Assessing Young Children's Social Competence

During the past two decades, a convincing body of evidence has accumulated to indicate that unless children achieve minimal social competence by about the age of 6 years, they have a high probability of being at risk into adulthood in several ways (Ladd, 2000; Parker & Asher, 1987). Recent research (Hartup & Moore, 1990; Kinsey, 2000; Ladd & Profilet, 1996; McClellan & Kinsey, 1999; Parker & Asher, 1987; Rogoff, 1990) suggests that a child's long-term social and emotional adaptation, academic and cognitive development, and citizenship are enhanced by frequent opportunities to strengthen social competence during childhood.

Hartup (1992) notes that peer relationships in particular contribute a great deal to both social and cognitive development and to the effectiveness with which we function as adults. He states that "the single best childhood predictor of adult adaptation is not school grades, and not classroom behavior, but rather, the adequacy with which the child gets along with other children. Children who are generally disliked, who are aggressive and disruptive, who are unable to sustain close relationships with other children, and who cannot establish a place for themselves in the peer culture are seriously at risk" (Hartup, 1992, p. 1). The risks are many: poor mental health, dropping out of school, low achievement and other school difficulties, and poor employment history (Katz & McClellan, 1997).

Children with ADHD, ODD, and other behavioral disorders are particularly vulnerable to low self-esteem. They frequently experience school problems, have difficulty making friends, and lag behind their peers in psychosocial development.

Because social development begins at birth and progresses rapidly during the preschool years, it is clear that early childhood programs should include regular opportunities for spontaneous child-initiated social play. Berk and Winsler (1995) suggest that it is through symbolic/pretend play that young children are most likely to develop both socially and intellectually. Thus, periodic assessment of children's progress in the acquisition of social competence is appropriate.

The set of items presented below is based on research on elements of social competence in young children and on studies in which the behavior of well-liked children has been compared with that of less-liked children (Katz & McClellan, 1997; Ladd & Profilet, 1996; McClellan & Kinsey, 1999).

The Social Attributes Checklist

The checklist provided in this digest includes attributes of a child's social behavior that teachers are encouraged to examine every three or four months. Consultations with parents and other caregivers help to provide a validity check. In using the checklist, teachers are advised to note whether the attributes are typical of the child. Any child can have a few really bad days, for a variety of reasons; if assessments are to be reasonably reliable, judgments of the overall pattern of functioning over a period of at least three or four weeks are required. The checklist is intended as one of a variety of ways the social well-being of children can be assessed.

How children act toward and are treated by their classmates (cooperatively or aggressively, helpfully or demandingly, etc.) appears to have a substantial impact on the relationships they develop (Ladd, 2000). However, healthy social development does not require that a child be a "social butterfly." The most important index to note is the quality rather than the quantity of a child's friendships. Children (even rejected children) who develop a close friend increase the degree to which they feel positively about school over time (Ladd, 1999). There is evidence (Rothbart & Bates, 1998; Kagan, 1992) that some children are simply more shy or more inhibited than others, and it may be counterproductive to push such children into social relations that make them uncomfortable (Katz & McClellan, 1997). Furthermore, unless that shyness is severe enough to prevent a child from enjoying most of the "good things of life," such as birthday parties, picnics, and family outings, it is reasonable to assume that, when handled sensitively, the shyness will be spontaneously outgrown.

Many of the attributes listed in the checklist below indicate adequate social growth if they characterize the child's usual behavior. This qualifier is included to ensure that occasional fluctuations do not lead to over-interpretation of children's temporary difficulties. On the basis of frequent direct contact with the child, observation in a variety of situations, and information obtained from parents and other caregivers, a teacher or caregiver can use the checklist as an informal research-based means of assessing each child's social and emotional well-being. It is intended to provide a guideline for teachers and parents and is based on several teacher rating scales (all demonstrating high internal reliability) used by researchers to measure children's social behavior. Most of these scales (Ladd, 2000; Ladd & Profilet, 1996; McClellan & Kinsey, 1999) have also been replicated on more than one occasion and have demonstrated high reliability over time.

Teachers can observe and monitor interactions among children and let children who rarely have difficulties attempt to solve conflicts by themselves before intervening. If a child appears to be doing well on most of the attributes and characteristics in the checklist, then it is reasonable to assume that occasional social difficulties will be outgrown without intervention. It is also reasonable to assume that children will strengthen their social skills, confidence, and independence by being entrusted to solve their social difficulties without adult assistance. However, if a child seems to be doing poorly on many of the items listed, the responsible adults can implement strategies that will help the child to overcome and outgrow the social difficulties. The checklist is not a prescription for "correct social behavior"; rather it is an aid to help teachers observe, understand, and support children as they grow in social skillfulness. If a child seems to be doing poorly on many of the items on the list, strategies can be implemented to help the child to establish more satisfying relationships with other children (Katz & McClellan, 1997).

Children's current and long-term social-emotional development, as well as cognitive and academic (Kinsey, 2000) development, are clearly affected by the child's social experiences with peers and adults. It is important to keep in mind that children vary in social behavior for a variety of reasons. Research indicates that children have distinct personalities and temperaments from birth (Rothbart & Bates, 1998; Kagan, 1992). In addition, nuclear and extended family relationships and cultural contexts also affect social behavior. What is appropriate or effective social behavior in one culture may not be in another. Many children thus may need help in bridging their differences and in finding ways to learn from and enjoy the company of one another. Teachers have a responsibility to be proactive in creating a classroom community that accepts and supports all children.

The Social Attributes Checklist

I. Individual AttributesThe child:

  • Is usually in a positive mood.
  • Is not excessively dependent on adults.
  • Usually comes to the program willingly.
  • Usually copes with rebuffs adequately.
  • Shows the capacity to empathize.
  • Has positive relationships with one or two peers; shows the capacity to really care about them and miss them if they are absent.
  • Displays the capacity for humor.
  • Does not seem to be acutely lonely.

II. Social Skills AttributesThe child usually:

  • Approaches others positively.
  • Expresses wishes and preferences clearly; gives reasons for actions and positions.
  • Asserts own rights and needs appropriately.
  • Is not easily intimidated by bullies.
  • Expresses frustrations and anger effectively and without escalating disagreements or harming others.
  • Gains access to ongoing groups at play and work.
  • Enters ongoing discussion on the subject; makes relevant contributions to ongoing activities.
  • Takes turns fairly easily.
  • Shows interest in others; exchanges information with and requests information from others appropriately.
  • Negotiates and compromises with others appropriately.
  • Does not draw inappropriate attention to self.
  • Accepts and enjoys peers and adults of ethnic groups other than his or her own.
  • Interacts nonverbally with other children with smiles, waves, nods, etc.

III. Peer Relationship AttributesThe child:

  • Is usually accepted versus neglected or rejected by other children.
  • Is sometimes invited by other children to join them in play, friendship, and work.
  • Is named by other children as someone they are friends with or like to play and work with.

Resources

Berk, L., & Winsler, A. (1995). Scaffolding children's learning: Vygotsky and early childhood education. Washington, DC: National Association for the Education of Young Children. ED 384 443.

Halberstadt, A. G., Denham, S. A., & Dunsmore, J. C. (2001). Affective social competence. Social Development, 10(1), 79-119.

Hartup, W. W. (1992). Having friends, making friends, and keeping friends: Relationships as educational contexts. ERIC Digest. Champaign, IL: ERIC Clearinghouse on Elementary and Early Childhood Education. ED 345 854.

