Disabled Village Children. A Guide for Community Health Workers, Rehabilitation Workers, and Families. First Edition.

Hesperian Health Guides (Where There Is No Doctor)

Hesperian

Werner, David, Hesperian Foundation, Palo Alto, Ca.

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Werner, David 

Disabled Village Children. A Guide for Community 
Health Workers, Rehabilitation Workers, and Families. 
First Edition. 

Hesperian Foundation. Palo Alto, CA. 
ISBN-0-942364-06-6 

May 87 

703p. 

Hesperian Foundation, P.O. Box 1692, Palo Alto, CA 
94302 ($9.00, 12 or more, $7.00 each). 

Guides - Non-Classroom Use (055) -- Reference 
Materials - General (130) 


MFO04/PC29 Plus Postage. 

Adaptive Behavior (of Disabled); Adolescents; 
*Assistive Devices (for Disabled); Attitude Change; 
Career Development; Child Development; Children; 
Clinical Diagnosis; *Community Health Services; 
*Developing Nations; *Disabilities; Educational 
Diagnosis; Family Programs; *Handicap Identification; 
Illustrations; Parent Child Relationship; *Parent 
Education; Prostheses; Rehabilitation; Self Care 
Skills; Sex Education; Teacher Attitudes; Young 
Adults 


This heavily illustrated volume is a reference book 


intended to bring together basic information to help community health 


workers, 


rehabilitation workers, and families in rural areas of 


developing countries meet the needs of village children with a wide 
range of disabilities. Part 1, "Working with the Child and Family," 
reviews the prevention of disabilities (examining and evaluating the 
disabled child) and simple ways to measure and record a child's 
progress. A guide for identifying disabilities includes detailed 
descriptions and illustrations of the most common disabilities found 
in developing countries. Also included is information on early 
stimulation and developmental activities for delayed infants and for 
young children with mental or physical delays, guidance on how to 
help children become more self-reliant, and exercises and techniques 
for managing physical disabilities. Part 2, "Working with the 
Community," includes sections on starting village-based 
rehabilitation activities, building playgrounds for all children, 
helping teachers and children understand disabled children, using 
popular theater to raise awareness and gain greater community 
participation, and establishing a children's workshop for making 
toys. It also discusses how to organize, manage, and finance a 
village rehabilitation program; adaptation of the home and community 
to the needs of the disabled; concerns of the disabled about love, 
sex, and social adjustment; the role of education at home, school, 
and work; work possibilities and training; and descriptions of 
successful community-directed programs. Part 3, "Working in the 
Shop," provides specific instructions and advice about setting up a 
workshop to make rehabilitation aids and procedures to be followed in 
providing aids such as braces and casts, developmental and walking 
aids, wheelchairs, and artificial limbs. The volume also includes a 
nine-page list of references, a glossary, and an index. This 
publication is announced in the May 1987 issue of "Newsletter from 
the Sierra Madre," which is appended. The newsletter includes a 
story, article, photographs, and illustrations which describe the 
work of Project Projimo and Project Piaxtla, of western Mexico, where 


this book had its start and was field tested. 


(JW) 


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foe) TIONAL RESOURCES INFORMATION 


CENTER (ERIC) 


OC) This document has been reproduced es 
received from the person or organization : —_—_ 
« [= onginating it i 
CD Minor changes have been made to improve 


Lil reproducticn quality 


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EST COPY AVAILABLE 


HOW TO USE THIS BOOK 


This is a reference book to help you meet the needs of disabled children. You need 
)t read it from cover to cover. Use |t to look up particular information as you need it. 
To learn how the book is n i 
organized, and why, we suggest ya ] a. ae YING 
you read ABOUT THIS BOOK at the hide Ht 
t "rn 


beginning. Also, please read Ho Introduction to PART 1 
the introduction to each of the 
3 main parts of the book. These 
chapters have page edges with a | 
short black line, to help you find | 
the beginning of PARTS 1, 2, and 3 . | 
| 


Home |e x 


1 to PART 2 
{=a to PART 3 


To work more effectively with disabled S| 
children, we strongly suggest that you read 
the first 5 chapters of PART 1. These wil! help you to examine a ch 
different disabilities, and to keep important records in an easy way 


THERE ARE SEVERAL WAYS TO FIND INFORMATION THAT YOU ARE 
LOOKING FOR: 


@ Check the list of CONTENTS at the beginning of the book. This tells you what 
each chapter is about and gives the page numbers. 


Look in the INDEX at the end of the book. It lists topics in alphabetical order 
(The edges of these pages are al! black.) 


If you do not know what disability a child has, use the GUIDE FOR 
IDENTIFYING DISABILITIES on p. 52 to 58. It lists the common signs of 
different disabilities and gives the page numbers. (There are several black lines 
on the edges of these pages. ) 


Throughout the book you will find this symbol Cr) in the margin of some pages. It 
appears where there is information for cerebral palsy. 


If you want more information than is in this book, see the list of books and teaching 
materials entitled REFERENCES (Where to Get More Information), p. 637. 


If you do not know what some words mean, !ook in the LIST OF SPECIAL OR 
DIFFICULT WORDS, p. 643. Words explained in this LIST are written in /ta/ics when 
first used in a chapter 


IMPORTANT: To find all the information you will need for one disabled child, you 
will usually need to look in several different chapters. To know where to look, follow 
the page references shown. These are explained inside the back cover. 


“Asterisk: This little star is called an asterisk. It is used to indicate that there is more 
information about a word or an idea at the bottom of the page 


panel x For more information on how to use this 
book, see the inside of the back cover 


J 


Disabled Village Children 


A guide for community health workers, rehabilitation 
workers, and families 


By David Werner 
with the help of many friends 


Library of Congress Cataloging in Publication Data 
Catalog Card No.: 86-81738 
Werner, David Bradford 
Disabled Village Children 
Palo Alto, CA: Hesperian Foundation 
672 p. 
ISBN: 0-942364-06-6 


PUBLISHED BY: 

The Hesperian Foundation 

P.O. Box 1692 

Palo Alto, CA 94302, U.S.A. 
Copyright © 1987 by the Hesperian Foundation 


First Edition, May, 1987 


Any parts of this book, including the illustrations, may be copied or adapted to 
meet local needs, without permission from the author or publisher, provided the parts 
copied are distributed free or at cost—not for profit. For any reproduction done 
commercially, permission must be obtained from the author or the Hesperian 
Foundation. The author would appreciate being sent a copy of any materials in which 
text or illustrations have been used. To avoid duplication of efforts, before beginning 
any translation, we suggest you contact the Hesperian Foundation. 


in order to keep down the cost, we are not using a commercial publisher. This means 
we need help with distribution. We are looking for ways to get this book to those it can 
serve best. |f you are able to help or have suggestions, please write to us. 


This book is dedicated to disabled children everywhere, 
with the hope that they and their families 

will help lead the world 

to be more loving, understanding, 

and just for everyone. 


REQUEST FOR YOUR SUGGESTIONS, 
CRITICISMS, AND IDEAS 


This book is an attempt to pull together basic 
information to help you meet the needs of 
village children with a wide range of disabilities 


We have done the best we can, given our 
limitations. We know the book is not perfect 
and that it has weaknesses and perhaps some 
mistakes 


We urge anyone reviewing or using the book 
whether a disabled person, parent, health 
worker, or professional, to send us all your 
criticism and suggestions. Help us to make 
improvements for a later edition. Thank you 


WE WOULD APPRECIATE ANY 
SUGGESTIONS YOU MAY HAVE 
FOR WAYS THAT THIS BOOK 
MIGHT BE IMPROVED TO SERVE 
YOUR RURAL AREA BETTER 
‘ . 


a \ 


CONTENTS 


Chapter 
¢ 


ABOUT THIS BOOK 


PART 1 WORKING WITH THE CHILD AND FAMILY: Information on Different Disabilities 


1. Introduction to PART 1: Making Therapy Functiona! and Fun 


A. Where Do We Start? 
2. Ideas for Sharing Information from This Book 
3. Prevention of Disabilities 
4. Examining and Evaluating the Disabled Child 
5. Simple Ways to Measure and Record a Child's Progress 


. Recognizing, Helping with, and Preventing Common Disabilities 
6. Guide For identifying Disabilities 

Polio 
Contractures: Limbs That No Longer Straighten 7 to 86 
Cerebral Palsy (difficulty with movements because of brain damaas 87 to 108 
Muscular Dystrophy: Gradual, Progressive Muscle Loss 109 to 112 
Club Feet, Flat Feet, Bow Legs, and Knock-knees 113to 118 
Common Birth Defects (cleft lip, extra or joined fingers 
incomplete limbs, and arthrogryposis) 119 to 124 
Children Who Stay Small or Have Weak Bones (includes Ricket 
Brittle Bone Disease, and Dwarfism 125 to 126 
Erb's Palsy: Arm Paralysis from Birth Injury 127 to 128 
Painful Joints (includes How to Use Aspirin 129 to 134 
Juvenile Arthritis 135 to 152 
Rheumatic Fever 153 to 154 
Hip Problems 155 to 158 
Bone Infections 159 to 160 
Spinal Curve and Other Back Deformities 161 to 164 
Tuberculosis of the Backbone: Pott's Disease 165 to 166 
Spina Bifida (babies born with a defect over their backbone 167 to 174 
Spinal Cord Injury 175 to 194 
Pressure Sores 195 to 202 
Urine and Bowel Management: With Spinal Cord Injury and Spina Bifida 
(includes Urinary Infections 203 to 214 
Leprosy 215 to 226 
Amputations 227 to 230 
Burns and Burn Deformities 231 to 232 
Fits: Epilepsy 233 to 242 
Blindness and Difficulty Seeing 243 to 256 

31. Deafness and Communication 257 to 276 

32. Mental Retardation: Down Syndrome, Cretinism, and Other Causes 277 to 282 

33. The Child With Several Severe Disabilities 283 to 286 


. Helping the Child Whose Mind and/or Body are Slow to Develop 
34. Child Development and Developmental Delay 287 to 300 
35. Early Stimulation and Development Activities 301 to 318 
1) Head Control and Use of Senses 
2) Rolling and Twisting 
3) Gripping, Reaching, and Hand-eye Coordination 
4) Body Control, Sitting, and Balance 


6) Standing, Walking, and Balance 
7 
8 


Communication and Speech 
Early Play Activities and Toys 


) 
) 
) 
5) Creeping and Crawling 
) 
) 
) 


D. Helping Children Develop and Become More Self-reliant 


36 
37 
38 
39 
40 
41 


Feeding 

Dressing 

Toilet Training 

Bathing (includes Care of the Teeth and Gums) 

Ways to Improve Learning and Behavior 

Learning Disabilities in Children with Normal Intelligence 


. Exercises and Techniques 


42 
43 


Range-of-motion and Other Exercises 
Crutch Use, Cane Use, and Wheelchair Transfers 


PART 2 WORKING WITH THE COMMUNITY: Village Involvement in the 
Rehabilitation, Social Integration, and Rights of Disabled Children 


44. 
45. 
46. 
47. 


48 
49 


50. 


51 


52. 
53. 
54. 


55 


Introduction to PART 2: Disabled Children in the Community 
Starting Village-based Rehabilitation Activities 

Playgrounds for All Children 

CHILD-to-child: Helping Teachers and Children Understand 
Disabled Children 

Popular Theater 

A Children's Workshop for Making Toys 

Organization, Management, and Financing of a Village 
Rehabilitation Program 

Adapting the Home and Community to the Needs of the Disabled 
Love, Sex, and Social Adjustment 

Education: At Home, at School, at Work 

Work: Possibilities and Training 

Examples of Community-Directed Programs 


PART 3 WORKING IN THE SHOP: Rehabilitation Aids and Procedures 


56. 


57 
58 


59. 


60 


61. 
62. 


63 


64. 
65. 
66. 
67. 


Introduction to PART 3: Making Sure Aids and Procedures Do 
More Good than Harm 

A ‘Shop for Making Aids’ Run by Disabled Villagers 

Braces (Calipers) 

Correcting Joint Contractures (with casts or braces) 
Correcting Club Feet (with tape or plaster casts) 
Homemade Casting Materials 

Developmental Aids (for lying, sitting, standing, balance, and 
communication) .... 

Walking Aids (bars, crutches, walkers, canes) 

Decisions about Special Seats and Wheelchairs 

Adaptations for Wheelchairs and Other Sitting Aids 

Designs for 6 Basic Wheelchairs 

Artificial Legs 


REFERENCE (Where To Get More Information) 


LIST OF SPECIAL OR DIFFICULT WORDS Used In This Book 


INDEX 


SHAS 


319 to 332 
333 to 336 
337 to 344 
345 to 348 
349 to 364 
365 to 366 


367 to 392 
393 to 398 


401 to 404 
405 to 414 
415 to 426 


427 to 454 
455 to 462 
463 to 476 


477 to 484 
485 to 490 
491 to 496 
497 to 502 
503 to 514 
515 to 522 


525 to 532 
533 to 538 
539 to 558 
559 to 564 
565 to 568 
569 to 570 


571 to 578 
579 to 588 
589 to 606 
607 to 612 
613 to 624 
625 to 636 


637 to 642 


643 to 644 


645 to 654 


THANKS 


This book has been a cooperative effort. Many persons have contributed in different ways. Some 
have helped to write or rewrite different sections. Some have criticized early drafts. Some have used it in 
their programs and sent us feedback. Some have sent original ideas or technologies that we have tested 
and then included. In all, persons or programs from 27 countries on 6 continents (North and South 
America, Africa, Asia, Europe, Australia) have contributed 


The entire book has been carefully reviewed by specialists in related fields: physical therapists (PTs) 
occupational therapists (OTs), orthotists, prosthetists, wheelchair designers, rehabilitation engineers 
and leaders from among the disabled. | cannot include the names of all those who have helped in so 
many ways, but the help of the following has been outstanding 


Sophie Levitt, PT: Ann Hallum, PT: Terry Nordstrom, PT 
Anne Affieck, OT; Mike Miles, rehab planner and critic 
Christine Miles, special educator, Farhat Rashid. PT. Bruce 
Curtis, peer disabled group counselor; Ralf Hotchkiss 
wheelchair rider/engineer: Alice Hadley, PT: Jan Postma 
PT, Jean-Baptiste Richardier, prosthetist; Claude Simonnot 
MD/prosthetist; Wayne Hampton, MD/prosthetist: Jim 
Breakey, prosthetist; Wally Motlock, orthotist: Valery Taylor 
PT. Dr P K. Sethi, orthopedic surgeon/prosthetist: Pam 
Zinkin, pediatrician/CBR expert: Paul Silva. wheelchair 
builder, David Morley, pediatrician; Elia Landeros, PT: Teresa 
Paez. social worker, Rafiq Jaffer, rehab specialist: Kris 
Buckner. parent of many adopted disabled children: Barbara 
Anderson, PT: Don Caston, rehab engineer; Greg Dixon 
Director, Partners Appropriate Technology In Health: Susan 
Hammerman, Director, Rehabilitation International: Carole 
Coleman, specialist in sign language; Suzanne Reier 
recreation therapist; Sarah Grossman, PT; Donald Laub 
plastic surgeon; Jean Kohn, MD in rehabilitation: Bob 
Fredricks, orthotist, Katherine Myers, spinal cord injury nurse 
Grace Warren, PT in leprosy, Jean M. Watson, PT in leprosy 
David Sanders, pediatrician; Jane Neville. leprosy expert 
Stanley Browne, MD. leprosy; Alexandra Enders, OT: John 
McGill, prosthetist, Victoria Sheffield, Rita Leavell, MD, Jeff 
Watson, J. Kirk Horton, Lawrence Campbell, Helen Keller 
International, Owen Wrigley, |IHAP; Roswitha and Kenneth 
Klee, Winfried Lichtemberger, Jeanne R. Kenmore 
Christoffel Bliindenmission, Judy Deutsch, PT: Jane Thiboutot 
PT. RL Huckstep, MD; Linda Goode, PT; Susan Johnson 
PT. David Hall, child health consultant: Ann Goerat, PT for 
WHO, Mira Shiva, MD, Nigel Shapcott, seating specialist 
Ann Yeadon, educator; Charles Reilly, sign language 
consultant, Eli Savanack, Gallaudet College; John Gray, MD 
Molly Thorburn, MD; Lonny Shavelson, MD: Margaret 
Mackenzie, medical anthropologist; Rainer Arnhold, MD 
Gulbadan Habibi, Caroline Arnold, Philip Kgosana, Garren 
Lumpkin, UNICEF 


Above all, | would like to thank the team of disabled village 
rehabilitation workers in Project PROJIMO, Ajoya, Sinaloa 
Mexico, along with the hundreds of disabled children and 
their families. Their involvement and interaction in exploring 
testing, inventing, and discovering simplified alternatives 
has led to the formation of this book. Key among the 
PROJIMO team are: Marcelo Acevedo, Miguel Alvarez 
Adelina Bastidas, Roberto Fajardo, Teresa Garate, Bruce 
Hobson, Concepcidn Lara, Inés Leén, Ramon Leon, Polo 
Leyva, Armando Nevarez, Maria Picos, Adelina Pliego, 
Elijio Reyes, Cecilia Rodriguez, Josefa Rodriguez, 
Concepcidn Rubio, Moisés Salas, Rosa Salcido, Asuncién 
Soto, Javier Valverde, Florentino Velazquez, Efrain Zamora, 
Miguel Zamora 


For this book we have borrowed information, ideas 
illustrations, methods, and designs from many sources 


published and unpublished Often credit has been given 
but not always. If you notice we have borrowed from your 
material and neglected to give you credit, please accept 
our unspoken thanks and apologies. Books in the Reference 
Section, p. 637 to 642, from which information or 
illustrations have been used are marked witha / 


For their excellent and dedicated work in preparing the 
manuscript for publication, special thanks go to: Carol 
Thuman, coordination, typing, correspondence; Janet Elliott 
graphics, artwork, and paste-up; Irene Yen, editing and 
paste-up; Jane Maxwell, editing, page design, and art 
production; Kathy Alberts, Elizabeth de Avila, Martin Bustos, 
Mary Klein, Carlos Romero and Marjorie Wang, paste-up 
Martin Bustos and Anna Mufioz-Briggs, Spanish translation 
Myra Polinger, typing: Lynn Gordon, Bill Bower, Phil 
Pasmanick and Dan Periman, general review; Alison Davis 
reference section research; Elizabeth de Avila, Don Baker 
Agnes Batteiger. Jane Bavelas. Leda Bosworth, Renée 
Burgard, Michael Lang, Betty Page, Pear! Snyder, Tinker 
Spar, Paula Tanous and Roger Wilson, proofreading; Lino 
Montebon, Joan Thompson and David Werner, drawings 
Richard Parker, Jonn Fago, Carolyn Watson, Tom Wells and 
David Werner, photography; Dyanne Ladine, art production 
Martin Bustos and Richard Parker, photo production; Hal 
Lockwood and Helen Epperson of Bookman Productions 
and Tim Anderson and Linda Inman of Reprographex 
typesetting and layout 


The main costs of preparing this book were met by grants 
from the Public Welfare Foundation, whose continued 
friendship and support of the Hesperian Foundation’s new 
publications is deeply appreciated. Additional funding 
was generously provided by the Gary Wang Memorial 
Fund, UNICEF, OXFAM UK, the Swedish International 
Development Agency, and MISEREOR. We would also 
like to thank the Thrasher Research Fund and Mulago 
Foundation for helping meet the costs of Project PROJ!MO 
from which this book evolved 


| would like to thank Trude Bock, who has given so 
wholeheartedly of herself and her home, not only for the 
preparation of this handbook, but also for the well-being 
of dozens of disabled children 

Finally, | want to give an extra word of thanks to Janet 
Elliott and Carol Thuman, who shared responsibility for the 
preparation and quality of this book. Their care, concern 
and thoughtful hard work is reflected on every page 


Pill. new. 


ABOUT THIS BOOK 


A TRUE STORY: CRUTCHES FOR PEPE 


A teacher of village health workers was helping as a volunteer in the mountains of 
western Mexico. One day he arrived on muleback at a smal! village. A father came up 
to him and asked if he could cure his son. The health worker went with the father to 
his hut. 


The boy, whose name was Pepe, was sitting on the floor. His legs had been paralyzed 
by polio, from when he was a baby. Now he was 13 years old. Pepe smiled and reached 
up a friendly hand. 


The health worker, who also had a physical disability, examined Pepe. ‘’Have you 
ever tried to walk with crutches?’’ he asked. Pepe shook his head 


“We live so far away from the city,”’ his father explained. 
“Let's try to make some crutches,”’ said the health worker. 
The next morning the health worker got up at dawn. 

He borrowed a long curved knife and went into the 


forest. He looked and looked until he found 2 forked 
branches the right size. 


He took the branches back to Pepe’s niga ee 
began to make them into crutches, like this. 


The father came and seeing the crutches, he said, ‘They won't work!” 


The health worker frowned. ‘Wait and see!’ he said 


When both crutches were finished, they showed them to Pepe, who was eager to try 
them. His father lifted Pepe to a standing position and the health worker placed the 
crutches under the boy’s arms. 


But as soon as Pepe put his weight on the crutches, 
they bent and broke. 


“| tried to tell you they wouldn't work,”’ said the 
father. ‘’It's the wrong kind of tree. Wood's weak as 
water! But now | see your idea. I'll go cut some branches 
of ‘jUtamo’. Wood's tough as iron, but iight! Don’t want 
the crutches too heavy.” 


He took the knife and went into the forest. Fifteen 
minutes later he was back with 2 forked branches of 
‘jdtamo’. He began making the crutches, his strong 
hands working rapidly. The health worker and Pepe 
helped him. 


ABOUT THIS BOOK 


When these crutches were finished, Pepe’s father tested 
them by putting his own weight on them. They supported 
him easily, yet were lightweight. Then Pepe tried them. At 
first, he had trouble balancing, but soon he could hold 
himself up. By afternoon, he was walking with the 
crutches! But they rubbed under his arms 


‘| have an idea,’’ said Pepe’s father. He ran to a wild 
kapok tree, and picked several of the large ripe fruits. He 
gathered the soft cotton from the pods and put a cushion 
kapok on the top crosspiece of each crutch. He wrapped 
the kapok in place with strips of cloth. Pepe tried the 
crutches again. They were comfortable 


‘Thanks, Papa, you fixed them great!’’ he said 
“Look how well | can walk now!"’ He moved ab 


“I'm proud of you, son!’ said his father, smiling tor 


As the health worker prepared to leave, the whole family came to say good-bye 


‘| can't thank you enough,”’ said Pepe’s father. ‘It’s so wonderful to see my son 
walking. | don't know why | never thought of making crutches before. 


‘| should be thanking you,” said the health worker. ‘“You have taught me a lot.”’ 


After leaving, the health worker smiled to 
himself. He thought, ‘‘How foolish of me not 
to have asked the father’s advice in the 
beginning. He knows the trees better than | 
do. And he is a better craftsperson. 


