FAS A Guide for Daily Living Parenting Children Affected by Fetal Alcohol Syndrome

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FAS
Parenting Children Affected
by Fetal Alcohol Syndrome
A Guide for Daily Living
Ministry for Children
and Families Edition
Ministry for Children and Families
To receive copies of this special Ministry for Children and Families (MCF) edition of the Parenting
Children Affected by Fetal Alcohol Syndrome: A Guide for Daily Living, please contact:
Warehouse Services
724 Vanalman Avenue
Victoria, British Columbia V8V 1X4
Canada
Ph. (250) 952-4563
Fax (250) 952-4559
Refer to document number MCF 089
For copies of the non MCF Parenting Children Affected by Fetal Alcohol Syndrome: A Guide for Daily Living, or for
further information about FAS, please contact:
The Society of Special Needs Adoptive Parents (SNAP)
Suite 1150, 409 Granville Street
Vancouver, British Columbia V6C 1T2
Canada
Ph. (604) 687-3114, toll free (in BC) 1-800-663-7627
Fax (604) 687-3364
e-mail: snap@snap.bc.ca
web: www.snap.bc.ca
Ce livret est aussi disponible en français. SVP contactez SNAP.
A previous edition of this book, edited by Rana Shaskin, was published by the Society of Special Needs Adoptive
Parents (SNAP) in 1994.
Principal writer for this edition: Sara Graefe, Society of Special Needs Adoptive Parents
Forewords by Ross Dawson, Ministry for Children and Families, and Dr. Julianne Conry, University of British
Columbia
This special MCF edition is based on the second, national edition, revised and expanded, published by SNAP in
1998 in both official languages, in cooperation with the Adoption Council of Canada and with the support of Queen
Alexandra Foundation for Children.
Copyright acknowledgements follow the Bibliography.
PARENTING CHILDREN AFFECTED BY FETAL A LCOHOL S YNDROME: A GUIDE FOR DAILY LIVING. MINISTRY FOR CHILDREN AND
FAMILIES EDITION (BRITISH COLUMBIA). Copyright © 1999 by the Society of Special Needs Adoptive Parents (SNAP).
Revised and updated by Sara Graefe, SNAP
Researched by Elspeth Ross, Adoption Council of Canada, with the assistance of Carole Julien, Canadian Centre
for Substance Abuse, and Sara Graefe, SNAP
Design and layout by Sara Graefe, SNAP
Published by the Society of Special Needs Adoptive Parents in cooperation with the B.C. Ministry for Children and
Families Child Protection Division.
ISBN 0-9698617-5-3
Contents
Introduction ........................................................................................... iii
Foreword by Ross Dawson .................................................................... v
Foreword by Dr. Conry ....................................................................... vii
Definitions and Facts ............................................................................. 1
Alcohol and Pregnancy .......................................................................................... 1
What is FAS? .......................................................................................................... 1
FAS Diagnostic Categories .................................................................................... 1
Other Terms............................................................................................................ 3
Facial Characteristics ............................................................................ 5
A Few Facts... ............................................................................................ 6
Common Manifestations ........................................................................ 7
Infancy .................................................................................................................... 7
Preschool ................................................................................................................. 8
Early School ............................................................................................................ 8
Middle School ......................................................................................................... 9
Adolescence ............................................................................................................. 9
Adulthood (18+) .................................................................................................... 10
Additional Behavioural Characteristics and Secondary Disabilities ................ 11
Overlapping Diagnoses ........................................................................................ 12
Positive Characteristics ....................................................................................... 12
Common Misconceptions .................................................................... 14
Information Processing ....................................................................... 17
Structure, Supervision, Simplicity, Steps and Context ................ 19
Parenting Suggestions ......................................................................... 20
Effective Communication .................................................................................... 20
Consequences and Positive Feedback ................................................................. 22
Transitions ........................................................................................................... 23
Structure and Routines ....................................................................................... 24
Supervision ........................................................................................................... 24
Advocacy ............................................................................................................... 25
Guidelines for Daily Living ................................................................ 26
Routines ................................................................................................................ 26
Dressing ................................................................................................................ 27
The Bathroom ....................................................................................................... 27
Mealtime ............................................................................................................... 28
Bedtime ................................................................................................................. 29
Sleep ...................................................................................................................... 30
Laundry ................................................................................................................ 30
Supervision ........................................................................................................... 31
i
Parenting Children Affected by FAS
Managing Hyperactivity ..................................................................................... 32
Managing Impulsivity .......................................................................................... 33
Sensory Considerations ....................................................................................... 33
Social Skills .......................................................................................................... 34
Telephone .............................................................................................................. 35
Handling Time ...................................................................................................... 35
Teaching Ownership ............................................................................................ 36
Handling Money ................................................................................................... 37
Special Considerations for Infants ................................................... 38
Sensitivity ............................................................................................................. 38
Illness .................................................................................................................... 38
Crying ................................................................................................................... 39
Feeding .................................................................................................................. 39
Sleep ...................................................................................................................... 39
Take Care of You ................................................................................................... 40
Special Considerations for Adolescents .......................................... 41
Structure and Supervision .................................................................................. 42
Life Skills .............................................................................................................. 42
Adolescents with FAS in the Justice System ..................................................... 43
Take Care of You ................................................................................................... 44
Parents’ Needs ........................................................................................ 45
Take Care of You ................................................................................................... 45
Respite .................................................................................................................. 46
Get Support .......................................................................................................... 46
Hang In There ...................................................................................................... 47
Assessment and Referrals ................................................................... 48
Referrals ............................................................................................................... 49
Medical Assessments ........................................................................................... 49
Dealing with a Diagnosis ..................................................................................... 50
Dealing with NOT Getting a Diagnosis .............................................................. 51
Talking to your Child about FAS ....................................................... 52
Young Children ..................................................................................................... 52
School-Aged Children ........................................................................................... 53
Adolescents ........................................................................................................... 53
Resource List.......................................................................................... 55
Books ..................................................................................................................... 56
Videos .................................................................................................................... 59
Informative Newsletters ...................................................................................... 60
Internet ................................................................................................................. 60
Organizations ....................................................................................................... 61
Bibliography........................................................................................... 68
Acknowledgements ............................................................................... 71
Appendix ............................................................................................... A-1
ii
Introduction
The Society of Special Needs Adoptive Parents (SNAP), a non-profit, provincially-funded organization in British Columbia, produced the first edition of this booklet in 1994 in response to
many requests from parents and professionals caring for children affected by Fetal Alcohol
Syndrome (FAS) and other alcohol-related birth defects (ARBD, ARND). The first edition received an overwhelming response from the community.
In the four years since this book was first published, there have been significant advancements in the field. Research in the field continues, and although there is still a long way to go,
awareness has been growing in society at large. In 1996, Health Canada issued a
groundbreaking, joint statement on the prevention of FAS, co-signed by eighteen national associations representing medical, nursing and midwifery disciplines, aboriginal and multicultural
groups, and other organizations known for their extensive work in the area of FAS and other
alcohol-related birth defects. Meanwhile, south of the border, the United States Congress
mandated the Institute of Medicine of the National Academy of Sciences to form an international committee to review FAS in response to confusion around terminology, diagnostic practices, and the disorder itself. A panel of fourteen experts in fields ranging from Pediatrics to
Psychiatry—including Dr. Joanne Weinberg, Professor of Anatomy at the University of British
Columbia—examined issues including those surrounding diagnostic categories and techniques,
the prevalence of FAS and related disorders, and the availability of treatment programs for
affected individuals. In 1996, based on the panel’s recommendations, the Institute of Medicine
published new terminology and diagnostic procedures for FAS.
In 1998, SNAP produced a new edition of the guide, to keep in step with the changing times
and the latest terminology and diagnostic criteria. With research assistance from the Adoption
Council of Canada (ACC) and the Canadian Centre on Substance Abuse (CCSA), the material
in the first edition was expanded and updated. There are also new sections outlining special
considerations for parenting infants and adolescents, as well as a section on parent’s needs
and caring for the caregiver—an important task that often gets overlooked when parenting
children with special needs.
Many sources of information written by parents and professionals contributed to the contents
of this publication. Their efforts to help children with FAS cope with special challenges are
gratefully acknowledged.
The information in this booklet represents the latest, most up-to-date information at the time
of publication. However, research and theories will continue to evolve, and you are encouraged
to contact agencies such as SNAP, ACC, CCSA, and other resources for updates. (Please see the
Resource List at the end of this manual)
Sara Graefe, MFA
Publications Coordinator
Society of Special Needs Adoptive Parents
editor and principal writer
September 1999
iii
Foreword by Ross Dawson
I am pleased to provide you with the FAS Guide for Daily Living. Developed in partnership
with the Society of Special Needs Adoptive Parents (SNAP), this guide book provides the most
up to date and accurate information on Fetal Alcohol Syndrome.
Fetal Alcohol Syndrome (FAS) is the leading cause of preventable birth defects. Consistent
and accurate information on FAS is essential in prevention, recognition and intervention of
FAS. Caregivers and others working with children with FAS will find valuable information in
this guide including how to obtain assessments and referrals and where to find supports for
children and families affected by FAS. Further information on resources available to social
workers, foster parents and parents are included at the back of the booklet.
I hope you will find this guide useful in your work with children and families affected by FAS.
Ross Dawson
Director of Child Protection
Ministry for Children and Families
v
Foreword by Dr. Conry
In 1994, the Society of Special Needs Adoptive Parents published the first edition of Parenting
Children Affected by Fetal Alcohol Syndrome: A Guide for Daily Living. Over 5,000 copies of
this manual have been distributed across Canada and the United Status which points to the
tremendous interest and need for information about this life-long disability. Requests for this
guide have come from parents, teachers, social workers, doctors and other interested professionals.
In British Columbia, the Society of Special Needs Adoptive Parents has been instrumental in
increasing our understanding of FAS/FAE by supporting workshops, disseminating information and making resources available to the parents of these children.
In 1996, the first comprehensive long-term follow-up into adolescence and adulthood of individuals with a diagnosis of FAS/FAE was published by the University of Washington (“Understanding the Occurrence of Secondary Disabilities in Clients with FAS and FAE”). The anecdotal stories we had been hearing from families raising a child with FAS/FAE were borne out
by the research. Many individuals with FAS/FAE , but not all, are prone to mental health
problems, disrupted school experiences, trouble with the law, alcohol and drug problems and
difficulties living independently in adulthood. On the positive side, the factors protecting the
child from this outcome include—not surprisingly—a nurturing, stable home environment and
an early diagnosis so that interventions can be put in place at an early age. This is where the
advocacy by determined individuals and organizations such as SNAP have played such an
important role in reducing the impact of FAS/FAE and improving the outcomes for families
having children affected by this disability.
Complex problems such as FAS/FAE do not have simple and quick solutions. There is no single
“right” way to parent a child with FAS/FAE. Each child is unique. Nor do we need to “reinvent
the wheel” in devising techniques to teach a child with FAS /FAE. By recognizing each child’s
particular strengths and weaknesses, it becomes possible to devise ways of teaching and parenting that will allow him/her to be successful. We recognize now that this is a life-long effort and
success is measured in small increments. Support for children, their families and communities
begins with knowledge and understanding of this invisible disability.
Dr. Julianne Conry, PhD
Assistant Professor
Department of Psychology and Special Education
University of British Columbia
July, 1998
vii
What
is FAS?
Definitions and Facts
Learning about Fetal Alcohol Syndrome and then applying it to our
son was quite a task. It reminded me of one of those “Choose Your Own
Adventure” books I often read to Luke. You thought you knew where the
journey was taking you and then they threw in three or four different
paths and endings. I thought I knew my boy and I did... but I grew to
know him better when I understood the diagnosis of FAS.
—Luke’s Mom
Alcohol and Pregnancy
When a pregnant woman consumes alcohol, she does not drink alone. Alcohol is a known
teratogen, which means it is a substance that can damage and disrupt the developing embryo
and fetus. The brain and central nervous system of the unborn child are particularly sensitive
to prenatal alcohol exposure (Health Canada, 1996; Streissguth, 1997).
What is FAS?
Fetal Alcohol Syndrome (FAS) refers to a constellation of physical and mental birth defects
that may develop in individuals whose mothers consumed alcohol during pregnancy. It is an
organic brain disorder which is characterized by central nervous system involvement, growth
retardation, and characteristic facial features (Stratton, Howe, & Battaglia, 1996).
FAS is a medical diagnosis that can only be made when a child has signs of abnormalities in
each of these three areas, plus known or suspected exposure to alcohol prenatally. Other
physical defects caused by prenatal exposure to alcohol may include malformation of major
organs (including heart, kidneys, liver) and other parts of the body (e.g. muscles, genitals,
bones) (Stratton, Howe, & Battaglia, 1996).
FAS is often called a “hidden” or “invisible” disability because its physical characteristics can
be subtle and may go unrecognized. Many alcohol-affected children are endearing and affectionate, and these qualities can mask the seriousness of this lifelong neurological disability. In
their early years, children with FAS are often described as the cutest child in their class.
FAS Diagnostic Categories
Fetal Alcohol Syndrome (FAS) was first defined over twenty years ago. Since then, researchers
and clinicians have encountered some confusion and clinical problems arising from certain
terminology used to describe the spectrum of effects caused by exposure to alcohol in the
womb (Clarren, 1996; Stratton, Howe, & Battaglia, 1996; Streissguth, 1997).
The United States government recently recognized the need to establish clear, consistent diagnostic criteria that more accurately reflects the range of disorders caused by prenatal exposure to alcohol. In 1996, the US Institute of Medicine (IOM) published new diagnostic procedures for FAS, based on the recommendations of a panel of experts from Canada and the USA.
1
Parenting Children Affected by FAS
In the past, a diagnosis of FAS required confirmation of the mother’s alcohol use during pregnancy, to make the distinction between FAS and other syndromes and conditions that look
very much like it. However, in the presence of clear features of FAS and the strong suspicion of
prenatal alcohol exposure, an experienced clinician may make a diagnosis of FAS in one of
three distinct categories.
The following is a brief introduction to the new terms. For full diagnostic criteria, please see
Appendix on page A-1, or refer to the IOM text Fetal Alcohol Syndrome: Diagnosis, Epidemiology, Prevention and Treatment (Eds. Stratton, Howe, & Battaglia), published in 1996 by the
National Academy of Sciences (see Bibliography, page 70).
1. FAS with Confirmed Maternal Alcohol Exposure
A diagnosis is made in this category when there is known, significant
prenatal exposure to alcohol and the child exhibits three characteristics:
i.
growth retardation (i.e. delayed prenatal and/or post-natal
growth)
This delay must result in height and/or weight very much below
normal—below the tenth percentile.
ii.
central nervous system involvement
This can result in one or more of the following conditions being
observed in the child: head circumference below the third percentile, developmental delay or intellectual disabilities, and/or
other less prevalent conditions.
iii.
characteristic facial features
These include short eye slits, elongated mid-face, thin upper lip
and flattened facial bone structure. These features are most noticeable during early childhood. (See diagram on page 5)
2. FAS without Confirmed Alcohol Exposure
This category is assigned to a child who has the necessary characteristics for a clear diagnosis of FAS, as above, but where there is no way to
accurately verify the mother’s alcohol use. This new diagnostic category (1996) is helpful for the many children with FAS in foster and
adoptive homes, where details about their prenatal histories may be
unavailable.
3. Partial FAS with Confirmed Maternal Alcohol Exposure
This applies to a child with a confirmed history of prenatal alcohol exposure who has some, but not all, of the characteristics of FAS. The
child does not display all of the characteristic facial features, but exhibits other signs such as growth deficiency, damage to the central nervous system, and/or a complex pattern of behaviour and cognitive abnormalities inconsistent with developmental level and cannot be explained
by family background or environment alone. Partial does not mean that
the condition is less severe than FAS. In fact, Partial FAS can have
equally serious implications for education, social functioning and voca-
2
A Guide for Daily Living
tional success.
Many children diagnosed as Partial FAS would have been designated
FAE (“Fetal Alcohol Effect”) under the old system. This new category, like FAE, still requires knowledge of the child’s pre-natal history,
which is not always available in adoption situations. However, because
children with Partial FAS do not exhibit all of the distinguishing characteristic facial features of full-blown FAS, the birth mother’s drinking
history becomes a crucial piece of the puzzle from a medical point of
view—a piece needed to rule out other medical conditions that may be
present. Nevertheless, the lack of a definitive diagnosis can be frustrating for adoptive parents whose children are exhibiting troubling
behaviours.
The Institute of Medicine has included two additional categories which are used to describe
very specific outcomes of prenatal alcohol exposure:
4. Alcohol-Related Birth Defects (ARBD)
This refers to a child who displays specific physical malformations resulting from confirmed maternal alcohol exposure. These may include
heart, skeletal, sight, hearing and visual problems.
5. Alcohol-Related Neurodevelopmental Disorder (ARND)
This applies to a child with a confirmed history of prenatal alcohol exposure who exhibits central nervous system damage as in FAS, inconsistent with developmental level and cannot be explained by family
background or environment alone (e.g. learning difficulties, poor impulse control, poor social skills, problems with memory, attention and
judgement). As children with disabilities due to prenatal alcohol exposure frequently come from environments where there has been neglect
and/or abuse, it can be difficult or impossible to separate which problems are due to alcohol effects and which can be explained by the family living situation. Usually there is a combined effect.