Hartup, W. W., & Moore, S. G. (1990). Early peer relations: Developmental significance and prognostic implications.Early Childhood Research Quarterly, 5(1), 1-18. EJ 405 887.

Kagan, J. (1992). Yesterday's premises, tomorrow's promises. Developmental Psychology, 28(6), 990-997. EJ 454 898.

Katz, L. G., & McClellan, D. E. (1997). Fostering children's social competence: The teacher's role. Washington, DC: National Association for the Education of Young Children. ED 413 073.

Kinsey, S. J. (2000). The relationship between prosocial behaviors and academic achievement in the primary multiage classroom. Unpublished doctoral dissertation, Loyola University, Chicago.

Ladd, G. W. (1999). Peer relationships and social competence during early and middle childhood. Annual Review of Psychology, 50, 333-359.

Ladd, G. W. (2000). The fourth R: Relationships as risks and resources following children's transition to school.American Educational Research Association Division E Newsletter, 19(1), 7, 9-11.

Ladd, G. W., & Profilet, S. M. (1996). The child behavior scale: A teacher-report measure of young children's aggressive, withdrawn, and prosocial behaviors. Developmental Psychology, 32(6), 1008-1024. EJ 543 361.

McClellan, D. E., & Kinsey, S. (1999) Children's social behavior in relation to participation in mixed-age or same-age classrooms. Early Childhood Research & Practice [Online], 1(1).

Parker, J. G., & Asher, S. R. (1987). Peer relations and later personal adjustment: Are low-accepted children at risk?Psychological Bulletin, 102(3), 357-389.

Rogoff, B. M. (1990). Apprenticeship in thinking: Cognitive development in social context. New York: Oxford University Press.

Rothbart, M., & Bates, J. (1998). Temperament. In W. Damon (Series Ed.) & N. Eisenberg (Vol. Ed.), Handbook of child psychology: Vol. 3. Social, emotional, and personality development (5th ed., pp. 105-176). New York: Wiley

Source: EDO-PS-01-2
Authors: Diane E. McClellan and Lilian G. Katz
March 2001

Page last modified or reviewed by athealth on January 29, 2014

Different Types of Parent-Child Relationships

There are different kinds of attachment relationships that can be put into different categories. These categories can describe children's relationships with both parents and childcare providers. Research has found that there are at least four attachment categories. The categories describe the ways that children act and the ways that adults act with the children. The strongest kind of attachment is called 'secure.' The way a parent or provider responds a child may lead to one of the four types of attachment categories. The way a child is attached to her parents also affects how she will behave around others when her parent is not around.

1. Secure relationships. This is the strongest type of attachment. A child in this category feels he can depend on his parent or provider. He knows that person will be there when he needs support. He knows what to expect.

  • The secure child usually plays well with other children his age.
  • He may cry when his mother leaves. He will usually settle down if a friendly adult is there to comfort him.
  • When parents pick him up from childcare, he is usually very happy to see them.
  • He may have a hard time leaving childcare, though. This can be confusing if the child was upset when the parents left at the beginning of the day. It does not mean that the child is not happy to see the parents.

How do adults build secure attachment relationships?

  • Adults are consistent when they respond to the child's needs.
  • When a child cries, the adult responds in a lovingly or caring way.
  • When a child is hungry, the adult feeds her fairly soon.
  • When a child is afraid, the adult is there to take care of her.
  • When the child is excited about something, the adults are excited about it, too.

Over time, a securely attached child has learned that he can rely on special adults to be there for him. He knows that, if he ever needs something, someone will be there to help. A child who believes this can then learn other things. He will use special adults as a secure base. He will smile at the adult and come to her to get a hug. Then he will move out and explore his world.

Note about different cultures: Parents and other caregivers show love in different ways in different cultures. In any culture, though, children can have good relationships with parents and providers. In all cultures, adults can build secure attachments if they are sensitive and respond to children's signals. They way they respond will be very different from one culture to another, however. Providers who work with children from different cultures should watch for differences. Ask parents and other people from that culture how they care for children.

2. Avoidant relationships. This is one category of attachment that is not secure. Avoidant children have learned that depending on parents won't get them that secure feeling they want, so they learn to take care of themselves.

  • Avoidant children may seem too independent.
  • They do not often ask for help, but they get frustrated easily.
  • They may have difficulty playing with other children their age. They may be aggressive at times.
  • Biting, hitting, pushing, and screaming are common for many children, but avoidant children do those things more than other children.
  • Avoidant children usually do not build strong relationships with providers in their childcare setting.
  • They don't complain when the parents leave them, and they usually do not greet them when the parents return. They know that the parents have returned, but it is almost like they want to punish them by ignoring them.
  • They seem to try to care for themselves.

What kind of parent behavior is linked to this category of attachment?

  • Parents respond to their children's needs, but it usually takes a while.
  • When a child is hungry, the child will be fed, but probably after she's been waiting for a long time.
  • When a child is frightened, she is usually left to deal with it on her own.
  • When a child is excited about something, the parent may turn away or ignore her.
  • The child gets used to not having her needs met, so she learns to take care of herself.

There are different reasons why parents might act this way. Some parents just don't know when their baby or child needs something. Other parents might think that it will make their child more independent if the parents do not give in to the child. Providers who have an avoidant child in their care may be able to help parents recognize and understand their children's needs.

3. Ambivalent relationships. Ambivalence (not being completely sure of something) is another way a child may be insecurely attached to his parents. Children who are ambivalent have learned that sometimes their needs are met, and sometimes they are not. They notice what behavior got their parents' attention in the past and use it over and over. They are always looking for that feeling of security that they sometimes get.

  • Ambivalent children are often very clingy.
  • They tend to act younger than they really are and may seem over-emotional.
  • When older preschoolers or early-elementary children want an adult's attention, they might use baby talk or act like a baby.
  • Ambivalent children often cry, get frustrated easily, and love to be the center of attention.
  • They get upset if people aren't paying attention to them and have a hard time doing things on their own.
  • Ambivalent children seem to latch onto everyone for short periods of time.
  • They have a very hard time letting parents go at the beginning of the day, and the crying may last a long time.

What kind of parent behavior is linked to this category of attachment?

  • When an infant is crying, these parents sometimes respond; sometimes they don't.
  • When a child is hungry, she might be fed, but it is more likely that she will be fed when she's not hungry.
  • When a child is frightened, she is ignored sometimes and overly comforted at other times.
  • When a child is excited about something, a parent doesn't understand the child's excitement or responds to her in a way that does not fit.

4. Disorganized relationships. Disorganized children don't know what to expect from their parents. Children with relationships in the other categories have organized attachments. This means that they have all learned ways to get what they need, even if it is not the best way. This happens because a child learns to predict how his parent will react, whether it is positive or negative. They also learn that doing certain things will make their parents do certain things.

  • Disorganized children will do things that seem to make no sense.
  • Sometimes these children will speak really fast and will be hard to understand.
  • Very young children might freeze in their footsteps for no apparent reason.
  • Most disorganized children have a hard time understanding the feelings of other children.
  • Disorganized children who are playing with dolls might act out scenes that are confusing and scary.
  • Disorganized children may be very hard to understand. They may seem very different from day to day.

There are two types of disorganized attachments:

  • Controlling-Disorganized. Children who are controlling tend to be extremely bossy with their friends.
  • Caregiving-Disorganized. Children who are caregiving might treat other children in a childish way, acting like a parent.