‘But it was good that the crutches | made 
broke. Making them was my idea, and the 
father felt bad for not thinking of it himself. 
But when my crutches broke, he made much 
better ones. That made us equal again!”’ 


So the health worker learned many things 
from Pepe's father—things that he had never 
learned in school. He learned what kind of 
wood is best for making crutches. He also 
learned how important it is to use the skills 
and knowledge of the local people—because a 
better job can be done, and because it helps 
maintain people's dignity. People feel equal 
when they learn from each other. 


ABOUT THIS BOOK ti 


HOW THIS BOOK WAS WRITTEN 


The story of Pepe’s crutches is an example of the lessons we have learned that helped 
to create this book. We are a group of village health and rehabilitation workers who 
have worked with people in farming communities of western Mexico to form a 
‘villager-run’ rehabilitation program. Most of us on the rehabilitation ‘team’ are 
disabled ourselves. 


From our experience of trying to help disabled children and their families to meet 
their needs, we have developed many of the methods, aids, and ideas in this book. We 
have also gathered ideas from books, persons, and other programs, and have adapted 
them to fit the limitations and possibilities of our village area. We hope this book wil! 
be useful to village people in many parts of the world. So we have asked for cooperation 
and included suggestions from community program leaders in more than 20 countries 


This book was Unlike most handbooks for village 

not written workers and families, this book was not 

by experts, written by ‘professionals’ and then ‘field 
tested’. Instead, it grew out of the practica 
experience of a team of disabled village 
health workers as we looked for 
information to help meet the most common 
problems we face 


However, a large number of professionals 
have helped in important ways. Many are 
well-known leaders in their fields. They 
include physical and occupational! 
therapists, special educators, nurses 
doctors, brace and l!imb makers, and 
rehabilitation engineers. They have 
carefully reviewed and even helped to 
rewrite sections of this book. Some have 
also helped to teach and advise our village 
and then team 
‘field tested’ 


with community 


workers 
Instead, it was and then reviewed 


written by and and corrected by 
with community experts. 
workers, 


ABOUT THIS BOOK 


HOW THIS BOOK DIFFERS FROM OTHER 
‘REHABILITATION MANUALS’ 


This book was written from the ‘bottom up’, working closely with disabled persons 
and their families. We believe that those with the most personal experience of disability 
can and should become leaders in resolving the needs of the disabled. In fact, the main 
author of this book (David Werner) and many of its contributors happen to be disabled. 
We are neither proud nor ashamed of this. But we do realize that in some ways our 
disabilities contribute to our abilities and strengths. 


In many rehabilitation manuals, disabled persons are treated as objects to be worked 
upon, to be ‘normalized’ or made as normal as possible. As disabled persons, we object 
to attempts by the experts to fit us into the mold of normal. Too often ‘normal’ 
behavior in our society is selfish, greedy, narrow-minded, prejudiced—and cruel to 
those who are weaker or different from others. We live in a world where too often it is 
‘normal’ and acceptable for the rich to live at the expense of the poor, and for health 
professionals to earn many times the wages of those who produce their food but cannot 
afford their services. We live on a wealthy planet where most children do not get 
enough to eat, where half the people have never seen a trained health worker, and 
where poverty is a major cause of disability and early death. And yet the world’s leaders 
spend 50 billion dollars every 3 weeks on the instruments of war—an amount that could 
provide primary health care to everyone on earth for an entire year! 


Instead of being ‘normalized’ into such an unkind, unfair, and unreasonable social 
structure, we disabled persons would do better to join together with all who are treated 
unfairly, in order to work for a new social order that is kinder, more just, and more 
sane. 


This large book, then, is a smali tool in the struggle not only for the liberation of the 
disabled, but for their solidarity in the larger effort to create a world where more value 
is placed on being human than on being ‘normal’—a world where war and poverty and 
despair no longer disable the children of today, who are the leaders of tomorrow. 


Top-down rehabilitation manuals too often only give orders telling the ‘local trainer’, 
family member, and disabled person exactly what they ‘must do’. We feel that this is a 
limiting rather than liberating approach. It encourages people to obediently fit the child 
into a standard ‘rehabilitation plan’, instead of creating a plan that fits and frees the 
child. Again and again we see exercises, lessons, braces, and aids incorrectly, painfully, 
and often harmfully applied. This is done both by community rehabilitation workers 
and by professionals, because they have been taught to follow standard instructions or 
pre-packaged solutions rather than to respond in a flexible and creative way to the 
needs of the whole child. 


In this book we try not to tell anyone what they must do. Instead we provide 
information, explanations, suggestions, examples, and ideas. We encourage an 
imaginative, adventurous, thoughtful, and even playful approach. After all, each 
disabled child is different and will be helped most by approaches and activities that are 
lovingly adapted to her specific abilities and needs. 


ABOUT THIS BOOK 


i3 


As much as we can, we try to explain basic principles and give reasons for doing 
things. After village rehabilitation workers and parents understand the basic principles 
behind different rehabilitation activities, exercises, or aids, they can begin to make 
adaptations. They can make better use of local resources and of the unique 
opportunities that exist in their own rural area. In this way many rehabilitation aids, 
exercises, and activities can be made or done in ways that integrate rather than separate 
the child from the day-to-day life in the community 


Ab Chat: 


This is not the first handbook of ‘simplified rehabilitation’. We have drawn on ideas 
from many other sources. We would like to give special credit to the World Health 
Organization's manual, Training the Disabled In the Community, and to UNICEF and 
Rehabilitation International's Childhood Disability: Prevention and Rehabilitation at 
the Community Level, a shortened and improved version of the WHO manual. The 
WHO manual has recently been rewritten in a friendlier style that invites users to take 
more of a problem-solving approach instead of simply following instructions. 


This handbook is not intended to replace these earlier manuals. It provides additional 
information. It is for those families, village health workers, and community 
rehabilitation workers who want to do a more complete job of meeting the needs of 
physically disabled children. 


HOW WE DECIDED WHICH DISABILITIES TO INCLUDE 


Because this book is written for village use in many countries, it was not easy to 
decide what to include. People in different parts of the world give importance to 
different disabilities. This is partly because some disabilities are much more common in 
one area than another. For example, 


@ polio in some countries is the most common disability. In others, it is rare because 
of effective vaccination programs. 


deafness and mental retardation are much more common in certain mountain 
regions because of lack of iodine in the diet (or in salt) 


blindness due to lack of vitamin A is common in some poor crowded communities, 
and depends a lot on local food habits. 


rickets is still common in regions where children are wrapped up or kept in dark 
places so much that they do not get enough sunlight. 


burn deformities are frequent where people cook and sleep on the ground near 
open fires. 


amputations are a big problem in war zones, refugee camps, and ‘shanty towns’ 
along railway tracks. 


disability from tuberculosis, leprosy, measles, malnutrition, and poor sanitation 
are especially common where lack of social justice lets some people live in great 
wealth while most live in extreme poverty. 


Local beliefs also affect how people see different disabilities. In an area where people 
believe that fits are the work of the devil, a child with fits may be feared, teased, or 
kept hidden. But in places where everyone accepts fits as ‘just something that happens 
to certain persons’ a child who sometimes has fits may participate fully in the day-to- 
day life of the community, without being seen as ‘handicapped’. Both of these children 
need medicine. But probably only the mistreated one needs ‘rehabilitation’. 


ABOUT THIS BOOK 


ig 


It is important to consider how local people see a child who is in some way 
‘different’. How do they accept or treat the child who learns slowly, limps a little, or 
occasionally has fits? 


Many reports say that in both rich and poor countries, 1 in 10 children are disabled. 
However, this number can be misleading. Although 1 child in 10 may show some defect 
if examined carefully, most of these defects are so minor that they do not affect the 
child's ability to lead a full, active life. In rural areas, children who are physically strong 
but are slow learners often fit into the life and work of the village without special 
notice. In India, a study found that only 1 in 7 of those recorded as mentally retarded 
by screening tests were seen as retarded by the community. 


Studies in several countries show that, on the average, only 2 or 3 children in 100 are 
considered disabled by the community. These are the children most likely to benefit 
from ‘rehabilitation’. 


CAUTION: \f the community does not consider a child ‘disabled’, and 
the child manages well, it may be wiser not to bring attention to her 
condition. To do so might actually ‘disable’ the child more in the 

eyes of the community, and make life harder for her. Think carefully 
before deciding to do a ‘complete survey’ on disability. 


When we started to write this book, we planned to include only physical disabilities. 
This is because concerned villagers and health workers in rural Mexico considered 
physical handicaps to be the area of greatest need. 


This is 

understandable. 
In poor farming 
communities, where 
many day-to-day 
activities depend 
on physical 
strength, and where 
schooling for most ; ; 

A child who is in a village but in a city 


children 's brief, mentally slow may not be very or in school 
the physically but physically handicapped, may be very 


disabled child can Rancroappee. 
have an especially 
difficult time 

fitting in. By 
contrast, ina 
middle-class city 
neighborhood, where 
children are judged 
mainly by their 
ability in school, but in a city 
it is the mentally A child who in a village or in school 


slow child who is physically may be very may not be 
often has the disabled but handicapped, especially 


a intelligent, handicapped. 
hardest time. 


ABOUT THIS BOOK 


The team of disabled village workers in Mexico was at first concerned mostly with 
physical disabilities. But they soon realized that they also had to learn about other 
disabilities. Even children whose main problem was physical, like polio, were often held 
back by other (secondary) emotional, social or behavioral disabilities. And many 
children with brain damage not only had difficulties with movement, but also were 
slow learners, had fits, or could not see or hear 


As the PROJIMO team’s need for information on different disabilities has grown, so 
has this book. The main focus is still on physical disabilities, which are covered in more 
detail. However, the book now includes a fairly complete (but less detailed) coverage of 
mental retardation and developmental delay (slow learning). Fits (epilepsy) are also 
covered. 


Blindness and deafness are included, but only in a very brief, beginner’s way. This is 
partly because we at PROJIMO still do not have much experience in these areas. And 
partly it is because seeing and hearing disabilities require so much special information 
that they need to be covered in separate books. Some fairly good instructional material 
is available on these disabilities, especially on blindness. We list some of the best 
materials that we know on p. 639 and 640. 


Note: This book does not include disabilities which are mainly in the area of internal medicine, 
such as asthma, chronic lung problems, severe allergies, heart defects, diabetes, bleeding problems, 
or cancers. And except for brief mention, it does not include very local disabilities such as 
lathyrism (parts of India). In local areas where such disabilities are common, rehabilitation workers 
should obtain information separately. 


To decide which disabilities to put in this book and how much importance to give to 
each, we used information from several sources, including the records of Project 
PROJIMC in Mexico. We found that the numbers of children with different disabilities 
who came to PROJIMO were fairly similar to those in studies done by WHO, UNICEF, 
and others in different areas of the world. 


On the next page is a chart showing how many children with each disability might be 
seen in a typical village area. (Of course, there is no such thing as a ‘typical’ village. The 
patterns of disability in some areas will be quite different from those shown on the 
chart.) The chart is based mainly or our records from PROJIMO over a 3-year period. 


Notice that in the chart, the number of children with each disability corresponds 
more or less to the relative importance that we give to each disability in this book. In 
certain cases we have made exceptions. For example, few persons with leprosy have 
come to PROJIMO. But we have included a long chapter on leprosy because we realize 
it is a big problem in some places. 


IMPORTANT: The disabilities discussed in this book are those that are most common in rural 
areas in many countries. But not all disabilities are included. Also, certain disabilities may be 
difficult to identify, or require special tests or analyses. When in doubt, try to get advice from 
persons with more training and experience. 


Clearly you cannot solve every problem. But there is much you can do. By asking 
questions, carefully examining the child, and using whatever information and resources 
you can find, you may be able to learn much about what these children need and to 
figure out ways to help them manage better. 


ABOUT THIS BOOK A7 


HOW COMMON ARE DIFFERENT DISABILITIES 


The little ‘stick people’ in this chart show how many children might have each 
disability in an average group of 100 significantly disab'ed village children. These 
figures are based on records of 700 children seen at PROJIMO, Mexico (1982-1985), 
and other studies. The numbers in your area may be similar or very different from 
these, depending on local factors. 


TYPICAL FREQUENCY OF DISABILITIES 
PER 100 SIGNIFICANTLY DISABLED CHILDREN 
(based on records of 700 children seen at PROJIMO, Mexico) 


Primary or main disabilities Secondary or additional disabilities 


A8 


Movement disabilities 


Brain damage and 
cerebral palsy 


Birth defects 
(includes club feet) 


Injury, burns, 
amputations 


Spina bifida 


Spinal cord injury 


Muscular dystrophy 
and atrophy 


Juvenile arthritis 
and other joint pain 


Bone infections 
(includes tuberculosis 
of the spine) 

Hip problems 
Leprosy 


Arthrogryposis 


Other 
Seeing disabilities 
Hearing and speech 
disabilities 


Fits 


Developmental delay 
(slow learners) 


Polio CEANARUCAPRRRRARCHE 
TAMEARAA AAT ARS 


athe 


PRAY S 


AAA A 
{ 4h 
RA 


if 4 


t 


AAR 
{ 


Contractures 
(mostly 

with polio and 
cerebral palsy) 


Spinal curve 


Developmental delay 
(mostly with 


_ palsy) 


Fits (mostly with 
cerebral palsy) 


Seeing (mostly with 
cerebral palsy) 


Hearing and speech 
(mostly with 
cerebral palsy) 


TRGT EAR 
AER ARE 


(plus those occurring 
cerebral palsy = 8 per 


> 


AGAGARARAS 
RGAK ART AA 


AREAEG 


ARRAN 


AT HAGRA 


AA 


ff 


with 


100) 


(plus those occurring with 
cerebral palsy = 10 per 100) 


AAA AG KA 
TE URACH 


(plus those occurring with 
cerebral palsy = 14 per 100) 


(plus those occurring with 


RACHA AA ATA 


(cerebral palsy = 16 per 100) 


Fa 


Behavioral 
problems 


{HAA 
RAR TY 
M4444 


Note: Seeing and hearing disabilities, fits, and developmental delay are listed in 2 places, depending on whether 
they are the main disability or occur in addition to some other disability. 


ABOUT THIS BOOK 


i7 


HOW THIS BOOK IS ORGANIZED 


This book is divided into 3 parts: 1, ‘Working with the Child and Family,” 
2, ‘Working with the Community,” and 3, ‘Working in the Shop.” 


The disabilities that villagers usually consider most important are discussed in early 
chapters, beginning with Chapter 7. In many countries, more than half of the disabled 
children have either polio or cerebral palsy. For this reason, we start with them. Other 
disabilities are arranged partly in order of their relative importance, and partly to place 
near to each other those disabilities that are similar, related, or easily confused. 


Notice that in the chart on p. A8, certain ‘secondary disabilities’ occur very often. 
(‘Secondary disabilities’ are problems that result after the main disability.) For example, 
contractures (joints that no longer straighten) can develop with many disabilities. In 
many villages, there will be more children who have contractures than who have any 
single primary disability. For this reason we include some of the important secondary 
problems in separate chapters. 


Common disabilities that are often ‘secondary’ to other disabilities include: 
Contractures, Chapter 8 
Dislocated Hips (either a primary or secondary disability), Chapter 18 
Spinal Curve (either primary or secondary), Chapter 20 


Pressure Sores (often occurs with spinal cord injury, spina bifida, or leprosy), 
Chapter 24 


Urine and Bowel Management (with spinal cord injury and spina bifida), Chapter 25 
Behavior Disturbances, Chapter 40 
Other disabilities that are often the primary problem but commonly occur with other 


disability—usually with cerebral palsy—include fits (Chapter 29), blindness (Chapter 
30), and deafness and speech problems (Chapter 31). 


IMPORTANT: Some important information in this book applies to many 
disabilities. In order not to make the book longer than it is now, we have 
not repeated all of this information in each chapter on specific disabilities. 
Instead we have put it in separate chapters. 


This means that to meet the needs of a specific child, you will often have 
to look in several different chapters. We have tried to make this as easy 
for you as possible (see ‘‘How To Use This Book,"’ inside the back cover). 


FOR MANY DISABILITIES IT IS VERY IMPORTANT THAT 
inl a YOU READ INFORMATION FROM SEVERAL CHAPTERS. 


ABOUT THIS BOOK AY 


LS 


a 


Note to 


REHABILITATION PROFESSIONALS, 
PROGRAM PLANNERS, AND THERAPISTS 


You may think that this book is ‘too complex’ or ‘too long’ for community health 
workers or rehabilitation workers, or family members. At first, for many, it may be. 
This is a book to grow into—a simplified but detailed work book and reference book. 


But remember, almost all the ideas and information in this book are right now 
being put into practice by village workers with little schooling, together with 
disabled children and their families. The book was developed for and with a team of 
village workers who have an average of 3 years primary school education. 


Some health workers and parents will be able to make fairly good use of the book, 
or parts of it, without special training. Others will not. 


This book is not intended to be a substitute for ‘learning through guided practice’. 
People learn best when someone with more experience shows and explains things to 
them in a real situation (working with disabled children and their families). Skills for 
making aids and teaching exercises are also learned best by working with an 
experienced rehabilitation worker or craftsperson. 


In some places, or when a village program is just beginning, this book may at first 
be used mainly by program leaders, therapists, and instructors to help you learn to 
teach in ways that communicate clearly and that encourage a problem-solving 
approach. The book can also be a resource to help you answer questions that village 
workers will have after they start working with disabled children. 


We have observed that when making decisions about what a child needs, some 
rehabilitation professionals, therapists, aid makers, and surgeons do not think 
enough about the whole child, the situation where she lives, the money problems, or 
the resources within the family and community. As a result, much too often the 
professionals make decisions that are not practical or that sometimes do more harm 
than good (see Chapter 56). Often their recommendations fail because they have 
tried to fit the child into their textbook, instead of adapting the textbook to fit the 
child and her situation. This comes partly from many years of conventional 
schooling, which encourages ‘following instructions’ more than ‘thinking things 
through’ and ‘being creative’. 


There will never be enough highly-trained rehabilitation professionals to attend to 
the needs of more than a small part of the world’s millions of disabled persons. Most 
rehabilitation and therapy can and should take place in the home and community 
with loving support of family, neighbors, and friends. 


A10 =ABOUT THIS BOOK 


~\ 


You rehabilitation professionals and therapists can play an extremely important 
role in ‘community-directed rehabilitation’. By simplifying and sharing your 
knowledge and skills, you can reach many more children. But to do this you will 
need to go out of the large city rehabilitation centers and into neighborhoods and 
villages. You will need to meet and work with the people on their terms, as learners, 
teachers, and information providers. You can help disabled persons, parents, and 
other concerned individuals to organize small, community-directed centers or 
programs. You can teach those who have the most interest to become teachers. You 
can help local craftspersons to figure out or improve low-cost designs for 
rehabilitation aids (and they can help you). You can encourage village leaders to 
improve paths and entrances to schools and public places. You can help local people 
to understand basic principles and to avoid common mistakes, so that they can be 
more effective leaders and participants in home and community rehabilitation. 


IMPORTANT: RESPECT THE KNOWLEDGE AND SKILLS 
OF THE PEOPLE 


Villagers are often much better than city persons at figuring out how to do 
things, at using whatever happens to be available, and at making and fixing 
things with their hands. In short, they are more ‘resourceful’. They have to 
be to survive! This ‘resourcefulness’ of village people can be one of the most 
valuable ‘resources’ for rehabilitation in rural areas. 


But for this to happen, we need to help people understand basic principles 
and ‘concepts’—not just tell them what to do. Above al!, we need to respect 
their intelligence, their knowledge of the local situation, and their ability to 
improve on our suggestions. 


Whenever possible, arrange for village workers to learn to use this book with 
guidance from experienced rehabilitation workers. Those rehabilitation workers 
should be able to listen to the people, respect their ideas, and relate to them as 
equals. 


For best learning, the teacher, or 
‘guide’ should stay as much in the 
background as possible, offering 
friendly advice when asked, and 
always asking the learners what they 
think before giving instructions and 
answers. 


It is our hope that this book may 
help disabled persons, their 
families, village workers, and 
rehabilitation professionals to learn 
more from each other, and to help A visiting therapist at PROJIMO teaches 
h other to b . bi the older brother of a disabled girl 
eacn other to become more capabie, how to do stretching exercises of her 


more caring, human beings. hip to correct a contracture. 


v4 


ABOUT THIS BOOK 


All 


NOTE ON LANGUAGE 
USED IN THIS BOOK 


Speaking of the Disabled Child — 
‘SHE’ or ‘HE’ 


Many studies have shown that more boys are disabled than girls. It is sometimes 
argued that this is because boys are more exposed to physical stress and danger, or 
because of sex-linked ‘genetic’ factors. 


But there may also be other, more disturbing reasons why reports show so many 
more disabled boys than girls: 


e@ Of those who are disabled, more of the boys than the girls are taken to medical 
centers where their disabilities are recorded 


e Disabled girls often are not cared for as well as disabled boys; therefore more of 
the girls die when they are babies or small children. 


In short, disabled boys often receive better attention than do disabled girls. This, of 
course, is not surprising: in most countries, non-disabled boys also get better treatment, 
more food, and more opportunities than do non-disabled girls 


Most literature on disabled children speaks of the disabled child as ‘he’. This is partly 
because male dominance is built into our language. However, we feel this can only add 
to the continued neglect of the so-called ‘weaker sex’ 


In this book, therefore, we have made an effort to be fair. But rather than to always 
speak of the child as ‘he-or-she’ or ‘they’, which is awkward, we sometimes refer to her 
as ‘she’ and sometimes as ‘he’. 


If at times this is confusing, please pardon us. And if we sometimes slip and give 


more prominence to ‘he’ than ‘she’, either in words or pictures, please criticize but 
forgive us. We too are products of our language and culture. But we are trying to 


Ab Chat 


Speaking of the Author(s): 
‘WE’ or ‘I’ 


Although one person has done most of the writing of this book, many persons have 
shared in its making (see the ‘Thanks’ page at the beginning of this book). Therefore, 
when speaking from our authors’ advisers’ viewpoint, we usually use ‘we’. This book 
is a group effort. 


A12 ABOUT THIS BOOK 


PART 1 


WORKING WITH THE CHILD 
AND FAMILY 


Information on 
Different Disabilities 


INTRODUCTION TO PART 1 


Making Therapy 
Functional and Fun 


CHAPTER 1 


Most disabled people in the world live 
in villages and poor communities where 
they never see a ‘rehabilitation expert’ or 
‘physical therapist’. But this does not 
always mean that they have no 
‘rehabilitation’ or ‘therapy’. In many 
villages and homes, family members, local 
craftspersons, traditional healers, and 
disabled people themselves have figured 
out ways for persons with disabilities to 
do things better and move about more 
easily. 