Other Terms
You may still encounter older terms relating to FAS. Previously, the term Fetal Alcohol
Effects (FAE) was used to describe an individual with a history of prenatal alcohol exposure,
but not manifesting all the physical or behavioural symptoms of FAS (Streissguth, 1997). Possible Fetal Alcohol Effects (PFAE) was an equivalent clinical term (Astley & Clarren, 1995;
Streissguth, 1997).
However, these terms were sometimes misinterpreted as meaning that FAE was less severe
than FAS. While a child designated FAE does not have all the physical abnormalities of FAS,
the cognitive and behavioural characteristics are similar. As a result, FAE poses similar lifetime challenges (Astley & Clarren, 1995; Clarren, 1996; Streissguth, 1997).
Clinicians and researchers discourage the use of FAE and PFAE because of these misunder-
3
Parenting Children Affected by FAS
standings, as well as other clinical problems the terms create. Further, FAE and PFAE are no
longer used in formal diagnostic procedures. With the gradual introduction of the new Institute of Medicine Criteria in clinical practice, the terms Partial FAS, ARBD and ARND will
come into more common usage. Some professionals suggest that better terminology is still
needed, and that these new definitions may evolve over time (Clarren, 1996).
Please note that this booklet only uses the term FAE if it was included in the original source
being cited, or in the name or description provided by an agency or organization. Terminology
aside, it is important not to minimize the impact of any alcohol-related birth defect.
For more information on diagnosis, please see the section on Assessment and Referral Information, page 48.
4
Figure
one
Facial Characteristics
5
Did you
know?
A Few Facts...
Then...we saw a news clip about FAS/E on TV. Shortly after we read The
Broken Cord and the missing pieces began to come together. With the discovery
of the probable cause of the behaviours of our children, came relief followed
by stages of grief. The questions that periodically haunt me about these times
are: “Why did we have to find such vital information through the media?
Where were the teachers, social workers and doctors? Why didn’t they share
this knowledge with us?
—adoptive parent
Ö
FAS is 100% preventable.
Ö
It is one of the leading causes of preventable birth defects and developmental delay in Canada and most countries of the world. It is also one of the leading known
causes of mental retardation, although not all persons with FAS are mentally retarded.
Ö
FAS leads to problems with learning, behaviour, and community living.
Ö
It is found in all economic and racial groups.
Ö
Health Canada (1996), based on incidence rates found in the United States, estimates that
there are one to two per 1000 children born with FAS in Canada.
Ö
FAS is not genetic or inherited. A woman who has FAS can give birth to unaffected
children.
Ö
FAS is more likely to occur following continuous or heavy intake of alcohol during pregnancy. However, some women who binge or drink sparingly have babies with alcohol-related damage. There is no definitive information regarding a safe quantity of alcohol use during pregnancy. Health Canada (1996) advises women who are or may become
pregnant to abstain from alcohol.
Ö
FAS prevention is not just a women’s issue. Many pregnant women need support from
their partners, extended family members and community in order to abstain from alcohol.
The role of paternal alcohol consumption is unclear. While the term FAS describes the
damage to the fetus caused by maternal alcohol exposure, recent research also suggests
that a father’s use of alcohol may cause damage to the sperm. The US Institute of Medicine
(1996) indicates that further research is required to clarify this issue. Since it is not yet
known whether this damage affects a fetus, it is advisable for men to abstain from alcohol
when planning or risking a pregnancy.
6
Children
with FAS
Common Manifestations
I wish I could repair myself;
I wish people didn’t throw me on the shelf.
I wish people wouldn’t use me soooo much,
I wish people would take advantage of how precious I am.
And...I wish they wouldn’t use too much touch.
—Nigel, age 16: “This refers to FAS/E people
as well as to electrical appliances.”
No two children with FAS are affected in exactly the same way. However, as a group, children
with FAS display more developmental and behavioural problems than other children. The
child with FAS may exhibit a number of the characteristics described here, but likely not all of
them. The clustering of these characteristics and behaviour patterns coupled with the history
of pre-natal exposure to alcohol are strong cues for identification.
Parents who identify reasons for their children’s problems are best equipped to plan effective
treatment and education strategies. The following is not an exhaustive list of FAS characteristics, but rather a place to start. However, an accurate diagnosis is important. There are
other disorders that have similar characteristics. Parents are advised to consult with a physician, pediatrician, pediatric neurologist, dysmorphologist or geneticist who has experience with
FAS—or a willingness to learn. For more information about diagnosis, please see the section on
Assessment and Referral Information on page 48 of this manual.
This list has been compiled from a number of sources and represents items common to several
reference sources. Please refer to the bibliography and resource list at the back of this manual
for further reading.
Infancy
When dealing with infants, you might also encounter the term, “Neonatal Abstinence Syndrome
(NAS), which refers to infants suffering through drug withdrawal after birth. We recognize that
many women are multiple drug users, and that the mother of a baby with NAS has likely been
using alcohol as well. Affected infants may exhibit a combination of lasting NAS symptoms and
emerging FAS symptoms.
n often tremulous and irritable; may cry a lot
n weak sucking reflex and muscle tone
n highly susceptible to illness
n feeding difficulties: often disinterested in food, feeding can take hours
n erratic sleep patterns; no predictable sleep-awake cycle
7
Parenting Children Affected by FAS
n sensitive to sights, sounds, and touch
n failure to thrive
n slow to master developmental milestones (e.g. walking, talking, imitating sounds)
n problems with bonding
Preschool
n disinterest in food and disrupted sleep continue
n poor motor coordination
n flits from one thing to another with “butterfly-like” movements
n more interested in people than objects
n overly friendly, highly social; indiscriminate with relationships
n expressive speech may be delayed; may have less in depth language than peers or may be
excessively talkative and intrusive, giving the superficial appearance that speech is not
impaired
n unable to comprehend danger; does not respond well to verbal warnings
n prone to temper tantrums and non-compliance
n short attention span
n easily distractible or hyperactive
n does not respond well to changes; prefers routines
Early School
n reading and writing skills during the first two years may not be noticeably delayed
n arithmetic may be more of a problem than spelling and reading
n attention deficits and poor impulse control become more apparent as the demands for class-
room attention increase
n inability to transfer learning from one situation to another—to learn from experience—
without more repetition than normal
n requires constant reminder for basic activities at home and school
n “Flow through” phenomena—information is learned, retained for a while and then lost; poor
performance of “learned” tasks may appear deliberate
8
A Guide for Daily Living
n gross motor control problems (e.g. clumsy)
n fine motor problems (e.g. trouble with handwriting, buttons, zippers, shoe laces, etc.)
n difficulties with social skills and interpersonal relationships: may be unable to share, to
wait for turn, to follow the rules or to cooperate; may be inappropriately intrusive
n poor peer relations and social isolation may be noted; may prefer to play with younger
children or adults rather than with peer group
n memory deficits
n exists in the “here and now,” seems to lack an internal time clock
n unable to monitor his/her own work or pace him/herself
n sleep disturbances continue
Middle School
n delayed physical and cognitive development
n reading and spelling skills usually reach peak
n increased difficulty maintaining attention, completing assignments and mastering new aca-
demic skills
n usually a very concrete thinker, may have trouble working with ideas—tends to fall farther
behind peers as the world becomes increasingly abstract and concept based
n continuing fine motor problems may make volume work production impossible
n good verbal skills, superficially friendly social manner and good intentions often mask the
seriousness of the problem
n psychological evaluation and remedial placement may be necessary
n a pattern of school suspensions may start
Adolescence
n increased truancy, school refusals and school dropouts
n increased behavioural disruption in school
n reading comprehension is poorer than word recognition
n math tends to be the most difficult task, suggesting poor memory, poor abstract thinking,
and difficulty with basic problem solving
9
Parenting Children Affected by FAS
n may be able to “talk the talk” while unable to “walk the walk”—for example, they may tell
you they understand your instructions, but are unable to carry them out. They may have
learned to act as though they understand, but cannot follow through on their own.
n often misjudged as being lazy, stubborn and unwilling to learn
n faulty logic; lacks basic types of critical thinking and judgement skills
n increased problems with abstract thinking and the ability to link cause and effect
n impulsive, total lack of inhibition and easily influenced, subject to peer manipulation and
exploitation
n difficulty showing remorse or taking responsibility for actions
n frequently behaves in ways that place him/herself or others at risk
n high risk for problems with the law and involvement in the criminal justice system
n problems managing time and money
n difficulty identifying and labelling feelings
n low motivation
n low self-esteem
n clinical depression may become evident
Adulthood (18+)
n perseverates with ideas or activities, may appear compulsive and rigid
n difficulty holding down jobs
n may be unable to live independently or parent children
n problems managing money
n poor social skills
n lack of reciprocal relationships
n unpredictable behaviour
n depression/suicidal ideation
n withdrawal and isolation
n drug or alcohol abuse; susceptible to chemical dependency
10
A Guide for Daily Living
Additional Behavioural Characteristics
and Secondary Disabilities
The frequently disabling characteristics of FAS often cause secondary disabilities—problems
that arise after birth as a result of the neurological deficits. These secondary conditions come at
a high cost to the individual, their family, and society, but may be reduced by early diagnosis,
appropriate intervention, better understanding, and a stable, nurturing home environment.
Additional behavioural characteristics and secondary disabilities that may be associated with
FAS include the following:
n behavioural deficits reported in many areas, including interpersonal relationships, commu-
nication, daily living skills, sexuality and adaptive skills
n communication deficits, including the inability to listen to a story for five minutes or longer,
to relate to an experience, to use a table of contents or to address an envelope
n problems with social skills include:
• talking too much and too quickly, but having little to say
• liking to be the centre of attention
• outgoing and friendly manner, often seen as positive in early childhood, often becomes
•
•
•
•
•
•
problematic as the child grows older because they are indiscriminate and/or overly intrusive;
impulsiveness, lack of inhibition, and naiveté regardless of age and gender
difficulty telling time, knowing the value of money, and interpreting social cues
problems sequencing tasks or instructions
low tolerance for frustration
difficulty distinguishing fantasy from real life
tending to gravitate to young children or adults rather than people their own age
n depression
n anger and aggression
n low self-esteem
n other mental health problems
n school problems and/or disrupted school experience
n running away
n substance abuse
n inappropriate sexual behaviour
n trouble with the law
n dependent living
11
Parenting Children Affected by FAS
n problems with employment
n violent or threatening behaviour
Overlapping Diagnoses
Disabling characteristics of FAS may also be compounded by “overlapping diagnoses,” meaning
that the child has been diagnosed with other conditions as well as FAS. Accurate identification
is important for developing an appropriate intervention and treatment plan.
Common overlapping psychiatric diagnoses include:
n Attention Deficit Disorder (ADD)/Attention Deficit Hyperactivity Disorder (ADHD)
n Attachment Disorder
n Autism
n Oppositional Defiant Disorder
n Conduct Disorder
Positive Characteristics
Characteristic features or behaviours associated with FAS may also serve as strengths. It is
important to recognize and reinforce these strengths so that they don’t wane. Some positives
may include the following:
n creative intelligence (e.g. artistic, musical)
n perseverance (determined, persistent, willing, committed hard workers, involved, energetic)
n highly moral, deep sense of fairness, rigid belief systems
n strong sense of self
n friendly, trusting
n loyal, loving
n affectionate, compassionate, gentle
n tactile, cuddly
n concerned, sensitive
n love children, animals, nurturing—devoted partners and parents
n highly verbal
12
A Guide for Daily Living
n exceptionally good long term visual memory
n spontaneous, have lots of energy
n curious and questioning, have sense of wonder
n rich fantasy life (poets, writers, wonderful story tellers)
n great sense of humour
13
Myths
Myths
Common Misconceptions
Our lives would have been
So much less complicated
If all those born with A.R.B.D.
(Alcohol Related Birth Defects,)
Were also born with F.B.H.
(Flourescent Blue Hair.)
—Leon’s Mom
Dr. Ann Streissguth (1997) identifies seven common myths surrounding FAS—based on more
than twenty years of work in the field—which she shares with us here:
There are several widespread misconceptions that can be detrimental to understanding the
complicated life circumstances of individuals with FAS/FAE and responding appropriately to
their needs. Before people can effectively help these individuals, they must understand the
true nature of their disability. The following seven statements that are frequently assumed to
be true are, in fact, common misconceptions:
1. Myth: People with FAS/FAE always have mental retardation.
Although it is true that FAS/FAE is caused by prenatal brain damage and every person
with FAS/FAE has specific, individualized cognitive strengths and weaknesses, not all people with FAS/FAE have mental retardation. For example, as one study (Streissguth, Barr,
Kogan, & Bookstein, 1996) found, only 25% of 178 individuals with the full FAS were classified as having mental retardation by an IQ score below 70. In fact, it is possible for an
individual with FAS/FAE to have an IQ score within the normal range. FAS/FAE diagnostic
centers such as the one at the University of Washington Medical School, see individuals
with broad spectrum of IQ scores. Only the most severely affected children—those with
clear microcephaly and other physical malformations—are easily detected at birth.
2. MYTH: The behavior problems associated with FAS/FAE are the
result of poor parenting or a bad environment.
Because people with FAS/FAE are born with some brain damage, they do not process information in the same way as most people and do not always behave in a manner that others
expect them to. This brain damage, in fact, can permeate even the best environments to
cause behaviour problems and present parenting challenges. Parents and caregivers need
help and support, not criticism. Of course, a loving and understanding environment helps a
child with FAS/FAE. But its absence isn’t the primary cause of the disability.
3. MYTH: Admitting that children with FAS/FAE have brain damage
means that society has given up on them.
Some people believe that acknowledging the brain damage that accompanies FAS/FAE will
depict these individuals as hopeless and devoid of treatment options. Yet, society spends
millions of dollars developing treatment procedures for children born with more obvious
14
A Guide for Daily Living
birth defects and for people sustaining brain damage in more noticeable ways (e.g. auto
accidents). As of 1997, the research to understand and ameliorate the specific neuropsychological and cognitive impairments associated with FAS/FAE has not yet been conducted.
These individuals are in no way hopeless, but their needs have been sadly overlooked in the
allocation of societal resources.
4. MYTH: Children eventually outgrow FAS/FAE.
FAS/FAE lasts a lifetime, although its manifestations and associated complications vary
with age. Children with brain damage (including those with FAS/FAE) usually require a
longer period of sheltered living, and many need a stronger than usual support system to
achieve their best level of adaptive living. Understanding this can help families plan effectively for structured transitions between school and work and can help them spare their
children with FAS/FAE the expectation that they should be or must be independent at age
18 or that it is shameful to ask for help.
5. MYTH: Diagnosing children with FAS/FAE will thwart their
development.
Diagnosing is the art or act of recognizing a disease from its symptoms. At a practical level,
it is a method of grouping people with some common characteristics together so others like
them can be identified, the cause can be identified, and treatments can be provided. The
problem is not the diagnosis, but the current lack of scientific knowledge about how to treat
the disease. An accurate diagnosis does not thwart development in any way whatsoever; it
simply alters unrealistic expectations. Most individuals who are diagnosed, and their families, actually feel a sense of relief.
6. MYTH: It is useless to diagnose FAS/FAE because there is no “real”
treatment approach.
This attitude isn’t taken toward any other incurable diseases (e.g., childhood autism). Why
should it be invoked for FAS/FAE? Any family is in a better position to raise a child once
members know the child’s diagnosis. Once an individual is diagnosed with FAS/FAE, family members and social services workers can customize developmental approaches and goals
to ensure that the individual reaches his or her personal potential. A diagnosis helps everyone to understand behaviors that would otherwise be incomprehensible and helps families
explain these behaviors to others and to respond more appropriately themselves. A diagnosis helps families build networks of support with others experienced with FAS/FAE. Parents and the individuals themselves need diagnostic information in order to behave rationally and respond realistically. In addition, when no treatment is known, then the acknowledgment of people with this diagnosis motivates the development of appropriate treatments
and remediations. Diagnosis provides visibility, and visibility prompts solutions.
7. MYTH: People with FAS/FAE are unmotivated and uncaring,
always missing appointments or acting in ways that society
considers irresponsible or inappropriate.
People with FAS/FAE usually care tremendously about pleasing others and want desperately to be accepted, but their basic organic problems with memory, distractibility, processing information and being overwhelmed by stimulation all work against their desires. They
simply have difficulty understanding the meaning and interrelationships of a complex world
15
Parenting Children Affected by FAS
that complicate their daily lives. In addition, the repeated experience of failing to meet
expectations can generate a general reluctance to meet challenges, even in someone with
the best intentions. Some people with FAS/FAE are now learning strategies and techniques
for working around these problems.
16
Brain
wiring
Information Processing
I am a brain cramp, never thinking of the right subject at the right time.
It seems like my brain goes on screen saver
or my input device has put a virus in my brain
to clear my memory of my train of thought
and needs a jolt to snap out of it.
But my brain is always chugging away.
—Ken, age 17
FAS significantly impairs information processing. This is one of the most devastating characteristics of FAS, since our ability to process information impacts so many areas of our day-today lives.
FAS affects at least four important components of information processing (adapted from Morse,
1993):
1. Cause and effect
the ability to translate information into appropriate action, or judge
the link between action and consequence
2. Generalization
the ability to take information learned from one situation and apply
it to another
3. Sorting, classification, inference and abstraction
the ability to perceive and understand similarities and differences
in people, places, things and events.
4. Prioritization, prediction, production and sequencing
the ability to assess a situation, request direction, or identify similar circumstances and take appropriate step-by-step action.
The Effect
FAS involves a serious information processing deficit.
The brain link between understanding the information supplied (request) and performing the
action required (response) is defective.