What kind of parent behavior is linked to this category of attachment?

  • The parents rarely respond to their needs when they are infants.
  • If the parent does respond, the response usually does not fit.
  • It is common for disorganized children to come from families in which some form of neglect or maltreatment is happening.
  • It is also possible that these children may have one or more parents suffering from depression.
Sidebar: Children with ADHD, ODD, and other behavioral disorders are particularly vulnerable to low self-esteem. They frequently experience school problems, have difficulty making friends, and lag behind their peers in psychosocial development. They are more likely than other children to bully and to be bullied. Parents of children with behavior problems experience highly elevated levels of child-rearing stress, and this may make it more difficult for them to respond to their children in positive, consistent, and supportive ways.

If you think you see a child with disorganized attachment, you may be very concerned. There are reasons to be concerned. At the same time, as a child care provider, it is not your job to fix the family. First, try to find out what is happening in the child's home. Sometimes, when a family is going through a major change (for example, a divorce, a death in the family, or a move), a parent-child relationship can look disorganized for a short time. It usually lasts only as long as the situation does. If you notice signs of disorganization that last for a long time, however, you may want to help the family find support.

Note: It is important to understand the family's culture when you are observing attachment. A secure attachment in one culture may look like an insecure attachment in another culture.

Source:

Provider-Parent Partnerships
http://www.ces.purdue.edu/providerparent/index.htm

Purdue University, School of Consumer and Family Sciences

Department of Child Development and Family Studies

Authors: Lynette C. Maga??a with Judith A. Myers-Walls and Dee Love

Page last reviewed by athealth.com on February 3, 2014

Attachment: A New Way of Understanding the Problems of Parents and Kids

WesselmannD
by Debra Wesselmann, MS, LPC

The Advantages of a Secure Attachment

The research in the field of attachment opens up a whole new world for all of us in understanding the problems of parents and children. Attachment is the emotional connection between any two people. However, life's first attachments are by far the most important, as they set a template for all later relationships. Attachment between kids and parents evolved naturally eons ago, as the infants and children who developed a strong need to remain near their parents were the ones who were most likely to survive - both physically and psychologically. Children who feel the most secure in their early relationships with parents have tremendous advantages in life. They tend to grow up feeling good about themselves and others. They cope well with life's ups and downs, and they have a strong capacity for empathy. These kids naturally form other healthy, close relationships as they go out into the world. Kids who have not developed a healthy, secure attachment with parents tend to grow up feeling more insecure, disconnected, and angry.

Three Ingredients of Attachment

There are three main ingredients to a secure attachment relationship. The first is physical connection, which means plenty of touch and eye contact. Such things as cradling an infant while feeding, cuddling with a toddler before bedtime, and hugging a teenager increase the sense of physical connection, especially if touch and eye contact take place on a daily basis throughout the childhood years. The second ingredient is emotional connection. Children sense their parents are connected on an emotional level when their parents are tuned into their feelings. Infants feel their parents' attunement when parents respond accurately to their infants' cries or when they share their infants' delight in new discoveries. Children sense the emotional connection when their parents empathize with their feelings or provide them with comfort or reassurance. Even discipline, when carried out with empathy, can increase the emotional connection. Finally, children need an environment that is consistent, predictable, and safe in order to develop a quality attachment. Children need to know that if their feelings or behaviors get out of control, their parents will remain steady and calm. They need to be able to depend on a consistent schedule, consistent limits, and consistent parental responses. Without this kind of safe, dependable environment a child will develop emotional walls which will prevent a secure attachment.

Obstacles to a Secure Attachment

All babies and children are biologically programmed to attach to their parents, but not all children develop quality attachments. There are several situations that can interfere with a good attachment. For example, children with a difficult temperament may be so highly active or so extreme in their emotions that their parents naturally have difficulty connecting with them either physically or emotionally. Children who endured an abusive or chaotic early life and who are later placed with an adoptive family may have emotional walls that are difficult to penetrate.

Parents who live in stressful circumstances may have difficulty creating secure attachments. Out of necessity they may be so preoccupied with solving the problems of living and coping that they are unable to tune into their children's feelings and needs. Parents with addictions are unable to stay attuned to their children or provide a consistent, safe environment because they are preoccupied with the addictive substance or behavior, and the whole family may be on the addictions roller coaster together.

Finally, parents who grew up without secure attachment relationships themselves often have difficulty providing the ingredients of a secure attachment relationship with their own children. Parents who did not experience nurturing and closeness growing up may feel uncomfortable with closeness, and may subsequently distance themselves from their kids. Parents who were mistreated as children may have a strong need to be in control in order to avoid feeling vulnerable, and may therefore become excessively controlling with their children. Parents who were mistreated may perceive normal child misbehaviors as attempts to mistreat or hurt them, and may overreact in these situations. Parents who feel unlovable may fear their children don't love them, and may attempt to placate their children or give them things to get them to love them more. Parents who were not securely attached in childhood may be disconnected from their own painful feelings, or they may be overwhelmed by painful feelings. Parents who experienced poor attachments are also more vulnerable to the use of addictive substances or behaviors to cope.

There is Hope for Parents and Kids

Most parents love their kids and want to give them the best start in life possible. By gaining a clear understanding of attachment and the obstacles present in their own relationships with their kids, parents can overcome these obstacles and strengthen the parent-child bonds. Parents who lacked quality bonds as children can be helped to identify and overcome the effects of their poor attachment histories so that they may give their children a better emotional start to life than the one they had.

The Whole Parent: How to Become a Terrific Parent Even If You Didn't Have One, by Debra Wesselmann, helps parents understand attachment, and teaches them how to provide the ingredients of a secure attachment for their children. The book helps parents who did not have the advantages of growing up with a quality attachment understand and overcome the effects of their early experiences in order to give their children a better emotional start to life than the one they had.

Click here to learn more about the book The Whole Parent: How to Become a Terrific Parent Even If You Didn't Have One

About the Author:

Debra Wesselmann, MS, LPC, is a therapist in private practice specializing in work with adults and kids, trauma, abuse, attachment, and breaking generational patterns of unhealthy relating. She is the mother of two step-children, two children by birth, and one child who joined the family through adoption. Debra lives with her husband and children in Omaha, Nebraska.

Page last modified or reviewed by athealth on January 29, 2014

Autism Spectrum Disorder

What is autism spectrum disorder (ASD)?

Autism is a group of developmental brain disorders, collectively called autism spectrum disorder (ASD). The term "spectrum" refers to the wide range of symptoms, skills, and levels of impairment, or disability, that children with ASD can have. Some children are mildly impaired by their symptoms, but others are severely disabled.

ASD is diagnosed according to guidelines listed in the Diagnostic and Statistical Manual of Mental Disorders, Fourth Edition - Text Revision (DSM-IV-TR).1 The manual currently defines five disorders, sometimes called pervasive developmental disorders (PDDs), as ASD:

  • Autistic disorder (classic autism)
  • Asperger's disorder (Asperger syndrome)
  • Pervasive developmental disorder not otherwise specified (PDD-NOS)
  • Rett's disorder (Rett syndrome)
  • Childhood disintegrative disorder (CDD).

This information packet will focus on autism, Asperger syndrome, and PDD-NOS, with brief descriptions of Rett syndrome and CDD in the section, "Related disorders."

What are the symptoms of ASD?