We have seen examples where local 
carpenters, tinsmiths, leatherworkers or 
blacksmiths have put together simple 
crutches, carts, wooden legs and other 
aids. We know parents who have figured 
out ways of adapting daily activities so 
that their children can help do farm work 


Two words often used by people who 
work with disabled persons are 
‘rehabilitation’ and ‘therapy’. 


Rehabilitation means returning of 
ability, or helping a disabled person 
to manage better at home and in the 
community. 


Therapy basically means treatment. 
Physical therapy —or physiotherapy— 
is the art of improving position, 
movement, strength, balance, and 
control of the body. Occupational 
therapy is the art of helping a disabled 
person learn to do useful or enjoyable 
activities 


We speak of ‘therapy’ as an art rather 
than a science because there are many 
different beliefs and approaches, and 


or housework—and at the same time get 
much of the exercise (therapy) they need. 


because the human feeling that goes 
into therapy is as important as the 
methods 


Sometimes the ‘rehabilitation’ that 
families and communities figure out by 
themselves works better in their situation 
than do methods or aids introduced by 
outside professionals. Here are 2 examples: 


1. In India, | met a villager who had lost a leg in 
a house-building accident. Using his 
imagination, he had made himself an artificial 
leg with a flexible foot out of strong wire 
with strips of an old cotton blanket for 
padding. After several months, he had the 
chance to go to a city where a professional 
‘leg maker’ (prosthetist) made him a costly 
modern fiberglass leg. The man tried using the 
new limb for a couple of months, but it was 
heavy and hot. It did not let his stump breathe 
like his ‘wire cage’ leg. And he could not squat 
to eat or do his toilet, as he could with his 
homemade leg. Finally, he stopped using the 
costly new leg and went back to the one he 
had made. For the climate and customs where 
he lived, it was more appropriate. 


All children, as much as possible, should 
get the exercise they need through daily 
work and play. (Morocco. Photo by 
Charles Trieschmann) 


4 CHAPTER! 


2. In asmall village in Mexico, over the years, the community together with its deaf 
citizens has developed a simple but expressive ‘sign language’ using their hands, 
faces, mouths, and whole bodies to communicate. As a result, children who are 
born deaf quickly and gracefully learn to express themselves. They are well 
accepted in the community, and some have grown up to become creative and 
respected craftspersons. This village method of ‘total communication’ allows the 
deaf children to learn a useful language more quickly, easily, and effectively than 
does the ‘lip reading and speech’ method now taught in the cities. For children 
who are born deaf, attempts to teach only |ip-reading-and-spoken-language often 
end in cruel disappointment (see p. 264). The ‘special educators’ in the cities 
could learn a lot from these villagers. 


Disabled children—if allowed—often show great imagination and energy in figuring 
out ways to move about, communicate, or get what they need. Much of what they do 
is, in effect, ‘therapy’, artfully adapted for and by each child. 


With a little help, encouragement, and freedom, the disabled child can often become 
her own best therapist. One thing is certain: she will make sure her therapy is 
‘functional’ (useful), always changing it to meet her immediate needs. A disabled child, 
like other children, instinctively knows that life is to be lived NOW and that her body 
and her world are there to be explored, used, and challenged. The best therapy is built 
into everyday activities: play, work, relationship, rest, and adventure. 


The challenge, then, for health workers and parents (as well as for therapists), is to 
look for ways that children can get the ‘therapy’ they need in ways that are easy, 
interesting, and functional. 


This takes imagination and ‘Physical therapy’ to improve control of the head, strength of 
flexibility on the part of all the back, and use of both arms and hands together: 
those working with disabled 
children. But mostly, it takes 
understanding. When family 
members clearly understand 
the reasons for a particular 
therapy and the basic 
principles involved, they can 
find many imaginative ways to 
do and adapt that therapy. 


(a) in acity clinic (b) in a village home 


Photo: Cheyne Photo: PROJIMO, 
Walk Spastic’s Centre Ajoya, Mexico 


Appropriate therapy helps the child to enjoy himself, be useful, and 
take part with others, while mastering the skills for daily living. 


INTRODUCTION PART 1 5 


Physical therapy and rehabilitation techniques have been developed mostly in cities. 
Yet most of the world’s disabled children live in villages and farms. Their parents are 
usually very busy growing the food and doing the chores to keep the family fed and 
alive from day to day. In some ways, this makes home therapy more difficult. But in 
other ways it provides a wide range of possibilities for exciting therapy in which the 
child and his family can meet life’s needs together. 


Here is a story that tells how therapy can be adapted to village life. 


Maricela’s family 
could not afford 
these costly things. 
So back in her 
village her father 
used whatever he 
could find to make 
similar aids at low 
cost. First he made 
a special seat of 
sticks. 


Maricela lives in a small village on a river. 
She has cerebral palsy. When she was 4 years 
old, she was just beginning to walk. 


But her knees bumped together when she 
tried to take steps. So she did not try often. 
Also, her arms and hands were weak and did 
not work very well. 


Later he made a better seat with pieces of 
wood, and an old bucket to hold her legs 


Then, using a 
board, corn cobs 
and rings cut 
from bamboo, 
he added a smal! 
table so that she 
could play games 
to develop hand 
control. 


Her family saved money and took 
Maricela to a rehabilitation center in the 
city. After a long wait, a therapist 
examined her. He explained that Maricela 
needed to stretch the muscles on the inner 
side of her thighs, so her knees would not 
press together as much. 


a Pamboo ring 


hi —— corn cob 


+— wood plank 


J 


He recommended 
that her parents do 
special exercises with 
her, and that they 
buy a special plastic 
seat to hold her 
knees wide apart. 


He also made a hand exerciser out of bamboo 


At first, while they were strange and new, 
Maricela used her special seat and played 
with her special toys. But soon, she got 
bored and stopped using them. She 
wanted to do the things that other children 
did. She wanted to go with her father and 


He said she also 
needed exercises to 
strengthen and 
increase the control 
of her hands and arms 


He suggested buying 
her some special toys, 
game boards, and aids 
to practice handling 
and gripping things 


brother to the cornfield. She wanted to help 
her mother prepare food and wash the 
clothes. She wanted to be helpful and grown 
uy. 

(story continued on next page) 


") 
rf 0) 


CHAPTER 1 


So she broke her special toys and refused 
to sit in her special seat. Her parents were 
furious with her—and she loved it! She 
would sit for hours with her knees together 
and her legs bent back. Walking began to get 
more difficult for her, so she did not walk 
much. 


Her parents then visited a smal! 
rehabilitation center in a neighboring village 
The village team suggested that they look for 
new ways to help Maricela keep her knees 
apart and improve control of her arms and 
hands—ways that would be exciting and help 
her to develop and practice useful skills 
together with the rest of her family. Here are 
some of the ideas that Maricela and her 
parents came up with 


When she was good (and sometimes even 
if she was not) her father would let her help 
shell corn with him and the other children 
Because she had trouble holding the corn 
and snapping off the grain with her finger: 
her father made a special holder and scraper 


piece of old 
holes to let saw blade 
grain drop between 
into basket 2 sticks 


cut out space 
stoppers to with nail 
hold board points coming 
on basket through bottom, 
to hold ear 
of corn 


The basket between her legs held her 
knees apart, and the shelling of the corn 
strengthened her arms, gave her practice 
gripping, and improved her coordination 
and control. 

shelling corn 
(taking the 
dried grain 
off the cobs) 


It was hard, important work that Maricela 
found she could do. And she loved it! 


Maricela’s mother sometimes invited her 
to help wash the clothes at the river. Maricela 
would sit at the river’s edge with a big 
‘washing rock’ between her legs. She would 
wash the clothes by squeezing and beating 
them against the rock—just like her mother. 


The rock kept her knees apart and the 
squeezing and banging strengthened her 
hands and improved her control. But what 
mattered was getting the clothes clean. It 
was hard work. But she found it easy—and 
fun! 


Coming back from 
the river, Maricela just 
had to walk. It was too 
far to crawl. And 
besides, she had to help 
her mother carry back 
the washed clothes. 
This was hard, but she 
tried hard, and could 
do it! 


Carrying the pails of 
clothes helped her learn 
to walk without bending 
and jerking her arms so much. 


To help Maricela grip the handle of the 
pail easier, her father wrapped a long strip of 
old bicycle inner tube very tightly around 
the handle. But when Maricela’s hand 
sweated, the smooth rubber got slippery. So 
her father wound a thin rope around the 
rubber. This way, Maricela could hold it 
better. 


As time passed she learned how to carry a 
bucket of clothes on her head—then a bucket 
of water. To do this took a lot of practice 
with balance and contro! of movement. She 
just had to keep her legs farther apart to 
keep her balance. 


Her mother was 
almost afraid to let her 
try carrying the water. 
But Maricela was 
stubborn—and she did 
it! Maricela also 
discovered that if she 
floated a gourd dipper 
(or a big leaf) on top of 
the water, it helped 
keep the water from 
splashing out. 


So, by trying different things, Maricela’s 
family, and Maricela herself, learned ways to 
create therapy and aids that were effective, 
useful, and enjoyable. 


Maricela did learn to walk better, and to 
use her hands and arms to do many things. 
But this took a long time. Sometimes she 
would try something that was too hard, and 
almost give up. But when her little brother 
would say she could not do it, she would 
keep trying until she succeeded. 


Even when Maricela liked doing 
something, because she was a child she 
would get bored and not keep doing it for 
long. Her parents always had to look for new 
ways for her to get her therapy. It became a 
challenge and a game for them, too. 


Of course, Maricela loved horses. So her 
father made her a rocking horse out of old 
logs, branches of trees, and a piece of rope 
for a tail. 


Her father noticed that she was beginning to 
walk on tiptoe, so he made special stirrups for 
the rocking horse. With 
these, when she rocked, 
her feet stretched up in 
a more normal position. 


The rocking horse kept her knees apart, 
strengthened her hands, and helped her 
improve her balance. Maricela loved her 
horse and sometimes rocked for an hour or 
more. When she got off, it seemed she could 


Soe better. 


INTRODUCTION PART 1 


After Maricela had learned to ride the 
rocking horse, she wanted to ride the real 
thing. She begged and begged. So one day 
her father let her ride with him to the corn- 
field on his donkey. He suggested she ride in 
front of him where he could hold her. But 
she insisted on riding behind, like other 
children do. 


So he fixed some stirrups and let her ride 
behind. Her legs were spread wide and she 
hung on tightly. It was excellent therapy— 
but nobody called it that. 


In the cornfield she helped her father and 
brother clean the weeds out from among the 
young corn plants. That was good for the 
young plants—and for her, too! But after 
several trips to the cornfield on the donkey 
with her father, Maricela begged him to let 
her ride alone. He was nervous, but he let 
her try. 


She could do it—and what confidence it 
gave her! Soon Maricela was preparing lunch 
for her father and brother and taking it to 
them in the cornfield—all by herself. Now 
she found she could do many other things 
she never thought she could. Although she 
was still awkward, and at times had to look 
for special ways to do things, she found she 
could do most anything she wanted or 
needed to. 


7 


fun 


7 


Recently, some ‘appropriate technology’ groups have tried to adapt standard 
‘rehabilitation aids’ to poor rural communities. However, many of their designs are 
modeled fairly closely after the same old city originals, using bamboo and string 

instead of plastic and aluminum. Some of these low-cost designs are excellent. But 
more effort is needed to make use of the unique possibilities for rehabilitation and 
therapy that exist in the village, farm, or fishing camp. 


Maricela’s family did just this. The basket of corn, the washing rock, the rocking 
horse, and the donkey all became ‘therapy aids’ to help Maricela spread her spastic legs, 
and at the same time, to take part in the life of her family and community. 


8 CHAPTER! 


The example of Maricela’s ‘therapy’ cannot and should not be copied—but instead, 
learned from. In fact, the story suggests that no approach to rehabilitation should be 

copied exactly. Our challenge is to understand each child's needs, and then to look for 
ways to adapt her rehabilitation to both the limitations and possibilities within her 
family and community. We must always look for ways to make therapy functional and 


But not every family shells corn in baskets, washes clothes on rocks, or has a donkey. 
And not every disabled child has Maricela’s needs and strengths. So we repeat: 


We should encourage each family to observe the specific needs and 
possibilities of their disabled child, to understand the basic 
principles of the therapy needed, and then to look for ways to 
adapt the therapy to the child’s and family’s daily life. 


Fed: Ds CoC oe S 
PeDees : 
IT rs NOT BEING ‘NORMAL’ . 
A THAT'S IMPORTANT ==: | 


me ie 
|. 


on § "BUT LEARNING TO ACCEPT 
oe =— OUR BEING DIFFERENT: TO LIVE* 


2. 


AND LOVE AS FULLY AS_ WE _ 
ee eee 


LV 


SAAS EG 


DKS) 


3 47 fe 
“© ’9 Wernev 86 


Sa 


Ideas for Sharing 2 
Information from This Book 


Most of the information in this book will be useful to health workers and village 
rehabilitation workers who see many disabled children. Some of the information wil 
also be useful for the family of a disabled child. However, a family with one disabled 
child will usually not need, or be able to afford this whole book. It has information 
about so many different disabilities, that parents may have difficulty finding the 
information that applies to their child. 


Also, learning from a book is often not the best way to learn something. A lot of 
methods, aids, and exercises can be learned more easily from other persons, through 
watching and through guided practice. But after a village worker has taught parents 
how to do certain exercises, or shown them an example of a homemade aid, printed 
instruction sheets with clear drawings can be a big help. Sometimes they can make the 
difference between whether the recommendations are followed at home, or not. 


There are certain pages or parts of this book that you may want to give to families 
after you explain and teach to them selected exercises or activities. For example, to the 
family of a girl with arthritis, you may want to give some of the ‘Exercise Instruction 
Sheets” at the end of Chapter 42, and the ‘Information Sheet on Aspirin’ on p. 134. 
You may also want to give them pages from Chapter 16 on arthritis, and to mark the 
exercises and activities that are important to their child 


To the family of a young child who is slow to develop, you may want to give pages 
from the chapters on child‘development and early stimulation activities (Chapters 34 
and 35). For a more advanced child you could give the family material from the 
chapters on self-care (Chapters 36 to 39). 


Depending on the interest and reading ability of the family, you may want to give 
them a whole chapter (or chapters) about their child’s disability. For example, the 
chapters on cerebral palsy (Chapter 9) or deafness (Chapter 31). An older child who is 
paralyzed from a broken back might appreciate having a copy of the chapter on spinal 
cord injury. Letting him and his family take home the 
chapters On pressure sores and urine and bowel control 
could even save his life! His family may also want to 
take home plans for making a low-cost wheelchair, to 
see if the carpenter and blacksmith in their village 
could make one. 


PAGES AND 
In Project PROJIMO in Mexico, the village CHAPTERS 
rehabilitation team keeps a big file box with copies of FOR GIVING 
the different pages and chapters that they have found TO PARENTS 
most useful for giving to families. (In fact, the 
exercise sheets at the end of Chapter 42 were Suggestion: Keep a file of pages, 
Originally prepared separately to give to families. chapters, and information sheets 
Later, we decided to include them in this book.) to give to families. 


OU 


CHAPTER 2 


Marking the information that applies to the child 


On any page or chapter 
that you give to parents, Lape ar hone «aes aa 
some of the information or 
suggestions will apply more 
than others to their child. 


We suggest that you 
circle the activities or ae 
suggestions that would be 
most helpful to the child You can do the sme thing with the 
in his present condition or wescvivintaeaics 
level of development. You meow your hand own 
could also put an ““X”’ so that he doped one 
through anything that should 
not be done or might be 
harmful for that child. eg) ode en Se on PUR inl Ie BAO 


on a large bal! 


Here is an example. 
If the child is spastic and 
beginning to sit, the first 
3 activities on p. 307 can 
help her to improve balance 
and to develop controlled spray cngoel saaeechereemieaaeme bh ge tr 
body movement. So circle sti pees 
these. The next 3 
activities will still 
be too difficult and could Rete: Vou con ste Go Dane PhS) = Geir eee 


exer ) tting the child 
ses by $ g 3 falling with his arms 


increase spasticity. Put an ogi ecard ecm 


“ s him backward, sideways. and «4 * = . Tilting him causes him 
forward But it is better to netiecrchincigger arch 
X"" through these so the nannaminen © his balance, which is a 


family does not do them. ; picts 


Making copies of pages can be 
costly. Or you may have to go a long 
way for them. Also, there will be 
times when you want to give a family 
written suggestions or drawings that 
you have not copied in advance. 


Perhaps some of the children or 
young people who are at the village 
center, either for rehabilitation or 
as learners-and-workers, can help 
trace drawings from the book. If 
they have some artistic skill, they 
can make the drawings larger, or make 
the child in the drawing look like 
the child that they are to be used mereieg a PROGR tes oak Gemeees 
with.* this book to the needs of specific children. 


*\Ideas for drawing and for copying drawings at larger size are in Helping Health Workers Learn, p. 12-1 to 12-21. 
(See p. 637.) 


3i 


SHARING INFORMATION 


\f someone prepares a set of large drawings in advance, perhaps a disabled child who 
visits the village center can trace the drawings of exercises he needs to do at home. 
Giving the child this responsibility from the start makes it more likely that he will do 
the exercises at home. 


If you make your own ‘hand out’ sheets (instead of just copying pages of this book) 
you can use the local language and villagers’ way of saying things. You can also adapt 
the drawings to the hair style and dress that people feel ‘at home’ with. 


Whatever you do, try to keep both your language and drawings simple and clear. 
Avoid unfamiliar words. 


@— 


Also, try to think of ways of adapting exercises or activities to the local situation. 


For example, suppose you live ina you might add a drawing like this one. 
fishing village, and want to make copies This will encourage parents to think of 
of a drawing showing an aid for ways to do exercises that involve their 
strengthening the wrist. Instead of just child in the life and action of their 
copying a method like this from a book, community. 


flexible 


and good for the whole child. 


Remember: Written pages and drawings can be a big help, but they should not be a 
substitute for teaching and showing. To help a family understand activities or exercises 
that are needed 


1. First show and explain 
2. Guide them in doing it until they do it right and understand why 


3. Then, give them the instruction sheet and explain the main points 
a 


These steps are explained with examples and drawings on p. 382. 


As much as you can, try not to use this book for giving exact 
instructions on how to do things. Instead, encourage everyone to use 
it as a source of ideas, in order to figure out better ways to help 

their children lead fuller lives and manage better in their communities. 


32 


12  CHAPTER2 


REMEMBER... 


One of the best ways to share information from this book is to: 


1. SHOW other people how to do things. 


Village rehabilitation 
workers and family members 
learn in an outdoor class. 
Here they practice a hip- 
stretching exercise. 

Behind them, drawings on 
the blackboard show which 
muscles are stretched. 


2. Then help them LEARN BY DOING it themselves—under your guidance. 


Teaching a village health 
worker how to stretch a 
tight heel cord (see p. 83.) 


3. And to help them remember, give them a DRAWING or INSTRUCTION SHEET. 


: 


IMPORTANT: Try to help people 
to understand not only what to 
do, but also why. Perhaps you 

can hold classes using information 
from this book. Try to combine 
hands-on practice with discussion 
of principles and reasons. 


CHAPTER 3 


Prevention of Disabilities 


Because this is a book on ‘rehabilitation’, it is mostly about children who are already 
disabled. However, preventing disabilities is also very important. For this reason, in 
most chapters on specific disabilities, we include suggestions for preventing them. 


Notice that we place the discussion of prevention at the end of each chapter, not at 
the beginning. This is because people are usually not concerned about disability until 
someone they love becomes disabled. Then their first concern is to help that person. 
After we have helped a family to do something for their disabled child, we can interest 
them in ways to prevent disability in other members of the family and community. 


We mention this because when health professionals design community programs, 
often they try to put prevention first—and find that people do not show much interest. 
However, when a group of parents comes together to help their disabled children, after 
their immediate needs are being met, they may work hard for disability prevention. 


For a community program to be successful, start with 
what the people feel is important, and work from there. 


To prevent disabilities, we must understand the causes. In most parts of the world, 
many causes of disability relate to poverty. For example: 


@ When mothers do not get enough to eat during pregnancy, often their babies are 
born early or underweight. These babies are much more likely to have cerebral 
palsy, which is one of the most common severe disabilities. Also, some birth 
defects are related to poor nutrition during the first months of pregnancy. 


When babies and young children do not get enough to eat, they get infections 
more easily and more seriously. Diarrhea in a fat baby is usually a mild illness 
But in a very thin, malnourished baby, diarrhea often leads to serious 
dehydration, high fever, and sometimes brain damage with fits or cerebral palsy. 


Poor sanitation and crowded living conditions, together with poor food, make 
diseases such as tuberculosis—and the severe disabilities it causes—much more 
common. 


Lack of basic health and rehabilitation services in poor communities makes 
disabilities more common and more severe. Often secondary disabilities develop 
that could be prevented with early care. 


To prevent the disabilities that result from poverty, big changes are needed in our 
social order. There needs to be fairer distribution of land, resources, information, and 
power. Such changes will happen only when the poor find the courage to organize, to 
work together, and to demand their rights. Disabled persons and their families can 
become leaders in this process. Only through a more just society can we hope for a 
long-term, far-reaching answer to the prevention of disabilities caused by poverty. 


34 


14 CHAPTERS 


Although the most complete 
prevention of disabilities related Why, since a good vaccine exists, is there 


still so much polio in so many countries? 


to poverty depends on social 
change, this will take time. 

However, more immediate actions at 
family, community, and national 
levels can help prevent some 
disabilities. For example, 


@ Polio, in certain situations, 
can be prevented through 
vaccination. (However, 
effective vaccination depends 
on much more than good 


vaccine. See the box.) ————————+ 


In places where vaccination 

is not available or not fully 
effective, families and 
communities can help to lower 
the chance of paralysis from 
polio in other ways: 


by breast feeding their 
children as long as 
possible (see p. 74). 


by not letting their 
children get unnecessary 
injections (see p. 18 to 21). 


EFFECTIVE VACCINATION DEPENDS ON 


MANY FACTORS: 


TECHNICAL 
Production 
and supply 
of safe, 
effective, 
vaccine. 


ECONOMIC (Cost 
of vaccine and 

of getting it to 

the children.) 
Leaders in 

poorer countries 
must decide that 
stopping polio 

is worth the 
expense. 


MANAGEMENT 
Knowledge of 
needs, planning, 
transportation, 
and distribution 
of the vaccine 


KEEPING POLIO VACCINE 
FROZEN (in many 
countries, 1/3 of 

vaccines are spoiled by 

the time they reach the 
children.) 


EDUCATION People must 
understand the value of 
vaccination and want to 
cooperate. Health workers 
must know how important it 
is to keep polio vaccine 
frozen 


POLITICAL Vaccination 
programs are most 
successful where the 
government fairly 
represents the people 

and has their full 
Participation in country- 
wide vaccination 
campaigns 


ETHICAL (Honesty and 
good will) Doctors, 
health workers, and 
citizens must try to see 
that vaccine reaches a// 
children. (In some 
countries, some doctors 
throw vaccines away and 
fill out false reports, 

and health inspectors do 
not care enough to try to 
stop what is happening.) 