An individual with FAS has difficulty translating knowledge learned from one situation into
another. For the FAS child, a similar situation is new and may bear no resemblance to anything which s/he may have previously experienced. Previous rules do not necessarily apply in
the new situation.
17
Parenting Children Affected by FAS
Asking a child with FAS to repeat instructions does not ensure compliance or understanding,
but asking them to demonstrate or to explain in their own words will help to ensure understanding.
Developmental delays become more obvious with age, as the gap widens between the alcoholaffected child and their age-peers.
The problems are neurologically-based, caused by damage to the developing brain. Affected
children often have behavioural and emotional problems—secondary disabilities. A good environment may reduce the impact of the neurological damage.
18
4 S’s
Plus C
Structure, Supervision,
Simplicity, Steps
and Context
The FAS/FAE child is not a hopeless case, he/she is simply a nowhere child,
never quite fitting into any setting.... There needs to be radical changes in our
classroom structures and attitudes if we are to give these children a chance to
develop and maximize their unique potential.
—Maureen Murphy
Taking these information processing deficits into account, clinicians and educators who have
worked with children affected by FAS stress the importance of the following factors, “The 4 S’s
+ C,” as described by Maureen Murphy (1991):
Structure
Create a structured environment for children with FAS which includes choices within clear
and predictable routines.
Supervision
Carefully supervise children with FAS so that they do not get into trouble or place themselves
in dangerous situations.
Simplicity
Offer simple directions and orders, stated briefly in simple language that you know the child
understands, rather than the elaborate verbal justifications and explanations often given by
parents and teachers.
Steps
Break down tasks into small steps and teach each step through repetition and reward.
Context
Teach skills in the context in which the skills are to be used, rather than assuming children
will generalize from one context to another or understand in which situations the behaviour is
appropriate and when it is not.
19
A place
to start
Parenting Suggestions
If you’ve told a child a thousand times and he still does not understand,
then it is not the child who is a slow learner.
—Walter Barbee
It is important to remember that all children, alcohol affected or not, are first and foremost
individuals with distinct personalities, preferences, and temperaments. Parenting tips which
may work wonders with one child may prove inappropriate and ineffective for another.
The following section offers suggestions for parenting a child with FAS which have been effective for some children. Based on the input of many parents and professionals, these strategies
focus on effective communication and positive parenting.
Please note that this is not a definitive list which will always lead to good communication and
daily living skills. Remember that you are the expert on your own child. You likely know which
parenting techniques may or may not work with your child. Keeping individual differences in
mind, we invite you to adapt the ideas to suit your children.
Effective Communication
Offer simple directions. Break down tasks into small steps and teach each through repetition
and concrete reward.
n Begin all conversations with the child’s name and make eye contact.
n Be specific when telling the child what to do, such as “sit on that chair” rather than “get out
of the kitchen,” and “hang your coat on the hanger in the closet” rather than “put your coat
away,” etc.
n Realize that many words or expressions have more than one meaning and teach these
meanings. Children with FAS may be very literal in their understanding.
n Use the same words to express directions for daily routines, such as “brush your teeth”
rather than “clean your teeth” or “get your teeth done.”
n Be brief and keep directions short. The child may have a short attention span, even though
they may appear to be listening. Multi-step directions should be given gradually and only
as the child exhibits the ability to follow more complex directions. There is no definite
time-line as to when this may occur. For some children, understanding multiple directions
may remain a problem throughout their life.
n Give the FAS child separate instructions using their name. The child may not realize that
s/he is to follow group-directed instructions.
20
A Guide for Daily Living
n Speak slowly and pause between sentences to allow for processing. Auditory processing
may lag behind rate of speech. Repeat and restructure information as needed.
n When the child needs to focus on a task or listen to you, you may need to keep the environ-
ment as free from the distractions as possible (i.e. TV, radios, video games, other people, etc.)
An F/M transmitter/receiver (known as a body pack hearing aid) is very useful for screening
out distracting noise at school.
n Lists for older children that give step-by-step simple instructions on how to do things can be
a useful lifeskill for both common and unexpected situations. Teach the child how to use a
list and practice with role-play and simulation games.
n If the child does not know what to do next, jog their memory. Tell, demonstrate, show and
then find a visual way to tap into their memory. If the child cannot remember, remind them
and move on.
n Gentle reminders help produce a positive attitude.
n Link one task with another to help establish sequences (e.g. dinner comes after homework;
the bus comes after breakfast; story time comes after the bath.)
n Use expressive gestures when talking. Try varying loudness, inflection, tone, coupled with
hand signals.
n Use as many visual cues as possible to trigger memory and to aid comprehension. Be spe-
cific when labelling inappropriate behaviour (e.g. “John doesn’t kick” with an exaggerated
shaking of the head) and include visual cues to emphasize the desired action.
n Touch can be useful for teaching appropriate social distance from others. (e.g. place your
hand straight on the child’s shoulder and say “This is where we stand when we stand to
talk.”)
n Teach the child a visual or verbal cue to help them understand it is time to begin the task.
For example, you might end instructions with the word “now.” Use exaggerated facial and
body language. Use hand signals for behaviour cues with language.
n Help the child interpret social and behavioural cues of others. (e.g. “That person looks happy
because...”) Encourage the child to self monitor and to recognize context, social cues (i.e.
facial expressions, tone of voice, posture, etc.) and their own feeling state. Model these skills
(e.g. “How do you think you are (I am) doing right now? Things are getting wild. You (I) need
to slow down and take ten deep breaths while doing nothing.”)
n Help the child to express their emotions in acceptable ways.
n Encourage the use of positive self talk: “I can do this!” “I need to pay attention.” “I’m smart!”
“ I can figure this out!”
n Help the child develop skills for safe expression of feelings through use of metaphor, art,
play, and anger management strategies to provide a bridge to verbalizing issues.
21
Parenting Children Affected by FAS
Consequences and Positive Feedback
Processing deficits may make it difficult for the child to connect consequences and feedback to
their behaviour. Creating structure in expectations and consequences will aid the child in predicting outcomes and feeling secure in their environment. FAS children may disobey instructions due to lack of comprehension, memory impairment, or—like any child—wilful disobedience. Ask yourself if the child’s misbehaviour is due to lack of comprehension or wilful lack of
compliance. Recognize your child’s unique strengths and weaknesses, build on their abilities
and interests, and set realistic goals for performance. (for more on structure, see pages 19 and
24)
n Often children with language disabilities have difficulty with“why”-type questions. Help
them learn this format by using alternate forms such as “what is the reason?” or “what
caused this to happen?”, or restating as who, what, where, how and show me to invite input.
n Spend time discussing cause and effect relationships. Be patient with their delayed ability
to learn this relationship.
n Tell the child what to do, not just what not to do. Letting children know what to do gives
them a direction to take the behaviour and focuses on the positives while defusing the
negatives (e.g. “Chris, put your feet on the floor, not on the table.”)
n Encourage the child to “help” as a valued member of the family.
n Give immediate rewards or consequences and remind the child what the consequence is for.
Parents of children with FAS often notice that rewards lose their effectiveness, and are
constantly searching for new ways to motivate behaviour. For some children, stars and
stickers on a chart work well, while for others time on the computer or videos are effective.
Older children often accept the “cost” for the behaviour (e.g. no telephone privileges or being
grounded for breaking curfew) as worth it. The goal may simply become keeping the child
out of harm’s way.
n Be firm. Set clear, consistent limits. Don’t debate or argue over rules. Post family rules in
simple words and/or with pictures.
n Separate the child from the behaviour. The action may be “bad,” but the child must never
feel that s/he is a “bad” person.
n When removing a child from a situation to diffuse and calm down, once again separate the
child (not a bad child) from the inappropriate behaviour (e.g. “Your behaviour tells me you
need a time-out.”) Always return to the child when calm and reinforce that s/he is a good
person.
n Do not make threats that you cannot carry out. These children may take you literally. Also,
the child learns that there is no consequence when the threat is not carried out.
n Be very specific with praise and criticism. (e.g. “Joey, good sitting” or “Susie, good listening”
with a smile and a touch rather than simply “Good boy/girl.”)
22
A Guide for Daily Living
n Intervene before inappropriate behaviour escalates (this is a difficult thing to do—the
caregiver must be tuned into the child’s feeling state and behavioural cues all the time.)
n Designate a place for “quiet time” when the child feels overwhelmed. Encourage the child to
choose a place where s/he will feel comfortable and secure.
n Give the child positive acknowledgement and regard for just being themselves—as well as
for desirable behaviour.
Transitions... Things Change
Changes in a child’s life, such as moving or starting school, can be traumatic. Children with
FAS may also experience difficulty in the simple changes that occur every day, such as moving
from one activity to another. This may even be the case when the child is being asked to change
their focus from a less pleasant task to a more pleasant one.
For the major changes:
n Develop “hello” and “farewell” rituals between you and your child.
n Use photographs of actual people, places, and important things to prepare a child for such
events as moving to a new home, going to the dentist/doctor, going to the hospital or going to
a new school.
n The absence of a family member can be upsetting to the child. Use photographs of the
person and the place where they will be to explain their absence.
n If a child must move to a new foster or adoptive home, or is even attending a sleep-over, try
to keep the child’s daily routines as normal as possible. Consistency and routine will minimize negative impact.
n Acknowledge the child’s fears about abandonment and other separation issues. Be as reas-
suring as you can while still being realistic. Help them work through separation issues in
advance of an impending move.
For more minor changes:
n Establish routines so that your child can predict coming events.
n Offer structured, limited choices and encourage decision making. Help the child shape
their environment.
n Teach the child a visual or verbal cue to help them understand it is time to begin the task.
n Egg timers are a useful way to clearly define the length of an activity.
n Give the child advance warning that an activity will be over soon.
n Prepare the child for school the night before and allow the child to direct as much of this
activity as possible. For example, in planning what to wear, offer some limited and structured choices.
23
Parenting Children Affected by FAS
Structure and Routines
Build security into the child’s day by maintaining consistency. Create a structured environment
for children with FAS which includes choices within clear and predictable routines.
n Write down or diagram what needs to be done for the completion of a task. For example,
you might post photographs of the child engaged in each step of an activity such as brushing
teeth.
n Break down daily activities into specific steps—plan mini-routines within the larger rou-
tine. Do everything in the same way and in the same order every day (e.g. wake the child in
the same predictable way each morning.) This may help the child become more comfortable
moving between activities, and able to operate more independently.
n Encourage imitation of daily activities through representational play.
n Avoid situations where the child will be overstimulated by people, sound, light or move-
ment.
n Have a place for everything and everything in its place. Allow only one item out at one time
if the child is overwhelmed by excessive stimulation. Storing things together by a system
(e.g. by type, size, colour, etc.) may assist the child in developing independence within their
own environment. For example, if all the blocks are stored together, the child may learn
where to go get them without your assistance.
n Place labels on the outside of drawers, cupboards, shelves, and so on. Use single words or
pictures to indicate contents.
n If the child has difficulty understanding boundaries and private spaces, such as shared
bedrooms, marking off areas with masking tape may be helpful.
n Create a homework corner in a quiet place. Have the minimal but necessary “tools of the
trade” there at all times. Use creative language to name this separate, personal space (e.g.
the child’s “office,” “workshop,” “private library,” etc.)
n Alternate active times with relaxation.
n Help your child to meet children who will be positive role models.
Supervision
Alcohol-affected children may need careful supervision so that they do not get into trouble or
place themselves in dangerous situations.
n Remember that it is impossible to be everywhere all the time and that structures in the
environment can help support supervision.
n Because children with FAS have trouble understanding the link between behaviour and
consequences, they are typically the child in the group who gets caught, even though they
may not have been the child who initiated or carried out the action.
24
A Guide for Daily Living
n Given that you too must sleep, keeping the child’s bedroom fairly sparse can minimize the
potential for disaster! For the child who wanders at night, an alarm on the bedroom door
may be necessary.
n If the child approaches strangers, deal with it immediately in front of the stranger (e.g.
“This is a stranger, this is someone we do not know. We do not talk to people we do not know.”)
This may be difficult and embarrassing, but essential for reinforcing the concept.
Advocacy
The ability to work effectively with schools, doctors and support workers may be challenging but
is critical. As a parent, you are likely the best advocate for your own child. Expand your advocacy skills. Look for advocacy resources and workshops in your own community, and check your
local library for books on self-advocacy.
n Continue learning about FAS. Search out magazines, books, newsletters, movies and tapes
for information and support. Attend workshops and conferences. Share your information
with professionals involved in your child’s life. (see the Resource List on page 55 of this
manual for some ideas and a place to start.)
n Work beyond the label. Remind yourself and others that a diagnosis of FAS should not be
used to label limitations. Each child has different potential. The goal is to facilitate their
development so that their fullest potential is realized.
n Recognize that FAS is a relatively new area, and that it will take time for a formal “system”
to develop to help affected individuals and their families. Find people who share an interest
in the area to work with you and help you through the existing system.
n Join a support group and share your information. Parents in some communities have started
FAS-focused self-help groups. Other parents have found much comfort and support in groups
for parents/adopted parents of special needs or high risk children. Check your local community resource directory or self-help resource association for listings of groups in your area.
n Find a child advocate if necessary, someone who will champion your cause within a sys-
tem—be it the school system, the legal system, the medical system or social services. There
are formal child advocates within the system, such as the Child, Youth and Family Advocate
for the Province of British Columbia, as well as outside help, such as community advocacy
groups. You can also tap into the support of an “informal” advocate—such as the friend who
walks into the principal’s office at your side when you lobby for better supports for your
child at school.
n Become active in efforts to shape legislation and support research endeavours.
n Make sure you get support for yourself! (see section on Parents Needs, page 45)
25
Day to
day basics
Guidelines for Daily Living
We’re the mothers who are “different;”
Special Needs Adoptive Parents.
—And the uninformed will find us
As peculiar as our children
Who are daily being challenged
With birth defects they can’t manage....
—Leon’s Mom
Expanding on the parenting suggestions outlined in the previous section, here are some strategies for dealing with specific situations that make up daily living.
Please keep in mind that these are loose guidelines only, a place to start. Once again, these
suggestions have been effective with some children, but do not necessarily work for everybody.
Remember that each child is unique. It is important to analyse your child’s problem areas as
well as their strengths and adapt the environment accordingly.
Routines
Daily routines are essential. They help maintain consistency, and build structure and security
into the child’s day. Without them, little gets done.
n Break down daily activities into specific steps. Plan mini-routines within the larger rou-
tine. Do everything in the same way and in the same order every day. For example, wake
the child up at the same time and in the same predictable way every morning. This could
look something like this:
• enter room and say “Chris, time to get up.”
• open drapes
• turn on light
• gently nudge, stroke child
• pull covers back to ease transition from sleep to awake
• aid child in sitting up; make sure their feet are on the floor
• tell them what comes next
n Use calendars in the kitchen and bedrooms to list events. Write down or diagram what
needs to be done. For example, morning needs before school might be listed like this:
• get up
• get dressed
• eat breakfast
• personal hygiene (wash face, brush teeth, comb hair)
• get school things together (books, backpack)
• prepare a lunch
• put on coat and shoes
26
A Guide for Daily Living
n Post key family rules in simple words:
• no hitting
• gentle hugs
• sit when eating
n Alternate active times with relaxation. Limit the time the child is expected to work quietly
at a desk. Take “action” breaks.
n Prepare the child for school the night before:
• choose clothes
• make lunch
• put homework in a designated spot
Dressing
Again, dressing is a task that needs to be handled in a routine, concrete manner to help the child
learn and retain the skill.
n If a child can’t choose clothing, put entire outfits together on individual hangers in the order
they go on. Teach the child to put on clothes in the same order.
n Teach children how to sort clothing by a system, to help them learn to coordinate what they
wear.
n Teach buttons from bottom to top to help the child “see” the match better. Try velcro instead
of buttons.
n Teach how to tie shoe laces, but if this is difficult for the child, use velcro instead, elastic coil
laces that do not require tying, or slip-on shoes.
n Keep outer clothes in the same place (e.g. only the front hall closet or only the mud-room.)
Have a hook, at the child’s level, with the child’s name on it for their coat. Label a place for
their boots.
n For winter climates, pin a hand drawn thermometer beside the door (inside) with a red line
drawn on it at the temperature where heavy clothing must be worn. On the outside of the
door hang a real thermometer. If the outside thermometer reads the same as or lower than
the hand drawn line, winter clothing is put on.
n Have an extra supply of mitts, hats, lunch bags, shoes and any other items likely to get lost.
n If your child wears eyeglasses, have two pairs and keep one at school.
The Bathroom
Structure and routine are also helpful in the bathroom.
n Keep all personal grooming aids together in a container. Assign a colour to the child to
indicate their toothbrush, comb, and so on.
27
Parenting Children Affected by FAS
n If overly long showers are a problem, put a timer on the shower that shuts it off. If overfill-
ing the tub is a problem, use indelible ink to draw a line on the bathtub to prevent the child
from overfilling the bath.
n Post bathroom routines on the mirror. Use simple words with pictures. Use a colour code
system for hot and cold taps (e.g. red and blue) or pictures (e.g. a sun and a snowman).
n Keep the hot water tank temperature down or invest in a scald-guard faucet. This is essen-
tial for children who do not have a normal sense of pain and temperature!