Symptoms of autism spectrum disorder (ASD) vary from one child to the next, but in general, they fall into three areas:

  • Social impairment
  • Communication difficulties
  • Repetitive and stereotyped behaviors

Children with ASD do not follow typical patterns when developing social and communication skills. Parents are usually the first to notice unusual behaviors in their child. Often, certain behaviors become more noticeable when comparing children of the same age.

In some cases, babies with ASD may seem different very early in their development. Even before their first birthday, some babies become overly focused on certain objects, rarely make eye contact, and fail to engage in typical back-and-forth play and babbling with their parents. Other children may develop normally until the second or even third year of life, but then start to lose interest in others and become silent, withdrawn, or indifferent to social signals. Loss or reversal of normal development is called regression and occurs in some children with ASD.2

Social impairment

Most children with ASD have trouble engaging in everyday social interactions. According to the Diagnostic and Statistical Manual of Mental Disorders, Fourth Edition - Text Revision, some children with ASD may:

  • Make little eye contact
  • Tend to look and listen less to people in their environment or fail to respond to other people
  • Do not readily seek to share their enjoyment of toys or activities by pointing or showing things to others
  • Respond unusually when others show anger, distress, or affection.

Recent research suggests that children with ASD do not respond to emotional cues in human social interactions because they may not pay attention to the social cues that others typically notice. For example, one study found that children with ASD focus on the mouth of the person speaking to them instead of on the eyes, which is where children with typical development tend to focus.3 A related study showed that children with ASD appear to be drawn to repetitive movements linked to a sound, such as hand-clapping during a game of pat-a-cake.4 More research is needed to confirm these findings, but such studies suggest that children with ASD may misread or not notice subtle social cues - a smile, a wink, or a grimace - that could help them understand social relationships and interactions. For these children, a question such as, "Can you wait a minute?" always means the same thing, whether the speaker is joking, asking a real question, or issuing a firm request. Without the ability to interpret another person's tone of voice as well as gestures, facial expressions, and other nonverbal communications, children with ASD may not properly respond.

Likewise, it can be hard for others to understand the body language of children with ASD. Their facial expressions, movements, and gestures are often vague or do not match what they are saying. Their tone of voice may not reflect their actual feelings either. Many older children with ASD speak with an unusual tone of voice and may sound sing-song or flat and robotlike.1

Children with ASD also may have trouble understanding another person's point of view. For example, by school age, most children understand that other people have different information, feelings, and goals than they have. Children with ASD may lack this understanding, leaving them unable to predict or understand other people's actions.

Communication issues

According to the American Academy of Pediatrics' developmental milestones, by the first birthday, typical toddlers can say one or two words, turn when they hear their name, and point when they want a toy. When offered something they do not want, toddlers make it clear with words, gestures, or facial expressions that the answer is "no."

For children with ASD, reaching such milestones may not be so straightforward. For example, some children with autism may:

  • Fail or be slow to respond to their name or other verbal attempts to gain their attention
  • Fail or be slow to develop gestures, such as pointing and showing things to others
  • Coo and babble in the first year of life, but then stop doing so
  • Develop language at a delayed pace
  • Learn to communicate using pictures or their own sign language
  • Speak only in single words or repeat certain phrases over and over, seeming unable to combine words into meaningful sentences
  • Repeat words or phrases that they hear, a condition called echolalia
  • Use words that seem odd, out of place, or have a special meaning known only to those familiar with the child's way of communicating.

Even children with ASD who have relatively good language skills often have difficulties with the back and forth of conversations. For example, because they find it difficult to understand and react to social cues, children with Asperger syndrome often talk at length about a favorite subject, but they won't allow anyone else a chance to respond or notice when others react indifferently.1

Children with ASD who have not yet developed meaningful gestures or language may simply scream or grab or otherwise act out until they are taught better ways to express their needs. As these children grow up, they can become aware of their difficulty in understanding others and in being understood. This awareness may cause them to become anxious or depressed. For more information on mental health issues in children with ASD, see the section: What are some other conditions that children with ASD may have?

Repetitive and stereotyped behaviors

Children with ASD often have repetitive motions or unusual behaviors. These behaviors may be extreme and very noticeable, or they can be mild and discreet. For example, some children may repeatedly flap their arms or walk in specific patterns, while others may subtly move their fingers by their eyes in what looks to be a gesture. These repetitive actions are sometimes called "stereotypy" or "stereotyped behaviors."

Children with ASD also tend to have overly focused interests. Children with ASD may become fascinated with moving objects or parts of objects, like the wheels on a moving car. They might spend a long time lining up toys in a certain way, rather than playing with them. They may also become very upset if someone accidentally moves one of the toys. Repetitive behavior can also take the form of a persistent, intense preoccupation.1 For example, they might be obsessed with learning all about vacuum cleaners, train schedules, or lighthouses. Children with ASD often have great interest in numbers, symbols, or science topics.

While children with ASD often do best with routine in their daily activities and surroundings, inflexibility may often be extreme and cause serious difficulties. They may insist on eating the same exact meals every day or taking the same exact route to school. A slight change in a specific routine can be extremely upsetting.1 Some children may even have emotional outbursts, especially when feeling angry or frustrated or when placed in a new or stimulating environment.

No two children express exactly the same types and severity of symptoms. In fact, many typically developing children occasionally display some of the behaviors common to children with ASD. However, if you notice your child has several ASD-related symptoms, have your child screened and evaluated by a health professional experienced with ASD.

Related Disorders

Rett syndrome and childhood disintegrative disorder (CDD) are two very rare forms of ASD that include a regression in development. Only 1 of every 10,000 to 22,000 girls has Rett syndrome.5,6 Even rarer, only 1 or 2 out of 100,000 children with ASD have CDD.7

Unlike other forms of ASD, Rett syndrome mostly affects girls. In general, children with Rett syndrome develop normally for 6-18 months before regression and autism-like symptoms begin to appear. Children with Rett syndrome may also have difficulties with coordination, movement, and speech. Physical, occupational, and speech therapy can help, but no specific treatment for Rett syndrome is available yet.

With funding from the Eunice Kennedy Shriver National Institute of Child Health and Human Development, scientists have discovered that a mutation in the sequence of a single gene is linked to most cases of Rett syndrome.8 This discovery may help scientists find ways to slow or stop the progress of the disorder. It may also improve doctors' ability to diagnose and treat children with Rett syndrome earlier, improving their overall quality of life.

CDD affects very few children, which makes it hard for researchers to learn about the disease. Symptoms of CDD may appear by age 2, but the average age of onset is between age 3 and 4. Until this time, children with CDD usually have age-appropriate communication and social skills. The long period of normal development before regression helps to set CDD apart from Rett syndrome. CDD may affect boys more often than girls.9

Children with CDD experience severe, wide-ranging and obvious loss of previously-obtained motor, language, and social skills.10 The loss of such skills as vocabulary is more dramatic in CDD than in classic autism.11 Other symptoms of CDD include loss of bowel and bladder control.1

How is ASD diagnosed?

ASD diagnosis is often a two-stage process. The first stage involves general developmental screening during well-child checkups with a pediatrician or an early childhood health care provider. Children who show some developmental problems are referred for additional evaluation. The second stage involves a thorough evaluation by a team of doctors and other health professionals with a wide range of specialities.12 At this stage, a child may be diagnosed as having autism or another developmental disorder.