Brain damage and fits can become less frequent if mothers and midwives take 
added precautions during pregnancy and childbirth, and if they vaccinate 


children against measles. (See p. 107.) 


Some birth defects and mental retardation can be prevented if mothers avoid 
most medicines during pregnancy, and spend the money they save on food. 


Spinal cord injury could be great 


y reduced if fathers would spend on education 


and community safety what they now spend on alcohol and guns. 


Leprosy could mostly be prevented if people would stop fearing and rejecting 
persons with leprosy. By being more supportive and encouraging early home 
treatment, the community could help prevent the spread of leprosy, since persons 
being treated no longer spread it. (See p. 215.) 


Blindness in young children in some countries is caused by not eating enough 
foods with vitamin A. Again this relates to poverty. However, many people do not 
know that they can prevent this blindness by feeding their children dark green 
leafy vegetables, yellow fruits, or even certain weeds and wild fruit. Also, some 
kinds of deafness and mental retardation can be prevented by using iodized salt 
during pregnancy (see p. 276 and 282). 


PREVENTION 


¢ Disability caused by poisons in TO PROTECT AGAINST PESTICIDE 
food, water, air, or workplace. POISONING 


The recent, common, worldwide @ Stand so that wind blows spray away from you. 
use of chemicals to kill insects @ Wear protective clothing, covering the whole 
and weeds has become a major 
health problem. Often villagers 
use these pesticides without any 
knowledge of their risks, or of 
the precautions they should take. 
As a result, many become 
paralyzed, blind, or disabled in clothes that 


other ways. —o" 


To prevent these problems, 
people need to learn about the : sandals) 

dangers, not only to themselves @ Wash whole body and change clothes 

and their children but to animals, rato es pots spraying. 

j ash clothes after spraying. 

birds, land, and to the whole Do not let wash water get into drinking supply. 
balance of nature’. Less Do not use spray containers for food or water. 
dangerous ways to contro! pests Do not let children play with spray containers. 

give better results over time. Pig. CAUTION: Make sure that children, and 
Laws are also needed to prohibit women who are pregnant or breast 

the most dangerous products feeding, stay away from all pesticides. 
and to provide clear warnings. 


Poisonous foods in some areas are a major cause of disability. In parts of India, 
thousands of farm workers who are paid with a poisonous variety of lentils suffer 
paralysis from ‘lathyrism’. The poor know the danger but have nothing else to eat. 
Fair wages and less corruption are needed to correct this situation. 


Fluoride poisoning (fluorosis), mainly from The 4 Bigeet cenes oF “cringive’ 
drinking water, is a common cause of bone in India, affecting over 2 million 
deformities (knock-knees) in parts of India people, are reported to be polio, 
d other place ts) blic health m r iodine deficiency, fluorosis, and 
ang otner places. Fublic nea €asures lathyrism. Given the political will, 


are needed to provide safe water.* all could be completely prevented! 


Dangerous work conditions, poisons in the air, and lack of basic safety measures 
result in many disabilities. These include burns, amputations, blindness, and back 
and head injuries. In some countries, the use of asbestos for roofs or walls in 
schools, work places, and homes causes disabling !ung diseases. Strict public health 
measures and an informed, organized people are needed to bring improvements. 


Certain dangerous medicines, known to sometimes cause disabilities, are now 
prohibited in the countries that make them, but are still sold in other countries. 

For example, diarrhea medicines containing clioquinol caused thousands of cases of 
biindness and paralysis in Japan. (A good book discussing dangerous medicines in poor 
countries is Bitter Pills by Dianna Melrose. See p. 641.) 


The high cost, overuse, and misuse of medicines in general adds greatly to the 
amount of poverty and disability in the world today. Better education of both doctors 
and people, and more effective international laws are needed to bring about more 
sensible supply and use of medicines 


*Note: Aithough too much fluoride is harmful, some is necessary for healthy bones and teeth. In some areas 
fluoride needs to be removed from drinking water, in other areas it needs to be added. 


CHAPTER 3 


WHO SHOULD BE RESPONSIBLE 
FOR DISABILITY PREVENTION 


Notice that many of the specific 
preventive measures we have discussed, 
just like the more general social measures, 
depend on increased awareness, community oe 
participation, and new ways of looking at HAPPEN 
things. These changes do not just happen. Aaa 
They require a process of education, 
organization, and struggle led by those 
who are most deeply concerned. 


Most able-bodied persons are not very 
concerned about disability or trying to 
prevent it. Often people think, ‘Oh, that 
could never happen to me!’’—until it does. 


Those who are most concerned about 
disability are usually disabled persons Mi 
themselves and their families. Based on this | 
concern, they can become leaders and 
community educators for disability x 


prevention. Disability can affect everybody, and 
sometime in our lives it usually does. 


They can do this in an informal, person-to-person way. 
For example, 
NO, I WOULDN'T TAKE HER FOR Or disabled children and families can join 
AN INJECTION. IF HER FEVER IS A together to form prevention campaigns. In 
eggs bests phen Pars ig one village, mothers put on short plays to 
THAT'S inform the whole community about the 
WHAT er importance of breast feeding and vaccination 
preilinyeodndd Fg (See p. 74.) In Project PROJIMO, Mexico, 
disabled rehabilitation workers have helped 
to vaccinate children in remote mountain 


villages. 


In PART i of this book, where we discuss 
different disabilities, we also include bas\ 
information on prevention. We hope that 
those of you who use this book for children 
who are already disabled, will also work 
actively towards disability prevention. 


PREVENTING SECONDARY DISABILITIES 


So far we have talked mainly about preventing original or ‘primary’ disabilities, 
such as polio or spinal cord injury. But the prevention of ‘secondary’ disabilities is 
also very important, and is one of the main concerns of rehabilitation. 


By ‘secondary’ disabilities we mean further disabilities or complications that can 
appear after, and because of, the original disability. 


3% 


PREVENTICN 


For example, consider a child with polio or cerebral palsy who at first is unable to 
walk. She gradually loses the normal range-of-motion of joints in her legs. Shortened 
muscles, called ‘contractures’, keep her legs from straightening. This secondary 
disability may limit the child's ability to function or to walk even more than the 
original paralysis 
This child, after polio The contractures (not /f the contractures had been 
gradually developed the original paralysis) prevented through early and 
contractures in her kept her from being continued range-of-motion 

able to stand or walk exercises, the child would 


have been able to stand and 
walk. 


Most contractures can be 
corrected. But it may take a 
long time and a lot of d 
expense—perhaps even surgery. 


It is far better to: 
J | PREVENT CONTRACTURES BEFORE THEY START. 


foot, and knee. 


Because contractures develop as a common complication in many disabilities, we 
discuss them in a separate chapter (Chapter 8). Range-of-motion exercises to help 
prevent and correct contractures are described in Chapter 42. Use of plaster casts to 
correct contractures is described in Chapter 59. 


Many other secondary disabilities wil! also develop unless preventive measures are 
taken. Some examples are pressure sores in children with spinal cord injury (see 
Chapter 24), spinal curve in a child with a weak back or with one leg shorter than the 
other (see Chapter 20), head injuries due to fits (see p. 235). Preventive measures for 
many other secondary disabilities are discussed in the chapters on the specific 
disabilities. 


In several places we discuss problems or disabilities that are commonly caused by 
medical treatment or orthopedic aids. For example, 


@ The medicine for fits, phenytoin, produces serious swelling of the gums in some 
children. This can partly be prevented by brushing the teeth regularly. (See 
p. 238.) 


Crutches that press hard under the armpit can damage nerves and gradually 
paralyze the hands. Shorter crutches, or lower-arm crutches (like those shown 
above) prevent this problem. (See p. 393.) 


Surgery is sometimes done to remove contractures that actually help a child to 
move or function better. So worse difficulties result. The benefits or possible 
harm of surgery should be carefully evaluated before it is done. (See p. 530.) 


Some braces or aids that help a child at first, may later actually hold her back. 
(See p. 526 to 529.) 


To prevent these mistakes, it is essentia! to evaluate the needs of each child carefully, 
and repeat evaluations periodically. We must take great care to prevent further 
disability caused by treatment. 


The first responsibility of a rehabilitation worker 
or parent, like the healer, should be to: 
DO NO HARM 


17 


CHAPTER 3 


In addition to secondary disabilities that are physical, others may be psychological 
or social (affecting the child’s mind, behavior, or place in the community). 


Some disabled children develop serious behavior problems. This is often because 
they find their bad behavior brings them more attention and ‘rewards’ than their good 
behavior. Chapter 40 discusses ways that parents can help prevent tantrums and bad 
behavior in disabled children. 


The biggest secondary handicap for many disabled children (and adults) usually 
comes from the lack of understanding and acceptance by other people. PART 2 of this 
book talks about how the community can be involved in taking a more active, 
supportive role in relating to the disabled and helping them to meet their needs. In 
PART 2 we also discuss what disabled persons and their families can do, in the 
community, to promote better understanding and prevent disability from becoming a 
serious handicap. 


Prevention of secondary disability is a basic part of rehabilitation. 


THE NEED FOR MORE SENSIBLE AND 
LIMITED USE OF INJECTIONS 


The overuse and misuse of medicines in the world today has become a major cause 
of health problems and disabilities. This is partly because medicines are so often 
prescribed or given wrongly (for example, certain medicines taken in pregnancy can 
cause birth defects, see p. 119). And it is partly because both poor families and poor 

nations spend a great deal of money 
on overpriced, unnecessary, or 
dangerous medicines. The money 
could be better spent on things that 
protect their health—such as food, 
vaccinations, better water, and more 
appropriate education. Some 
medicines, of course, when correctly 
used are of great importance to health. 
But most are not. Of the 30,000 
medicinal products sold in most 
countries, the World Health 


In most of the world, doctors, health workers, Organization says that only about 250 
and the people make giving and getting 
injections too big a part of health care are needed. 


In many countries, — 
injections have become the : eae | PRESCRIBE 


‘modern magic’. People Tarte we SO MANY 
demand them because doctors INJECTIONS e ‘ INJECTIONS 
and health workers often BECAUSE BECAUSE 

. My DOCTOR MAN PATIENTS 
prescribe them, and doctors PAE SCRIBES HAVE FAITH 
and health workers prescribe THEM. d IN THEM. 
them too often because people 


demand them. 


PREVENTION 


HOW INJECTIONS DISABLE CHILDREN 


Giving injections with an unclean 
needle or syringe is a common cause 
of infection. Sometimes these 
infections can lead to paralysis, or 
spinal cord injury (see the story on 
p. 192), or death. 


Also, some injected medicines can 
do harm. Dangerous allergic reactions, 
poisoning, and deafness are sometimes 
caused by injecting certain medicines— 
often when they are not needed. 


Overuse by doctors and midwives of 


This child was injected with a needle that was not sterile injectable hormones to speed up child- 
(clean). The dirty needle caused an infected abscess birth and ‘give force’ to the mother 


(pocket of pus) that in time burst and drained. The child . . 
had been injected for a cold. It would have been better has become a major cause of babies 


to give him no medicine at all. born with brain damage, cerebral 
palsy, and fits in many countries. 


NRE 
The disability most often caused by injections is 
paralysis from polio. Some experts say that each year up 
to 2 million children are paralyzed by polio because of 


injections. Nearly all of these injections are given when 
they are not needed. 


It happens like this. Children who are infected by the 
polio virus usually only have signs of a bad cold or ‘flu’. 1 out of every 3 cases of 
Most get well in a few days, without developing polio is caused by injections. 
paralysis. But the risk of paralysis increases if the child's 
muscles are injured or irritated. Injections of any kind of medicine irritate the muscles. 
Messages from the irritated muscles travel up the nerves to the spina/ cord, and cause 
changes that let the polio virus produce paralysis 


Unfortunately, when children develop a cold or ‘flu’ caused by the polio virus, their 
parents often take them to a doctor or health worker for an injection. Many times the 
result is paralysis, which is usually worse in the leg on the side that was injected. Many 
people used to think that paralysis in a leg after an injection was caused because the 
needle ‘hit a nerve’. We now know that in most cases the paralysis was caused by polio. 
Because it was brought on or ‘provoked’ by an injection, this is called ‘provocation 
polio’. 


It is very important that mothers—and doctors—remember that children should not 
be given injections when they have signs of a cold with fever or ‘flu’. It might be polio, 
and an injection could bring on paralysis. 


If injections are given to children only when they are really 
needed, millions of cases of polio could be prevented. 


20 3s CHAPTER3 


The worldwide epidemic of unnecessary injections each year sickens, kills, or 
disables millions of persons, especially children. An international campaign is needed to 
re-educate doctors. health workers, traditional healers (many of whom also now 
overuse injections), and the people themselves. 


Combatting misuse and overuse of medicines is as important a preventive measure as 
is vaccination, clean water, or the correct use of latrines. 


Health workers, schoolteachers, and community organizers should all work to 
‘de-mystify’ or take the magic out of injections, and to help peopie always to weigh 
the possible risks and benefits before using any medication. 


For skits and ideas on teaching people about the danger of unnecessary injections, 
see Helping Health Workers Learn, Chapters 18, 19, and 27. 


Note: When used correctly, certain injected medicines are important 


to health. Vaccinations, including those that are injected, are very 
important to protect a child’s health and prevent disability. However, 
to avoid paralysis from polio, it is best not to give vaccinations 


(immunizations) or any other injection when a child has a fever or 
signs of a cold. This could be a mild polio infection, and giving an 
injection could cause paralysis. 


AVOID UNNECESSARY 
INJECTIONS 


WAR AS A CAUSE OF CHILD DISABILITY 


Armed violence is increasing. Since 1980, 45 
countries have been involved in 40 wars, with over 
four million soldiers. In today’s wars, more civilians 
than soldiers are killed or disabled, and most are 
women and children. |n World War One, only 5 
percent of persons killed or injured were civilians. 
Today, 80 to 90 percent are civilians. At least 3 times 
as many people are injured as are killed. 


The increased poverty and ‘hard times’ caused by 
war also lead to many disabilities. There are 25 to 30 
million refugees, many living under dangerous and 
unhealthy conditions. One-third of the world’s 
children lack adequate food and basic health care. 
Millions are homeless. Yet in 1985, world leaders 
spent 1,000 billion US dollars on war and arms—twice 


as much as in 1981. by a ‘Contra’ 


bomb. The Contras are rebel troops 


, supported by the United States 
War, terrorism, and torture have become tools of rn cso quetieen the cow 


the powerful for economic, political and social government in Nicaragua. (Photo by 
control. When the peoples of poor countries dare to Marc Krizack, Links) 

get rid of their dictators and form popular 
governments that work toward fairer distribution, the Terrorism is too often fought 
rich, powerful countries often try to destroy those with terrorism. During the U.S. 
new governments. They pay for terrorism, long wars, attack on Libya in April, 1986, 
and the destruction of schools, health centers, and bombs hit a school for disabled 
production. The result is still more poverty, disease, children. Such actions do not 
and disability. stop terrorism; they merely kill 
ies . . and disable innocent persons. 
To help change this situation, we disabled persons “AN EYE FOR AN EYE WILL 


of the world must join with all who are disadvantaged MAKE THE WHOLE WORLD 
or treated unfairly, to struggle for a new, more truly BLIND.”’—Mahetma Gandhi. 
human, world order. 


Examining and Evaluating cre ae 
the Disabled Child 


To decide what kind of special help, if any, a disabled child 
may need, first we need to learn as much as we can about the 
child. Although we may be concerned about her difficulties, we 
must always try to look at the whole child. Remember that: 


A child's abilities are more 
important than her disabilities. 


The aim of rehabilitation is to help the child to function 
better at home and in the community. So when you examine a 
child, try to relate all your observations to what the child can 


do, cannot do, and might be able to do. LOok Fiast 
AT MY 
STRENGTHS, 


What a child is and does depends partly on other persons. So wi Rachael 
we must also look at the child’s abilities and difficulties in j 
relation to her home, her family, and her village or neighborhood. 


To evaluate a child’s needs, try to answer these questions: y 


@ What can the child do and not do? How does this compare with other children the 
same age in your community? 


What problems does the child have? How and when did they begin? Are they 
getting better, worse, or are they the same? 


In what ways are the child's body, mind, senses, or behavior affected? How does 
each specific problem affect what she does? 


What secondary problems are developing? (Problems that result after and because 
of the original problem.) 


What is the home situation |ike? What are the resources and limitations within the 
family and community that may increase or hold back the child’s possibilities? 


In what way has the child adjusted to her disability, or learned to manage? 
To find the answers to these questions, a health or rehabilitation worker needs to do 
3 things: 


1. Observe the child carefully—including her interaction with the family and with 
other persons. 


2. Take a ‘history’. Ask the parents and child (if old enough) for al! information they 
can provide. Obtain medical records if possible. 


3. Examine the child to find out how well and in what way different parts of her 
body and mind work, how developed they are, and how much they affect her 
strengths, weaknesses or problems. 


BE SURE TO LOOK AT THE WHOLE CHILD-—NOT JUST THE DISABILITY 


+2 
ad 


CHAPTER 4 


Observation of the child can begin from the first moment the health worker or 
rehabilitation worker sees the child and her family. It can begin in the waiting area of a 
village center, the home, or the street, and should continue through the history-taking, 
examination, and follow-up visits. Therefore, we do not discuss ‘observation’ separately, 
but include it with these other areas. 


It is usually best to ask questions BEFORE beginning to examine the child—so that 
we have a better idea what to look for. Therefore, we will discuss history-taking and 
then examination. But first a word about keeping records. 


RECORD KEEPING 


For a village rehabilitation worker who helps many children, writing notes or records 
can be important for following their progress. Also, parents of a disabled child may 
find that keeping simple records gives them a better sense of how their child is doing. 


Six sample RECORD 
SHEETS are on pages 37 to 
41, 50, 292, and 293. You 
can use these as a guide for 


Sample RECORD SHEETS RECORD SHEET 
included in this book page 


37 and 38 


Child history 


getting and recording basic 
information. But you will 
want to follow with more 
detailed questions and 


Physical examination . 


Tests of nervous system . eer 
Factors affecting child development 


Measuring a child's progress . 


examination, depending on . 292 and 293 


what you find. 


Child development chart . 


Sheets 1 and 2 will be useful for most disabled children. Sheets 3, 4, and 6 are for 
children who may have brain damage or seem slow for their age. Sheet 5 is a simple 
form for evaluating the progress of children 5 years old or older. 


HISTORY TAKING 


On pages 37 and 38 you will find a record sheet for taking a child’s history. You can 
use it as a guide for the kinds of questions it is important to ask. (Of course, some of 
the questions will apply more to some children than others, so ask only where the 
information might be helpful.) 


When asking questions, we rehabilitation workers must always remember that 
parents and family are the only real ‘experts’ on their child. They know what she can 
and cannot do, what she likes and does not like, in what ways she manages well, and 
where she has difficulties. 


However, sometimes part of the parents’ knowledge is hidden. They may not have 
put all the pieces of knowledge together to form a clear picture of the child’s needs and 
possibilities. The suggestions in this chapter, and the questions on the RECORD 
SHEETS, may help both rehabilitation workers and parents to form a clearer picture of 
their child’s needs and possibilities. 


Rehabilitation workers and parents can work 
together to figure out the child’s needs. 


EXAMINATION 


EXAMINING THE DISABLED CHILD 


After finding out what we can by asking questions, our next step is to examine the 
child. In as friendly a way as possible, we carefully observe or test what parts of the 
child work well, what parts work poorly, and how this affects the child’s ability to do 
things and respond to the world around him. 


CAUTION: Although we sometimes examine separately different aspects of the 

child’s body and mind, our main purpose is to find out how well the child’s body 
and mind work together as a whole: what can the child do and not do, and why? 
This information helps us decide how to help the child to do things better. 


In examination of a disabled child, we may check on many things: 


@ The senses: How well does the child see? dd Ode hear? ) fee|? <a 


@ Movement: How well does the child move or control her movements? 
ras 
@ Form and structure: How well formed, deformed, or damaged are different parts 
of the body: the joints, J os the backbone, nN and skin? 


A) = 


@ Mind, brain, and nervous system: How much does the child i 
understand? How well do different parts of the body work Sie 
together? For example, balance or eye-to-hand coordination. ( 


@ Developmental level: How wel! does the child do things, compared to other local 
children her age? 


In addition, a complete physical examination would include checking the health of 
systems inside the body. Aithough this part of the examination, if needed, is usually 
done by health workers, rehabilitation workers need to know that with certain 
disabilities inner body systems may also be affected. Depending on the disability, these 
may include: 


the the body’s the heart the food 
breathing cleaning A>r~r~XK and blood processing 
system system system system 
(respiratory (urinary (circulation (digestive 
system) tract) system) system) 


Rehabilitation workers need to work in close cooperation with health workers. 


A detailed examination of a// a child's parts and functions could take hours or days. 
Fortunately, in most children this is not necessary. Instead, start by observing the child 
in a general way. Based on the questions you have already asked and your general 
observations, try to find anything that seems unusual or not quite right. Then examine 
in detail any body parts or functions that might relate to the disability. 


44 


CHAPTER 4 


Part of the art of examining a child is KNOWING WHEN TO STOP. It is important 
to check everything that might help us understand the child's needs. But it is equally 
important to win the child’s confidence and friendship. Too much examining and 
testing can push any child to the point of fear and anger. Some children reach their 
limit long before others. So we must learn how much each child can take—and try to 
examine the child in ways that she accepts. 


Some children require a much more complete examination than others. For example 


uan lost one hand in an accident 2 years 

ago, but otherwise seems normal. Probably 

he will need little or no physical 

examination other than to see how he uses 

his arms, stump, and hand. You will also 
want to check how 
much he can do with 
his other hand, with 
only his stump, and 
when using both 
together. 


The Physical 
Examination Form 
(RECORD SHEET 2 
on p. 39) is probably 
the only examination 
form you need to fill 
out. 


However, it would be wise to learn about 
how Juan’s family and others treat him 
now, and how he feels about himself and 
his ability to do things. Does he keep his 
stump hidden when he is with strangers? 
With family members? What are his hopes 
and fears? You can write this information 


n the back of the form. 


uncontrolled movements. She does not play with toys or respond 
much to her parents. 


fon is 2 years old and still does not sit by herself. She has strange \ 


Ana seems to have many problems. 


We wil! need to check: 


how well she sees and hears. 

how strong, weak, or stiff different 
parts of her body are. 

in what ways her development is 
slow (what she can do and not do). 
how much she understands. 

signs of brain damage, and how 
severe. 

her sense of balance and position. 
what positioning or support gives her 
better control and function. 