Mealtime
Eating problems are common for alcohol-affected children. Some children over-eat, some undereat, some eat very slowly, while others never seem to feel hungry. Many children use food as a
comfort. Also, since children with FAS have poor impulse control, mealtime itself can be a
problem because the dinner table is full of impulsive things—play things like silverware, napkins, glasses and food. Anticipate that meals could be a problem and be flexible in your expectations.
n Children with FAS are often slow to gain weight, despite good nutrition. However, if the
child starts to lose weight for no obvious reason, or has persistent vomiting or diarrhea, a
medical check-up is needed.
n Allow ample time to eat.
n Establish a firm routine for meals at the table (e.g. we all choose what we eat from what is
prepared; the child must ask to be excused; etc.)
n Avoid spicy foods for young children if they react to strong flavours. Some children do not
have a distinct taste sense and prefer strong flavours, like lemon.
n Require that the child take at least one bite of everything. Have reasonable expectations of
portion size.
n If “eating all night long” or late night eating is a problem, establish rules about eating at the
table only and one light snack just before bed. You may find that sugar and food additives
are a problem.
n Use plastic tags on frozen food and use non-metallic wrap on left-leftovers or convenience
foods so that children do not inadvertently damage the microwave. Get rid of plates, mugs
and other dishes with metallic rims.
n A child with FAS may eat slowly because of poor muscle control or poor swallowing reflex.
Accept that FAS children may be sloppy eaters and have sensitive gag reflexes.
n Carefully control the temperature and texture of foods. The child may have hypersensitiv-
ity toward certain food textures. Food without some sort of texture may be rejected. Try
mixing in something a little rough. Conversely, a rough texture may be rejected.
28
A Guide for Daily Living
n Some infants seem not to “feel” nipples or spoons in their mouth. Some have a high palate
which hampers the use of a nipple.
n Manipulating forks and knives may be a problem. Allow use of fingers or a spoon, even for
older children.
n If the child is agitated or confused at meal time, you may need to keep routines the same
every meal:
• Use the same dishes for the child at every meal.
• Serve meals at the same time daily.
• Give the child a specific seat at the table. If possible, seat the child at the end of the table
away from others’ elbows. Seat the child beside a high tolerance child and avoid the
one(s) with whom the FAS child fights.
• Consider having the same meals on the same days. This helps children with sequencing
difficulties to “know” the day of the week. You can try this for school lunches, as well.
n Serve the FAS child first if they have trouble waiting for others to be served first. You may
want to try having the child serve: this lets them get up and do something physical several
times during the meal and gives them an important role to play during dinner time.
n Avoid putting dessert on the table until after dinner.
n If the child cannot reach the floor when seated and finds this uncomfortable, allow the child
to stand instead or place a step-stool under the child’s feet.
n Work on one kind of table manner at a time. Integrate a new “manner” only when the
previous one has been successfully used for a time.
n Avoid fast food restaurants at peak times when eating out. Look for quiet eateries with low
light and minimal noise.
n Reduce distractions at mealtimes. Avoid TV, radio and too much conversation. Save dis-
tracting socializing for after the meal—although this may be difficult to do as meals are
often a key socializing time for families.
Bedtime
Children with FAS often have difficulties with transitional periods and activities where there is
little or no structure. Bedtime contains elements of both, and can pose problems for children
with FAS from a very early age. Again, the key is to establish a firm and calm routine, as in the
following examples.
n Establish a definite bedtime and stick to it, even during summer holidays.
n Have a calming routine that starts an hour before bedtime (the child picks up their toys, has
a bath, brushes their teeth, gets into their pj’s, gets their hugs, goes to their room for story
time/quiet time, etc.)
n If the child wishes, have one light in the room, by the bed—all lights out except that light.
29
Parenting Children Affected by FAS
n The child may have one toy or book in bed with them—only the one they choose for that
night.
n If they wish, the child can have the radio on very low with reasonable relaxing music. “White”
noise in the bedroom (such as a fan or humidifier, very low music, or anything that makes a
low hum) can be calming. This helps relax them so they can go to sleep.
n Every time the child gets out of bed repeat the same identical words like a broken record.
(e.g. “This is your bed. This is where you are supposed to be.” If another light is turned on,
“This is the only light left on.”) Accept that the child might be in bed but not sleeping.
Sleep
Sleeping problems are also common, particularly for younger children. Patterns vary from
child to child. Many children with FAS need extra hours of sleep each night, while others seem
to require little sleep.
n A warm bath before bed may help the child fall asleep. A warm bath after a stressful day of
school can also be calming.
n Snug bedclothes are also helpful.
n A rocking crib can be useful.
n Establish bedtime rituals for saying goodnight which visually allow a transition from the
“getting ready for bed” routine to the bed itself.
n Keep furnishings in the child’s bedroom to a minimum.
n For children who wake up at night, have a list of acceptable things for the child to do in an
acceptable place.
n Safety-proof the house for night time wandering. Lock doors. Place locks near the top of the
doors so the child cannot reach the lock. Consider installing a single alarm system that lets
you know when the child has passed a certain point. Before that point, let the child wander.
Make sure that this area is entirely child-proofed. A gate across the bedroom door may be
useful.
n Encourage the habit of having the child sleep in their own bed.
n Many parents have found that it does get easier as the child gets older!!
Laundry
Laundry is an example of a complex life skill that may present difficulties for a child with FAS.
Laundry can be challenging as it involves following an elaborate sequence of steps, making
judgment calls (e.g. sorting clothes appropriately) and generalizing (e.g. dealing with different
combinations of clothing each time). Again, it is helpful to teach this skill step by step, with
demonstration and simple language.
n
30
Teach the child/teen to do laundry sorting by colour of clothing.
A Guide for Daily Living
n Break down laundry into specific steps. [i.e. open door, put in clothes, add 1 soap (only have
1 measuring cup available), shut lid, turn dial to dot, push in knob, etc.] Provide visual cues
with drawings.
n Buy an iron with an automatic shut-off.
Supervision
Children with FAS can easily get themselves into trouble due to poor impulse control and difficulties understanding cause and effect. They also tend to be overly friendly and trusting, even
towards strangers. It is important to supervise children with FAS so that they do not get into
trouble or place themselves in dangerous situations.
n Small children and most pre-teens should be in direct line of vision at all times. One-to-one
supervision is mandatory in strange places, on field trips, in stores, and so on. Do the best
you possibly can, but keep in mind that even supervision is bound to occasionally fail to
prevent problems.
n Some parents use a bungee cord to keep a small child close to them in public.
n If hyperactivity for the FAS child tends to increase with the day, shop with them first thing
in the morning. Shop at small stores where there is low noise, fewer people and good service.
n Teach your child how to protect themselves from danger. For example, meeting a new per-
son on the street does not mean that the person is no longer a stranger.
n Help the child to be aware of their environment. Walk in your neighbourhood together and
point out the landmarks. Make trial runs of new trips on foot or on the bus. It is helpful to
do this repeatedly from pre-school to adulthood.
n Make a telephone book for the child with addresses and phone numbers. This should be
small enough for the child to keep in their pocket. Keep a copy for yourself.
n Safety-proof the home. Place locks on outer doors. Lock up all medication, household clean-
ers, other potential poisons and power tools. Safely store knives, scissors, matches and
lighters. Cover electrical outlets. Erect high fences and keep gates locked. Give away any
poisonous plants. Never leave a lit cigarette unattended and dispose of used cigarette butts.
n Fire extinguishers are advisable in the kitchen.
n Always be on hand if a child/teen is cooking.
n Never leave a child with someone you do not know well.
n Assess whether the child can be left alone. Even some teenagers need supervision.
n Escort children to and from all activities.
31
Parenting Children Affected by FAS
n Arrange for recess and noon hour supervision at school.
n Try not to let the child know that you are supervising all the time. The child needs to feel as
independent as other children. Plan concurrent activities that legitimately keep you in the
child’s proximity.
Managing Hyperactivity
Hyperactivity is a common problem for children with FAS. Parents can help control the problem by carefully structuring the child’s activities and by reducing the amount of external stimulation.
n Limit TV-watching and avoid video games if this causes the child to become overstimulated.
Keep in mind that highly-charged social activities such as birthday parties may be overwhelming for a child with FAS.
n Alternate activities requiring attention (e.g. studying, washing dishes, etc.) with physical
exercise (e.g. running, tumbling, dancing, trampoline, etc.). Give your child opportunities to
be physically active. Sports such as soccer and gymnastics—and skiing/snowboarding for
older children—are excellent ways to use all that energy. These activities also promote
healthy self-esteem. Swimming is also a good physical outlet for many hyperactive children. However, group swimming lessons may be counter-productive. Private lessons may
be preferable.
n Avoid cluttered space. Clutter may increase hyperactivity.
n Make the home a calm place.
n Calming music is preferable to loud, frenetic music.
n Fluorescent lights may be bothersome. Children with FAS may be more sensitive to flicker
that others don’t notice. Use low or recessed lighting.
n Avoid situations where the child may be overstimulated by light, movement, sound, toys,
noise, colour, activities or crowds.
n Designate a calm, cosy, comfortable place for “quiet time” where the child can go when they
are overwhelmed. Make it clear that “quiet time” is not a punishment. It is best that an
adult be present while the child calms down.
n Avoid trying to have a child concentrate for long periods of time. Concentration is hard
work and physically tiring.
n Limit the number of visitors if this is overwhelming for the child. Try to have people over
when the child is asleep or not at home. Many parents have found a substantial increase in
energy levels when extra people are around, especially people the child doesn’t know.
n If anger is a problem, have a safe place for the child to express it in some physical manner
(i.e. screaming, kicking a ball.)
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A Guide for Daily Living
n Avoid activities such as pillow fighting or wrestling which can cause over-stimulation. Make
sure extracurricular activities do not cause over-stimulation. At the same time, do not
deprive your child of extracurricular opportunities. Sports or Boy Scouts/Girl Guides may
provide an excellent channel for the child’s energy, while boosting self-esteem and encouraging personal interests. The child needs the outlet, and you probably need the break!
n Ask yourself, “Does it really matter?” Don’t sweat the small stuff.
Managing Impulsivity
Children with FAS and Attention Deficit Hyperactivity Disorder (ADHD) tend to have poor
impulse control. They often have difficulties understanding cause and effect relationships, or
foreseeing long-term consequences for their actions.
n Teach the concept of “your turn” by using a physical object such as a “talking stick” which
could be a pebble or any small, portable object that is easily passed around—“if the object is
in your hand, it’s your turn.”
n Teach “walk, don’t run” by counting numbers between steps.
n Verbally label and redirect unacceptable impulsive behaviour as early as possible in the
child’s life (i.e. toddlerhood) and on each occasion. Do so in a calm, consistent manner with
visual cues.
n Learn to recognize the signs that the child is going to have a “negative event” and step in as
soon as the signs begin. Avoid, anticipate, act!
n If time out is needed, consistently use the same designated place. Avoid places used for
other important or fun activities (e.g. bedroom, play table, book corner, etc.). If possible,
choose a calm, uncluttered space that is used for no other purpose.
n Don’t hook into tantrums!! Allow each one to run its course. Help the child to calm. Make
sure the child is in a safe place where they cannot hurt themselves. If necessary, move the
child to a safer place (i.e. a carpeted floor.)
n In order to “look before they leap” (reflection), a child must have the language (words) for the
situation. Try to teach in simple terms with visual cues.
n FAS children have “good” days and “bad” days. Do not expect compliance today because
they had it yesterday. Always have a fall-back plan.
n Limit choices. Inability to choose from a variety of options causes intense frustration and
impulse control problems.
Sensory Considerations
Many children with FAS are hypersensitive to noises, touch, bright lights, hot and cold, sudden
movements, and pain. They may also be sensitive to small amounts of various stimuli (e.g.
people, noise and movement) all at once. This problem of overstimulation is noted in newborns,
33
Parenting Children Affected by FAS
especially those with NAS, and apparently some alcohol-affected individuals remain hypersensitive to sensory stimulation most of their lives. On the other hand, some individuals with FAS
are hyposensitive, meaning they have extremely high tolerance to sensory input and may even
seem impervious to pain.
n If the child is hypersensitive, avoid itchy clothing. Soft, loose material is more easily toler-
ated. Elastic, sock seams, ties under the chin, labels in the neck, tags, jeans seams, appliqués
with a scratchy backside, hair bands, barrettes and stiff shoes may cause problems. Solutions include:
• Remove tags from clothing.
• Wash all clothes 2 or 3 times before wearing.
• Turn socks and gloves with seams inside out.
n Avoid bright lights (particularly fluorescent) and sunlight reflecting from water, snow or
vehicles.
n Use sunglasses and tinted glasses (prescription and non-prescription) to reduce glare.
n Loud noises may be quite painful for the child’s ears, but use earplugs only under supervi-
sion.
n Loud music is often distractive because it seems to “switch off” what is being seen visually.
It is as though the child can have either visual stimulus or auditory stimulus, but not both
at once.
n Avoid crowded situations. Place child at the beginning or end of a line, not in the middle.
n Learn which foods seem to be too smooth or too rough. (see section on mealtime, page 28)
n Use soft play-dough or other smooth surfaces with which the child can feel and play.
n Use routine calming techniques when the child is overstimulated (e.g. sitting in a bean bag
chair, rocker, or hammock; taking a warm bath or shower; listening to quiet music through
headphones; etc.)
Social Skills
Individuals with FAS have difficulty relating cause and effect, generalizing, and learning from
non-verbal cues. As a result, a child with FAS may have trouble picking up social cues and may
not realize when they are acting inappropriately. Other children and adults tend to reject peers
who are not skilled socially or who act differently. Teaching social competence and how to
communicate with others serves to bolster their self-esteem and enhance their social well-being.
n Teach social skills carefully, consistently, and repetitively through modelling, role play and/
or practice.
n Teach appropriate social skills, such as:
• how to share and take turns
• how to ask for help
34
A Guide for Daily Living
•
•
•
•
•
•
how to interpret facial expressions, tone of voice, posture, etc.
how to deal with rebellious behaviour in peers
how to react when there is a disagreement with a supervisor
how to make choices
how to ask others if they can join in an activity
how to say “no”
and so on. Talk about each situation in some detail. Try to seize “teachable moments.”
Keep the tone light and natural, and the “lesson” brief.
n Teach what is inappropriate, such as:
•
•
•
•
standing too close
interrupting and talking non-stop
throwing things
not asking for help
n For a child who requires excessive body contact, structure the physical contact so that the
child learns what is acceptable and what is not. Gradually replace the excessive amount of
physical contact with visual and verbal assurances (i.e. a key word, phrase or sign).
Telephone
Telephone manners and taking messages pose problems for children with FAS because these
skills require memory work as well as understanding abstract concepts and appropriate social
skills. Teach by role-play:
n Have a large, erasable message board next to the telephone.
n Have an answering machine with a “record” function so that messages do not get lost or
numbers mixed up. Some parents have found the voice mail service through their local
telephone company very effective.
n You may consider having two phone lines, one for the children and a second which only the
adults answer.
Handling Time
Children with FAS have great difficulty telling time and understanding how much time has
passed. Dealing with time involves abstract concepts, and understanding abstract concepts is a
common difficulty for people with FAS. A 12 year-old child with FAS may still be unable to tell
time on an analog watch.
n Make time visual with paper chains, time-lines or other concrete objects to represent peri-
ods of time (e.g. 5 minutes). The adult takes responsibility for removing one object/link
every 5 minutes so the child can “see” time pass. Sand-timers and egg timers also work
well.
n Teach time using an analog watch or a clock face with hands that the child can manipulate.
Digital watches seem to work only if the child is looking at the watch when the specific time
rolls around.
35
Parenting Children Affected by FAS
n Even when a child has started to master telling time, they may still have difficulty under-
standing the concept that 9:45 is the same thing as quarter to ten, or that 10:30 and 10:40
are roughly the same time.
n The child may also have a poor sense of time. The idea of when time occurs has no meaning.
“Dinner is at 5 o’clock” means nothing, while “Dinner comes after...” may be easier for the
child to comprehend. Always relate events to other events to create a sense of the day and
the usual order of things. The words “after” and “before” are helpful when referring to time.
n FAS children who are in an established routine will follow that routine regardless of the
time. The fact that dinner may be delayed due to a late lunch is complicated information for
the child with FAS to process.
n Do not have high expectations about handling time. It may not be reasonable to expect a
child to be able to complete a certain amount of work in a specific amount of time. It is also
best to send a child from point A to B with an escort if you need them to be there at a specific
time. Give the child lots of time to get ready for an event and supervise closely.
n The responsibility for making sure FAS children/teens are where they are supposed to be
on time rests with the adult. Even some adults with FAS may require help in this area,
although many find this skill improves with age.
Teaching Ownership
Similarly, ownership and personal belongings are abstract concepts that are difficult for many
alcohol-affected children to understand. A child with FAS will often pick up something that
catches their eye and then drop it whenever they lose interest. Or, the child may take something
they recognize as having been left by someone else with the good intention of returning it. Unfortunately, short term memory dysfunction, distractions and other problems may cause them to
forget, leaving them open to charges of stealing. Work on teaching the child to ask before they
touch anything that is not theirs.
n Teach the child what belongs to them by placing a colour code or an initial on all their
possessions. The child then knows what to take (e.g. the item with the purple “J”) and what
not to take (everything without the purple “J”).
n Connect ownership to visual cues. The child may understand that a specific person owns a
specific item as long as the person and object are together, but not if the two are apart (e.g.
the child finds an object that’s been left somewhere.)
n If the child takes something that is not theirs, do not get caught up in an argument. Simply
state, “This .... belongs to ....” and return the object. Stealing should be dealt with firmly
with appropriate consequences.
n Objects of value should not be left around where a child may come across them.
n Keep in mind that malls are neither recreation centres, nor suitable places to hang out. It
is best not to allow unsupervised trips to stores. You cannot expect store managers to
understand FAS.