Children with autism spectrum disorder (ASD) can usually be reliably diagnosed by age 2, though research suggests that some screening tests can be helpful at 18 months or even younger.12,13

Many people - including pediatricians, family doctors, teachers, and parents - may minimize signs of ASD at first, believing that children will "catch up" with their peers. While you may be concerned about labeling your young child with ASD, the earlier the disorder is diagnosed, the sooner specific interventions may begin. Early intervention can reduce or prevent the more severe disabilities associated with ASD. Early intervention may also improve your child's IQ, language, and everyday functional skills, also called adaptive behavior.14

Screening

A well-child checkup should include a developmental screening test, with specific ASD screening at 18 and 24 months as recommended by the American Academy of Pediatrics.14 Screening for ASD is not the same as diagnosing ASD. Screening instruments are used as a first step to tell the doctor whether a child needs more testing. If your child's pediatrician does not routinely screen your child for ASD, ask that it be done.

For parents, your own experiences and concerns about your child's development will be very important in the screening process. Keep your own notes about your child's development and look through family videos, photos, and baby albums to help you remember when you first noticed each behavior and when your child reached certain developmental milestones.

Types of ASD screening instruments

Sometimes the doctor will ask parents questions about the child's symptoms to screen for ASD. Other screening instruments combine information from parents with the doctor's own observations of the child. Examples of screening instruments for toddlers and preschoolers include:

  • Checklist of Autism in Toddlers (CHAT)
  • Modified Checklist for Autism in Toddlers (M-CHAT)
  • Screening Tool for Autism in Two-Year-Olds (STAT)
  • Social Communication Questionnaire (SCQ)
  • Communication and Symbolic Behavior Scales (CSBS).

To screen for mild ASD or Asperger syndrome in older children, the doctor may rely on different screening instruments, such as:

  • Autism Spectrum Screening Questionnaire (ASSQ)
  • Australian Scale for Asperger's Syndrome (ASAS)
  • Childhood Asperger Syndrome Test (CAST).

Some helpful resources on ASD screening include the Center for Disease Control and Prevention's General Developmental Screening tools and ASD Specific Screening tools on their website.

Comprehensive diagnostic evaluation

The second stage of diagnosis must be thorough in order to find whether other conditions may be causing your child's symptoms. For more information, see the section: What are some other conditions that children with ASD may have?

A team that includes a psychologist, a neurologist, a psychiatrist, a speech therapist, or other professionals experienced in diagnosing ASD may do this evaluation. The evaluation may assess the child's cognitive level (thinking skills), language level, and adaptive behavior (age-appropriate skills needed to complete daily activities independently, for example eating, dressing, and toileting).

Because ASD is a complex disorder that sometimes occurs along with other illnesses or learning disorders, the comprehensive evaluation may include brain imaging and gene tests, along with in-depth memory, problem-solving, and language testing.12 Children with any delayed development should also get a hearing test and be screened for lead poisoning as part of the comprehensive evaluation.

Although children can lose their hearing along with developing ASD, common ASD symptoms (such as not turning to face a person calling their name) can also make it seem that children cannot hear when in fact they can. If a child is not responding to speech, especially to his or her name, it's important for the doctor to test whether a child has hearing loss.

The evaluation process is a good time for parents and caregivers to ask questions and get advice from the whole evaluation team. The outcome of the evaluation will help plan for treatment and interventions to help your child. Be sure to ask who you can contact with follow-up questions.

What are some other conditions that children with ASD may have?

Sensory problems

Many children with autism spectrum disorder (ASD) either overreact or underreact to certain sights, sounds, smells, textures, and tastes. For example, some may:

  • Dislike or show discomfort from a light touch or the feel of clothes on their skin
  • Experience pain from certain sounds, like a vacuum cleaner, a ringing telephone, or a sudden storm; sometimes they will cover their ears and scream
  • Have no reaction to intense cold or pain.

Researchers are trying to determine if these unusual reactions are related to differences in integrating multiple types of information from the senses.

Sleep problems

Children with ASD tend to have problems falling asleep or staying asleep, or have other sleep problems.15 These problems make it harder for them to pay attention, reduce their ability to function, and lead to poor behavior. In addition, parents of children with ASD and sleep problems tend to report greater family stress and poorer overall health among themselves.

Fortunately, sleep problems can often be treated with changes in behavior, such as following a sleep schedule or creating a bedtime routine. Some children may sleep better using medications such as melatonin, which is a hormone that helps regulate the body's sleep-wake cycle. Like any medication, melatonin can have unwanted side effects. Talk to your child's doctor about possible risks and benefits before giving your child melatonin. Treating sleep problems in children with ASD may improve the child's overall behavior and functioning, as well as relieve family stress.16

Intellectual disability

Many children with ASD have some degree of intellectual disability. When tested, some areas of ability may be normal, while others - especially cognitive (thinking) and language abilities - may be relatively weak. For example, a child with ASD may do well on tasks related to sight (such as putting a puzzle together) but may not do as well on language-based problem-solving tasks. Children with a form of ASD like Asperger syndrome often have average or above-average language skills and do not show delays in cognitive ability or speech.

Seizures

One in four children with ASD has seizures, often starting either in early childhood or during the teen years.17 Seizures, caused by abnormal electrical activity in the brain, can result in

  • A short-term loss of consciousness, or a blackout
  • Convulsions, which are uncontrollable shaking of the whole body, or unusual movements
  • Staring spells.

Sometimes lack of sleep or a high fever can trigger a seizure. An electroencephalogram (EEG), a nonsurgical test that records electrical activity in the brain, can help confirm whether a child is having seizures. However, some children with ASD have abnormal EEGs even if they are not having seizures.

Seizures can be treated with medicines called anticonvulsants. Some seizure medicines affect behavior; changes in behavior should be closely watched in children with ASD. In most cases, a doctor will use the lowest dose of medicine that works for the child. Anticonvulsants usually reduce the number of seizures but may not prevent all of them.

For more information about medications, see the NIMH online booklet, "Medications". None of these medications have been approved by the FDA to specifically treat symptoms of ASD.

Fragile X syndrome

Fragile X syndrome is a genetic disorder and is the most common form of inherited intellectual disability,18 causing symptoms similar to ASD. The name refers to one part of the X chromosome that has a defective piece that appears pinched and fragile when viewed with a microscope. Fragile X syndrome results from a change, called a mutation, on a single gene. This mutation, in effect, turns off the gene. Some people may have only a small mutation and not show any symptoms, while others have a larger mutation and more severe symptoms.19

Around 1 in 3 children who have Fragile X syndrome also meet the diagnostic criteria for ASD, and about 1 in 25 children diagnosed with ASD have the mutation that causes Fragile X syndrome.19

Because this disorder is inherited, children with ASD should be checked for Fragile X, especially if the parents want to have more children. Other family members who are planning to have children may also want to be checked for Fragile X syndrome. For more information on Fragile X, see the Eunice Kennedy Shriver National Institute of Child Health and Human Development website.

Tuberous sclerosis

Tuberous sclerosis is a rare genetic disorder that causes noncancerous tumors to grow in the brain and other vital organs. Tuberous sclerosis occurs in 1 to 4 percent of people with ASD.18,20 A genetic mutation causes the disorder, which has also been linked to mental retardation, epilepsy, and many other physical and mental health problems. There is no cure for tuberous sclerosis, but many symptoms can be treated.

Gastrointestinal problems

Some parents of children with ASD report that their child has frequent gastrointestinal (GI) or digestion problems, including stomach pain, diarrhea, constipation, acid reflux, vomiting, or bloating. Food allergies may also cause problems for children with ASD.21 It's unclear whether children with ASD are more likely to have GI problems than typically developing children.22,23 If your child has GI problems, a doctor who specializes in GI problems, called a gastroenterologist, can help find the cause and suggest appropriate treatment.