It may take weeks or months of repeated examining and testing 
to figure out all of Ana’s difficulties, and how to best help her 
to function better. It could be a mistake to try to do all the 
needed examining at one time. 


To record all the useful information on a child like Ana, you will 
find RECORD SHEETS 1, 2, 3, 4, and 6 helpful. ) 


Examining techniques: Winning the child’s confidence 


Depending on how you go about it, the physical examination can help you become a 
child's friend or turn you into his enemy. Here are a few suggestions: 


e@ Dress as one of the people, not as a 
professional. White uniforms often 


scare a child—especially if at some : 4 
time he was injected by a nurse or a § YOUR CONFIDENCE 


doctor. 


an interest in the child as a person. 


=e Tage , BEFORE 
Before starting the examination, take y EY EXAMINING 
Speak to him in a gentle, friendly way. >. 


WE TRY TO WIN, 


A we BEGIN / 


Help him relax. Touch him in ways 


that show you are a friend. 


Approach the child from the same 
height, not from above. (Try to have 
your head at the same level as his.) 


Start the examination with the child 
sitting or lying on mother’s lap, on the 
floor, or wherever he feels most safe 


and comfortable. 


EXAMINATION 25 


PLEASE ASK HER 
TO STRAIGHTEN 


HER KNEE AS . 
MUCH AS SHE CAN. OUCH MY FINGER 
WITH YOUR FOOT, 


e@ If the child seems DARLING. 
nervous about a 
stranger touching 
or examining her, 
have the parent do 
as much of it for 
you as possible. This 
will let the mother 
know that you 
respect and want to 
include her. And she 
may learn more. 


NOw TRY TO 


@ Make the waiting area and 
place where you do the 
examining as pleasant and 
as much like home as you 
can. Have lots of toys, 
from very simple to 
complex, where the 
children can choose and 
play with them. By 
watching if, how, for how 
long, with what, and with 
whom a child plays, you 
can learn a lot about what 
a child can and cannot do, 
his level of physical and 
mental development, the 
types of problems he has, 
and the ways he has (or 
has not yet) adapted to 
them. 


Watching how a child plays— 
| by herself, with people, and 


ae 6 a7 
aw with toys—is an essential 1 ~< é 
_ part of evaluating the child. ia) Lf (NLS 


*0 


26 CHAPTER 4 


@ Try to make the examination interesting and fun for the child. Turn it into a game 
whenever possible. For example: 


When you want to test a child’s ( Or ee eee, 
‘eye-to-hand coordination’ (for - 
possible balance problems or 

brain damage) you might make a 

game out of having the child 

touch the nose of a doll. Or 

have her turn ona flashlight 

(torch) by pushing its button 


Also, when he begins to get 
restless, stop examining for 

a while and play with him, or 
let him rest. 


GEST 


tf It is best to examine a child when he is we//-rested, 
“,.7 4) well-fed, and in a ‘good mood’—and when you are, too. 
= (We know this will not always be possible.) 


@ When achild is weaker or has less control on one side than the other, 
first test the stronger side, and then the weaker side. 


NOW LET'S SEE IF YOU 
PLEASE LIFT THIS KNEE CAN LIFT YOUR OTHER 
OCF THE FLOOR, KNEE OFF THE FLOOR. 


O.K. THANKS 
FOR TRYING. 


By testing the good side first, you start by giving the child encouragement with what 
he can do well. Also, if the child does not move the weaker side, you will know it is 
because he cannot, and not because he does not understand or is not trying. 


GOOD FOR 
e As you examine the child, give Ane You, MENA! 
her lots of praise and < pote sg 
encouragement. When she tries Le ST aS YOURSELF / 
to do something for you and 2 
cannot, praise her warmly for 


trying. 


Ask her to do things she can 
do well and not just the things 
she finds difficult, so that she 
gains a stronger sense of 
SUCCESS. 


EXAMINATION 


TESTING RANGE OF MOTION OF JOINTS 
AND STRENGTH OF MUSCLES 


Children who have disabilities that affect how they move often have some muscles 
that are weak or ‘para/yzed’. As a result, they often do not move parts of their bodies 
as much as is normal. 


Loss of strength and active movement may in time lead to a stiffening of joints or 
shortening of muscles (contractures, see Chapter 8). As a result, the affected part can 
no longer be moved through its complete, normal range of motion. 


ACTIVE MOVEMENT PASSIVE MOVEMENT 


When the shoulder 
muscles are 
paralyzed, the 
child can no 
longer actively 

lift his arm. 


Normally the shoulder 
muscles can raise the arm 
until it is straight up. 


At first the 
paralyzed arm can 
be lifted straight 

up with help. 

This is called 
PASSIVE MOTION. 


Unless the normal range 
of motion is kept through 
daily exercises, the 
Passive range of motion 
will steadily become less 
and less. 


shoulder 
muscles , 


small 
and weak 


(( 


shoulder 
muscles 
used to 
raise arm 


of, 


tcp) £0 RANGE 


Lifting the arm like this 
VE moTio 


with the arm’s own muscles 


is called ACTIVE MOTION. Now the arm cannot be 


raised straight up, even 
with help. 


In the physical examination of a child with any weakness or paralysis of muscles, or 
joint pain, or scarring from injuries or burns, it is a good idea to test and record both 
RANGE OF MOTION and MUSCLE STRENGTH of all parts of the body that might 
have contractures or be affected. There are 2 reasons for this: 


@ Knowing which parts of the body have contractures or are weak, and how much, 
can help us to understand why a child moves or limps as she does. This helps us to 
decide what activities, exercises, braces, or other measures may be useful. 


@ Keeping accurate records of changes in muscle strength and range of motion can 
help tell us if certain problems are getting better or worse. Regular testing 
therefore helps us evaluate how well exercises, braces, casts, or other measures are 
working, and whether the child’s condition is improving, and how quickly. 


For testing range of motion and muscle strength, it helps to first know what is 
normal. You can practice testing non-disabled, active persons. They should be of the 
same ages as the disabled children you will test. Age matters because babies are usually 
weaker and have much more flexible joints than older children. For example: 


A baby’s back and 
hips bend so much 
he can lie across 
his straight legs. 


A young child bends 
less but can usually 
touch his toes with 
his legs straight. 


Around 11 to 14 it 

is narder to touch toes. 
His legs grow faster and 
become longer than his 
upper body. 


48 


Later, upper body growth 
catches up with legs. 

He can again touch toes 
more easily. 


CHAPTER 4 


In different children (and sometimes in the same child) you may need to check range 
of motion and strength in the hips, knees, ankles, feet, toes, shoulders, elbows, wrists, 
hands, fingers, back, shoulder blades, neck, and jaw. Some joints have 6 or more 
movements to test: bending, straightening, opening, closing, twisting in, and twisting 
out. See, for example, the different hip movements (range-of-motion exercises) on 
p. 380 in Chapter 42 


To test both ‘range of motion’ and ‘strength’, first check ‘range of motion’. Then 
you will know that when a cl it, it is Not just because of 
weakness. 


g cannot straiqnten ator 


Range-of-motion testing: Example: 


Knee With your hands, 
support the joint 
on each side as 


you Straighten it. 


1. Ask the 
child to 
straighten 
it as much 
as she can 


t straighten 

Rast tall tne way 

YOUR FOOT row fer vou car 
AND TOUCH 
Ay fineece 


agentiy see 
straighten 


t without forcing. 


If at first the (see Chapter 8 

joint will not 

If it gradually straightens, spasticity (muscle spasms) 
may be what makes it difficult (see p. 79). (If it 
stops before it straightens completely, contractures 
may also be developing.) 


Straighten, keep 
trying with gentle 
continuous pressure 
for 2 or 3 minutes 


NOw '!T ii, 
STRAIGHTENS 
For exampie, a / 


fA ee” 


For this reason, 
each time you test 
range of motion to 
measure changes, 
be sure the child 

is in the same 
position. 


If a joint will 
not straighten 
completely, try not 
with the child as much witt 
in different } 
positions . as 
’ hips straight 


knee often does 
straignter 


the hips bent 


with the 


Position affects how much certain joints straighten or bend. This is true in any child, but 
especially in a child with spasticity (see pages 101 to 103). 


In addition to 
checking how 


THATS ALL IT 
Witt BEND’ 


If joints are kept straight and never bent, they 
may stiffen or develop contractures that do not 


let them bend. (This can happen with joint 
infection, arthritis, and other conditions, or 
when a joint is kept in a cast for a long time.) 


much a joint 
straightens, 
check how much 
it bends. 


«= he same thing can 
happen to the child 
with weak arms who 
uses crutches (or 
crawls). 


A child who walks on a weak leg often 
‘locks’ her knee backward to keep from 
falling. In time, the knee stretches 

back more and more, like this. ———___> 


Also check 
for too much 
range of 
motion. 


Usually the best positions for checking range of motion are the same as those for 
doing range-of-motion and stretching exercises. These are shown in Chapter 42. 


For methods of measuring and recording range of motion, see Chapter 5 


49 


EXAMINATION 29 


Precautions when testing for contractures 


Testing range of motion of the ankles, knees, and hips is important for evaluating 
many disabled children. We have already discussed knees. Here are a few precautions 
when testing for contractures of ankles and hips. 


Ankle With the knee bent, the foot will 
Test the range of motion usually bend up more. But for 
with the knee as straight walking, we need to know how far 


as it will go. it bends with the knee straight. 
i= normal ) 
S upward 
bend 


Feel the tight 
heel cord here. 


Note: Tocheck ankle range of motion in a child with spasticity: 
So first bend his neck, body, Then slowly straighten his 


With his body and knee straight, and knees and then slowly knee while keeping the 
it may be hard to bend the ankle. bend up the ankle. ankle bent. 


Other precautions for testing ankle range of motion are on p. 383. 


Hip 


To check how far the hip joint 

straightens, have the child hold his +— 
other knee to his chest, like this, so 

that his lower back is flat against the | | Feel the tight cord here 
table. If his thigh will not lower to the 

table without the back lifting, he has a nye oy 
bent-hip contracture. (See p. 79.) edge of a table. 


CAUTION The hips will often straighten 
more at an angle to the body. So be sure to 
lower the leg in a straight line with the 
body, or you can miss contractures that 
need to be corrected before the child can 
walk. 


CHAPTER 4 


Muscle testing 


Muscle strength can be anywhere between normal and zero. Test it like this 


Test the strength of all muscles that might be affected. Here are some of the muscle 
tests that are most useful for figuring out the difficulties and needs of different 


children. 


If the child can lift the 
weight of leg all the way, 
press down on it, to check 
if she can hold up as much 
weight as is normal for a 
girl her age. If she can, 

her strength is NORMAL. 


Press down 
strongly. 


rates 


NORMAL 
strength 


If she can hold 
some extra weight, 
but not as much 
as is normal, she 


Press down 
ey 


GOOD 
strength 


GOOD 


If she can just hold up 
the weight of her leg, 
but no added weight, she 
rates FAIR. 


If she cannot hold up the 
weight of her leg, have her 
lie on her side and try to 
straighten it. If she can, 


If she cannot straighten her knee at 

all, put your hand over the muscles as 
she tries to straighten it. If you can 

feel her muscles tighten, rate her TRACE. 


she rates POOR. 


Muscles move, 
but not leg: 


TRY AS HARD AS YOU 
CAN TO STRAIGHTEN 
YOUR LEG. 

TRACE 


strength strength 


strength 
8g No muscle 


movement: 


ZERO 
strength 


Note: These tests are simple and mostly test the strength of groups of muscles. 
Physical therapists know ways to test for strength of individual muscles. 


ae NORMAL 
foot-lift 
muscle 


If the child can 
walk, see if she 
can stand and walk 
on her heels and 
her toes. 


Ankle and Foot 


DOWN BEND IN BEND OUT 


— 


NORMAL 
calf-—— 


muscle 


Note: Sometimes when the muscles that 
Normally lift the feet are weak, the child uses 
his toe-lifting muscles to lift his foot. 


EXAMPLES OF REASONS FOR TESTING 
1. If strength to lift up the foot is 
WEAK and strength to push down 
is STRONG, tiptoe contractures C 
may develop—unless steps are 
taken to prevent them. (See p. 
383.) 


. Anankle with POOR or very uneven 
strength may be helped by an 
ankle brace. But if strength is 
FAIR, exercise may strengthen it— 
and a brace may weaken it more! 


If he lifts 

his foot with 
his toes bent 
up, like this, 


see if he can 

lift it with his 
toes bent down, 
like this. 


L AQ, 


Also notice if the foot tips or pulls more to 
one side. This may show ‘muscle imbalance’. 
(See p. 78.) 


. Lifting the foot with only 
the toe muscles may lead 
to a high-arch deformity. 


L 


EXAMINATION 


To learn about which muscles move body parts in different ways, as 
you test muscle strength, feel which muscles and cords tighten. 


EXAMPLES OF REASONS FOR TESTING 


1. POOR or NO strength 
STRAIGHTEN for straightening knee 

} may mean an above-knee 
brace is needed. 


Stronger muscles 
in back of the 


You can feel Feel the muscles Feel the f thigh than in \ 
the muscle tighten on the tight cords 7 | front can lead 
tighten on top back of the pull here. to a bent-knee 


of the thigh thigh contracture. 


Hips 


ROTATING HIP OUT ROTATING HIP IN 
OPENING CLOSING (and leg in) (and leg out) 


pA Pe 
‘o ) 


} | 


| 


STRAIGHTENING 


BENDING Feel the butt lf the hip has contractures, 
muscles tighten. test with legs off end of table. 


padding 


TEST FOR WEAK SIDE-OF-HIP MUSCLES IN THE CHILD 
WHO CAN STAND 

SIDEWAYS LIFT Have the child stand on the weaker leg. 

Feel the side-of-hip muscles tighten NORMAL NOT NORMAL 

The child stands The hip tilts Or the child shifts 
straight. The down on the his whole weight so 
hip tilts up on lifted side. it balances over the 
the lifted leg. weak hip. 


This child dips 
to the side on 
Note: Weak hip muscles sometimes each step of 
lead to dislocation of the hip. Be sure vee or ) the weak leg. 
to check for this, too. (See p. 155.) — (This is often 
Testing side-of-hip muscles is of-hip seen with 
important for evaluating why a child muscles polio.) 

limps or whether a hip-band may be 
needed on a long-leg brace Note: Dipping to one side when walking is caused more by weak 
side-of-hip muscles than by a shorter leg. But a shorter leg can 
make dipping worse. 


ct 
JC 


CHAPTER 4 


Stomach and Back 


To find out how strong the stomach muscles To test the back muscles, 
are, see if the child can do ‘sit ups’ (or see if he can bend 
at least raise his head and chest). backward like this. 


Sitting up with knees bent Sitting up with knees Feel the muscles tighten 

uses (and tests) mainly Straight uses the hip- on either side of the 

the stomach muscles. Feel bending muscles and backbone. Notice if 

stomach muscles tighten. stomach muscles they look and feel the 
same or if one side 
seems stronger. 


You can check a child's trunk If achild’s 
control and strength of stomach and 


° back | sure to check 
stomach, back, and side eegpbirngrey for curvature 


muscles like this. Have him may need ak of the spine— 
hold his body upright over braces with T presale 
his hips, then lean forward nx AD my muscie imbalance 
and back, and side to side, ewheucher. A T\ or weakness of 


and twist his body. the trunk. 


IMPORTANT: Be 


Shoulders, Arms, and Hands 


When a child's legs are severely Therefore, an 
paralyzed but she has FAIR or important test pa 
better trunk strength, she may be is this: If she can, 
able to walk with crutches /f her she has a 
shoulders, arms, and hands good chance 
are strong enough. for walking 
with crutches. 


Can she lift her 
butt off the 
seat like this? 


If she cannot lift herself, check the strength in her shoulders and arms: 
SHOULDERS 


Puen bach g 
Dow we 


2 


Muscles Muscles 
tighten here. tighten here. 


lf the shoulder pushes ¢ Or, if her elbow 

down strongly but her range of motion is 
elbow-straightening | | normal, she may learn 
muscles are weak, she elbow AF to ‘lock’ her elbow 
may be able to use a oppor | back like this. 

crutch with an elbow | However, this can lead 
support. | to elbow problems. 


EXAMINATION 


You may want to make a chart something like this and hang it in your examining 
area, as a reminder. 


In muscle 
testing, it 

is especially 
important to 
note the 
difference 
between FAIR 
and POOR. 


This is 
because FAIR 
is often 
strong enough 
to be fairly 
useful (for 
standing, 
walking, or 
lifting arm 

to eat). 
POOR is 
usually too 
weak to be 
of much use. 


Strong enough 
to be useful 


EVALUATING STRENGTH OR WEAKNESS OF MUSCLES 


CAUTION: To avoid misleading results, check 
range of motion BEFORE testing muscle strength. 


A. 


Strength 
rating 


ie <a 


- 
NORMAL 
(5) 


GOOD 


lifts and holds 
against strong 
resistance 


lifts and holds 
against some 
resistance 


lifts own weight 
but no more 


Too weak to be of much use for 
lifting or bearing weight. 


Ji 


ad 


cannot Tt own 


weight but moves 


well w 
weight 


barely moves 


no sign of 
movement 


Test with the child positioned 
so that he lifts the weight of 
the limb 


thout any 


Test with the child positioned 
so that he can move the limb 

without lifting its weight (by 

lying on his side). 


Sometimes with exercise POOR muscles can be strengthened to FAIR; this can 
greatly increase their usefulness. It is much less common for a TRACE muscle to 
increase to a useful strength (FAIR), no matter how much it is exercised. (However, 
if muscle weakness is due to lack of use, as in severe arthritis, rather than to paralysis, 
a POOR muscle can sometimes be strengthened with exercise to GOOD or even 
NORMAL. Also, in very early stages of recovery from polio or other causes of 
weakness, POOR or TRACE strength sometimes returns to FAIR or better.) 


x 
ou 4 


CHAPTER 4 


Other things to check in a physical examination 


Difference in leg length. When one leg is weaker, it usually grows slower, and becomes 
shorter than the other leg. An extra thick sole on the sandal might help the child stand 
straighter, limp less, and avoid curving of the spine. A short leg may also be a sign of a 
dislocated hip. So it helps to check for, and to measure, difference in leg length. (For 


tests, see p. 155 and 156.) 


If the child can stand, 


look fora 
tilt of the 
hip bones, 


then raise 
the foot of 
the short 
leg until 
the hips 
are level. 


P 


and measure the difference’ 


Curve of the spine 


If she cannot stand, 


have her lie as straight as she can. Feel 
nN both sides of her body 


then mark 


the top front 


f the hip bone 


Then measure from here to here 
with a tape measure or string. 
Measure each leg and record the 
difference. If you used a string, 
just draw lines on your record 
sheet showing the actual 


difference in leg length. 


Pass tape 
along inner 
side of knee. 


LOLI'S DIFFERENCE 
IN LEG LENGTH 
(LYING DOWN) 


JUNE 314986 ~— 4 
SEPT 10 14t6 
DEC 2.1986 + 


Especially when one leg is shorter or there are signs of muscle imbalance in the 
stomach or back, be sure to check for abnormal curve of the spine (back bone). The 
3 main types of spinal curve (which may occur separately or in combination) are: 


Sideways curve (scoliosis) 


shoulder 


short leg 2 

a \ 
Check for /} ) Have the 
weaker child bend 
muscles over 
on this Check for 
side of 
spine | | on outer 


Some spinal curves will straighten when 
a child changes her position, lies down 
or bends over. Other spinal curves wil! 
not straighten, and these are usually 
more serious. For more information 
about examining spinal curve and 
deformities of the back, see Chapter 20. 


arib hump 


Hunch back, 
rounded back 
(kyphosis) 


May result 
from weak 
back 
muscles, — 
yr poor 


posture 


Swayback 
(lordosis) 


May result 
from weak 
stomach 


\\ p> muscles 
NY, or bent-hip 


contractures. 
(Be sure to 
check for 
these.) 


of the 


backbone 


Vg S pace 


Ure 


EXAMINING THE 
NERVOUS SYSTEM 


Sometimes physical disability 
results from problems in the 
muscles, bones, or joints 
themselves. But often it comes 
from a problem in, or damage to, 
the nervous system. 


Depending on what part of the 
nervous system is affected, the 
disability will have different 
patterns. 


For example, polio affects only 
certain action nerves at points in 
the spinal cord (or brain stem). It 
therefore affects movement. It 
never affects sensory nerves, so 
sight, hearing, and feeling stay 
normal. (See Chapter 7.) 


EXAMINATION 35 


THE NERVOUS SYSTEM 


The nervous system 

is the body's 
communication system. 
The ‘central 
switchboard’ is the 
brain, from which 
electrical messages 
run back and forth, to 
all parts of the body, 
through ‘wires’ 

called nerves. 


Sensory nerves bring 
messages from parts 
of the body about 
what the body sees 
(eyes), hears (ears), 
smells (nose), and 
feels (skin). 


Action nerves (motor 
nerves) carry messages 
to parts of the body, 
telling muscles to move. 


The brain is 
the main 
control 
center of 
the nervous 
system. 


The ‘trunk 
line’ of the 
nerves is 

the spinal 
cord. It runs 
from the 
brain down 
the middle of 
the spine. 
Nerves come 
out from 
between 
each back 
bone and 
communicate 
to a part 
lower down 
in the body. 


A spinal-cord injury, however, can damage or cut both the sensory and action 
nerves, so that both movement and feeling are lost. (See Chapter 23.) 


Unlike polio and spinal-cord injury, which come from damage to nerves in the 
spine, cerebral palsy comes from damage to the brain itself. Because any part or parts 
of the brain may be damaged, any or all parts of the body may be affected: movement, 
sense of balance, seeing, hearing, speech, and mental ability. (See Chapter 9.) 


Therefore, how completely you examine the workings of the nervous system will 
depend partly on what disability the child appears to have. If it is fairly clear the 
disability comes from polio, little examination of the nervous system is needed. But 
sometimes polio and cerebral palsy can be confused. If you have any suspicion that the 
disability might be caused by brain damage, you will want to do a fairly complete exam 
of nervous system function. Damage to the brain or nervous system can cause problems 


in any of these areas: 


®@ seeing (See Chapter 30.) 


hearing (See Chapter 31.) 


unusual or strange behaviors; 
signs of self-damage (See page 364.) 


use of mouth and 
tongue, and speech 
(See pages 313 to 315.) 


@ eye movement or 
position 
(See pages 40 and 301.) 


muscle tone (patterns of unusual 
floppiness, tightness, spasms, or 
movements). 

fits or seizures (See Chapter 9.) 
(epilepsy) 

(See Chapter 29.) 


mental ability; 

level of development 
(See pages 278 and 288.) reflexes; muscle jerks 
(See pages 40 and 88.) 
balance, coordination, 
and sense of position 


(See pages 90 and 105.) 


feeling 
(pain and touch) 
(See pages 39 and 216.) 


urine and bowel control 
(See Chapter 25.) 


