that you could do anything you really
gave your all to, but maybe there are just some things you can’t do.” I was
disheartened, but felt that I had no choice but to just keep working. I received
a C and then a C+ on my next two exams, but my overall class grade was still
very low. My professor spoke to me and said that as long as I received at least a
C+ on the final exam, he would pass me. I did all I could to prepare for the test
and took the exam without reservation, simply willing to accept the results,
whatever they might be. I ran into my professor a week after the final exam
and was told that not only had I passed the final exam, but that I had received
an A, one of the highest grades in the class. As you might expect, I was
ecstatic. I looked back on the day when I had thought, “Maybe there really are
things that I just can’t do,” and smiled, because I proved myself wrong. On top
of that, I had accomplished it without the help of medication. That was when I
truly felt that I had overcome my ADHD and learning disabilities.
In fact, some of the most important activities in my life are things that at first
glance you wouldn’t think someone with ADHD would find attractive. I medi-
tate every day, which involves sitting in one place and not moving for long pe-
riods of time. When I meditate, I am actually watching how my mind works.
I see how easily I am distracted from simply sitting by thinking about all kinds
of things, like what I did yesterday or what I am going to do later. Neverthe-
less, I keep bringing myself back, over and over again, and sometimes my
mind becomes very quiet and clear. I find that this has had a positive impact
xxix
on all aspects of my life. I was talking with my older brother, Michael, after
attending my first 3-day meditation retreat, and he told me how proud he was
of me. He said that after seeing me bounce off the walls and have such diffi-
culty concentrating while growing up, he was amazed that I could sit still and
meditate for 3 days.
After 4 years, including 6 months at the University of York in England, I
graduated from Vassar College with a B.A. in Computer Science in May 1999.
After graduation, I worked for a year as a software engineer and then started
my own company with my brother and a friend. Unfortunately, after devel-
oping the company for a year, we became one of the many casualties of the
dot-com collapse. Naturally, I was very disappointed, but it was an incredible
experience that I will always value. It sparked in me a passion for entrepre-
neurship that led to my decision to attend business school.
Throughout the process of applying to business school, it became clear to me
how my learning disability had been transformed from a hindrance to an asset.
The work habits I had developed to overcome my disability allowed me to
stick to a rigorous preparation program for my business school entrance
exams. As a result, I scored in the 98th percentile. In addition, when preparing
my applications, I chose to include an essay about how overcoming a disability
had taught me to treat failure as a natural and necessary part of important
accomplishments. Furthermore, it instilled in me a drive to achieve and to
take calculated risks that are essential to being successful in business. I will be
attending the University of Southern California Business School with a full
scholarship.
Drew Batshaw
April
2002 2002
xxx
Five eventful years have passed since I wrote my foreword to the fifth edition
of this text. I graduated from business school, fell in love and married an amaz-
ing woman, and have been pursuing a career in business. Through all of these
experiences, my ADHD and learning disability continue to impact my life in
both subtle and not-so-subtle ways.
At the end of my last letter, I spoke about pursuing an MBA at the University
of Southern California. My experience in business school was positive, both
academically and socially. I’d come a long way from my childhood struggles;
my ADHD and learning deficits had little effect on my performance. I ex-
celled, my teachers respected me, and other students regularly sought me out
to work on projects with them.
For me, business school was easier than college for a number of reasons. The
subject matter was generally more engaging and played to my strengths: think-
ing on my feet, presenting ideas orally, and using analytical reasoning. In addi-
tion, much of the learning took place in an interactive and experiential envi-
ronment that kept my interest and attention. For example, we discussed real
situations that companies have had in the past and how we would have man-
aged them, and we role-played as consultants with 90 minutes to prepare a
thorough presentation for the class. Another significant factor was that writing
(which historically has been my most challenging form of communication) is
different and easier for me in a business setting than an academic one. In busi-
ness writing, lengthy discourse is discouraged and traditional writing rules are
far less important than presenting information in a clear and concise way; plus,
of course, I’d had many years to hone my writing skills since I entered Vassar.
Finally, I’d learned to manage my disability and identify environments like
business school where I would be most successful.
After graduating with my MBA, I launched a company that provided coaching
services for young executives and business owners. My job as a coach was to as-
sist clients in their effectively working through problems, as opposed to the
traditional consultant model of doing the work for them. After about 18
months, I realized that my heart was no longer in building the business; I
missed managing tangible projects and found coaching to be lonely. I had
many clients but no peers to interact with on a daily basis. I then moved to my
current job, where I run the operations and technology of an education tech-
nology company that helps low-income children improve their reading skills.