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A Guide for Daily Living
Handling Money
Money, and the value associated to it, are also abstract concepts. Not surprisingly, FAS-affected
children do not typically handle money well. The ability to handle money has a significant
impact on the potential for independent living.
n Children with FAS do not associate value to items and have difficulties making judgements
about the sum of money asked for an item. For example, $10 for a candy bar or for a bicycle
may both appear acceptable to a child with FAS.
n FAS children are at risk for being victimized by others. Children and teens should have a
very limited access to money without direct supervision. Money should be given in small
amounts. Pay for lunches at school ahead of time, or be at the store when expensive items
are being purchased. Use an account book to record every cent the child spends with the
child present.
n Monitor the child’s money. Where did it come from? The child may have sold a personal or
household item just because they were asked.
n Teach the child about money whenever you go to the store or in other real life situations.
n Be very cautious about the use of cheques, credit cards or banking machines. Set up a bank
account where cheques are not allowed and withdrawal amounts are limited. Many parents suggest that bank cards and cheques should not be used because they are open to
misuse.
37
Babies
with FAS
Special Considerations
for Infants
The Social Worker brought him;
A little warm blue bundle
With straight silky hair and huge dark eyes.
She said, “His mother had some problems,
But he will be fine....
—Leon’s Mom
The difficult task of caring for any newborn (adjusting sleep routines, feeding, etc.) is multiplied when caring for an infant with FAS. FAS affected babies tend to have a very hard time
during their first few months. They can be difficult to care for because of their various developmental problems (see Common Manifestations section, page 7). Most significantly, they have
troubles sleeping regularly, and eating and napping at predictable times.
Here are some additional parenting suggestions geared specifically to the special needs of
infants with FAS. Again, please keep in mind that these are suggestions only—not every
technique will work with every alcohol-exposed infant. Adapt to suit the needs of your own
baby.
Sensitivity
Infants with FAS, and especially those with NAS, may be extra-sensitive to the stimulation
around them, particularly to sound and touch.
n Speak softly and hold them gently. Don’t rush when picking them up.
n Many babies with FAS are unable to “screen out” all the stimulation around them. Control
the amount of stimulation the baby is exposed to.
n Each baby is unique in how they are affected by sound and touch. Notice what upsets them,
as well as what calms them.
Illness
Some infants with FAS have weaker immune systems and are more susceptible to illness than
other babies.
n The infant should not be exposed to environmental irritants such as tobacco smoke.
n Keep the infant away from people who are sick because of their compromised immune
system response.
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A Guide for Daily Living
Crying
Alcohol-affected babies are often tremulous and irritable. It may seem that they are crying
constantly. Avoid, if you can, letting your baby get to a state of frantic crying. Get to know what
your baby likes, and tell other caregivers how the baby likes to be handled.
n Wrap the infant snugly in a receiving blanket, with the arms tucked in close to the baby’s
chest and legs wrapped in a bent position towards their tummy.
n Babies are soothed by sucking. Guide the child to its thumb. A pacifier may also be helpful.
Do not add incentives such as honey on a pacifier or leave the child to nurse alone on a
bottle of juice or formulae/milk, because this may cause ear infections and/or serious tooth
decay. It is advisable to consult with your dentist.
n Other kinds of gentle motion, such as walking or slow movement in a baby swing or stroller
may help. A car ride may be soothing, as well as any motion that produces gentle vibration
and a low, soothing, humming sound.
n Comforting sounds may also help. Try quiet music, singing or gentle talking.
n If your baby usually enjoys being bathed, a warm bath may help to settle and calm them.
Feeding
Feeding difficulties are common. Infants with FAS often have poor coordination and weak
sucking reflexes which contribute to nursing difficulties. They can easily become fussy because
they can’t get the nourishment they need—nourishment which is crucial because of their low
birth weights.
n Reduce external stimulation. For example, feeding the baby in a darkened, quiet room will
help them relax and focus on sucking.
n Wrapping them in a blanket may help to calm them during feeding.
n Press chin upward in a gentle, rhythmic pattern.
n Stroke lips and gums gently before giving breast or bottle.
n If bottle feeding, try nipples with different shapes until you find one that works well.
Sleep
Infants with FAS may have erratic sleep patterns, and no predictable sleep-awake cycle. They
may have trouble getting and staying asleep. Also, many tend to have short sleep periods, both
day and night. This can be exhausting for parents.
n During sleep times, place in a quiet area, lower lights, and wrap snugly in a blanket.
n When the baby starts to wake up, gently rock the bed or rub the infant’s back, either to ease
back to sleep or to aid transition to being awake.
39
Parenting Children Affected by FAS
n Bedtime routines are very important (see Guidelines to Daily Living). Put them to bed in
the same bed each night, and provide a constant soft sound to drown out other noise (e.g.
gentle music, humming of a fan, etc.)
n If your baby usually enjoys being bathed, a warm bath may help them sleep.
n Singing softly to them may also help.
Take Care of You
Caring for any infant is tiring, but looking after a baby with FAS can be particularly exhausting. In the first few weeks and months, when everything’s still so new, parents of infants with
FAS often experience frustration and feelings of inadequacy. It is important to take care of
yourself to avoid burnout. Your baby depends on you. Building a support structure and connecting with health professionals can help you feel more successful in meeting your infant’s
special needs. Organizing supports and arranging for respite care is crucial for your own wellbeing.
n If the baby’s crying happens at the same time every day, try to call someone before it starts
to give yourself a change before you reach your limit. If you have a partner, take turns with
the baby. Treat yourself with extra kindness. Sleep when your baby sleeps, take a hot bath
and make sure you eat properly.
Please refer to the section Parent’s Needs on page 45 for more ideas on taking care of yourself.
40
Teens
with FAS
Special Considerations
for Adolescents
Driving north along Highway 101, from northern California into Oregon, we
see spectacular scenery.... On a recent trip with my husband, Ron, along that
route, I noticed a relationship to our lives as parents of 14 year-old twins with
ARBD. At the time, I had no idea of the crisis we would face when we returned
home from that trip nor the months of panic and pleading for help just ahead
of us. Rather, I had a brief glimpse of beauty rather than tragedy, of being
formed rather than falling apart.
Soon we were home again, and reality struck a heavy blow. The lesson I had
begun to learn was forgotten as we faced anger, swearing, being called losers,
doors slamming, being pushed out of the way, stealing from us and friends,
lying, and running away repeatedly for different lengths of time. Most of
these behaviours were new and we panicked. We had no idea how to deal with
them.
—Bev, adoptive parent
Adolescence is a transitional period from childhood to adulthood. Like any major life transition, it is usually accompanied by crisis. People with FAS often experience many of the same
crises as other adolescents—adjusting to sexual maturity, becoming less reliant on parents
and family, establishing areas of independence, and planning for a fulfilling role in society as
an adult (Streissguth, Ladue & Randels, 1988).
It is often difficult to separate these “typical” teen issues from the disability issues caused by
FAS. However, teens with FAS—like those with any developmental disability—have special
needs during adolescence.
Parents of a teen with FAS are faced with a range of challenging issues such as:
• sexual maturity in a developmentally disabled person
• their teen’s plateauing academic skills and decreasing satisfaction with school, and need
for work and social skills
• their teen’s high risk for exploitation, peer manipulation, school expulsion and/or involvement in the criminal justice system
• managing their adolescent’s leisure time, interpersonal relationships and independence
(Please see section on adolescents in Common Manifestations, page 9.)
The following strategies build further on the Parenting Suggestions and Guidelines for Daily
Living outlined earlier in this guide, and are geared for coping with adolescents with FAS.
Again, while these suggestions have been effective with some adolescents, they may not be
appropriate for everybody. As always, remember that your teen is unique. Adapt your strategy
to suit their individual needs.
41
Parenting Children Affected by FAS
Structure and Supervision
Streissguth, Ladue & Randels (1988) summarize the best method of coping with adolescents
with FAS in three words: “STRUCTURE! STRUCTURE! STRUCTURE!” Parents have the
difficult task of finding a balance between permitting freedom appropriate to the child’s developmental level, while providing enough structure for protection and growth. Follow your instincts and resist pressure from family members, other adults involved with your child, and the
teen him/herself to lessen control and let the teen “learn from their mistakes.” The risks are too
great.
n Continue to provide a safe, structured environment and clear, predictable routines.
n Clear, consistent expectations and behavioural consequences are still necessary.
n Supervision cannot be decreased in adolescence. Although a child may be chronologically
fifteen, their mental/emotional functioning may be at a lower level.
n Teens with FAS are easily influenced, and vulnerable to peer manipulation and negative,
destructive behaviours such as sex, drugs, alcohol and crime. Carefully monitor social activities and structuring of leisure time. Do not leave alone for an extended period of time.
n Encourage the teen’s talents (e.g. music, art, athletics, Special Olympics, etc.) to discourage
non-constructive use of leisure time. Identifying strengths and interests is also useful when
looking for an appropriate job setting.
Life Skills
As the teen’s academic skills plateau, it is important to emphasize work, social and daily living
skills. Adolescents need help with day-to-day language skills, interpersonal relationships, managing money, making purchases, looking after their own health, looking after their appearance
and clothes, and so on.
n Teach the teen about sex and birth control as you would any hygiene or care issue (i.e. be
open, use language and concepts appropriate to the child’s developmental age, repeat regularly, seize the teachable moment, have appropriate teaching aids and methods available,
etc.) Sex and birth control are important issues for teens with FAS. They have a normal sex
drive, which causes problems when coupled with their poor judgement and impulsivity—
they are often easy targets for sexual exploitation, both as a victim and a victimizer. Again,
supervision is key—like all teens, don’t expect that they won’t want to try sex just because
they’ve been told not to.
n Children with FAS are at high risk for becoming chemically dependent because of family
histories of alcoholism. Studies show that alcoholism is a disease that is passed on from
generation to generation, whether the child lives with the alcoholic parent(s) or not. Adolescents are particularly vulnerable as they are exposed to many more negative influences.
A teen’s desire to fit in, coupled by poor judgement and impulsivity, can lead them to substance abuse. Show them alternate ways of having fun, dealing with their feelings, and
being accepted by others.
n Help the teen find “sheltered” employment opportunities where the employer understands
that they have hired an individual with a significant disability. The job environment should
42
A Guide for Daily Living
be one where there is structure, order, and routine, and where the adolescent will be supervised by adults who are patient and understanding of the teen’s limitations.
n You may need to accompany your teen to and from work to make sure they get to their
destination, or designate someone else to do this.
n Individually structured volunteer placements can help a teen with FAS contribute to the
community and develop a sense of participation, accomplishment and responsibility.
n You may always have to “remind” the individual with FAS when things must be paid, even
into the adult years. Ideally, establish the routine of paying bills as soon as possible.
n Teens with FAS are susceptible to depression and loneliness. They may be rejected by their
peers due to impaired social skills or because they are different. For people who have
difficulties making and keeping friends, holding down a job or achieving at school, depression, loneliness and low self-esteem are normal. Psychological counselling is a healthy
option to deal with depression and other mental health issues that may arise. It is important to find a counsellor who is experienced working with individuals with FAS or other
neurologically-based disabilities.
n Let go of high expectations. Relax about your child’s level of achievement and focus on their
feelings of self-worth, satisfaction and well-being.
Adolescents with FAS in the Justice System
As children with FAS reach adolescence, they are at increased risk for involvement with the
justice system. Their poor judgment, impulsiveness, inability to anticipate consequences, and
seeming inability to alter their behavior as a result of those consequences appears to make
them particularly susceptible to trouble with the law. Streissguth et al.’s (1996) follow-up
study of adolescents and adults with FAS /FAE found that approximately 60% had experienced some involvement with the law. Forty percent did not!
Teens with FAS/FAE have been charged with offences ranging from vandalism or mischief to
more serious offences of theft and assault. They may be easily led and manipulated by more
street-wise teens. However, in a recent study in B.C., youth with FAS were no more likely to
commit the offence with a group than on their own.
Teens with FAS/FAE are also victims. Their inability to anticipate dangerous situations may
put them in the wrong place at the wrong time. They may be too trusting of people, including
strangers, whom they consider to be “friends”. Inappropriate social skills may make them the
scapegoats in the teen peer group.
For both perpetrators and victims, alcohol and drug use is often the driving influence.
It is important to remember that having FAS in and of itself does not cause criminal behaviour.
Many other factors combine to result in this outcome. The advice to parents to closely monitor
their teen’s activities is the key factor in preventing involvement with the justice system.
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Parenting Children Affected by FAS
Take Care of You
Respite care is just as important for caregivers of adolescents affected by FAS as it is for
parents of younger children. The adolescent years can be particularly exhausting as you are
dealing with new stressors on top of the many special needs you have been coping with since
infancy and childhood.
Please see section on Parents’ Needs on the next page.
44
Take care
of you!!
Parents’ Needs
We felt like prisoners in our own home because we
dared not expect friends or grandparents to manage the children in our absence. We had never heard
the word “respite.”
—adoptive parent
Parenting can be challenging even at the best of times. Parenting a child with FAS is often
even more demanding, frustrating and exhausting. As a parent, it’s important not to lose sight
of your own needs—those things that get lost or overlooked when you’re preoccupied with
meeting your child’s special needs on a day to day basis. Taking good care of yourself is a
crucial part of your job. After all, you are probably the most important person in your child’s
world. How can you effectively support your child if you burn out yourself?
Take Care of You
n Get adequate sleep. Children with FAS have difficulty sleeping, so you will likely have
trouble getting enough rest for yourself. Learn to rest when your child is napping. If your
child doesn’t nap, arrange for someone to take over once a day so you can rest.
n Develop a repertoire of stress reduction strategies that work for you. Most people have
difficulty making time to deal with stress, but it’s so important for your physical, emotional
and mental health—particularly if you’re dealing with the extraordinary stress of caring
for a child with special needs.
n Make time for yourself (and your partner). Get some fresh air, keep a journal, or read a
book.
n Do something physical (e.g. walk, jog, swim, etc.)
n Nurture yourself.
n Maintain a sense of humour. Let yourself laugh.
n Maintain a sense of yourself beyond your child.
n Don’t forget to breathe.
n Let the crisis pass. There may be another, but keep in mind that this too will pass.
n Try to maintain a positive attitude about your ability to manage the day-to-day and long-
term stresses associated with parenting your child.
45
Parenting Children Affected by FAS
n Establish reasonable expectations. Don’t expect yourself to be able to do everything for
your child. Focus on what you can do and seek help for things you can’t.
n Let go.
Respite
n Arrange time away for yourself on a regular basis. Caring for children, adolescents or even
adults with FAS can be demanding and tiring. If you are co-parenting, make an arrangement with your partner so that one of you gets a night or afternoon off while the other stays
at home, and vice-versa. You might also consider trading time with another family raising a
child with FAS. It is also important to consider arranging substitute child care or longer
term respite care which can be arranged through a social worker or formal program. Many
parents of children with FAS find that respite care is crucial to the well-being of the family.
n Babysitters typically burn out because they often don’t have the experience of dealing with
children with FAS. Have the sitter come to visit a few times when you are home, and give
them tips on how to deal with your child’s behaviour. Prepare your child for the babysitter
by talking about what s/he will be like, and rehearsing appropriate behaviours.
n Speak to a social worker at the Ministry for Children and Families to find out more about
respite care or other family support services that are available.
Get Support
It is important to get support for your own needs, issues and feelings.
n Make a list of every person you know who can help you. Include family, friends and commu-
nity groups. You have an important, difficult job, and you don’t have to face it alone—it
takes a whole community to raise a child, particularly a child with special needs.
n Tap into available resources, like the ones listed at the back of this booklet.
n Find other parents in your community who have children with FAS. Nobody understands
your struggle like someone who’s “lived it.” Share information and support. Join or create
a support group. Surround yourself by people who “get it.”
n The Warm Line (604) 589-1854 volunteers are knowledgeable and experienced caregivers
of children with FAS. Staff can provide information and support on caring for children
affected by FAS. The Warm Line staff are available, on call, 24 hours a day.
n If you have access to the INTERNET, join an FAS chat group or listserve like FASLink,
hosted by the Canadian Centre on Substance Abuse in Ottawa. (for more information, see
page 60 of the Resource section)
n Talk to a counsellor. Consider getting counselling for the rest of the family as well. Be sure
to find a therapist who has experience with FAS and other neurologically-based disabilities.
Unfortunately, there are still professionals who are not sensitive to FAS and related issues
who may simply see families struggling with challenging children as dysfunctional families.
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A Guide for Daily Living
Get referrals to appropriate professionals through FAS resources (see listing in the back of
this manual, starting on page 55) or from other families touched by FAS.
n Keep on educating yourself about FAS. Books, magazines, newsletters, movies and tapes
can provide not only practical information but also a source of support and inspiration.
n Take a realistic and practical approach to getting professional and community support.
Recognize that FAS is a relatively new area—it will take time for a formal system to develop to meet the needs of people with FAS and their families. Advocate for yourself and
your child. Educate the professionals who work with your child, and the community at
large. Find people with a strong interest in the area to work with you and help you through
the system. (for more on advocacy, please see page 25)
n If you are a foster parent, contact the After Hours Foster Families Support Line at 1-888-
495-4440. (for more information, see page 66 of the Resource section)
n The 53 hour B.C. Foster Care Education Program includes a module on FAS/E, NAS for
foster parents. This module assists foster parents in understanding the implications of
caring for children whose development and behaviours may be influenced by these conditions.