Methods for testing some of these things are included on the next few pages and on the 
RECORD SHEETS 2, 3, and 4. Other tests that you will need less often, we include 
with specific cisabilities. Refer to the page numbers listed above. 


Ub 


CHAPTER 4 


EVALUATION OF A CHILD WHOSE 
DEVELOPMENT IS SLOW 


For the child who cannot do as much as other children do at the same age, a special 
developmental evaluation may be helpful. Additional information about the child's 
mother during pregnancy, or any difficulties during or after birth may explain possible 
causes. Measurement of the distance around the head may show possible causes of 
problems or other important factors. Repeated head-size measurements (once a month 
at first) may tell us even more. 


For example, a child who has had meningitis (brain infection) at age 1, and 
> whose head almost stops growing from that age on, will probably remain quite 
retarded. We should not expect a lot. However, if the child's head continues to 
= grow normally, the child may have better possibilities for learning and doing 
= more (although we cannot be sure). 


A child who is born with a ‘sack on the back’ (spina bifida, see p. 167) may have a head 
that is bigger than average. If the head continues to grow rapidly, this is a danger sign (see 
p. 41 and 169). Unless the child has surgery, she may become severely retarded or die. If, 
however, the monthly measurements show that the head has stopped growing too fast, 
the problem may have corrected itself. She may not need surgery. 


RECORD SHEET 4, on page 41, covers additional questions relating to child 
development, and includes a chart for recording and evaluating head size. 


To help the child who is developmentally delayed, you will first want to evaluate her 
level of physical and mental development. Chapter 34, pages 287 to 300, explains ways 
to do this. 


You can use the Child Development Chart on pages 292 and 293 to find a child’s 
developmental level, to plan her step-by-step activities, and to evaluate and record her 
progress. We have marked this 2-page chart, RECORD SHEET 6. 


RECORD SHEETS 


On the next 5 pages are the sample RECORD SHEETS that we discussed on p. 22. 
You are welcome to copy and use them. However, they are not perfect. They were 
developed for use by the village rehabilitation team in Mexico, and we are still trying 
to improve them. Before you make copies, we suggest that you adapt them to meet the 
needs of your area. 


Be sure you have copies made of the RECORD SHEETS 
you will need before you need to use them. 


In addition to the 4 RECORD SHEETS here, you may also want copies of RECORD 
SHEET 5 ‘‘Evaluation of Progress,’ page 50, and RECORD SHEET 6, “Child 
Development Chart,"’ pages 292 and 293. 


Note on RECORD SHEET 1 (CHILD HISTORY): 


The box at the top of RECORD SHEET 1 is to be filled out after you examine the child. It gives 
brief, essential information. This will make it easier to find out which disabilities you have seen 
most often, and to check on what you still need to do for different children. 


The last few questions on page 2 of RECORD SHEET 1 are for a study PROJIMO is doing on 
medical causes of disability. Adapt them to study special concerns in your area. 


EXAMINATION 37 


Movement RECORD 
Deformity Future action: : SHEET 

—— come back again ; 
Blindness . (page 1) 
Deafness refer to specialist 
Speech 
Fits 
Behavior other 
Other 


File 
Number 


visit at home 


TYPE OF DISABILITY 


Specific disability if known: 


CHILD’S HISTORY (First visit) 


Name: 
Date of birth: Address: 
| 
Mother: 
Father: Telephone: 
How did you learn about the program? 


WHAT IS THE CHILD’S MAIN PROBLEM? 


When did it begin? How? (Cause?) 
Other problems? 
Is the disability improving?____ Getting. worse?____ Aout the same? 
Explain: 
How do you hope your child will benefit from coming here? 

Do other family members or relatives have a similar problem? 
Has the child received medical attention? What? 
Where? 
Use any braces or other aids? _ What? 
Has he used any in the past?___ Explain: 


How is the child’s general health? 
Is he fat? Very thin? Other? 
Hears and sees well? _--_-_EE—sdEExpiain: 
Comment on the child’s developmental abilities or difficulties: normal for age? 
head control 
use of hands 
creeping or crawling 
Standing, walking 
play 
feeding or drinking 
toileting 
personal hygiene 
dressing 
Does the child speak? _____»_ How much or wee ||? L______ Began. wher? 
What other things can the child do? 


What things can the child not do? 


What new skills or abilities would you like to see your child gain? 


CHAPTER 4 


Is the child mentally normal? 


Retarded?_______ How severely? 


RECORD 
SHEET 
1 


(page 2) 


Why do you think so? 


Does the child have fits? How often? 


Describe: 


Takes medicine? _--__. What? 


For what? Results (good or bad): 


Behavior normal for age? 


Behavioral or emotional problems? Explain: 


Goes to school? What year? 


With whom does the child live? 


Number of brothers and sisters: — 
Father works? At what? 


_ Ages: 


AVERAGE EARNINGS 


Mother works? At what? 


The child seems: well-cared for? spoiled or overprotected? 


self-confident? withdrawn? 


neglected? happy? 
other? 


Important details of family situation: 


What has the family done, made, or obtained to help the child function better? 


Other observations, information or drawings: 
(Use an additional sheet if necessary.) 


History of illness Date Vaccinations: How many Allergies 


measles 
chicken pox 


whooping cough 


polio 


D.P.T. 


measles 


other BCG (TB) 
Other 


How much have you spent for your child’s disability? For what? 


Were disability or complications caused by improper medical treatment or therapy? 


Explain: 


FOR CHILDREN WITH POLIO: 
Was your child injected within 2 weeks before getting polio? 


If so, was he or she injected on the side that became most paralyzed? 


ug 


EXAMINATION 39 


SAMPLE RECORD SHEET FOR PHYSICAL EXAM 
RECORD 
Child’s name (...) SHEET 


File number is \ 2 
R b 


Mark on the drawings 
where you find the problems. 


Use lines and circles together 
with abbreviations shown Ow-Jee at 
on this page. For example: —« 

R L 


Where necessary, make new 24 2% cre 
drawings on another sheet. 4 


Parts of body affected Strength or weakness of muscles: Use this code 


NORMAL lifts and holds ‘} POOR” moves some but 
against strong 2 cannot lift = 
resistance Mf own weight ii 


moves against TRACE barely moves 
LorR other some resistance 1 
(indicate) 


— lifts own weight ZERO no sign of 
OW: Pain OW-} pain in joints but no more 0 movement 
OW-M pain in muscles Pi 


Onone 
+little 


++a lot Wd T: ability to feel, touch, pain, etc. Problems with 
+++so much that she __ *Eyes or sight. 
does not move it aa | ef RorL | normal | *reduced hae: 


———P 


CTR: contractures SP: spasticity 


tight muscles do | —— *tight muscles ee —— *Ears or hearing. 
not yield with yield slowly other 4) What: 
Pressure with pressure 


me Deep tendon reflexes: : : 
wife? oy *nothing | *little normal *extreme 
Soy ; 0 + ++ ++++ 
= Right knee 


Left knee 
Other 


Spine 


sideways 
hunchback curve swayback bump 
(kyphosis) (scoliosis) (lordosis) (TB?) DL: dislocations: 


HT: hips tilt 


df hi (BS 


R leg shorter __ \eaittow 


L leg shorter __ el 


other 


curve fixed___ curve can straighten_— 
(See p. 161.) 


*Spina bifida *Spinal cord injury Other problems 
back already operated date what level _. *pressure sores 


soft sac 


head already operated date —_— *unusual 
4 movements 
extent of paralysis " : — 
owe ; 
i — *fits 


control 
“targe head extent of feeling lost = — *poor balance 
(hydrocephalus) Bladder _ *developmental 


delay 


control 


IMPORTANT: This form does not cover all the tests *If you check any problem area marked with a star (*), 
and information you will want to record when a more complete check of the nervous system is 
examining a child. Put other information on the back of needed. You can use the RECORD SHEETS 3, 4, and 6. 
this sheet. Or use separate sheets or forms. 


GU 


40 3s CHAPTER4 


RECORD SHEET: ADDITIONAL TESTS AND OBSERVATIONS OF THE 

NERVOUS SYSTEM aa 
These tests are often not needed but may sometimes be useful when you are not 3 
sure if a child has brain damage. For other signs of brain damage, see Chapter 9 
on Cerebral Palsy. For tests of seeing and hearing, see p. 447 to 454. 


Eye movement Balance 


—— eyes jerk, flutter, or roll up unexpectedly and With the child in a sitting or standing position, 
repeatedly (brain damage, possible epilepsy — gently rock or push him off balance. 
p. 233) ___CHILD DOES NOT TRY TO KEEP FROM FALLING 
—— one eye looks in a different direction or moves (poor balance—sign of brain damage in child over 1 
differently from the other (possible brain damage) year) 
Move finger or toy yl —— CHILD TRIES NOT TO FALL by putting out his 
in front of eyes hands (fair balance) 
from side to side —— CHILD KEEPS FROM FALLING by correcting 
and up and down. a> body position (good balance) 


— eyes follow smoothly (normal) 


—— eyes follow in jumps or jerks (possible brain 
damage) 


Eye to hand coordination 


—— moves finger from nose to 
object and back again ‘ Have child stand with feet together. 


almost without error— __ balance difficulty with eyes open— 
with eyes open, and also may be brain damage (or muscle-joint 
closed (normal) problem) 

—— misses or has difficulty —— has much more 
with eyes open (poor difficulty with 
coordination, poor balance, eyes closed 
or loss of position sense) (loss of position 

sense) 


—— balance difficulty much greater 
with eyes closed (probably nervous 
system damage) 


‘Knee jerks’ and other ‘muscle jump’ reflexes 


Body movements . With the leg relaxed and partly bent, tap the 
—— awkwardness or difficulty in controlling cord just below the knee cap. 


movements NORMAL REDUCED OVER KEEPS 


—— sudden or rhythmic uncontrolled movements ACTIVE JUMPING 
—— Parts of body twist or move strangely when child = = 

tries to move, reach, walk, speak, or do certain 4 

things \\ 74 y ( $ \ 


(All these may be signs of brain damage; The leg moves )) . 

see Chapter 9.) S SS The knee __-very /ittle ee wy 
A jumpsa or not at all. A slight 

Details of any of the above: little. tap causes One tap 

a big jump. Causes the 
Typical of limb to 
spasticity jerk many 


other floppy nie a 2 
. ° . rom cereodra imes. 
Fits of different kinds (See Chapter 29.) paralyses. ociy,tpledt | Wanner 


—— sudden loss of consciousness with strange cord injury, with spinal 
movements, > tap the heel and other cord injury 


\\ cord and | brain or and some 
3 othercords | spinal cord cerebral 
7 —- 
a\ near joint. | damage. palsy. 


Typical of 
polio, muscular 
dystrophy, and 


—— brief periods of strange movements or positions, 
—— blank stares, __ eye fluttering, _ twitching. 


Developmental delay: Is the child unable to do Great toe reflex 
many different things that others her age can do? 


Which? (See Chapter 34.) Stroke the foot toward the toe witha 


somewhat pointed object (like a pen). ——»— 


—— head control — sucking NORMAL NOT NORMAL 
—— use of hands —— eating (in achild over 2) thie is a sign of 
r 


«*% 


— rolling —— playing Pe ~ brain or spinal 
_—— creeping and crawling —— communication or cord damage 
me a (Babinski’s sign) 
sittin speech : 
—_ 8 ; May occur ina 
—— Standing and walking —— behavior toes bend down toes bend up normal child 
—— self-care activities and spread under 2 years. 


61 


EXAMINATION 


RECORDS OF FACTORS POSSIBLY AFFECTING CHILD DEVELOPMENT RECORD 
(mainly for children with possible brain damage or developmental delay) SHEET 


4 


Added history 


Was the child born before 9 months? _____ at how manny months? 


Was the child born smaller or thinner than normal? weight at birth? 


Was the birth of the child normal?___ slow or difficult? 


Explain: 
Did the child seem normal at birth? ________ If not, describe problems: delayed breathing? 


very floppy? __-__ other? 
Did the mother have problems in pregnancy? German measles at months. 
Other? Medicines or drugs during pregnancy: What? 


Age of mother _____and father_________ att. time  f child’ birth. 


Physical exam 


Does the child show signs of brain damage? (Use RECORD SHEETS 3 and 4.) 
What? 


Does the child show signs of Down syndrome (mongolism)? 
What? (wide, slanted eyes _______,, crease in hand - , other . See p. 279.) 
Other physical signs, possibly related to retardation 


Does the child’s head seem smaller _____ or larger —__ than normal? 
Distance around head? cm. Difference from normal 
Average at her age (from chart) cm. Difference from average 


AVERAGE DISTANCE AROUND HEAD IN FIRST 18 YEARS OF LIFE 


Record of the child’s head size 


r - T —_—— 
4 —_ 


mal 


Co 
On the chart put a dot on 


where the up-and-down 

line of the child’s age Measure around 
crosses the sideways line the widest part 
of her head size: of the head. 


If the dot is be/ow the 
shaded area the head is 
smaller than normal. The 
child may be microcephalic 


(small-brained, see p. 278). 


If the dot falls above the 
shaded area, the head is 

bigger than normal. The 
child may have 


hydrocephalus (see p. 169). _/” Note: Boys’ heads average from %4 to 1 cm. larger than 
girls’ heads. Also head size may vary somewhat with 
different races. If possible get local charts. 


->————— DISTANCE AROUND HEAD IN INCHES ——————> 


A A. 4 i i i A i 4 i 
2 4 6 8 10 12 14 16 18 20 22 2 4 6 8 10 12 14 16 18 
———————_ ACE IN MONTHS ————»  <——— AGE IN YEARS ——> 


Use the chart for a continuing record. Every month put a new dot on the chart.* If the difference 
from normal increases, the problem is more likely to be serious. For example, 


Brain not Brain ape! Head too big; Large head. 

growing much. growing well. growing fast. ant, 4 Probably 

Probably -— Probably not Hy drocephalus -— P nota 

microcephalic. hd +h serious. el. or tumor. Ta © problem. 
+4 ++ Getting worse. 


*Filling out this chart every month is especially important for children with spina bifida or suspected 
hydrocephalus (see p. 169). If you do not know how to use the chart, ask a local schoolteacher. 


Las 12 


~~ 
ae 


+—————— DISTANCE AROUND HEAD IN CM. —————_> 


41 


42 = CHAPTER4 


Simple Ways to Measureand 9 “""" § 
Record a Child’s Progress 


It is important to keep records of each child's progress. Careful records help workers 
and parents to follow the change in the individual child, and to evaluate the 
effectiveness of advice, therapy, and aids. 


We need a clear view of the progress of the whole child in all areas—physical, mental, 
and social. The Child Development Chart on p. 292 and 293 will help us to do this for 
younger children. For children over 5, at the end of this chapter there is a simple chart 
(RECORD SHEET 5) for evaluating a child’s increasing ability to do things. 


When the parents and child themselves regularly measure and record a child's 
progress, they become more aware of gradual improvements. This encourages them to 
continue with important exercises, aids, and activities. 


Unfortunately, the standard way of recording physical deformities and contractures 
requires knowledge of angles, degrees, and symbols that many people do not 
understand. For evaluation to become a family tool, we need a way to measure, record, 
and interpret information that is as simple, clear, and enjoyable as possible. Here are 
some ideas. 


MEASURING JOINT POSITIONS AND CONTRACTURES 


You can make a simple 1. Rivet the pieces 2. Line them up 
measuring tool using é; together on one end. exactly with 


flat pieces of wood, spice 
plastic, or cardboard. 
(Tongue depressors work 


. Do this again 


well ) every 1 or 2 March ~ 
: weeks to see 
3. Trace the Aprit “—s 


Other simple methods ak on if the joint is 
for recording joint paper. prion 
positions are on p. 79. piace 


The ‘flexikin’ —an aid to measure and encourage progress 


Flexikins are cardboard dolls with joints. Disabled 
and non-disabled children can make and play with 
them. They are so easy to use that even parents who 
cannot read can measure and record their children’s 
contractures. Because the periodic measurements are 
recorded as a line of pictures, anyone can see the child’s 
progress at a glance. 


We have found that when families 
follow their child’s progress using 
flexikins, both the child and parents are a 
more likely to keep doing stretching Children making and playing with 
exercises. As a result, many contractures _ flexikins. In the PROJIMO 
can be partly or completely straightened _ village rehabilitation center, 
. : he h d th is | d f all the flexikins used are made 
Flexikins—front and! the home, and there Is less need for by disabled children and the 
side view models casting and surgery. local school children. 


64 


CHAPTER 5 


Examples of how flexikins are used 


Village rehabilitation workers have 
just made a brace for a child with 
polio whose leg bends back 
severely. They want to know if 
the leg will gradually get better 
(bend back less). So they ask the 
mother to measure it every month. 


The mother 
places the 
flexikin’s 

leg in the 

same position # 
as her son’s 

leg, bent 

back as far 

as it goes. 

She then 

traces it 

onto a large sheet of paper. 


FEBQ 


bt MAR APR MAY 
6 10 10 


JUNE JUY4 AUGT7 SEPT! 


CUM 


Each month she does 
the same and records 
the date. (In April her 
son did not use the 
brace for 2 weeks and 
she saw the knee was 
getting worse. This 
convinced both mother 
and boy of the 
importance of using the 
brace.) 


The flexikins can be used to record a wide variety of positions, deformities, 
contractures, and limitations in range of motion, mainly of the arms and legs but also 


of the neck, back, hips, and body: 


head leans 
Pd 


sway back backward 


neck forward 
hand bent up 


knees bent 
backward 


knees together 
and feet separated 


L 


feet turned inward" 


lactone 


contracture 


hunch-backed 


contracted 
bent (twisted) 
downward 


forward 


trunk 
twisted 


You can draw both 
arms and legs. First 
one and then the 
other, like this: 


elbow 
and hand 
contracted 


contracted 


a this shoulder higher 


than the other 


spine curved 


hip tilts 
to one side 


(Draw the spine by 


looking at the child 
after you have 


marked each vertebr 
with a marker.) 


as wy 


In addition to using the small flexikins for record keeping, you can make large 
flexikins for group teaching. Or use them to keep body proportions correct when 
making drawings for instruction sheets. 


Note: For recording contractures, we have found the side-view flexikin more useful 
than the front-view one. The side-view flexikin is also easier to make. It is probably 
the only one you will need for evaluating a child’s progress. 


FLEXIKIN 


How to make the flexikins 


1. Trace the patterns of different pieces (p. 47 and 48) onto very thick paper or thin, 
firm cardboard. Or use old X-ray film. 


You can do this using carbon paper. 
(Make your own carbon paper by 
completely blackening a sheet of 


paper with a soft-leaded pencil.) 
cardboard 


Or you can glue a copy of 
the pattern sheet directly GLUE carbon paper 


to the cardboard. 
pattern sheet 


({f your program plans to make many 
flexikins, or have children make 

them, we suggest you have the patterns 
printed or mimeographed directly 

on sheets of thin, firm cardboard.) 


\) 
2. Cut out the pieces with strong scissors, SD —- piece of razor 


shears, or a piece of razor blade. blade in the split 
end of a stick 


. Place the pieces 
together as shown 
in the drawings. ~“—— Put this piece 
Make sure the 
pieces that overlap 
with dotted lines ~“——. and put this piece, 


go behind those 
with complete lines. behind this. 


behind this piece, 


4. Fasten the pieces together at the black dots with rivets, pins or thread. 


Use the Or string the joints Or use sewing pins; 
smallest together with thread Or use thin 

rivets you or yarn (this does wire or string 

can find. not work as well). and tie knots. 


noe ee cut here and put a drop 
of very strong glue 
(like epoxy) here. 


Rivets usually work best. First punch a hole through each black dot. Put the rivets 
through and hammer them just enough so that the cardboard joints are tight enough to 
hold their positions but can be moved without tearing. 


66 


46 CHAPTERS 


You can copy this sheet, or one like it, and give it to parents together with a flexikin. 
Be sure that you also show them how to use it and then watch them use it. 


INSTRUCTIONS FOR USING THE FLEXIKIN 


We have given you a ‘flexikin’ so that you can measure and see the progress that 
your child is making with his exercises or aids. 


We suggest you take a new measurement every 
Do it like this: 


. Have your child take the position you want 
to measure (for example, straighten his 
knee as much as he can). 


. Put the flexikin in 
exactly the position 
the child is in. To do : . 
this hold the flexikin GN 
at a distance between = fay 
your eye and the child il Ny Ay 
so that it appears the one 
same size as the child. WY 
This will let you line 
it up exactly. 


. Without moving the Pal example 


position of the flexikin, — , 5 phere 
trace it onto a large piece | 
A oar & exercises 
—e 


of paper. The first time have helped 
trace the whole body. straighten a 
Each time measure the contracted 

child in the same posture. knee. 


For later recordings, you only need to trace the part or parts you are measuring 
Each time you record a measurement, write the date. 


In certain cases you may want to | Make 2 columns. 
measure how far the child can In one, record Problem: Right Mame: Marfa Lopez 
straighten an arm or leg by how far the child Nona 

. Date (1983) Range-of Motion: 
herself, a a Ma Riayat hg can move it by “T cilgaane tno 
to straighten it Tor ner (little by herself. In the 
little without forcing). other column MorchI OA, OAR 
record how far April WNW ay 
she can move it May! AY ——~) 
with help. June 10 ay 


SS July5 ~~) —J 


Here you see the -——> August 6 =~ 
CAUTION: When you progress of a leg (she got with 
straighten the limb, until it became ag bees ae 
support it close to straight and a brace . pene with 

the joint. This could be made for it, | SOS =" Sine 
prevents injury. 


FLEXIKIN 


EVALUATING THE PROGRESS OF THE WHOLE CHILD 


A simple way for rehabilitation workers and parents to evaluate how a child is 
progressing as a whole is to keep a record of her ability to do different things. Each 
month, or during each visit to the community rehabilitation center, the child's 
different abilities are reviewed, tested, or observed. Any changes are recorded. 


For children under 5 years old, one way of evaluating a child's development is to use 
the RECORD SHEET 6 (p. 292). This chart shows the developmental levels 
(‘milestones’) for different skills and activities. The first time the child is evaluated, 
circle the drawing that shows what the child can do in each area. 


Each time the child is evaluated, on the same sheet, again circle the appropriate 
drawing, but use a different color (or a dotted, dashed, or zigzag line). This way, you 
can see where the child is moving ahead well and where he is behind. 


4 Mts with 
{hand ‘ . twists and moves 


; 


Casily while sitting 


Dk 


‘« pis br cr awts 
ms. 


hel 


begins to reach 
towards objects 


“ee |< 


Sen 2 1 eyes aa on 
\ Pst laces J tar object 


a 


$ responds to enjoys Thy omic understa hears clearly and understands 
at aloud none mother's vone muse most wmople language 


For evaluating the progress of children over age 5, the charts on the next page may 
help. Two different approaches are used. Chart A is more objective (requires less 
personal judgment or opinion) but does not allow for small improvements. Chart B is 
more subjective (is based more on personal judgments). It considers quality of 
improvement, not just quantity. You can try both and see which you think gives truer, 
more useful results. 