It is very satisfying to be involved in a business that helps children who have
reading difficulties like I had. In contrast to the coaching work, this job allows
me to manage many different projects and work with a great team.
xxxi
I have also found that I reap unexpected benefits from my ADHD. Profession-
ally, I am known for my ability to effectively problem-solve with limited infor-
mation. Unlike others who are intimidated by their lack of knowledge or in-
formation, I delight in jumping right into the problem and figuring it out as I
go (much like how I used to raise my hand all the time in grade school even
though I didn’t know the answer). In addition, I juggle many different projects
and priorities with finesse. I thrive in environments that offer variety, allow me
to wear many different hats, and require the use of a broad set of skills
throughout the course of each day. Perhaps because of this I have changed jobs
every 1 to 2 years since graduating from college (7 years ago): I have been a
software developer, a dot-com founder, a business school student, and an exec-
utive coach, and now I am a manager of technology and finance. When I first
start a job, I’m very excited and engaged in the work, but after I become profi-
cient, I start to itch to do something different. Does my ADHD cause me to
need a certain kind of sustained and varied stimulation that I have not yet
found? I’m not sure, but I do know that I require a high level of change and
stimulation to stay engaged and productive.
My ADHD impacted my early adulthood in other ways. For many years, no
matter how much I achieved or how well I succeeded, I was still left with the
shame of not being good enough during my formative years. As a child, my
disability affected my self-image as well as my academic performance. Despite
my mother telling me, “You are intelligent. It’s just your learning disability that
affects how you do in school,” I still measured my worth in comparison to
everyone else—for example, how far I got in a spelling bee, how long it took
me to read a book, or what grade I received on a writing assignment. Through
much of my twenties, when something didn’t go well in my life—profession-
ally, personally, or sometimes even when I was just sick—I would feel like that
little boy again who just couldn’t do anything right. I can see now that no
amount of achievement would have transformed those feelings of inadequacy.
What has helped me most in dealing with this legacy is counseling and reward-
ing intimate relationships. Counseling has helped me to recognize when this
old shame is triggered and how to notice it and move on. Through intimate
relationships, I’ve come to understand and own my worth in a greater sense—
how I offer so much more than just what I can achieve. For example, I have a
positive impact on others by just being in their lives, and I can move people
with my emotions and words. These things are all effortless. I don’t have to try
or work hard to make them happen. They simply occur as a natural result of
who I am inherently.
xxxii
My greatest teacher in this has been my wife, Amy. We were married in August
2005 after dating for 2 years. Her capacity for love, joy, and compassion
amazes me. While preparing this letter, I asked her how my disability impacts
our relationship. She smiled and said, “Well, you don’t like to wash the dishes
or go clothes shopping with me!” Much as I’d like to blame that on ADHD,
I’m not sure that would be fair. What I have noticed are some of Amy’s quali-
ties that make her an especially good match for someone like me with ADHD.
Professionally, she is a coach and organizing consultant, and, as a result, natu-
rally provides structure and organization to our lives. In addition, she gives me
a lot of space and honors the transition time I need between being by myself
and being with her. Finally, she is very accepting and offers me constant
appreciation and encouragement. I am a lucky man!
In sum, I lead an extraordinarily blissful life. I have a wonderful wife, my
current work is stimulating and meaningful, and my relationships with family
and friends are warm and fulfilling. I am immensely grateful for all I have been
given and all I have been able to accomplish—in spite of and because of my
disability.
Andrew Batshaw
2007
xxxiii
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ally,
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struck by how little impact I still feel. At the age of 33, I appreciate with limited infor-
mation.
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and reward-
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ing intimate relationships. Counseling has helped me to recognize when this I have a disability (in fact,
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tempted to say “had” a disability instead of “have”).
is triggered and how to notice it and move on. Through intimate
relationships,
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the emotions in a greater
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ability is witnessing others with disabilities. A few years ago, I happened I have a
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and play because things were so challenging for his brother.
His thoughtfulness and commitment to creating joy for his brother still move
me today.