Some studies have reported that children with ASD seem to have more GI symptoms, but these findings may not apply to all children with ASD. For example, a recent study found that children with ASD in Minnesota were more likely to have physical and behavioral difficulties related to diet (for example, lactose intolerance or insisting on certain foods), as well as constipation, than children without ASD.23 The researchers suggested that children with ASD may not have underlying GI problems, but that their behavior may create GI symptoms - for example, a child who insists on eating only certain foods may not get enough fiber or fluids in his or her diet, which leads to constipation.

Some parents may try to put their child on a special diet to control ASD or GI symptoms. While some children may benefit from limiting certain foods, there is no strong evidence that these special diets reduce ASD symptoms.24 If you want to try a special diet, first talk with a doctor or a nutrition expert to make sure your child's nutritional needs are being met.

Co-occurring mental disorders

Children with ASD can also develop mental disorders such as anxiety disorders, attention deficit hyperactivity disorder (ADHD), or depression. Research shows that people with ASD are at higher risk for some mental disorders than people without ASD.25 Managing these co-occurring conditions with medications or behavioral therapy, which teaches children how to control their behavior, can reduce symptoms that appear to worsen a child's ASD symptoms. Controlling these conditions will allow children with ASD to focus more on managing the ASD.26

How is ASD treated?

While there's no proven cure yet for autism spectrum disorder (ASD), treating ASD early, using school-based programs, and getting proper medical care can greatly reduce ASD symptoms and increase your child's ability to grow and learn new skills.

Early Intervention

Research has shown that intensive behavioral therapy during the toddler or preschool years can significantly improve cognitive and language skills in young children with ASD.27,28 There is no single best treatment for all children with ASD, but the American Academy of Pediatrics recently noted common features of effective early intervention programs.29 These include:

  • Starting as soon as a child has been diagnosed with ASD
  • Providing focused and challenging learning activities at the proper developmental level for the child for at least 25 hours per week and 12 months per year
  • Having small classes to allow each child to have one-on-one time with the therapist or teacher and small group learning activities
  • Having special training for parents and family
  • Encouraging activities that include typically developing children, as long as such activities help meet a specific learning goal
  • Measuring and recording each child's progress and adjusting the intervention program as needed
  • Providing a high degree of structure, routine, and visual cues, such as posted activity schedules and clearly defined boundaries, to reduce distractions
  • Guiding the child in adapting learned skills to new situations and settings and maintaining learned skills
  • Using a curriculum that focuses on
    • Language and communication
    • Social skills, such as joint attention (looking at other people to draw attention to something interesting and share in experiencing it)
    • Self-help and daily living skills, such as dressing and grooming
    • Research-based methods to reduce challenging behaviors, such as aggression and tantrums
    • Cognitive skills, such as pretend play or seeing someone else's point of view
    • Typical school-readiness skills, such as letter recognition and counting.

One type of a widely accepted treatment is applied behavior analysis (ABA). The goals of ABA are to shape and reinforce new behaviors, such as learning to speak and play, and reduce undesirable ones. ABA, which can involve intensive, one-on-one child-teacher interaction for up to 40 hours a week, has inspired the development of other, similar interventions that aim to help those with ASD reach their full potential.30,31 ABA-based interventions include:

  • Verbal Behavior - focuses on teaching language using a sequenced curriculum that guides children from simple verbal behaviors (echoing) to more functional communication skills through techniques such as errorless teaching and
  • Pivotal Response Training - aims at identifying pivotal skills, such as initiation and self-management, that affect a broad range of behavioral responses. This intervention incorporates parent and family education aimed at providing skills that enable the child to function in inclusive settings.33,34

Other types of early interventions include:

  • Developmental, Individual Difference, Relationship-based(DIR)/Floortime Model - aims to build healthy and meaningful relationships and abilities by following the natural emotions and interests of the child.35 One particular example is the Early Start Denver Model, which fosters improvements in communication, thinking, language, and other social skills and seeks to reduce atypical behaviors. Using developmental and relationship-based approaches, this therapy can be delivered in natural settings such as the home or pre-school.33,34
  • TEACCH (Treatment and Education of Autistic and related Communication handicapped Children) - emphasizes adapting the child's physical environment and using visual cues (for example, having classroom materials clearly marked and located so that students can access them independently). Using individualized plans for each student, TEACCH builds on the child's strengths and emerging skills.34,36
  • Interpersonal Synchrony - targets social development and imitation skills, and focuses on teaching children how to establish and maintain engagement with others.

For children younger than age 3, these interventions usually take place at home or in a child care center. Because parents are a child's earliest teachers, more programs are beginning to train parents to continue the therapy at home.

Students with ASD may benefit from some type of social skills training program.37 While these programs need more research, they generally seek to increase and improve skills necessary for creating positive social interactions and avoiding negative responses. For example, Children's Friendship Training focuses on improving children's conversation and interaction skills and teaches them how to make friends, be a good sport, and respond appropriately to teasing.38

Working with your child's school

Start by speaking with your child's teacher, school counselor, or the school's student support team to begin an evaluation. Each state has a Parent Training and Information Center and a Protection and Advocacy Agency that can help you get an evaluation. A team of professionals conducts the evaluation using a variety of tools and measures. The evaluation will look at all areas related to your child's abilities and needs.

Once your child has been evaluated, he or she has several options, depending on the specific needs. If your child needs special education services and is eligible under the Individuals with Disabilities Education Act (IDEA), the school district (or the government agency administering the program) must develop an individualized education plan, or IEP specifically for your child within 30 days.

IDEA provides free screenings and early intervention services to children from birth to age 3. IDEA also provides special education and related services from ages 3 to 21. Information is available from the U.S. Department of Education.

If your child is not eligible for special education services - not all children with ASD are eligible - he or she can still get free public education suited to his or her needs, which is available to all public-school children with disabilities under Section 504 of the Rehabilitation Act of 1973, regardless of the type or severity of the disability.

The U.S. Department of Education's Office for Civil Rights enforces Section 504 in programs and activities that receive Federal education funds. More information on Section 504 is available on the Department of Education website.

More information about U.S. Department of Education programs for children with disabilities is available on their website.

During middle and high school years, your child's teachers will begin to discuss practical issues such as work, living away from a parent or caregiver's home, and hobbies. These lessons should include gaining work experience, using public transportation, and learning skills that will be important in community living.29

Medications

Some medications can help reduce symptoms that cause problems for your child in school or at home. Many other medications may be prescribed off-label, meaning they have not been approved by the U.S. Food and Drug Administration (FDA) for a certain use or for certain people. Doctors may prescribe medications off-label if they have been approved to treat other disorders that have similar symptoms to ASD, or if they have been effective in treating adults or older children with ASD. Doctors prescribe medications off-label to try to help the youngest patients, but more research is needed to be sure that these medicines are safe and effective for children and teens with ASD.

At this time, the only medications approved by the FDA to treat aspects of ASD are the antipsychotics risperidone (Risperdal) and aripripazole (Abilify). These medications can help reduce irritability—meaning aggression, self-harming acts, or temper tantrums—in children ages 5 to 16 who have ASD.