To use Chart A: For each skill, circle whether the child can do it ‘‘without help,” 
“with a little help,’’ or ‘‘with lots of help.’’ Add all the numbers you circle. Compare 
the scores of the first and second visits. For example: 


First visit | Second visit Here we see the 
| child has 
| 
| 
| 
| 


without little lots of 

help help help 
How does the child eat? 4 Q) 0 
How does the child drink? 4 @) 0 


without little lots of improved his 
help help help eating skills but 
@ : 0 not his drinking 


4 @) 0 skills. 


To use Chart B: In each area, on the second visit, circle whether the child is doing a 
lot better, a little better, or the same. Add it all up. The higher the score, the more the 
child has improved. 


NOTE: We question whether the use of numbers may not be misleading. But 
we think the questions themselves may be a useful guideline. None of 

these evaluation forms will show all areas of change or improvement. 

They are not substitutes for detailed notes, drawings, and a good memory! 


fau 


CHAPTER 5 


EVALUATION OF PROGRESS — CHILD OVER AGE 5 


Name Age 


RECORD 
SHEET 
5 


Disability 


CHART A 
Daily activities 


First visit (date 


little 
help 


without 
help 
Feeding 

1. How does the childeat? .. . . « «© « © « 2 
2. How does the childdrink? . . . . . . 2 


Dressing and washing 
3. Does child wash face and body? 
4. Does child dress? . ‘ 
5. Does child put on orthopedic equipment? . 


Bowel and bladder care and control 
6. Does child stay clean (bowel control)? . 
7. Does child clean herself after shitting? . 
8. Does child stay dry during the day? 
9. Does child stay dry at night? 


Mobility /transfers 
10. Does child move from chair to bed and back? 
11. Does child move from floor to bed and back? 


Movement 

12. Walks on flat surface? 

13. Walks on uneven surface? 

14. Climbs up and down stairs? . 

15. Uses a wheelboard or wheelchair? 
16. Does child crawl? . 


Social activities/communication 

17. Does child help with housework or farm work? 
18. Does child play with other children? 

19. Does child go to school? . : 

20. Does child speak? , 

21. Does child communicate with signs « or gestures? 


) 


lots of 
help 


Second visit (date ) 


little 
help 


lots of 
help 


without 
help 


4 2 


0 0 
0 4 2 0 


| 
| 
| 
| 
| 
| 
| 
| 
| 
| 
| 
| 
| 
| 
| 
| 
| 
| 
| 
| 
| 
| 
| 
| 


CHART B 
Quality of activities 


First visit 


make notes for 
comparison here 


Does child move about better? 

Does he sit in a better position? . : 

Does he walk better (straighter, with less limp, or 
with less support)? : 

Does he walk farther, faster, or easier? ‘ 

Are his joints straighter (less contractures) ? 
hip?. 
knee? 
ankle? 

Can the child do things he could not do before? 
feeding? cant 
bathing? 
dressing? 
toileting? ‘ 

Does he play with things better? 

Does he speak or communicate better? 

Does he get along with other children better? . 

Does he seem happier or more self-confident? . 

Has he improved or got worse in other ways? . 
In what ways? 


| 
| 
| 
| 
| 
| 
| 
| 
| 
| 
| 
| 
| 
| 


Second visit 


a little 
better 


much 
better 


same worse 


nN 
oo 


4 
4 


nh 


NR 
-FHotrt SHAH HHAHHA HAH 


NM CWOHNHNMNN NNN NNN ND NY ND LP 
oooocoocjcoooocjoooq”;tooco 


= 
=) 

mad 
~, 


Guide for ew 6 
Identifying Disabilities 


This chapter has a chart, 7 pages long, to help you find out what disability a child 
possibly has, and where to look up that disability in this book. 


In the first column of the chart, we list the more noticeable signs of different 
disabilities. Some of these signs are found in more than one disability. So in the second 
column we add other signs that can help you tell apart similar disabilities. The third 
column names the disability or disabilities that are most likely to have these signs. And 
the fourth column gives the page numbers where you should look in this book. (Where 
it says WTND and then a number, this refers to the page in Where There Is No Doctor.) 


If you do not find the sign you are looking for in the first column, look for another 
sign. Or check the signs in the second column. 


This chart will help you find out which disabilities a child might have. It is wise to 
look up each possibility. The first page of each chapter on a disability describes the 
signs in more detail. 


IMPORTANT: Some disabilities can easily be confused. Others 
are not included in this book. When you are not sure, try to 

get help from someone with more experience. At times, special 
tests or X-rays may be needed to be sure what the problem is. 


Fortunately, it is not always necessary to know exactly what disability a child has. 
For example, if a child has developed weakness in his legs and you are not sure of the 
cause, you can still do a lot to help him. Read the chapters on disabilities that cause 
similar weakness, and the chapters on other problems that the child may have. For this 
child, you might find useful information in the chapters on polio, contractures, 
exercises, braces, walking aids or wheelchairs, and many others. 


Sometimes it is important to identify the specific disability. Some disabilities require 
specific medicines or foods—for example, night blindness, rickets, or cretinism. Others 
urgently need surgery—for example, spina bifida or cleft lip and palate. Others require 
special ways of doing therapy or exercises —for example, cerebral palsy. And others 
need specific precautions to avoid additional problems—for example, spinal cord injury 
and leprosy. For this reason, it helps to learn as much about the disability as you can. 
Whenever possible, seek information and advice from more experienced persons. 
(However, even experts are not always right. Do not follow anyone’s advice without 
understanding the reasons for doing something, and considering /f and why the advice 


applies to the individual child.) 


In addition to this chart, 2 other guides for identifying disabilities are in this book: 


GUIDE FOR IDENTIFYING CAUSES OF JOINT PAIN, p. 130. 
GUIDE FOR IDENTIFYING AND TREATING DIFFERENT FORMS OF FITS 
(EPILEPSY), p. 240. 


CHAPTER 6 


GUIDE FOR IDENTIFYING DISABILITIES 


SIGNS PRESENT AT OR SOON AFTER BIRTH 


IF THE CHILD HAS THIS 


AND ALSO THIS HE MAY HAVE 


SEE PAGE 


born weak 
or ‘floppy’ 


slow to begin 
to lift head 
or move arms 


often a difficult birth 

delayed breathing 

born blue and limp 

or born before 9 months and very smal! 


cerebral palsy 
developmental delay 


87 
277 


round face 
slant eyes 


: cretinism 
thick tongue 


Down syndrome (mongolism) 


small head, 
or small top 
part of head 


microcephalia (smal! 
brain) mental retardation 


developmental delay for 
other reasons 


none of above 


does not suck 
well or chokes 
on milk wt! 


or food w Fs 
u 


pushes milk back out with tongue 


k cerebral palsy 
or will not suck 


cannot suck well check for cleft palate 
chokes or milk comes out nose 


possibly severe retardation 


one or both 
feet turned 
in or back 


no other signs club foot 


hands weak, stiff ee. f 
or clubbed » 


some joints stiff, in bent ; S 
or straight positions a 


arthrogryposis 


dark lump on back spina bifida 


‘bag’ or 
dark lump 
on back 


clubbed feet 

or feet bend 

up too far —© 

or feet lack movement and feeling 


spina bifida 

(sometimes no ‘bag’ is 
seen, but foot signs may 
be present) 


head too 
big; keeps 
growing 


hydrocephalus (water on 
may develop the brain) 
@ eyes like 
‘setting SUN! —— 
@ increasing mental 
and/or physical disability 
blindness 


At birth, this is usually 
a sign of spina bifida. 


in an older child, 
possibly tapeworm in 
brain, or a brain tumor 


upper !ip and/or 
roof of mouth 
incomplete 


cleft lip (hare lip) 


and cleft palate 


difficulty feeding o> 
later, speech difficulties @B) 


birth deformities, 2) 
defects, or 


missing parts 


meds 


See 


@ birth defects 

@ amputations 

@ Down syndrome 

@ developmental delay 


(may or may not be associated 
with other problems) 


abnormal 
stiffness 
or position 


from birth 

some muscles weak 

some joints stiff 

head control and mind normal 


arthrogryposis 


Muscles tighten more in certain spastic cerebral palsy 
positions. 


: : Note: muscle tightness 
may grip thumb tightly 


(spasticity) usually does 
not appear until weeks 
or months after birth. 


DISABILITY GUIDE 


IF THE CHILD HAS THIS 


AND ALSO THIS 


HE MAY HAVE 


SEE PAGE 


one arm 
weak or in 
strange 
position 


does not move the arm much ¢ 
s 
holds it like “. i” 


Erb’s palsy (weakness 
from damage to nerves in 
shoulder during birth) 


leg on same side often affected 


hemiplegic (one-sided) 
cerebral palsy 


dislocated hip 
at birth 


leg held 
differently, 
shorter; fla 
covers part 
of vulva 


On opening legs 
like this, leg 
‘pops’ into place 
or does not open 
as far. 


dislocated hip from birth 
(often both hips) 


may be present with 


@ spina bifida 
@ Down syndrome 
@ arthrogryposis 


Also see p. 156. 


slow to respond 
to sound or to 


(may be due to one ora 


look at things ey. i> combination of problems) 


Check for signs of 


developmental delay 
cerebral palsy 
blindness 

deafness 


SIGNS IN CHILDREN 


slower than other 
children to do things 
(roll, sit, use hands, 
show interest, walk, talk) 


slow in most or all areas: 


Developmental delay, 
check for signs of 


round face 
slant eyes 
single deep 
crease in hand 


Down syndrome (mongolism) 


movements and response slow 

skin dry and cool , 
hair often low on forehead (5) 
puffy eyelids 


cretinism 


has continuous 

strange movements or 
positions, and/or can 
stiffness ae 


Vv 


cerebral palsy 


also check tor 

@ blindness 

@ deafness 

@ mainutrition 


does not respond 
to sounds, does 
not begin to 
speak by age 3 


may respond to some 
sounds but not others 


Check for ear infection (pus) 


Check for 


@ deafness 

@ severe developmental 
delay (with or without 
deafness) 

@ severe cerebral palsy 


does not turn head to 
look at things, or reach 
for things until 

they touch her 


Eyes may or may not look normal 


@ blindness and/or 

@ severe mental 
retardation 

@ severe cerebral palsy 


Eyelids or 
eyes make 
quick, 
jerky, or 
strange 
movements. 


Check for one or a 
combination of these. 


@ blindness 

@ fits 

@ too much medicine 

@ cerebral palsy 

@ other problems affecting 
or damaging the brain 


53 


ao 


CHAPTER 6 


IF THE CHILD HAS THIS 


AND ALSO THIS 


HE MAY HAVE 


SEE PAGE 


All or part of body makes 
strange, uncontrolled 
movements. 


begins suddenly, child 

may fall or lose consciousness 
child is normal (or more normal) 
between ‘fits’ 


epileptic fits 

(Pattern varies a lot in 
different children—or 
even in the same child.) 


233 


slow, sudden, or rhythmic ¢ 
movements; fairly 
continuous (except in sleep); 
no loss of consciousness 


athetoid cerebral palsy 


(Note: Fits and cerebral 
palsy may occur in the 
same child.) 


Body, or parts of it, 
stiffens when in certain 
positions: poor control 

of some or all movements. 


different positions 
in different children 


Body may stiffen 
backward and legs 
cross. 


spastic cerebral! palsy 


PARTS OF BODY WEAK OR PARALYZED 


floppy or limp weakness 
in part or all of body 


no loss of feeling in 
affected parts 


no spasticity 
(muscles that tighten 
without control) 


normal at birth 


usually began 
with a ‘bad cold’ 
and fever before 
age 2 


irregular pattern of parts weakened. 
Often one or both legs—sometimes 
arm, shoulder, hand, etc. 


begins little by little 

and steadily gets worse ff \ 
about the same on } 
both sides of body 

often others in the family 

also have it 


@ muscular dystrophy 


@ muscular atrophy 


2, 
Css yy fom 
a a 


Paralysis starts in legs and moves 
up; may affect whole body. 


or, pattern of paralysis variable 


tick paralysis 
Guillain-Barré paralysis 
(usually temporary) 


paralysis from pesticides, 
chemicals, foods (lathyrism) 


lump on back (See p. 57.) 


tuberculosis of spine 


floppy or limp weakness 


usually some loss of 
feeling 


one or both 

hands or feet 

develops slowly in older 
child. Gets worse and worse. 


Pt... 


leprosy 


born with bag on back 
(Look for scar.) 

feet weak, often without 
feeling 


spina bifida 


usually from back or neck injury 
weakness, loss of feeling below 

level of injury 

may or may not have muscle spasms 
loss of bladder and bowel control 


spinal cord injury 


paraplegia 
(lower body) 


quadriplegia 
(upper and 
lower body) 


injury to nerves going to 
one part of body 


hand weakness sometimes caused 
by using crutches wrongly 


DISABILITY GUIDE 


IF THE CHILD HAS THIS 


AND ALSO THIS 


HE MAY HAVE 


SEE PAGE 


weakness usually 
with stiffness or 
spasticity of 
muscles 


no loss of feeling 


usually affects body in 
one of these patterns 


% 2. 
whole body 


one side both legs 


@ 1: cerebral palsy 
(or stroke, usually older 
persons) 


@ 2and 3: cerebral palsy 


@ occasional other causes 


Muscles tighten and resist 
movement because of joint pain. 


JOINT PAIN 


(many causes—see below) 


JOINT PAIN 


one or more 
painful joints 


< 


slyoe ; \ 
@ begins with or without fever .) 
@ gradually gets worse, but there 
are better and worse periods 


2 


juvenile arthritis 


other causes of joint pain 
See chart on joint pain 


WALKS WITH DIFFICULTY OR LIMPS 


dips to one 
side with 
each step 


one leg often weaker and shorter 


Check for 
@ polio 
@ cerebral palsy 
@ dislocated hip 


usually begins age 4 to 8 
may complain of knee pain 


damaged hip joint 


walks with 
knees 
pressed 
together 


muscle spasm and tightness 
upper body little affected 


spastic diplegic or 
paraplegic cerebral palsy 


stands and walks 
with knees 
together and 
feet apart 


no other problems 


feet less than 3” 
apart at age 3 


normal from ages 2 to 12 


feet more than 3" 
apart at age 3 


IN 
IN 


knock-kneed 


walks awkwardly 
with one 
foot tiptoe 


muscle spasms and poor control 
on that side. Hand on that 
side often affected. 


hemiplegic cerebral palsy 


(stroke in older persons) 


walks awkwardly 
with knees bent 
and legs 

usually 
separated 


jerky steps, poor balance 
sudden, uncontrolled movements 
that may cause falling 


athetoid cerebral palsy 


slow ‘drunken’ way of walking 
learns to walk late and falls often 


poor balance (ataxia) — 

often with cerebral palsy 
Down syndrome (mongolism) 
cretinism 


walks with 
both feet 
tiptoe 


weakness, especially in legs and feet 
gradually gets worse and worse 


muscular dystrophy 


legs and feet stiffen 
(spasticity of muscle) 


spastic cerebral palsy 


no other problems 


normal? (some normal children 
at first walk on tiptoes) 


46k 


ib 


55 


56 CHAPTER 6 


IF THE CHILD HAS THIS AND ALSO THIS 


HE MAY HAVE 


SEE PAGE 


i 


walks with hand(s) pushing 
thigh(s) or with knee(s) weak thigh muscle 
bent back ~ 


difficulty 
lifting leg 


' 


polio 

muscular dystrophy 
arthritis (joint pain) 
other causes of muscle 
weakness 


Foot hangs 

down weakly 

(foot drop) Child lifts foot high 
with each step so that 
it will not drag. 


polio 

spina bifida 

muscular dystrophy 
muscular atrophy 

nerve or muscle injury 
other cause of weakness 


dips from 


side to side 2. 
with each ‘ 
step &, 
due to muscle weakness at 
side of hips, or double 
| dislocated hips, or both 


polio 

cerebral palsy 

spina bifida 

Down syndrome 
muscular dystrophy 
child who stays small 
arthrogryposis 
dislocated hips (may 
occur with any of the 
above) 


walks with 

one (or both) r 5) 

hip, knee, or , : 

onkin that J joints cannot be slowly 

] straightened when child 
relaxes (see page 79) 


Stays bent 


J/ 
y ( 


@ contractures 
(shortened muscles) 
@ joined or fused joints 


may be secondary to 
@ polio 


@ joint infection 
@ other causes 


Joints can gradually be 
straightened when child relaxes 


spasticity, often 
cerebral palsy 


Knees wide apart when under 18 months old 


often normal 


feet together (bow 


legs). Waddles or Any combination of these 
ips TrOM sie tO @ Joints look big or thick 
@ Child is short for age 
@ Bones weak, bent, or break 
easily 
Arms and legs may seem 
too short for body, or 
‘out of proportion’. 
Belly and butt stick outa lot 


side (if he walks) 


Consider 

@ rickets (lack of vitamin 
D and sunlight) 

@ brittle bone disease 

@ children who stay very 
short (dwarfism) 

@ cretinism 

@ Down syndrome 

@ dislocated hips 


flat feet no pain or other problems 


normal in many children 


@ Pain may occur in arch of foot. 
@ Deformity may get worse. 


may be problems in 
@ cerebral palsy 
polio 
spina bifida 
Down syndrome 


BACK CURVES AND DEFORMITIES 


sideways Curve 

of backbone 
When child bends 
over, look for a 
lump on one side. 


‘scoliosis'—may occur alone 
or as complication of 


@ polio 

@ cerebral palsy 

@ muscular dystrophy 

@ spina difida 

@ other physical disability 


DISABILITY GUIDE 


IF THE CHILD HAS THIS 


AND ALSO THIS 


HE MAY HAVE SEE PAGE 


belly often sticks out 
may be due to 
contractures here, or 
weak stomach muscles 


rounded back 


S 


‘lordosis’—may occur in: 


polio 59 
spina bifida 167 
cerebral palsy 87 
muscular dystrophy 109 
Down syndrome 279 
cretinism 282 
child who stays small 126 
many other disabilities 161 


hard, sharp bend 
of or bump in 
back bone ™. 


Starts slowly and without pain 
often family history of 
tuberculosis 

may lead to paralysis of 

lower body 


‘kyphosis’—often occurs with: 


arthritis © 

spinal cord injury 
severe polio 

brittle bone disease 


tuberculosis of the spine 


dark soft 
lump over 
backbone 


present at birth 

sometimes only a soft or slightly 
swollen area over spine 
weakness and loss of feeling in 
feet or lower body 


spina bifida 
(‘sack on the back’) 


OTHER DEFORMITIES 


missing body parts 


a“ 


born that way = 


born with missing or 
incomplete parts 


accidental or surgical loss of limbs 
(amputation) 


amputations 


gradual loss of fingers, 

toes, hands, or feet, é 
often in persons who z 
lack feeling 


@ osteomyelitis (bone 
infections) 


sometimes seen with 


@® leprosy (hands or feet) 
@ spina bifida (feet only) 


hand problems 


(For hand problems from 
birth, see p. 305.) 


floppy AL ; 
Paralysis \ 
(no spasticity) ; aa 


without care may lead to 
contractures so that 
fingers cannot be opened 


may occur with 


@ polio 

@ muscular dystrophy 

@® muscular atrophy 

@ spinal cord injury (at 
neck level) 

@® leprosy 

@ damage to nerves or 
cords of arms 


All may lead to contractures 


uncontrolled muscle eS iy, 


tightness (spasticity) 
strange movements 
or hand in tight fist 


spastic cerebral palsy 


may lead to contractures 


burn scars and deformities =23 


burns 


clubbing or 
bending of feet 


(For club feet from 
birth, see p. 114.) 


may begin as floppy weakness and 
become stiff from contractures, 
if not prevented 


OF 


may occur with many physical 
disabilities, including 
@ polio 
cerebral palsy 
@ spina bifida 
@ muscular dystrophy 
@ arthritis 
@ spinal cord injury 


57 


- 68  CHAPTERG 


DISABILITIES THAT OFTEN OCCUR WITH 


OR ARE SECONDARY TO OTHER DISABILITIES 


Developmental delay: 


caused by slow or 


often seen in 


hild si incomplete brain function @ mental retardation 277 
7 , paragiad or by severe physical @ cerebral palsy 87 
prt eis disability, or both @ severely or multiply 283 
use her Body disabled children 
or develop 
basic skills caused by overprotection 

treating children like some delay can occur with 287 
babies when they could do almost any disability 
more for themselves 
Contractures often secondary to: 
* Ily due to muscle , 
: peciakls vs @ polio 59 
joints that no longer weakness or spasticity 
: @ cerebral palsy 87 
straighten because > ina bifida 167 
muscles have shortened e@ Often, muscles that pull a joint . ota 135 
one way are much weaker than 4 id des tees 109 
Joints those that pull it the other 6 dg Lethal 127 
hy way (muscle imbalance). 
a will not ay Senet @ amputations 227 
/) ne FH _, Straighten @ leprosy 215 
* ie 
if #6 
oI ee ——wn sometimes due to scarring 
i burns 231 
from burns or injuries 
behavior problems common with 
may come from 
@ mental retardation 277 
© brain damage @ fits (epilepsy) 233 
@ difficulty understanding things © cerebral palsy 87 
® overprotection 
@ difficult home situation and for emotional reasons, 
with 
(Some children with epilepsy @ spinal cord injury 175 
from brain damage may pull out @ muscular dystrophy 109 
hair, bite themselves, etc.) @ deafness 257 
@ learning disability 365 
oe 7 sp ca @ often over-active or nervous disabil 365 
oer Senay eee @ sometimes behavior problems well Saal La 
intelligent. 
Speech and @ often, but not always, may occur with 
i i f 
communication problems due to deafness or @ deafness 257 
retardation (or both) 
@ developmental delay 287 
@ Some children can hear ‘ 
soe @ cerebral palsy 87 
datas noe @ Down syndrome 279 
@ cretinism 282 
@ children who stay small 126 
@ brittle bone disease 125 
re @ cleft lip and palate 120 
still (Deafness may occur 
cannot together with these and 
speak. other disabilities.) 
other problems that Main disability Common secondary disabilities 
sometimes occur secondary 4 
to other disabilities @ blindness 243 
@ deafness 257 
@ cerebral palsy e 233 
(Some of thesewehave § 0 Nee OO 
wher included in this @ many disabilities with paralysis @ spinal curve 161 
chert.) 0 aaa a nawenenucel 
@ pressure sores 195 
@ persons who have lost @ osteomyelitis (bone 159 
feeling: leprosy, spinal infection) 
cord injury, spina bifida @ loss of urine and bowel 203 
control 


My 


Polio 


Infantile Paralysis 


CHAPTER 7 


HOW TO RECOGNIZE PARALYSIS CAUSED BY POLIO 


e@ Paralysis (muscle weakness) 
usually begins when the child 
is small, often during an 
illness like a bad cold with 
fever and sometimes diarrhea. 