xxxiv
Another random document with
no related content on Scribd:
DANCE ON STILTS AT THE GIRLS’ UNYAGO, NIUCHI
I see increasing reason to believe that the view formed some time
back as to the origin of the Makonde bush is the correct one. I have
no doubt that it is not a natural product, but the result of human
occupation. Those parts of the high country where man—as a very
slight amount of practice enables the eye to perceive at once—has not
yet penetrated with axe and hoe, are still occupied by a splendid
timber forest quite able to sustain a comparison with our mixed
forests in Germany. But wherever man has once built his hut or tilled
his field, this horrible bush springs up. Every phase of this process
may be seen in the course of a couple of hours’ walk along the main
road. From the bush to right or left, one hears the sound of the axe—
not from one spot only, but from several directions at once. A few
steps further on, we can see what is taking place. The brush has been
cut down and piled up in heaps to the height of a yard or more,
between which the trunks of the large trees stand up like the last
pillars of a magnificent ruined building. These, too, present a
melancholy spectacle: the destructive Makonde have ringed them—
cut a broad strip of bark all round to ensure their dying off—and also
piled up pyramids of brush round them. Father and son, mother and
son-in-law, are chopping away perseveringly in the background—too
busy, almost, to look round at the white stranger, who usually excites
so much interest. If you pass by the same place a week later, the piles
of brushwood have disappeared and a thick layer of ashes has taken
the place of the green forest. The large trees stretch their
smouldering trunks and branches in dumb accusation to heaven—if
they have not already fallen and been more or less reduced to ashes,
perhaps only showing as a white stripe on the dark ground.
This work of destruction is carried out by the Makonde alike on the
virgin forest and on the bush which has sprung up on sites already
cultivated and deserted. In the second case they are saved the trouble
of burning the large trees, these being entirely absent in the
secondary bush.
After burning this piece of forest ground and loosening it with the
hoe, the native sows his corn and plants his vegetables. All over the
country, he goes in for bed-culture, which requires, and, in fact,
receives, the most careful attention. Weeds are nowhere tolerated in
the south of German East Africa. The crops may fail on the plains,
where droughts are frequent, but never on the plateau with its
abundant rains and heavy dews. Its fortunate inhabitants even have
the satisfaction of seeing the proud Wayao and Wamakua working
for them as labourers, driven by hunger to serve where they were
accustomed to rule.
But the light, sandy soil is soon exhausted, and would yield no
harvest the second year if cultivated twice running. This fact has
been familiar to the native for ages; consequently he provides in
time, and, while his crop is growing, prepares the next plot with axe
and firebrand. Next year he plants this with his various crops and
lets the first piece lie fallow. For a short time it remains waste and
desolate; then nature steps in to repair the destruction wrought by
man; a thousand new growths spring out of the exhausted soil, and
even the old stumps put forth fresh shoots. Next year the new growth
is up to one’s knees, and in a few years more it is that terrible,
impenetrable bush, which maintains its position till the black
occupier of the land has made the round of all the available sites and
come back to his starting point.
The Makonde are, body and soul, so to speak, one with this bush.
According to my Yao informants, indeed, their name means nothing
else but “bush people.” Their own tradition says that they have been
settled up here for a very long time, but to my surprise they laid great
stress on an original immigration. Their old homes were in the
south-east, near Mikindani and the mouth of the Rovuma, whence
their peaceful forefathers were driven by the continual raids of the
Sakalavas from Madagascar and the warlike Shirazis[47] of the coast,
to take refuge on the almost inaccessible plateau. I have studied
African ethnology for twenty years, but the fact that changes of
population in this apparently quiet and peaceable corner of the earth
could have been occasioned by outside enterprises taking place on
the high seas, was completely new to me. It is, no doubt, however,
correct.
The charming tribal legend of the Makonde—besides informing us
of other interesting matters—explains why they have to live in the
thickest of the bush and a long way from the edge of the plateau,
instead of making their permanent homes beside the purling brooks
and springs of the low country.
“The place where the tribe originated is Mahuta, on the southern
side of the plateau towards the Rovuma, where of old time there was
nothing but thick bush. Out of this bush came a man who never
washed himself or shaved his head, and who ate and drank but little.
He went out and made a human figure from the wood of a tree
growing in the open country, which he took home to his abode in the
bush and there set it upright. In the night this image came to life and
was a woman. The man and woman went down together to the
Rovuma to wash themselves. Here the woman gave birth to a still-
born child. They left that place and passed over the high land into the
valley of the Mbemkuru, where the woman had another child, which
was also born dead. Then they returned to the high bush country of
Mahuta, where the third child was born, which lived and grew up. In
course of time, the couple had many more children, and called
themselves Wamatanda. These were the ancestral stock of the
Makonde, also called Wamakonde,[48] i.e., aborigines. Their
forefather, the man from the bush, gave his children the command to
bury their dead upright, in memory of the mother of their race who
was cut out of wood and awoke to life when standing upright. He also
warned them against settling in the valleys and near large streams,
for sickness and death dwelt there. They were to make it a rule to
have their huts at least an hour’s walk from the nearest watering-
place; then their children would thrive and escape illness.”