Some medications that may be prescribed off-label for children with ASD include the following:

Antipsychotic medications are more commonly used to treat serious mental illnesses such as schizophrenia. These medicines may help reduce aggression and other serious behavioral problems in children, including children with ASD. They may also help reduce repetitive behaviors, hyperactivity, and attention problems.29

Antidepressant medications, such as fluoxetine (Prozac) or sertraline (Zoloft), are usually prescribed to treat depression and anxiety but are sometimes prescribed to reduce repetitive behaviors. Some antidepressants may also help control aggression and anxiety in children with ASD.29 However, researchers still are not sure if these medications are useful; a recent study suggested that the antidepressant citalopram (Celexa) was no more effective than a placebo (sugar pill) at reducing repetitive behaviors in children with ASD.39

Stimulant medications, such as methylphenidate (Ritalin), are safe and effective in treating people with attention deficit hyperactivity disorder (ADHD). Methylphenidate has been shown to effectively treat hyperactivity in children with ASD as well. But not as many children with ASD respond to treatment, and those who do have shown more side effects than children with ADHD and not ASD.40

All medications carry a risk of side effects. For details on the side effects of common psychiatric medications, see the NIMH website on "Medications".

FDA warning about antidepressants

Antidepressants are safe and popular, but some studies have suggested that they may have unintended effects on some people, especially in teens and young adults. The FDA warning says that patients of all ages taking antidepressants should be watched closely, especially during the first few weeks of treatment. Possible side effects to look for are depression that gets worse, suicidal thinking or behavior, or any unusual changes in behavior such as trouble sleeping, agitation, or withdrawal from normal social situations. Families and caregivers should report any changes to the doctor. The latest information is available on the FDA website.

A child with ASD may not respond in the same way to medications as typically developing children. You should work with a doctor who has experience treating children with ASD. The doctor will usually start your child on the lowest dose that helps control problem symptoms. Ask the doctor about any side effects of the medication and keep a record of how your child reacts to the medication. The doctor should regularly check your child's response to the treatment.

You have many options for treating your child's ASD. However, not all of them have been proven to work through scientific studies. Read the patient information that comes with your child's medication. Some people keep these patient inserts along with their other notes for easy reference. This is most useful when dealing with several different prescription medications. You should get all the facts about possible risks and benefits and talk to more than one expert when possible before trying a new treatment on your child.

How common is ASD?

Studies measuring autism spectrum disorder (ASD) prevalence—the number of children affected by ASD over a given time period—have reported varying results, depending on when and where the studies were conducted and how the studies defined ASD.

In a 2009 government survey on ASD prevalence, the Centers for Disease Control and Prevention (CDC) found that the rate of ASD was higher than in past U.S. studies. Based on health and school records of 8-year-olds in 14 communities throughout the country, the CDC survey found that around 1 in 110 children has ASD.41 Boys face about four to five times higher risk than girls.

Experts disagree about whether this shows a true increase in ASD prevalence. Since the earlier studies were completed, guidelines for diagnosis have changed. Also, many more parents and doctors now know about ASD, so parents are more likely to take their children to be diagnosed, and more doctors are able to properly diagnose ASD. These and other changes may help explain some differences in prevalence numbers. Even so, the CDC report confirms other recent studies showing that more children are being diagnosed with ASD than ever before. For more information, please visit the autism section of the CDC website.

What causes ASD?

Scientists don't know the exact causes of autism spectrum disorder (ASD), but research suggests that both genes and environment play important roles.

Genetic factors

In identical twins who share the exact same genetic code, if one has ASD, the other twin also has ASD in nearly 9 out of 10 cases. If one sibling has ASD, the other siblings have 35 times the normal risk of also developing the disorder. Researchers are starting to identify particular genes that may increase the risk for ASD.42,43

Still, scientists have only had some success in finding exactly which genes are involved. For more information about such cases, see the section, "What are some other conditions that children with ASD may also have?" which describes Fragile X syndrome and tuberous sclerosis.

Most people who develop ASD have no reported family history of autism, suggesting that random, rare, and possibly many gene mutations are likely to affect a person's risk.44,45 Any change to normal genetic information is called a mutation. Mutations can be inherited, but some arise for no reason. Mutations can be helpful, harmful, or have no effect.

Having increased genetic risk does not mean a child will definitely develop ASD. Many researchers are focusing on how various genes interact with each other and environmental factors to better understand how they increase the risk of this disorder.

Environmental factors

In medicine, "environment" refers to anything outside of the body that can affect health. This includes the air we breathe, the water we drink and bathe in, the food we eat, the medicines we take, and many other things that our bodies may come in contact with. Environment also includes our surroundings in the womb, when our mother's health directly affects our growth and earliest development.

Researchers are studying many environmental factors such as family medical conditions, parental age and other demographic factors, exposure to toxins, and complications during birth or pregnancy.29,46-48

As with genes, it's likely that more than one environmental factor is involved in increasing risk for ASD. And, like genes, any one of these risk factors raises the risk by only a small amount. Most people who have been exposed to environmental risk factors do not develop ASD. The National Institute of Environmental Health Sciences is also conducting research in this area. More information is available on their website.

Scientists are studying how certain environmental factors may affect certain genes—turning them on or off, or increasing or decreasing their normal activity. This process is called epigenetics and is providing researchers with many new ways to study how disorders like ASD develop and possibly change over time.

ASD and vaccines

Health experts recommend that children receive a number of vaccines early in life to protect against dangerous, infectious diseases, such as measles. Since pediatricians in the United States started giving these vaccines during regular checkups, the number of children getting sick, becoming disabled, or dying from these diseases has dropped to almost zero.

Children in the United States receive several vaccines during their first 2 years of life, around the same age that ASD symptoms often appear or become noticeable. A minority of parents suspect that vaccines are somehow related to their child's disorder. Some may be concerned about these vaccines due to the unproven theory that ASD may be caused by thimerosal. Thimerosal is a mercury-based chemical once added to some, but not all, vaccines to help extend their shelf life. However, except for some flu vaccines, no vaccine routinely given to preschool aged children in the United States has contained thimerosal since 2001. Despite this change, the rate of children diagnosed with ASD has continued to rise.

Other parents believe their child's illness might be linked to vaccines designed to protect against more than one disease, such as the measles-mumps-rubella (MMR) vaccine, which never contained thimerosal.

Many studies have been conducted to try to determine if vaccines are a possible cause of autism. As of 2010, none of the studies has linked autism and vaccines.49,50

Following extensive hearings, a special court of Federal judges ruled against several test cases that tried to prove that vaccines containing thimerosal, either by themselves or combined with the MMR vaccine, caused autism. More information about these hearings is available on the U.S. Court of Federal Claims' website.

The latest information about research on autism and vaccines is available from the Centers for Disease Control and Prevention. This website provides information from the Federal Government and independent organizations.

What efforts are under way to improve the detection and treatment of ASD?

Many recent research studies have focused on finding the earliest signs of autism spectrum disorder (ASD). These studies aim to help doctors diagnose children at a younger age so they can get needed interventions as quickly as possible.

For example, one early sign of ASD may be increased head size or rapid head growth. Brain imaging studies have shown that abnormal brain development beginning in an infant's first months may have a role in ASD. This theory suggests that genetic defects in growth factors, which direct proper brain development, cause the brain abnormalities seen in autism. It's possible that an infant's sudden, rapid head growth may be an early warning signal, which could help in early diagnosis and treatment or possible prevention of ASD.51

Current studies on ASD treatment are exploring many approaches, such as:

  • A computer-based training program designed to teach children with ASD how to create and respond to facial expressions appropriately52
  • A medication that may help improve functioning in children with Fragile X syndrome53
  • New social interventions that can be used in the classroom or other "everyday" settings
  • An intervention parents can follow to reduce and prevent ASD-related disability in children at high risk for the disorder.54
  • More information about clinical trials on ASD funded by the National Institute of Mental Health is available on the website.