Paralysis may affect any 
muscles of the body, but is 


most common in the legs. muscies that 


Muscles most often affected straighten 


are shown in the drawing. or bend hip, 


or that 
Paralysis is of the ‘floppy’ type spread or 
. close legs 
(not stiff). Some muscles may 
be only partly weakened, 


MUSCLES COMMONLY WEAKENED BY POLIO 


shoulder muscles 


muscles behind 
arm (weakness 
straightening 


_— arm) 


back muscles 
(either side 
of backbone) 


thumb 


others limp or floppy. muscles 


In time the affected limb may 


that 
straighten 


not be able to straighten all — 


the way, due to shortening, or contractures 


‘contractures’, of certain causing 
muscles tight cords 


muscles ———e 


The muscles and bones of the that lift 
affected limb become thinner foot 
than the other limb. The affected limb 
does not grow as fast, and so is shorter. 


Unaffected arms or legs often become extra strong to make up for parts that are 
weak. 


Intelligence and the mind are not affected. 
Feeling is not affected. 


‘Knee jerks’ and other tendon reflexes in the affected limb are 
reduced or absent. (!n cerebral palsy, ‘knee jerks’ often jump more 
than normal. See p. 88.) Also, the paralysis of polio is ‘floppy’; 
limbs affected by cerebral palsy often are tense and resist when 
straightened or bent (see p. 102). 


The paralysis does not get worse with time. However, secondary problems like 
contractures, curve of the backbone and dislocations may occur. 


Of children who become paralyzed by polio: Sih sis Soler hemi 


30% recover 30% have 30% have of difficulty breathing 
completely mild moderate ‘ or swallowing). 

in the paralysis. or severe 

first weeks paralysis. 

or months. 


CHAPTER 7 


BASIC QUESTIONS AND ANSWERS ABOUT POLIO 


How common is it? In many countries, polio—or ‘poliomyelitis’— 
is still the most common cause of physical disability in children. 
In some areas, at least one of every 100 children may have some 
paralysis from polio. Where vaccination programs are effective, 
polio has been greatly reduced. 


What causes it? A virus (infection). The infection attacks parts of 
the spinal cord, where it damages only the nerves that control 
movement. In areas with poor hygiene and lack of latrines, the 
polio infection spreads when the stool (shit) of a sick child 
reaches the mouth of a healthy child. Where sanitation is better, 
polio spreads mostly through coughing and sneezing. 


Do all children who become infected with the polio virus 
become paralyzed? No, only a small percentage become 
paralyzed. Most only get what looks like a bad cold, with 
fever. However, if a child with a ‘cold’ caused by the polio 
virus is given an injection of any medication, the irritation 
caused by the injection can bring on paralysis. (See warning 
on p. 19.) 


Is the paralysis contagious? No, not after 2 weeks from » ee 
when a child first gets sick with polio. In fact, most polio is ~ és < 
spread through the stoo/ of non-paralyzed children who LE 
have ‘only a cold’ caused by the polio virus. severe parayses 


eget et CZ 


At what age do children get polio? |n areas with poor sanitation, polio most often 
attacks babies from 8 to 24 months old, but occasionally children up to age 4 or 5. As 
sanitation improves, polio tends to strike older children and even young adults 


Who does it most often affect? Boys, a little more than girls. Unvaccinated children 
much more often than vaccinated children. (See p. 74). Young children who are given 
injections unnecessarily are paralyzed by polio more often those who are not. 


How does the paralysis begin? |t begins after signs of a cold and fever, sometimes with 
diarrhea or vomiting. After a few days the neck becomes stiff and painful and parts of 
the body become limp. Parents may notice the weakness right away, or only after the 
child recovers from the acute illness. 


Once a child is paralyzed, what changes or improvements can be expected? Often the 
paralysis will gradually go away, partly or completely. Any paralysis left after 7 months 
is usually permanent. The paralysis wi!l not get worse. However, certain secondary 
problems may develop—especially if precautions are not taken to prevent them. 


What are the child’s chances of leading a happy, productive life? Usually very good— 
provided the child is encouraged to do things for himself, to get the most out of 
school, and to learn useful skills within his physical limitations (see p. 497). 


Can persons with polio marry and have normal children? Yes. Polio is not inherited 
(familial) and does not affect ability to have children. 


Si 


SECONDARY PROBLEMS TO LOOK FOR WITH POLIO 


(By secondary problems, we mean problems that do not come from the original 
disease or disability, but appear later, as complications.) 


CONTRACTURES OF JOINTS 

| 3 TYPICAL CONTRACTURES IN POLIO 
A contracture is a shortening of A child with paralysis who crawls around like this and 

muscles and tendons (cords) so that never straightens her legs will gradually develop 


the full range of limb movement is contractures so that her hips, knees, and ankles can no 
prevented. longer be straightened. 


Unless preventive steps are taken, 
joint contractures will form in many wrist 
paralyzed children. Once formed, 
often they must be corrected before 
braces can be fitted and walking is 
possible. Correction of advanced 
contractures, whether through 
exercises, Casts, or surgery (or a 
combination), is costly, takes time TYPICAL DEFORMITIES 
and causes discomfort. Therefore OF ANKLE AND FOOT 
early prevention of contractures is 


very important. ! 
A full discussion of contractures, - cy 
their causes, prevention, and \y 


treatment is in the next chapter beading 
(Chapter 8). Methods and aids for down at bending bending bending 


correcting contractures are described ankle (tiptoe = down at out at in at 
in Chapter 59. contracture) mid-foot ankle ankle 


fingers 


OTHER COMMON DEFORMITIES 


Weight bearing (supporting the body's weight) on weak joints can cause deformities, 
including: 


OVER-STRETCHED JOINTS DISLOCATIONS 


partly WARNING: 
—«—— dislocated Dislocations 
knee like these are 


dislocated joints sometimes 
knee points (especially knee, caused by 
forward foot, hip, stretching 
foot points shoulder, elbow, contractures 
err i thumb) incorrectly. 
to the side) partly 
(See p. 28.) 
dislocated foot 


bending swayback.. 
out at Tout out of partly or 
knee— line with back-knee completely 


knee (when 


SPINAL CURVE a severely paralyzed child 


More serious curve of the ‘ dislocated 
spine is caused by muscle ARS shoulder 
weakness of the back or 

body muscles. The curve elbow bent 
can become so severe backward 
that it endangers life by Z 
leaving too little room 
leg. for the lungs and heart. 


At first, the spinal 
curve straightens 
when the child is 
positioned better. 
But in time the 
curve becomes more 
apparent fixed (will not 
hunchback straighten any more). 
from bulge For information 
dislocated of ribs on spinal curves, 
contracture hip see Chapter 20. 


Minor curve 
of spine can 
be caused by 
tilted hips, 
as a result 
of a short 


62 CHAPTER? 


WHAT OTHER DISABILITIES CAN BE CONFUSED WITH POLIO? 
© Sometimes cerebral palsy can be mistaken for polio—especially cerebral palsy of 
the ‘floppy’ type. 


However, cerebral palsy usually affects Polio has a more irregular 
the body in typical patterns: pattern of paralysis 


all arm and both 
CEREBRAL 4 leg on legs POLIO 
PALSY limbs same 
side 


In cerebral palsy, usually you can find other signs of brain damage: over-active 
knee jerks and abnormal reflexes (see p. 88), developmenta! delay, awkward or 
\ uncontrolled movement, or at least some muscle tenseness (spasticity ) 


@ In muscular dystrophy, paralysis begins little by little and steadily gets worse 
(see p. 109) 


Hip problems (see p. 155) can cause limping, and Note: Polio 
muscles may become thin and weak. Check hips for can occur 
pain or dislocations. (Note: Dislocated hip may also | before or 
occur secondary to polio.) )) after a child 
( has any of 
Cb @ Clubbed foot is present from birth (see p. 114) these other 
problems 
Check 


aretully 


‘Erb’s palsy’, or partial paralysis in one arm and 
hand, comes from birth injury to the shoulder 
(see p. 127) 


@ Leprosy. Foot and hand paralysis begins gradual! 
Gi in older child. Often there are skin patches and loss 
of feeling (see p. 215) 


- , - wy Pr oersgees 
@ Spina bifida is present from birth. There is ( —@~—— » ALWAYS 


reduced feeling in the feet, and often a lump Xe wn EXAMINE THE 
(or scar from surgery) on the back (see p. 167) Vv Ch BACK INA 
CHILD WITH 
@ Injuries to the spinal cord (see p. 175) or te at Se 
to particular nerves going to the arms pod a c % 
-~ L o 
legs. There is usually a history of a severe ; on § FEELING 


4 
AY 
Tuberculosis of the spine can cause gradual or \\ \ 
suddenly increasing paralysis of the lower body 
Look for typical bump on spine (see p. 165) 

cs 


&< 


Other causes of paralysis or muscle weakness. There are many causes of floppy 
paralysis similar to polio. One of the most common is ‘Guillain-Barré’ paralysis. 
This can result from a virus infection, from poisoning, or from unknown causes 

It usually begins without warning in the legs, and may spread within a few days to 
paralyze the whole body. Sometimes feeling is also reduced. Usually strength 
slowly returns, partly or completely, in several weeks or months. Rehabilitation 
and prevention of secondary oroblems are basically the same as for polio 


WHAT CAN BE DONE? 


DURING THE ORIGINAL ILLNESS, when the child first becomes paralyzed: 


No medicines help, either during the first illness, or later 


Rest is important. Avoid forceful exercise because this may increase paralysis 
Avoid injections. 


Good food during recovery helps the child become stronger. (But take care that the 
child does not eat too much and get fat. An overweight child will have more 
problems with walking and other movements.) For suggestions about good food, see 
Where There /s No Doctor, Chapter 11 


Position the child to 

be comfortable and to 
avoid contractures. At 
first the muscles wil! 

be painful, and the 
child will not want to 
straighten his joints. 
Slowly and gently try to 
straighten his arms and 
legs so that the child 

lies in as good a Note: To reduce pain, you may need to put cushions under the knees, 
position as possible. but try to keep the knees as straight as you can 

(See Chapter 8.) 


GOOD POSITION BAD POSITION 


Arms, hips, and legs as Bent arms, hips, and 
Straight as possible. legs. Feet in 
Feet supported. tiptoe position 


FOLLOWING THE ORIGINAL ILLNESS: 


Continue with good food and good positions. 


As soon as the fever drops, start exercises to prevent contractures and return 
strength. Range-of-motion exercises are described in Chapter 42. Whenever 
possible, make exercises fun. Active games, swimming, and other activities to keep 
limbs moving as much as they can are important throughout the child's 
rehabilitation. 


Crutches, leg braces (ca/ipers), and other aids may 
help the child to move better and may prevent 
contractures or deformities 


In special cases, surgery may be needed to correct 
contractures, or to change the place where strong muscles 
attach, so that they help do the work of weak ones. When 
a foot is very floppy or bends to one side, surgery to join 
certain bones of the foot may help. But because bone 
surgery stops the growth of the foot, usually it should not 
be done before age 12 or 13. 


Encourage the child to use his body and mind as much as 

possible, to play actively with other children, to take care of his daily needs, to 
help with work, and to go to school. As much as possible, treat him like any other 
child. 


CHAPTER 7 


REHABILITATION OF THE CHILD WITH PARALYSIS 


All children paralyzed by polio can be helped by 
certain basic rehabilitation measures—such as exercise 
to keep a full range of motion in the affected limbs. 


However, each child will have a different 
combination and severity of paralyzed muscles, and 
therefore will have his own special needs. 


For some children, normal exercise and play may be 
all that are needed. Others may require special 
exercises and playthings. Still others may need braces 
or other aids to help them move about better, do things 
more easily, or keep their bodies in healthier, more For this child, walking 
p : . s a provides exercise that stretches 
useful positions. Those who are severely paralyzed may 


his legs and feet, and prevents 
be helped most by a wheelboard (trolley) or wheelchair. contractures. (Tilonia, India) 


Every child needs to be carefully examined and evaluated in order to best meet his 
or her particular needs. The earlier you evaluate a child’s needs, and take steps to meet 
them, the better. 


Unfortunately, in 
most areas where polio is 
still common, village 
rehabilitation programs 
do not exist or are just 
beginning. Many children 
(and adults) who have 
been paralyzed for a long 
time already have severe 


deformities or joint 

contractures. Often This child, who had polio as a It took several months of 
baby, already had severe exercises at home and then a 

these must be corrected contractures in the hips, knees, series of plaster casts in the 

before a child can use and teet. (PROJIMO) village rehabilitation center 


braces or in to walk to straighten the contractures 
. beg ore. so he could walk with braces. 


Because contractures are such a common problem, not only with polio but with 
many other disabilities, we discuss them separately in the next chapter. Before 
evaluating a child with polio, we strongly suggest you read Chapter 8 on contractures. 


WARNING: Before deciding on any aid or procedure, carefully 
consider its advantages and disadvantages. For example, some 
deformities may be best left uncorrected because they actually help the 
paralyzed child stand straighter or walk better (see p. 530). And some 
aids or braces may prevent a child from developing strength to walk 
without aids (see p. 526). Before decidirg what aid or procedure to use, 
we suggest you read Chapter 56, ‘Making Sure Aids and Procedures Do 
More Good Than Harm.” 


PROGRESS OF A CHILD WITH POLIO: 
THE CHANGING NEEDS FOR AIDS AND ASSISTANCE 


1. exercises to keep full 2. supported sitting 3. active exercises 
range of motion, in positions that with limbs supported, 
starting within days help prevent to gain strength and 
after paralysis contractures maintain full motion 
appears and continuing 
throughout 4, a; P< 


. exercise in water— 
walking, floating, and 
swimming, with the 
weight of the limbs 
supported by the water 


. wheelboard or wheelchair with supports to prevent 6. braces to prevent 
or correct early contractures. contractures and 


j prepare for walking 


Note: These also provide good arm exercise 
in preparation for walking with crutches. 


7. parallel bars for 8. walking machine or 9. crutches modified as 
beginning to balance ‘walker’ walker for balance 
and walk , and extra 


support 


10. under arm 11. forearm and perhaps 12. acane or no arm 
crutches crutches in time supports 
at all 


Note: These pictures are only an example—but most of the steps are necessary for 
many children. Chiidren who begin rehabilitation late may also have contractures or 
deformities requiring corrective steps not shown here. 


© 
OD 


CHAPTER 7 


EVALUATING A CHILD’S NEEDS FOR AIDS AND PROCEDURES 


Step 1: Start by learning what you can through talking with the child and family (see 
Child's History, p. 37 to 38). As you do this, watch the child move about. Observe 
carefully which parts of the body seem strong, and which seem weak. Look for any 
differences between one side of the body and the other—such as differences in the 
length or thickness of the legs. Are there any obvious deformities, or joints that do not 
seem to straighten all the way? If the child walks, what is unusual about the way she 
does it? Does she dip forward or to one side? Does she he!p support one leg with her 
hand? Is one hip lower than the other? Or one shoulder? Does she have a humpback, a 
swayback, or a sideways curve of the back? 


These early observations will help you know what parts of the body you most need 
to check for strength and range of motion. Often, by watching a child you can begin to 
get an idea about what kind of aids or assistance may help. For example 


Carmen appears to She will probably 
have severe never walk, and will 
paralysis need a wheelchair or 
affecting both wheelboard 

legs and her right 
arm. Weakness in 
her trunk (main 
part of the body) 
appears to have 
caused a severe 
S-shaped curve of 


You may want also to 
make her a body brace, 
or help her in other 
ways to sit more 
upright and try to 


keep the spine from 


Sai spine bending more 


r 


Pedro appears to have severe paralysis in his legs and hips. It 
looks as if his hips, knees, and feet cannot straighten _' 
(contractures). Weak stomach muscles and severe hip // { 
contractures may be the cause of his swayback 


Because his arms look 
strong, Pedro will ee mnag? Ey 
strap T casts 


probably be able to sradually straighten 


walk with crutches and straighten knees and of rng 
leg braces. But first hips ankles weakness, 
his contractures must x \ he may 
be straightened.——>_ { i aap abet 


with a 
If the contractures 


cannot be straightened 
by gradual stretching, 


hip band 


‘ he may need surgery 


ow) 


a. 


Manuel walks with the help of a stick. He appears to have paralysis 
mainly in his right leg and foot. Because of weak thigh muscles, he 
‘locks’ his knee backward in order to bear weight on it. This ‘back- 
kneeing’ has become more and more extreme as the cords behind the floppy 
knee stretch. The foot is very unstable and flops to one side. The 

weaker leg looks somewhat shorter—and for walking is much shorter 

because of the bent-back knee and bent-over foot. 


back-knee 


He might be able to walk without the stick if he uses a below-knee 


brace to stabilize his foot. (See p. 550.) 
pad holds 


knee forward 


But the back-knee would become worse and worse until he could 
not walk. So probably he should have a long-leg brace. The brace firm ankle 
might allow his knee to bend backward just a little for stability 
Tes that no knee lock is needed. 


support 


raised sole —___ 


Onis leans forward and pushes her weak left thigh Or she may need Or she may oe 
with her hand when she walks. Her left knee an above-knee need a below 
cannot quite straighten. Her weak leg looks a brace with a knee brace that 
little shorter than the other. strap to pull helps push her 


‘ the knee back knee back. 


: 5 Exercises to get her knee 

straighter or so it can bend very 

slightly backward may be all nes 
that is needed for Afia to walk knee 
without using her hand back 


Pad 


The brace bends the foot down just a little, 
so that by bearing weight on toes (rather than 
heel) her knee is pushed back. 


To get a better idea about which of the three solutions may work best for Afia, you will need 
to do a careful physical examination, testing range of motion and muscle strength of the hip, 


knee, and ankle joints. 
ae ) 


Step. 2: This is the physical examination. |t shou!d usually include: 


1. Range-of-motion testing, especially where you think there might be contractures. 
(See ‘‘Physical Examination,” p. 27 to 29, and ‘‘Contractures,”’ p. 79 and 80.) 


2. Muscle testing, especially of muscles that you think may be weak. Also test 
muscles that need to be strong to make up for weak ones (such as arm and 
shoulder strength for crutch use). (See p. 27 and p. 30 to 33.) 


3. Check for deformities: contractures; dislocations (hip, knee, foot, shoulder, 
elbow); difference in leg length; tilt of hips; and curve or abnormal shape of the 
back. (See p. 34.) 


CHAPTER 7 


Step 3: After the physical exam, again observe how the child moves or walks. Try to 
relate her particular way of moving and walking with your physical findings (such as 
weakness of certain muscles, contractures, and leg length). (For an example, see p. 70.) 


Step 4: Based on your observations and tests, try to figure out what kind of exercises, 
aids, or assistance might help the child most. Consider the advantages of different 
possibilities: benefit, cost, comfort, appearance, availability of materials, and whether 
the child is likely to use the aid you make. Ask the child and parents for their opinions 
and suggestions 


Step 5: Before making a final brace or aid to fit the child, if possible test to see how 
well it may work by using a temporary aid or old brace from another child. For 
example, 


Ifa re iki But before nailing and 
child’s on the glueing in the lift, 
ankle outer side quickly make a trial 
bends of the sole one of cardboard or 
over to like this, something else and 
the may help to fasten it temporarily 
outside keep the to the sandal or shoe 
like foot with tape or string. 
Svs: straighter. Then have the child 
walk. 


Note: For afew children, a lift like this will help 
For many it will not. 


| Ask the child what she thinks. 


Step 6: After the child, her parents, and you have decided what kind of brace or aid 
might work best, take the necessary measurements and make the brace or aid. When 
making it, once again it is wise to put it together temporarily so that you can make 
adjustments before you rivet, glue, or nail it into its final form. (See p. 540.) 


Step 7: Have the child try the brace 
or aid for a few days to get used to 
it and to see how well it works. Ask 
the child and parents if it seems to 
help. Does it hurt? Are there any 
problems? How could it be 
improved? Is there something that 
might work better? Make what 
adjustments are necessary. But 
remember that no brace or aid is 
likely to meet the needs of a child 
perfectly. Do the best you can. 


Mari and Chelo making a child’s Brace 


SY 


POLIO 69 


Here is a story of how workers in a small village rehabilitation program figured out 
what kind of aids a child needed. How many of the steps we have just discussed did 
they follow? Was each step important? 


A STORY: A BRACE FOR SAUL 


Saul’s mother 


One day a mother from a neighboring “Don't worry, Saul. Maybe we can do 
village arrived at the village center with her something simpler,’ said Mari. ‘But first 
6 year old son, Saul. Mari and Chelo, 2 of let’s examine you, okay?’’ Saul nodded 
the village rehabilitation workers, welcomed 
them warmly. Learning that Saul had polio 
as a baby, they asked him to walk, and then 
to run, while they watched carefully. Saul 
limped a lot and one leg looked thinner and 


shorter. With each step it bent back at the THAT'S AS 


On muscle testing Saul, they found he 
could not straighten his knee at all. But he 
had fair strength for bending his knee back 


‘He walks quite well, really,’’ said Mari. 
“But he has to ‘lock’ his knee back in order 
to put weight on it. That knee is going to 
keep stretching back and some day it will 
give out.” 


“A long-leg brace would protect his and his hip forward 
knee,’’ suggested Chelo 


“Oh, please, no!"’ said Saul’s mother. 
“A year ago we took Saul to the city and 
the doctors had a big metal brace made for 
him. It cost so much we are still in debt! 
Saul hated it! He would always take it off 
and hide it. We tried and tried to get him to 
use it, but he wouldn’t.”’ 


_- 


Ly and good strength for bending his hip back 


“That's not surprising,’’ said Mari. ‘‘Often 
a child who can walk without a brace will 
refuse to use one—even if he walks better 
with it. We could make him a long-leg brace 
out of plastic. It would be much lighter. 
What do you say, Saul?’’ Sau! began to cry. 


70 


CHAPTER 7 


“With the hip and thigh strength he has, 
he should almost be able to stand on that leg 
without the knee bending back,"’ said Mari. 
“Saul, let’s see you try it like this. Pretend 
you're a stork!'’ For a moment Saul could 
do it. ““Good!"’ said Mari. ‘‘Every day stand 
like that and see how high you can count 
without letting your knee go back. Every day 
try to beat your old record! Okay?” 


“Okay,” said Saul. 
Sounds like fun!”’ 


@ 


“The stork exercises may help,” said 
Chelo. ‘But | still think he needs a brace. At 
least at first.”’ 


We must weigh the advantages against the 
disadvantages,’ said Mari. ‘‘A long-leg brace 
would keep his knee straight. But it could 
weaken the muscles he needs to strengthen. 
Since the brace would keep his leg from 
bending back, he wouldn't have to use his 
muscles to do it 


A long-leg brace 

; might weaken the 

…[truncated]