Hang In There
You’ve already demonstrated your commitment to your child and to yourself by making it this
far—by weathering the struggles of parenting a child with special needs, hanging in there no
matter how much your child has tested or challenged you, and even just by picking up this
book. It’s probably been hard, but you’ve made it this far. Keep on hanging in there the best
you can, and don’t forget to take care of yourself.
Even if you’re faced with what seems like the worst case scenario—the interventions have
failed or come too late, the child has left home or the child has been removed from the home—
this doesn’t mean you’ve failed as a parent. It is helpful to remember that you’re not there to
make a person’s life—you’re there to be with them while they live it. You can help them, hold
their hand and support them, but there are some things you cannot control. Being a parent
doesn’t mean you have to live with the child twenty-four hours a day. Being a parent means
being an advocate, somebody sending that child love from somewhere in the world, making
sure that the child gets services, and providing a safe place for the child to phone home to. In
some circumstances, parenting from a distance is the best way of taking care of yourself and
taking care of your child.
47
Getting a
diagnosis
Assessment and Referrals
Sunnyhill Hospital, in Vancouver.
A gloriously blue and gold September day...
But I felt myself dying, just a little,
With that first positive diagnosis...
—Leon’s Mom
A medical diagnosis of FAS is important. There are other disorders that have similar symptoms to FAS (“look-alike” syndromes such as Williams Syndrome, Noonan Syndrome, DiGeorge
Syndrome, etc.) that may need to be ruled out before a diagnosis is made.
An accurate diagnosis helps parents and professionals better plan for the child’s needs and
care. It is important for implementing appropriate medical, educational and social strategies,
and for accessing needed services and supports.
Early diagnosis is recommended to help maximize the potential outcome for the child. Also, by
adolescence, many physical features change, making diagnosis more difficult. However, it is
never too late. If you suspect your older child or teen has FAS, it is still important to get an
assessment as soon as possible.
FAS is a medical diagnosis—not a label
Some parents worry that a diagnosis will place a negative “label” on the child—a label which
will handicap them unfairly in school and in social situations.
However, FAS is an invisible disability—it is still not widely known, nor is it easily recognizable by physical characteristics. For example, when a child is in a wheelchair, there is no
question that the child has a disability. When people do not recognize what is different about
a child with an invisible disability, they may be inefficient in trying to help that child reach
their potential. The child may already be labelled as “bad,” “slow,” or “hyper” by a teacher or
other adults who wrongly attribute the child’s misbehaviour to laziness, lack of motivation,
obstinacy or bad parenting rather than a deficit in information processing. An accurate diagnosis is a relief for many parents, as it helps to explain the academic, social and behavioural
difficulties they have been encountering at home and at school. It serves as an important first
step for getting outside recognition and support for the child’s special needs.
It is also important to remember that each child with FAS is first (and foremost) a child—a
child who happens to have symptoms of an invisible disability. As a parent, you can choose
which people you tell that your child has FAS. You may decide only to tell people in those
situations (e.g. school, hospital, respite care, social worker’s office, etc.) where it may be helpful
to you and your child.
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A Guide for Daily Living
Referrals
Assessment at any age should be multi-faceted and cover all aspects of functioning. It is
recommended that your child be assessed by a doctor who has experience with FAS. A background in dysmorphology (birth defects), paediatric neurology or genetics is especially important where Partial FAS, ARBD and ARND are concerned. A diagnosis of Partial FAS or ARND
is usually made in conjunction with a psychologist after a psycho-educational evaluation. Again,
it is important that the psychologist be knowledgeable about FAS.
In British Columbia, Sunny Hill Health Centre for Children offers medical assessment and
referrals through its Child Development and Rehabilitation Program—call (604) 453-8300 for
more information. Questions relating to clinical service, consultation or educational support
may be directed to one of the five geographic liaison staff or the Team Leader of the Substance
Exposure Resource Team (S.E.R.T).
If you are a foster parent and believe that the child placed in your care could benefit from an
assessment of FAS, talk to the child’s social worker about arranging a referral for the child.
Keep in mind that FAS is still a growing area, and it is taking time for the medical community
to develop a fully-coordinated response. In some parts of the country, there are very limited
services available. When services do exist, there are frequently long wait-lists. Don’t let this
discourage you. If you are told there are no options in your region, keep looking! Provincial
contacts listed in the Resource section of this guide can help direct you to the nearest available
help. The FASLink service on the INTERNET may be useful for connecting with other people
(both parents and professional) who can guide you to resources.
See Resource List on page 55.
Medical Assessments
Unfortunately, there is currently no “laboratory test” that confirms whether or not a child has
FAS. Diagnosis is a clinical judgement based on assessment of the child with regard to specific
symptoms and criteria (see FAS Diagnostic categories, pages 2-3, and the Appendix, A-1-A-3),
and a medical history which may include the mother’s drinking pattern during pregnancy.
To prepare for an assessment, gather an extensive history of the child and their family background. If possible, include the following information:
• maternal alcohol, drug or tobacco use during pregnancy
• mother’s illnesses during pregnancy
• birth and health history (birth weight, developmental milestones)
• placement history
• assessments by other professionals
• records of height and weight over the years
• photographs (it’s helpful to provide one good full-face picture per year if available)
• any siblings known to have FAS or other alcohol related birth defects
• any history of Neonatal Abstinence Syndrome (NAS)
• a list of “problem” areas in social, behavioural and adaptive functioning (a compilation of
information by parents, other caregivers and professionals)
Assessments should be updated every 2-3 years.
49
Parenting Children Affected by FAS
Adoptive parents can request pertinent data about their adopted child through the agency or
provincial Ministry office that finalized the adoption—usually in the city where the adoption
occurred. In British Columbia, you may obtain non-identifying information about your child’s
birth family and pre-natal history through Vital Statistics in Victoria. Send the relevant office
or agency proof of your adoptive parent status, and ask for information pertaining to alcohol/
drug use in the birth family. This should be done well before proceeding with an assessment.
Adopted persons over the age of eighteen in most provinces (fourteen in Quebec) may place
their names on a provincial adoption disclosure registry to start the process of obtaining identifying information and possible contact and/or reunion with birth relatives. They must register in the province in which their adoption was finalized.
Dealing with a Diagnosis
Receiving a medical diagnosis is typically an intense, emotionally charged process. While it
may be a relief to have a reason for the child’s behaviour, it is normal for parents to experience
a range of emotions and discomfort when they first hear that their child has been diagnosed
with FAS.
As a parent, you may experience intense guilt or anger about your child’s condition. You may
feel anxious about the medical outcome, and be worried about future complications and risks.
You might be overwhelmed with feelings of helplessness and panic about how to manage the
condition, and be anxious about how to plan for the future. You will likely have to grieve the
loss of certain life goals for your child, and come to terms with the necessary changes in living
patterns due to the condition (Rathbun, n.d.b).
Dealing with a diagnosis of FAS or other medical conditions in children involves phases of
grief—impact, denial, anger, bargaining, mourning, acceptance and focusing outward. Families need recognition and support to work through this grieving process (see section on Parents’
Needs). Families can move towards acceptance and management of their child’s condition by
learning about the condition, getting support though the stages of grief and adjustment, and
actively developing strategies based on family and individual strengths.
Rathbun (n.d.d) has identified the following psychosocial tasks for successfully coping after
diagnosis:
1. Maintaining emotional distress within manageable limits (learning how to care while
detaching from overreaction)
2. Understanding medical and developmental needs, and how to meet them with new knowledge, motivation and skills
3. Preserving important relationships with others in a support network (stepping out of
isolation)
4. Regaining hope for the future (alleviating burnout)
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A Guide for Daily Living
5. Encouraging adaptive development for the child with FAS in family, peer, and school
roles/responsibilities by building on the child’s potential (including the characteristics of
having a chronic condition)
6. Maintaining stable, equitable family functioning (learning solution-focused instead of
problem-focused ways of coping)
Dealing with NOT Getting a Diagnosis
Some parents, after years of concerted effort, remain unable to get an accurate diagnosis for
their child. This can be extremely frustrating, distressing and invalidating. You may feel
stuck in limbo, unable to get on with the grieving process described above. The child’s difficult
behaviour continues without an explanation, and others may continue to blame your parenting.
An accurate diagnosis may be impossible to obtain for a number of reasons. There may be
limited information about the child’s pre-natal history, particularly in adoption situations,
making it impossible to confirm the birth mother’s use of alcohol during pregnancy. Also, it
may be difficult to accurately diagnose an adolescent or adult because many of the physical
features—particularly the characteristic facial features and growth deficiency—change and
become less pronounced with age. This is why childhood photographs are recommended to
accompany the diagnostic process, but even these are not always reliable as smiling faces can
distort the appearance of some of the classic facial features.
In situations where an accurate diagnosis is not possible due to gaps in the prenatal history,
the new Institute of Medicine diagnostic category “FAS without confirmed Alcohol Exposure”
may now be applied in some circumstances. In other cases, medical professionals have been
able to construct evidence of pre-natal exposure through the information that is available in
order to make a diagnosis of Partial FAS or ARND (e.g. alcohol consumption during pregnancy
may not be confirmed, but if the birth mother is a known alcoholic, that may be sufficient
evidence to presume she drank during the pregnancy).
Other parents who have been unable to get a diagnosis due to gaps in the child’s prenatal
history, or features obscured by growth in an older child, have found it useful to act as if their
child has a diagnosis. This is NOT to be confused with self-diagnosis, which can be dangerous.
An inaccurate diagnosis can be more damaging than no diagnosis! Your child should
be assessed by a knowledgeable doctor. Some parents have obtained a professional opinion
that their child has “suspected FAS” or “unexplained neurological damage,” which at the very
least has opened the door to helpful services, supports and intervention strategies. It also goes
a long way to taking the pressure off you, the parent, by reminding yourself and others that
the problem isn’t poor parenting.
51
Let’s
chat!
Talking to your Child
about FAS
Most parents who decide to “tell”
Add an important bottom line—
“This is a medical condition
And it’s not your fault.”
—Leon’s Mom
It is important to discuss FAS with your child, in order to help them better understand and
face the challenge of their chronic condition. Children with disabilities often know they are
different from their peers, which typically causes feelings of anger and frustration. Self-esteem increases when children’s truths about themselves are talked about, listened to, and
taken into consideration.
Talk about FAS openly and honestly in a safe environment, using language and concepts appropriate for the child’s age and developmental level. Talking about common symptoms can be
a unifying place to start. Discussions may be revisited as the child grows older. Some parents
have found that as they personally became more comfortable with the reality of FAS, the child
began to ask more questions about how they were affected and what to expect.
Rathbun (n.d.e) offers some suggestions for talking to your child about FAS at different ages:
Young Children
Young children are very immediate. They need consistent, warm, reassuring support from parents and medical personnel.
n Use concrete language (“picture-talk”) about animals or plants to describe differences (e.g.
dogs have special ears that hear things well, owls like things darker and wake up at night,
flowers have tender petals like tender skin, etc.)
n Help the child belong in the natural world with other living things by pointing out and
appreciating differences (i.e. differences are normal in nature, not sameness)
n The child needs to know that they are accepted and not blamed when they get stuck. They
need to know that they are safe. They have as much trouble accepting themselves when
things aren’t working as adults do, only they have less ability to put this into words.
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A Guide for Daily Living
School-Aged Children
The child may understand simple explanations of the condition and want to know what is
different about their bodies. Children are often concerned about what caused their difficulties.
n Talk about symptoms and strengths, while validating struggles and successes. Use visual
metaphors (instead of medical slides designed for adult audiences) to help the child describe their experiences (e.g. “it’s like a wall in my brain and sometimes a mouse gets through”
or “it’s like snow on a TV screen in my head—it’s hard to tune in on one thing.”)
n The child may ask you if any other children have it or if they are the only one. It is often
helpful for them to know that someone else has felt the same way they have. They also may
want to know how other children with FAS cope with their feelings and their condition.
n Help the child come to terms with the realness of the condition. The child will probably
want to know if it will go away. Be honest with your child, and use specific examples that
they will understand. (e.g. “Some things might change, and some won’t. Your ears will always hear noises better than mine. You might always like activity the child likes better than
some other activity like math,” etc.) Minimizing or pretending that it will all go away or
there’s nothing to worry about patronises the child’s effort to make sense out of their daily
reality.
n Repeated questions about why the birth mother drank during pregnancy may be less about
why (because life is not about fairness), and more about how sad and frustrated the child
feels when things are hard for them. The child may be struggling to accept what is unacceptable—that they were hurt by someone they depended on. The child often needs honesty, encouragement and reassurance more than technical explanations. Use simple answers and ask what it’s like for them.
n Encourage children to take a role in their own self-care. At all ages, children feel more
powerful when they help to create solutions for coping with their tougher symptoms. This
may include choosing certain soothing methods when agitated or facing challenging circumstances.
Adolescents
Talk honestly, realistically, and constructively about the dilemmas posed by the condition. Discuss possible options. Questions need to be answered honestly and respectfully. Be direct. Adolescents generally hate to be patronised—they have low tolerance for adults who beat around the
bush.
n Teens may want to know what to tell their friends if asked. Encourage simple, honest
discussion. (e.g. “I do it this way instead because that works better for me. Everybody’s different and people do things different ways.”) Walk it through and role play if the adolescent
wants to, or explore situations in your own life and ask for your teen’s advice as a teachable
moment.
n Help them set clear boundaries—let them know that they get to choose what they want
others to know (e.g. only telling helpers but not peers if the teen is worried about being
teased.) Respect choices about disclosure.
53
Parenting Children Affected by FAS
n Adolescents may benefit from talking with other adolescents or even adults who are suc-
cessfully coping with FAS. This will not only help the teen feel less alone, but also provide
an opportunity for them to learn from role models who embody “togetherness” and good
functioning. Peer support groups are also helpful, as they can provide guidance and mutual
encouragement while supporting diversity.
54
Help &
support
Resource List
In this new edition of A Guide for Daily Living, we have updated and substantially expanded
our Resource List.
Compiling an extensive list of this nature requires hours of research and attention to detail.
We would like to acknowledge the following individuals for their contribution: Elspeth Ross,
Adoption Council of Canada; Verna Booth, Society of Special Needs Adoptive Parents; Carole
Legge, Provincial FAS/E Prevention Coordinator, British Columbia; Carole Julien and Karen
Palmer, Canadian Centre on Substance Abuse.
The books, other media, and organizations listed here are intended as suggestions about where
to look for help, not as endorsements. Please use care and sound judgment when selecting an
information source, organization or program. Does the resource meet your individual needs?
Does the information you receive come from an accurate source? Pay attention to your instincts,
get a second opinion when necessary, and be open to “shopping around.”
Resource guides tend to get dated very quickly. By the time you read this, some of the information may be out of date. Books go in and out of print; publishers go out of business; organizations move, rename themselves or go under; contact people change. And in a growing field like
FAS, new resources will become available.
Also, it’s impossible to include everything that may be relevant—the SNAP library alone has
hundreds of materials related to FAS. But what we’ve listed here provides a solid place to
start.
We will continue to update these resources in later editions of the Guide, and on the SNAP web
site (currently http://www.snap.bc.ca). Please help us keep up to date by providing your feedback. Let us know if you encounter a book that is out of print, a phone number out of service,
an information source providing inaccurate information, or an organization that is not very
helpful, or perhaps even disrespectful—and so on. Also, please send in your suggestions for
additions—your favourite book that we left out, the resource in your community that we didn’t
know about, or a new resource you would like us to consider listing. Contact us at SNAP, 1150409 Granville Street, Vancouver, B.C. V6C 1T2, Canada, phone (604) 687-3114, toll-free (in
B.C.) 1-800-663-7627, fax: (604) 687-3364, e-mail <snap@snap.bc.ca>.
55
Parenting Children Affected by FAS
Books
Alberta Alcohol and Drug Abuse Commission. Fetal Alcohol Syndrome & Other Birth Defects,
2nd Edition. Edmonton: AADAC, 1996.
Alberta Alcohol and Drug Abuse Commission, Production and Distribution, 200 Pacific Plaza,
1099 Jasper, Edmonton, AB T5J 3M9. 1-800-280-9616 or (403) 427-7319; fax (403) 422-5237;
email: aadacrdm@compusmart.ab.ca . Features a comprehensive literature review. The identification, effects, safe drinking level, father’s contribution, incidences, labelling children
and the prevention of FAS/E are covered.
British Columbia, Ministry of Education and Training, Special Programs Branch. Teaching
Students with Fetal Alcohol Syndrome/Effects: A Resource Guide for Teachers. Victoria: British
Columbia, Ministry of Education and Training, 1996.
Contact Crown Publications (250) 386-4636; fax (250) 386-0221. Available in full-text on the
Internet at http://www.est.gov.bc.ca/specialed/fas/title.html. Dr. Julie Conry (see Forword
in this copy of SNAP’S Guide for Daily Living) is the principal writer and researcher for this
valuable teacher’s resource.
Burd, Larry. Fetal Alcohol Syndrome. Grand Forks, ND: Author, 1995.
Larry Burd, 1300 S. Columbia Road, Grand Forks, ND 58202. This handbook covers: diagnosis of FAS; development of children with FAS; behaviour; costs; treatment; medication; attention deficit hyperactivity disorder and FAS; the future; prevention; management; education; support; and social skills.
Copeland, Brenda and Deborah Rutman. Young Adults with Fetal Alcohol Syndrome or Fetal
Alcohol Effects: Experiences, Needs and Support Strategies. Victoria, British Columbia: School
of Social Work, University of Victoria, 1996.