The explanation of the name Makonde given by my informants is
somewhat different from that contained in the above legend, which I
extract from a little book (small, but packed with information), by
Pater Adams, entitled Lindi und sein Hinterland. Otherwise, my
results agree exactly with the statements of the legend. Washing?
Hapana—there is no such thing. Why should they do so? As it is, the
supply of water scarcely suffices for cooking and drinking; other
people do not wash, so why should the Makonde distinguish himself
by such needless eccentricity? As for shaving the head, the short,
woolly crop scarcely needs it,[49] so the second ancestral precept is
likewise easy enough to follow. Beyond this, however, there is
nothing ridiculous in the ancestor’s advice. I have obtained from
various local artists a fairly large number of figures carved in wood,
ranging from fifteen to twenty-three inches in height, and
representing women belonging to the great group of the Mavia,
Makonde, and Matambwe tribes. The carving is remarkably well
done and renders the female type with great accuracy, especially the
keloid ornamentation, to be described later on. As to the object and
meaning of their works the sculptors either could or (more probably)
would tell me nothing, and I was forced to content myself with the
scanty information vouchsafed by one man, who said that the figures
were merely intended to represent the nembo—the artificial
deformations of pelele, ear-discs, and keloids. The legend recorded
by Pater Adams places these figures in a new light. They must surely
be more than mere dolls; and we may even venture to assume that
they are—though the majority of present-day Makonde are probably
unaware of the fact—representations of the tribal ancestress.
The references in the legend to the descent from Mahuta to the
Rovuma, and to a journey across the highlands into the Mbekuru
valley, undoubtedly indicate the previous history of the tribe, the
travels of the ancestral pair typifying the migrations of their
descendants. The descent to the neighbouring Rovuma valley, with
its extraordinary fertility and great abundance of game, is intelligible
at a glance—but the crossing of the Lukuledi depression, the ascent
to the Rondo Plateau and the descent to the Mbemkuru, also lie
within the bounds of probability, for all these districts have exactly
the same character as the extreme south. Now, however, comes a
point of especial interest for our bacteriological age. The primitive
Makonde did not enjoy their lives in the marshy river-valleys.
Disease raged among them, and many died. It was only after they
had returned to their original home near Mahuta, that the health
conditions of these people improved. We are very apt to think of the
African as a stupid person whose ignorance of nature is only equalled
by his fear of it, and who looks on all mishaps as caused by evil
spirits and malignant natural powers. It is much more correct to
assume in this case that the people very early learnt to distinguish
districts infested with malaria from those where it is absent.
This knowledge is crystallized in the
ancestral warning against settling in the
valleys and near the great waters, the
dwelling-places of disease and death. At the
same time, for security against the hostile
Mavia south of the Rovuma, it was enacted
that every settlement must be not less than a
certain distance from the southern edge of the
plateau. Such in fact is their mode of life at the
present day. It is not such a bad one, and
certainly they are both safer and more
comfortable than the Makua, the recent
intruders from the south, who have made USUAL METHOD OF
good their footing on the western edge of the CLOSING HUT-DOOR
plateau, extending over a fairly wide belt of
country. Neither Makua nor Makonde show in their dwellings
anything of the size and comeliness of the Yao houses in the plain,
especially at Masasi, Chingulungulu and Zuza’s. Jumbe Chauro, a
Makonde hamlet not far from Newala, on the road to Mahuta, is the
most important settlement of the tribe I have yet seen, and has fairly
spacious huts. But how slovenly is their construction compared with
the palatial residences of the elephant-hunters living in the plain.
The roofs are still more untidy than in the general run of huts during
the dry season, the walls show here and there the scanty beginnings
or the lamentable remains of the mud plastering, and the interior is a
veritable dog-kennel; dirt, dust and disorder everywhere. A few huts
only show any attempt at division into rooms, and this consists
merely of very roughly-made bamboo partitions. In one point alone
have I noticed any indication of progress—in the method of fastening
the door. Houses all over the south are secured in a simple but
ingenious manner. The door consists of a set of stout pieces of wood
or bamboo, tied with bark-string to two cross-pieces, and moving in
two grooves round one of the door-posts, so as to open inwards. If
the owner wishes to leave home, he takes two logs as thick as a man’s
upper arm and about a yard long. One of these is placed obliquely
against the middle of the door from the inside, so as to form an angle
of from 60° to 75° with the ground. He then places the second piece
horizontally across the first, pressing it downward with all his might.
It is kept in place by two strong posts planted in the ground a few
inches inside the door. This fastening is absolutely safe, but of course
cannot be applied to both doors at once, otherwise how could the
owner leave or enter his house? I have not yet succeeded in finding
out how the back door is fastened.