Child, Family and Community Research Program, School of Social Work, Box 1700, University of Victoria, Victoria, BC V8W 2Y2; email cfcrp@hsd.uvic.ca. Living with FAS is a life
long challenge. This study addresses issues faced by young adults with FAS, such as pregnancy, parenting, and developing independent living skills.
Dorris, Michael. The Broken Cord. New York: Harper Collins, 1989.
Dorris recounts his struggle to find the cause of his adopted son Adam’s physical, behavioural and learning difficulties. This is the groundbreaking book that had a huge impact on
public awareness of FAS when it was first published in the late 80s.
Edelstein, Susan. Children with Prenatal Alcohol and/or Other Drug Exposure: Weighing the
Risks of Adoption. Washington, D.C.: CWLA Press, 1995.
Child Welfare League Press, 440 First Street, NW, Suite 310, Washington, DC 20001-2085,
phone (202) 638-2952; fax (202) 638-4004. Designed primarily for professionals, this book
offers practical suggestions, recommendations, and food for thought for preparing, counselling, and working with those who are considering adoption of a child who has been prenatally
exposed to alcohol or drugs.
Fernandez Villarreal, S. Handle with Care: Helping Children Prenatally Exposed to Drugs and
Alcohol. Scott Valley, CA: ETR, 1992.
ETR Associates, 19 Janis Way, Scott Valley, CA 95066-4200. Suggestions for teachers, parents and other care providers of children to age ten.
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A Guide for Daily Living
Fetal Alcohol Syndrome/Effects (5 part series): Booklet 1: Identifying FAS/FAE; Booklet 2:
Parenting Children (0-12 Years) Affected by FAS/E; Booklet 3: Parenting Adolescents Affected
by FAS/E: A Guide for Daily Living; Booklet 4: Educational Approaches for Children with
FAS/E: A Guide for Caregivers; and Booklet 5: Working with FAS/E Adults. Compiled by Nykola
Dubienski. Winnipeg: Association for Community Living, 1996-97.
This series features information compiled from existing publications, including substantial
material from the first edition of SNAP’s Guide for Daily Living. To order, please contact
(204) 786-1607; fax: (204) 786-1607.
George, Anne. FAS, FAE, NAS Resource. Includes: FAS/FAE & NAS Community Prevention
Guide; Guide for Parents, Teachers and Others Caring for Children with FAS/FAE or NAS;
FAS/FAE and NAS Guide to Resources. Vancouver: YWCA Crabtree Corner, Fetal Alcohol Syndrome, Neonatal Abstinence Syndrome Prevention Project, 1996, 1993.
Contact YWCA Crabtree Corner for more information, at (604) 689-2808; fax: (604) 6895469.
Kleinfeld, Judith and Siobhan Wescott, eds. Fantastic Antone Succeeds! Experiences in Educating Children with Fetal Alcohol Syndrome. Fairbanks: University of Alaska Press, 1993.
Available from the B.C. FAS/E Support Network. (604) 525-5069; fax: (604) 521-1958 or
through NOFAS (National Organization on Fetal Alcohol Syndrome U.S.) (202) 785-4585;
fax: (202) 466-6456. The reality of FAS is far more hopeful and far more complex than the
stories we hear about those with FAS.
Leon’s Mom. And Have Not Love. Duncan, BC: Metaphor Publishing, 1997.
Available through the SNAP office, 1150-409 Granville Street, Vancouver, B.C. V6C 1T2,
phone (604) 687-3114 or toll-free (in BC) 1-800-663-7627, or directly from the Duncan SNAP
FAS/E Parent Support Group, Box 1217, Lake Cowichan, B.C. V0R 1G0. Leon’s Mom began
writing poetry in 1995 in her FAS/E Parent Support Group as a way of sharing the difficulties of parenting teens and young adults struggling with alcohol related birth defects. A
selection of poems have been put together in this collection to share these experiences more
widely, and to increase public awareness.
Malbin, Diane. Fetal Alcohol Syndrome Fetal Alcohol Effects Strategies for Professionals
Hazelden. Center City, MN: Author, 1993.
15251 Pleasant Valley Road, Box 176 Center City, MN 55012-176. Ideal book for the professional who deals with FAS clients. Some information for the adult with FAS.
McIntyre-Palmer, Florence. Two Sides of the Coin. Calgary: Author, 1995.
The author shares her daughter’s story. Available through Florence McIntyre-Palmer, (403)
276-1577; fax: (403) 277-2933.
Normand, Claude and Deborah Rutman. Caring for Children with Fetal Alcohol Syndrome.
Victoria, British Columbia: School of Social Work, University of Victoria, 1996.
Child, Family and Community Research Program, School of Social Work, Box 1700, University of Victoria, Victoria, BC V8W 2Y2; email cfcrp@hsd.uvic.ca. This book covers: getting a
diagnosis, financial costs, emotional toll, education issues, advocacy, attachment issues, and
long term support needs. The issues for the families who have children with FAS that are
addressed are: disbelief, isolation, blame, denial, access to information and access to services (including the need for respite) and resources.
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Parenting Children Affected by FAS
Rutman, Deborah and Claude Louise Normand. Working with Families Affected by Fetal Alcohol Syndrome/Effects. Victoria, British Columbia: School of Social Work, University of Victoria, 1996.
Child, Family and Community Research Program, School of Social Work, Box 1700, University of Victoria, Victoria, BC V8W 2Y2; email cfcrp@hsd.uvic.ca. This is a collaborative research project funded by the B.C. Ministry for Children and Families, out of the University
of Victoria School of Social Work Child, Family and Community Research Program. Several
recommendations are made regarding the needs of those working with families who either
foster or adopt children affected by FAS.
Slinn, Jim. FAS/FAE a Practical Guide for Parents. Anchorage, AK: PARENTS, 1994.
Call SNAP office for purchasing information, (604) 687-3114 or toll-free in B.C. 1-800-6637627. A small book full of practical tips for parents of FAS affected children.
Stratton, Kathleen, Cynthia Howe, and Frederick Battaglia. Fetal Alcohol Syndrome: Diagnosis, Epidemiology, Prevention And Treatment. Washington, DC: National Academy Press, 1996.
National Academy Press, 2101 Constitution Avenue, NW Washington, DC 20418. A source
book for clinicians and researchers, this book presents the 1996 findings of the Institute of
Medicine’s Committee to Study Fetal Alcohol Syndrome. This volume discusses diagnosis,
surveillance, prevention, and treatment of FAS and other possible alcohol-related effects
from a broad perspective, problems associated with FAS epidemiology, and surveillance.
Streissguth, Ann. Fetal Alcohol Syndrome: A Guide For Families and Communities. Baltimore:
Paul H. Brookes, 1997.
Based on the life work of Dr. Streissguth, one of the pioneers in the field, this guidebook
presents an overview of FAS and explains how to identify the disorder, how to work with
children (and adults) who have it, how to talk to parents about it, and how to prevent its
occurrence through sensitive education of prospective mothers and society at large.
Streissguth, Ann, Fred L. Bookstein, Helen M. Barr, and Paul D. Sampson. The Enduring Effects of Prenatal Alcohol Exposure on Child Development. Ann Arbor: University of Michigan
Press, 1996.
University of Michigan Press, 839 Green Street, Box 1104, Ann Arbor, MI 48106-1104 Phone
(313) 764-4392. Alcohol is the most common neurobehavioural teratogenic drug used by
pregnant women. Its effects are particularly harmful if it is consumed during the fetus’s
early gestation period. This volume reports the results of a study of the systematic effects
of prenatal alcohol exposure on 500 children, followed from gestation for seven years. It is
the first major longitudinal inquiry designed within the framework of behaviours teratology to illustrate the long-term effects of alcohol on the development—both mental and physical—of a child.
Streissguth, Ann, and Jonathan Kanter. The Challenge of Fetal Alcohol Syndrome: Overcoming
Secondary Disabilities. Seattle: University of Washington Press, 1997.
In Canada, available through UBC Press, Vancouver, phone (604) 822-5959. In this book,
various experts describe how to help people with FAS. A summary of recent findings and
recommendations is presented by the team who conducted the largest study ever done on
people of all ages with FAS and FAE. Twenty two experts, conference participants from the
field of human services, education, and criminal justice, respond by describing their solutions to this problem of a birth defect that targets the brain and has lifelong consequences.
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A Guide for Daily Living
Streissguth, Ann, Robin A. Ladue, Sandra P. Randels. A Manual on Adolescents And Adults
With FAS With Special Reference to American Indians. Seattle: University of Washington,
1988.
For ordering information, phone (206) 543-7155. This manual provides succinct information
about FAS, focusing on older children and adolescents with special reference to America’s
First Peoples. (It is an older book but still has pertinent information.)
Videos
Cardinal, Gil. David with FAS: A Story of Fetal Alcohol Syndrome. 1996. Kanata Productions
in co-production with the National Film Board of Canada and the CBC. NFB 1-800-267-7710.
David’s condition went undiagnosed for the first 18 years of his life, causing confusion, anger, and pain for both David and his adoptive family.
Caring Together. 1996. Native Physicians Association in Canada, 103 1785 Alta Vista Drive,
Ottawa, ON K1G 3Y6, Phone (613) 521-6582.
This is a video about caring and pregnancy for community caregivers who provide
preconceptual and prenatal health information to Aboriginal people. There is an accompanying discussion guide.
Fetal Alcohol Syndrome and Effect: Stories of Help and Hope. 1994.
Hazelden 15251 Pleasant Valley Road, Box 176 Center City, MN 55012-176. This video
presents a balanced view of the medical and social consequences of FAS and FAE. Excellent
for women in treatment, addiction professionals, and community education programs, the
video is centered on current work being done with children affected by FAS and their families. It provides a factual definition of FAS and FAE, explains how children are diagnosed,
and most importantly, vividly illustrates the positive prognosis possible for FAS-affected
children.
Helping Families-Helping Children. 1997. Yellowknife Films, for Yellowknife Association for
Community Living, P.O. Box 981, Yellowknife, NT X1A 2N7 Phone 403-920-2644.
This video describes what FAS is, how it is diagnosed and how it affects the child who has it.
A case for early intervention is made. Specific suggestions are given on how to educate
these children, how to make abstract ideas seem real, and how to discipline.
Preventable Tragedy Fetal Alcohol Syndrome/Effects. 1991. NCA/Long Beach Area Council on
Alcoholism and Other Drug Dependencies, 836 Atlantic Avenue, Long Beach, CA 90813.
This video shows interviews with birth and adoptive mothers of FAS/FAE victims. Parents
talk about their expectations for their children and how they deal with them.
Rakel, Bob. Family Practice Update: Fetal Alcohol Syndrome. 1992. Lifetime Television, NY,
NY.
This is a video with three parts from Lifetime Television’s Family Practice Update. Dr. Bob
Rakel has Dr. Ken Jones, Dr. Ann Streissguth, and Dr. Larry Culpepper discussing FAS,
recognition of it, managing pregnancies, children and debunking myths.
A Series about FAS Program (3 parts), 1991: 1: What Is FAS?, 2: Preventing FAS, and 3: Living
with FAS. Ministry of Health, 5th Floor, 1515 Blanshard Street, Victoria, B.C. V8W 3C8.
Wherever alcohol is abused, children are born with FAS. This video, designed for families,
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Parenting Children Affected by FAS
educators and health professionals, examines the cause, treatment, and prevention of alcohol related birth defects.
What’s Wrong with My Child? 1991. Marlin Motion Pictures Ltd., 211 Watline Avenue,
Mississauga, ON L4Z 1P3.
This 20/20 segment introduces researchers Dr. Sterling Clarren and Ann Streissguth. Clarren
notes the alcohol consumed by a pregnant woman reaches the brain of the fetus which is
developing continually during pregnancy.
Informative Newsletters
About FASE: A Publication of the FAS/E Support Network of B.C. Quarterly. $30/year. (604)
525-5069; fax (604) 521-1958; email: fasnet@istar.ca
F.A.S. Times: Fetal Alcohol Syndrome/Family Resource Institute Newsletter. Quarterly. US$20
(family) or US$30 (professional). FAS/FAE, P.O. Box 2525, Lynnwood, WA 98036, U.S.A.
Iceberg: an Educational Newsletter for People Concerned about Fetal Alcohol Syndrome (FAS)
and Fetal Alcohol Effects (FAE). Quarterly. Includes Canadian information. Seattle, Washington. $12 Can (family) or $25 Can (professional). P.O. Box 95597, Seattle, WA 98145-2597, U.S.A.
(206) 827-1773
Society of Special Needs Adoptive Parents Newsletter. Quarterly. $25 (family) or $35 (group/
society). Provides the latest information for parents, professionals and others interested in
special needs and adoption issues, including FAS. SNAP, 1150-409 Granville Street, Vancouver, BC V6C 1T2. (604) 687-3114; fax (604) 687-3364, e-mail: snap@snap.bc.ca
Internet
The FASlink listserv, maintained by the Canadian Centre on Substance Abuse in Ottawa, is an
electronic support group and forum for the discussion of issues and concerns related to FAS.
To join, send an e-mail to manager@list.ccsa.ca with the message “join faslink.” Those who do
not have the time or energy to read a large number of e-mail messages each day may subscribe
to a digest version. Contact CCSA for details at (613) 235-4048 or toll-free 1-800-559-4514, or
by e-mail: kpalmer@ccsa.ca
The Canadian Centre on Substance Abuse also provides information on FAS on the World
Wide Web: http://www.ccsa.fasgen.htm
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A Guide for Daily Living
Organizations
This is a list of FAS-related organizations and agencies providing services to British Columbians.
Agencies with a national mandate are noted first, followed by a listing of services within the
province. This is not intended to be an exhaustive list. We have included central agencies who
will be able to refer you to more specific resources in your area.
National
FAS/FAE Information Service
Canadian Centre on Substance Abuse
75 Albert Street, Suite 300
Ottawa, ON K1P 5E7
tel: 1-800-559-4514; or (613) 235-4048, ext. 223, fax (613) 235-8101
email: fas@ccsa.ca; http://www.ccsa.ca/fasgen.htm
CCSA maintains the data-base of FAS/FAE support groups and contacts for all of Canada,
which is available both on the INTERNET and in book form. Faslink—an electronic listserv
for discussion of FAS/FAE issues—is also available. See section on INTERNET resources.
Adoption Council of Canada
180 Argyle Ave., #329
Ottawa, ON K2P 1B7
tel: (613) 235-1566; fax: (613) 235-1728
email: acc@adoption.ca; http://www.adoption.ca
Aboriginal Nurses Association of Canada
Marilyn Van Bibber
192 Bank Street
Ottawa, ON K2P 1W8
tel: (613) 236-3373; fax: (613) 236-3599
e-mail: info@anac.on.ca
Motherisk Program
Division of Clinical Pharmacology and Toxicology
Hospital for Sick Children
555 University Avenue
Toronto, ON M5G 1X8
tel: 1-877-327-4636
Bilingual service offered to callers throughout Canada. This toll-free information line provides information on the possible risks of consuming alcohol and drugs during pregnancy. Wherever possible, referrals are provided to services in the caller’s home region.
Health Units
Local health units throughout Canada have resources and educational materials on the subject of FAS/FAE and on healthy pregnancies. Check your local phone directory for a health
unit in your community.
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Parenting Children Affected by FAS
Canadian Association for Community Living
Kinsmen Building
York University
4700 Keele Street
Toronto, ON M3J 1P3
tel: (416) 661-9611
The Canadian Association for Community Living is a federation of local associations across
Canada. There are 90 associations in B.C. that serve individuals with mental disabilities and
their families. The Association as a whole lobbies, educates with and for individuals to ensure
opportunities, access, justice and rights in all areas of their lives. There are a number of local
organizations throughout B.C. which have included work with individuals affected by FAS as
part of their mandate.
Contact for B.C.:
B.C. Association for Community Living
#300 - 30 East 6th Avenue
Vancouver, B.C. V5T 4P4
tel: (604) 875-1119; fax: (604) 875-6744
e-mail: info@bcacl.org
British Columbia
Provincial FAS Prevention Coordinator
Women’s Health Centre
5th Floor Rm E501
4500 Oak Street
Vancouver, B.C. V6H 3N1
tel: (604) 875-3599; fax: (604) 875-2039
The coordinator provides an information and referral service for the public on how to access
information, resources, expertise and services related to FAS/E. The coordinator also helps
with networking among health, education, justice and social service agencies and provides
support to community groups addressing FAS issues. The position is fully funded by the Ministry for Children and Families.
Society of Special Needs Adoptive Parents (SNAP)
#1150 - 409 Granville Street
Vancouver, BC V6C 1T2
tel: (604) 687-3114; toll free in B.C.: 1-800-663-7627; fax: (604) 687-3364]
e-mail: snap@snap.bc.ca; web site: http://www.snap.bc.ca
SNAP is a provincial organization dedicated to assisting special needs adoptive families through
mutual support, information sharing and advocacy. SNAP provides support groups and oneto-one contact resource parents throughout B.C. The Society operates a toll-free (in B.C.)
telephone contact line and publishes a quarterly newsletter, as well as publishing booklets
such as this one! SNAP also maintains a large resource library of books, periodicals, reports,
audio tapes and videos on adoption and special needs-related issues.
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A Guide for Daily Living
BCANDS Resource Centre
1179 Kosapsum Crescent
Victoria, B.C. V9A 7K7
Toll Free: 1-888-815-5511
tel: (250) 381-7303; fax: (250) 381-7312
Resources are available to First Nations parents, groups and educators. There are videos, kits,
manuals, displays and brochures dealing with FAS and the effects of alcohol on pregnancy.
B.C. FAS Resource Society
Sunny Hill Health Centre for Children
3644 Slocan Street
Vancouver, B.C. V5M 3E8
Project Office:
#302 11965 Fraser Street
Maple Ridge, B.C. V2X 8H7
tel: (604) 465-5211; fax: (604) 465-8204
The B.C. FAS Resource Society encourages the provision of information, support and services
to families, professionals and the broader community around prevention, intervention and
treatment issues relating to alcohol and other drug related developmental disabilities including FAS/E. Publications include: B.C. FAS Resource Society Newsletter; information pamphlets;
FAS Community Action Guide: Youth in the Criminal Justice System; Identifying FAS and
Other Alcohol Related Neurodevelopmental Disabilities; and a series of videos about FAS:
What’s FAS?; Prevention of FAS; and Living and Learning with FAS.
FAS/E Support Network of B.C.
Suite 187 151 10090 152nd Street
Surrey, B.C. V3R 8XA
tel: (604) 589-1854; fax: (604) 589-8438
e-mail: fasnet@istar.ca
The FAS/E Support Network, a parent-based group, provides information, support, consultation and advocacy services for individuals, families, professionals and the broader community
around prevention, intervention and treatment issues pertaining to alcohol related birth defects caused by alcohol use during pregnancy. Included in the services are the WARMLINE
and FAS support groups and publications
Vancouver Aboriginal Friendship Centre Society
1607 East Hastings Street
Vancouver, B.C. V5L 1S7
tel: (604) 251-4844; fax: (604) 251-1986
The Vancouver Aboriginal Friendship Centre Society’s Fetal Alcohol Syndrome Program offers
the following services: support services for children, youth, parents, elders, professionals; support groups for individuals diagnosed with FAS/E assessment, A/D counselling, residential
treatment, and family violence; FAS/E outreach services for women who drank alcohol and
took other drugs during pregnancy; information about pregnancy and liaison between VAFCS
and the Aboriginal community; and FAS Workshops.
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Parenting Children Affected by FAS
YWCA Crabtree Corner FAS/NAS Prevention Project
101 East Cordova Street
Vancouver, B.C. V6A 1K7
tel: (604) 689-2808; fax: (604) 689-5463
YWCA Crabtree Corner FAS/NAS Prevention Project offers FAS/NAS educational workshops,
a resource lending library, a peer support group for moms with children with FAS/NAS and
information and crisis counselling. Crabtree Corner has published posters and pamphlets, as
well as three guides.
Fetal Alcohol and Drug Effects Resource Coalition
Regional Coordinator
Box 1249
Vanderhoof, BC V0J 3A0
tel: (250) 567-9205; fax: (250) 567-3939
Contacts for the eight sites:
Burns Lake
(250) 692-1722
Fraser Lake
(250) 699-8386
Vanderhoof
(250) 576-9205
Fort St. James
(250) 996-7645
Prince George
(250) 561-2689
Quesnel
(250) 992-8347
Williams Lake
(250) 392-4481
100 Mile House
(250) 395-5500
Each site delivers services required to meet local needs. Services may include direct support
for at-risk prenatal and postnatal women through counselling, referrals, education and advocacy; work with caregivers, parents or foster parents of affected children or with preschool
children themselves; and information and education about fetal alcohol and drug effects presented to school children, school staff, partner agencies, community groups and the general
public.
Prevention Source B.C.
2730 Commercial Drive, Suite 210
Vancouver, B.C. V5N 5P4
tel: (604) 874-8452; toll free: 1-800-663-1880; fax: (604) 874-9348
e-mail: info@preventionsource.bc.ca
Prevention Source provides a toll-free information service for residents of the province seeking information about prevention contacts, organizations, programs, materials and research in
the area of substance misuse. The Centre also has a collection of prevention resource materials
for on-site use. Included in this collection are a variety of FAS and NAS resource materials.
Substance Exposure Resource Team
Sunny Hill Centre for Children’s Health, B.C. Children and Women’s Hospital
3644 Slocan Street
Vancouver, B.C. V5M 3E8
tel: (604) 453-8300, Local 8221; fax: (604) 453-8301
web: http://www.cw.bc.ca
Sunny Hill provides in patient and outpatient service to children (birth to 19) and their families where questions have arisen around the possible impact of prenatal exposure to alcohol
and/or other drugs. Service may take the form of consultation and initial linking to available
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A Guide for Daily Living
community resources, diagnosis and developmental assessment, medical and social support to
inpatient infants experiencing withdrawals. Community education is a vital component to all
of Sunny Hill’s clinical outreach.
Federation of Invisible Disabilities
1818 Belmont Avenue
Victoria, B.C. V8R 3Z2
tel: (250) 595-3569; fax: (250) 370-9309
e-mail: noise@islandnet.com
The Federation of Invisible Disabilities establishes a collective and united organization to
create and direct change on behalf of and with children, youth and adults with invisible disabilities. The federation promotes awareness and public education regarding invisible disabilities, and provides information and support to parents and caregivers.
Family Support Institute
Suite 300, 30 East 6th Avenue
Vancouver, B.C. V5T 4P4
tel: (604) 875-1119; fax: (604) 875-6744
e-mail: info@bcacl.org
Family Support Institute provides information, training and province-wide networking to assist families and their communities to build upon and share strengths.
NISHA Family and Children’s Services Society
Vancouver Region
#201 - 2830 Grandview Highway
Vancouver, B.C. V5M 2C9
tel: (604) 412-7950; fax: (604) 412-7951
e-mail: mailbox@nisha.org
NISHA Family and Children Services offers a variety of homes, programs and services for
children, youth and families.
Learning Disabilities Association of B.C.
Provincial Office
1524 Fort Street
Victoria, B.C. V8S 5J2
tel: (250) 370-9513; fax: (250) 370-9421
e-mail: Ida-svi@commercial.net
The Leaning Disabilities Association advances the education and general well-being of children and adults who have learning disabilities through the provision of information, referrals
and support. The Association operates a resource centre where books, tapes and films may be
borrowed. Speakers are available on request. The Learning Disabilities Association has 17
local chapters. Chapters with offices are in:
Vancouver
873-9511
Vernon
542-5033
South Vancouver Island
386-9511
Williams Lake
392-7801
Hours are from 9:00 am to 4:00 pm, Monday to Friday.
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Parenting Children Affected by FAS
Kindale Developmental Association
Box 94
Armstrong, B.C. V0E 1B0
tel: (250) 546-3005; fax: (250) 546-3035
e-mail: kindale@mindlink.bc.ca
Kindale Developmental Association is a non-profit society which has been serving persons
with mental and physical disabilities in the North Okanagan. The Society offers residential
and a broad range of day programming to both children and adults.
Office of the Child, Youth and Family Advocate
Box 6, Suite 600, 595 Howe Street
Vancouver, B.C. V6C 2T5
tel: (604) 775-3203; toll-free: 1-800-476-3933; TTY (604) 775-3680; fax: (604) 775-3205
e-mail: info@advokids.org
web: www.advokids.org
The Office of the Child, Youth and Family Advocate has staff who help children and youth and
their families when they feel they’re not getting the services they need from the provincial
government.
After Hours Foster Families Support Line Program
This service is designed to support foster parents who are dealing with difficult child behaviour issues by providing immediate support and expertise outside of regular Ministry for Children and Families office hours.
The After Hours Foster Families Support Line is staffed by professional caregivers with experience in a therapeutic foster care setting and/or a child and youth care residential setting.
The staff provide professional consultation and support related to living with and managing
difficult behaviour of children and youth in the Ministry’s care, including difficult behaviour
presented by children affected by FAS.
Call toll-free: 1-888-495-4440.
Hours of operation are Monday to Friday, 4:00 pm to 12:45 am, statutory Holidays and Weekends, 8:00 am to 12:45 am.
B.C. Federation for Foster Parents Association
3680 East Hastings, #301
Vancouver, B.C. V5K 2A9
tel: (604) 660-7696 or toll-free (in B.C.): 1-800-663-9999
Federation of Aboriginal Foster Parents Association
300-3680 East Hastings Street
Vancouver, B.C. V5K 2A9
tel: (604) 291-7091; fax: (604) 291-7098
e-mail: fafp@direct.ca
web: http://mypage.direct.ca/f/fafp
The Federation of Aboriginal Foster Parents is a non-profit organization run by and for Aboriginal caregivers throughout B.C. The Federation works in partnership with the B.C. Federation of Foster Parent Associations to provide support and training to Aboriginal caregivers and
non-Aboriginal people caring for Aboriginal children in a way that respects Aboriginal culture
and traditions.
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A Guide for Daily Living
Infant Development Program of British Columbia
2765 Osoyoos Crescent
Vancouver, B.C. V6T 1X7
tel: (604) 822-4014; fax: (604) 822-9556
e-mail: infantdv@unixg.ubc.ca
Infant Development Programs in B.C. provide home visits and group experiences for families
with children aged birth through three at risk for, or living with, a developmental challenge.
For families with a child with FAS or where a parent has FAS, information and support is
given to the family that will promote the child’s development and strengthen family capacity.
(Member, B.C. Association for Child Development & Rehabilitation.)
FAS/NAS Early Intervention Consultant
Aurora Centre, B.C. Children & Women’s Hospital
4500 Oak Street, 5th Floor
Vancouver, B.C. V6H 3N1
tel: (604) 875-2017; fax: (604) 875-2039
e-mail: jamos@cw.bc.ca
The early intervention consultant works with health and social service providers towards the
provision of improved early intervention approaches with women at risk; develops and supports policy work regarding appropriate and accessible treatment options for women using
alcohol and other drugs during pregnancy; and gathers and disseminates information on effective early intervention strategies for women who are pregnant and using substances.
67
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A Guide for Daily Living
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Parenting Children Affected by FAS
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in Fetal Alcohol Syndrome. In A. Streissguth & J. Kanter (Eds.), The Challenge of Fetal
Alcohol Syndrome: Overcoming Secondary Disabilities (pp. 25-39). Seattle: University of
Washington Press.
Streissguth, A. P. (1997). Fetal Alcohol Syndrome: a Guide for Families and Communities.
Baltimore: Paul H. Brookes Publishing Co.
Streissguth, A. P., Aase, J. M., Clarren, S. K., Randels, S. P., LaDue, R. A., & Smith, D. F. (1991).
Fetal Alcohol Syndrome in adolescents and adults. JAMA 265 (15), 1961-1967.
Steissguth, A.P., Barr, H.M., Kogan, J., & Bookstein, F.L. (1996). Understanding the Occurrence
of Secondary Disabilities in Clients with Fetal Alcohol Syndrome (FAS) and Fetal Alcohol
Effects (FAE): Final Report to the Centers for Disease Control and Prevention (CDC) on Grant
No. R04/CCR008515 (Tech. Report No. 96-06). Seattle, University of Washington, Fetal
Alcohol and Drug Unit.
Streissguth, A. P., Bookstein, F. L., Sampson, P. D., & Barr, H. M. (1993). The Enduring Effects
of Prenatal Alcohol Exposure on Child Development: Birth through seven years, a partial
least squares solution. Ann Arbor: University of Michigan Press.
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University of Washington.
Streissguth, A. P., & Little, R. E. (1994). Alcohol: Pregnancy and the Fetal Alcohol Syndrome.
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70
Acknowledgements
Grateful acknowledgement is made to the following authors and publishers for permission to
reprint:
Excerpts from And Have Not Love, by Leon’s Mom, copyright © 1997 by Leon’s Mom and
SNAP FAS/E Support Group, Duncan. Reprinted by permission of the author.
Quotes from an adoptive parent, Ken, Luke’s Mom, Nigel, and Bev, excerpted from back
issues of The Society of Special Needs Adoptive Parents Newsletter, copyright © 1994, 1997, The
Society of Special Needs Adoptive Parents (SNAP).
Facial Characteristics diagram from Streissguth and Little, “Alcohol: Pregnancy and the
Fetal Alcohol Syndrome,” Krock Foundation Slide Curriculum on Alcoholism, Unit 9: Alcohol
and Pregnancy. Timonium, MD: Milner-Fenwick, 1994. Reprinted by permission of Dr. Ann
Streissguth, University of Washington Fetal Alcohol and Drug Unit.
Seven Common Misconceptions about FAS/FAE by Dr. Ann Streissguth, from Streissguth,
A.P. (1997). Fetal Alcohol Syndrome: A Guide for Families and Communities (306pp). Baltimore: Paul H. Brookes Publishing Co. Reprinted by permission of the author.
Excerpts from Hope for the FAS/FAE Nowhere Child, by Maureen Murphy, © 1991 by
Maureen Murphy. Reprinted with permission of the author.
71
Appendix
Diagnostic Criteria for Fetal Alcohol Syndrome (FAS) and Alcohol-Related Effects, as recommended by the Institute of Medicine (IOM), 1996. For further details and analysis, see Stratton,
K., Howe, C., & Battaglia, F. (1996), Fetal Alcohol Syndrome: Diagnosis, Epidemiology, Prevention, and Treatment.
Fetal Alcohol Syndrome
1. FAS with confirmed maternal alcohol exposurea
A. Confirmed maternal alcohol exposurea
B. Evidence of a characteristic pattern of facial anomalies that includes features such as short
palpebral fissures and abnormalities in the premaxillary zone (e.g., flat upper lip, flattened
philtrum, and flat midface)
C. Evidence of growth retardation, as in at least one of the following:
C low birth weight for gestational age
C decelerating weight over time not due to nutrition
C disproportional low weight to height
D. Evidence of CNS neurodevelopmental abnormalities, as in at least one of the following:
C decreased cranial size at birth
C structural brain abnormalities (e.g., microcephaly, partial or complete agenesis of the
corpus callosum, cerebellar hypoplasia)
C neurological hard or soft signs (as age appropriate), such as impaired fine motor skills,
neurosensory hearing loss, poor tandem gait, poor eye-hand coordination
2. FAS without confirmed maternal alcohol exposure
B, C, and D as above
3. Partial FAS with confirmed maternal alcohol exposure
A. Confirmed maternal alcohol exposurea
B. Evidence of some components of the pattern of characteristic facial anomalies
Either C or D or E
C. Evidence of growth retardation, as in at least one of the following:
C low birth weight for gestational age
C decelerating weight over time not due to nutrition
C disproportional low weight to height
D. Evidence of CNS neurodevelopmental abnormalities, as in:
C decreased cranial size at birth
C structural brain abnormalities (e.g., microcephaly, partial or complete agenesis of the
corpus callosum, cerebellar hypoplasia)
C neurological hard or soft signs (as age appropriate) such as impaired fine motor skills,
neurosensory hearing loss, poor tandem gait, poor eye-hand coordination
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Parenting Children Affected by FAS
E. Evidence of a complex pattern of behaviour or cognitive abnormalities that are inconsistent
with developmental level and cannot be explained by familial background or environment
alone, such as learning difficulties; deficits in school performance; poor impulse control;
problems in social perception; deficits in higher level receptive and expressive language;
poor capacity for abstraction or metacognition; specific deficits in mathematical skills; or
problems in memory, attention, or judgment
Alcohol-Related Effects
Clinical conditions in which there is a history of maternal alcohol exposure,a,b and
where clinical or animal research has linked maternal alcohol ingestion to an observed outcome.
There are two categories, which may co-occur. If both diagnoses are present, then both diagnoses should be rendered:
4. Alcohol-related birth defects (ARBD)
List of congenital anomalies, including malformations and dysplasias
Cardiac
Atrial septal defects
Ventricular septal defects
Aberrant great vessels
Tetralogy of Fallot
Skeletal
Hypoplastic nails
Shortened fifth digits
Radioulnar synostosis
Flexion contractures
Camptodactyly
Clinodactyly
Pectus excavatum and carinatum
Klippel-Feil syndrome
Hemivertebrae
Scoliosis
Renal
Aplastic, dysplastic,
hypoplastic kidneys
Horseshoe kidneys
Ureteral duplications
Hydronephrosis
Ocular
Strabismus
Retinal vascular anomalies
Refractive problems secondary to small globes
Auditory
Conductive hearing loss
Neurosensory hearing loss
Other
Virtually every malformation has been described in some patient with FAS. The
etiologic specificity of most of these anomalies to alcohol teratogenisis remains
uncertain.
5. Alcohol-related neurodevelopmental disorder (ARND)
Presence of:
A. Evidence of CNS neurodevelopmental abnormalities, as in any one of the following:
C decreased cranial size at birth
C structural brain abnormalities (e.g., microcephaly, partial or complete agenesis of the corpus callosum, cerebellar hypoplasia)
C neurological hard or soft signs (as age appropriate), such as impaired fine motor skills,
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A Guide for Daily Living
neurosensory hearing loss, poor tandem gait, poor eye-hand coordination
and/or:
B. Evidence of a complex pattern of behaviour or cognitive abnormalities that are inconsistent with developmental level and cannot be explained by familial background or environment alone, such as learning difficulties; deficits in school performance; poor impulse control; problems in social perception; deficits in higher level receptive and expressive language; poor capacity for abstraction or metacognition; specific deficits in mathematical skills;
or problems in memory, attention, or judgment
a
A pattern of excessive intake characterized by substantial, regular intake or heavy
episodic drinking. Evidence of this pattern may include frequent episodes of intoxication,
development of tolerance or withdrawal, social problems related to drinking, legal problems
related to drinking, engaging in physically hazardous behaviour while drinking, or alcoholrelated medical problems such as hepatic disease.
b
As further research is completed and as, or if, lower quantities or variable patterns of
alcohol use are associated with ARBD or ARND, these patterns of alcohol use should be incorporated into the diagnostic criteria.
A-3
ISBN 0-9698617-5-3

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