How can I help a child who has ASD?

After your child is diagnosed with autism spectrum disorder (ASD), you may feel unprepared or unable to provide your child with the necessary care and education. Know that there are many treatment options, social services and programs, and other resources that can help.

Some tips that can help you and your child are:

  • Keep a record of conversations, meetings with health care providers and teachers, and other sources of information. This will help you remember the different treatment options and decide which would help your child most.
  • Keep a record of the doctors' reports and your child's evaluation. This information may help your child qualify for special programs.
  • Contact your local health department or autism advocacy groups to learn about the special programs available in your state and local community.
  • Talk with your child's pediatrician, school system, or an autism support group to find an autism expert in your area who can help you develop an intervention plan and find other local resources.

Understanding teens with ASD

The teen years can be a time of stress and confusion for any growing child, including teenagers with autism spectrum disorder (ASD).

During the teenage years, adolescents become more aware of other people and their relationships with them. While most teenagers are concerned with acne, popularity, grades, and dates, teens with ASD may become painfully aware that they are different from their peers. For some, this awareness may encourage them to learn new behaviors and try to improve their social skills. For others, hurt feelings and problems connecting with others may lead to depression, anxiety, or other mental disorders. One way that some teens with ASD may express the tension and confusion that can occur during adolescence is through increased autistic or aggressive behavior. Teens with ASD will also need support to help them understand the physical changes and sexual maturation they experience during adolescence.

If your teen seems to have trouble coping, talk with his or her doctor about possible co-occurring mental disorders and what you can do. Behavioral therapies and medications often help.

Preparing for your child's transition to adulthood

The public schools' responsibility for providing services ends when a child with ASD reaches the age of 22. At that time, some families may struggle to find jobs to match their adult child's needs. If your family cannot continue caring for an adult child at home, you may need to look for other living arrangements. For more information, see the section, "Living arrangements for adults with ASD."

Long before your child finishes school, you should search for the best programs and facilities for young adults with ASD. If you know other parents of adults with ASD, ask them about the services available in your community. Local support and advocacy groups may be able to help you find programs and services that your child is eligible to receive as an adult.

Another important part of this transition is teaching youth with ASD to self-advocate. This means that they start to take on more responsibility for their education, employment, health care, and living arrangements. Adults with ASD or other disabilities must self-advocate for their rights under the Americans with Disabilities Act at work, in higher education, in the community, and elsewhere.

Living arrangements for adults with ASD

There are many options for adults living with ASD. Helping your adult child choose the right one will largely depend on what is available in your state and local community, as well as your child's skills and symptoms. Below are some examples of living arrangements you may want to consider:

Independent living. Some adults with ASD are able to live on their own. Others can live in their own home or apartment if they get help dealing with major issues, such as managing personal finances, obtaining necessary health care, and interacting with government or social service agencies. Family members, professional agencies, or other types of providers can offer this assistance.
Living at home. Government funds are available for families who choose to have their adult child with ASD live at home. These programs include Supplemental Security Income, Social Security Disability Insurance, and Medicaid waivers. Information about these programs and others is available from the Social Security Administration (SSA). Make an appointment with your local SSA office to find out which programs would be right for your adult child.

Other home alternatives. Some families open their homes to provide long-term care to adults with disabilities who are not related to them. If the home teaches self-care and housekeeping skills and arranges leisure activities, it is called a "skill-development" home.
Supervised group living. People with disabilities often live in group homes or apartments staffed by professionals who help with basic needs. These needs often include meal preparation, housekeeping, and personal care. People who are more independent may be able to live in a home or apartment where staff only visit a few times a week. Such residents generally prepare their own meals, go to work, and conduct other daily activities on their own.
Long-term care facilities. This alternative is available for those with ASD who need intensive, constant supervision.

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25. Leyfer OT, Folstein SE, Bacalman S, Davis NO, Dinh E, Morgan J, Tager-Flusberg H, Lainhart JE. Comorbid psychiatric disorders in children with autism: interview development and rates of disorders. Journal of Autism and Developmental Disorders, 2006 Oct;36(7):849–61.

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27. Reichow B, Wolery M. Comprehensive synthesis of early intensive behavioral interventions for young children with autism based on the UCLA young autism project model. Journal of Autism and Developmental Disorders, 2009 Jan;39(1):23–41.

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34. Autism Speaks. How Is Autism Treated? http://www.autismspeaks.org/docs/family_services_docs/100day2/Treatment_Version_2_0.pdf. Accessed on October 22, 2010.

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39. King BH, Hollander E, Sikich L, McCracken JT, Scahill L, Bregman JD, Donnelly CL, Anagnostou E, Dukes K, Sullivan L, Hirtz D, Wagner A, Ritz L. Lack of efficacy of citalopram in children with autism spectrum disorders and high levels of repetitive behavior: citalopram ineffective in children with autism. Archives of General Psychiatry, 2009 Jun;66(6): 583–90.

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42. Campbell DB, Sutcliffe JS, Ebert PJ, Militerni R, Bravaccio C, Trillo S, Elia M, Schneider C, Melmed R, Sacco R, Persico AM, Levitt P. A genetic variant that disrupts MET transcription is associated with autism. Proceedings of the National Academy of Sciences of the United States of America, 2006 Nov 7;103(45):16834–9.

43. Arking DE, Cutler DJ, Brune CW, Teslovich TM, West K, Ikeda M, Rea A, Guy M, Lin S, Cook EH, Chakravarti A. A common genetic variant in the neurexin superfamily member CNTNAP2 increases familial risk of autism. American Journal of Human Genetics, 2008 Jan;82(1):160–4.

44. Sebat J, Lakshmi B, Malhotra D, Troge J, Lese-Martin C, Walsh T, Yamrom B, Yoon S, Krasnitz A, Kendall J, Leotta A, Pai D, Zhang R, Lee YH, Hicks J, Spence SJ, Lee AT, Puura K, Lehtimaki T, Ledbetter D, Gregersen PK, Bregman J, Sutcliffe JS, Jobanputra V, Chung W, Warburton D, King MC, Skuse D, Geschwind DH, Gilliam TC, Ye K, Wigler M. Strong association of de novo copy number mutations with autism. Science, 2007 Apr 20;316(5823):445–9.

45. Morrow EM, Yoo SY, Flavell SW, Kim TK, Lin Y, Hill RS, Mukaddes NM, Balkhy S, Gascon G, Hashmi A, Al-Saad S, Ware J, Joseph RM, Greenblatt R, Gleason D, Ertelt JA, Apse KA, Bodell A, Partlow JN, Barry B, Yao H, Markianos K, Ferland RJ, Greenberg ME, Walsh CA. Identifying autism loci and genes by tracing recent shared ancestry. Science, 2008 Jul 11;321(5886):218–23.

46. Kolevzon A, Gross R, Reichenberg A. Prenatal and perinatal risk factors for autism: a review and integration of findings. Archives of Pediatric and Adolescent Medicine, 2007 Apr;161(4):326–33.

47. Lawler CP, Croen LA, Grether JK, Van de Water J. Identifying environmental contributions to autism: provocative clues and false leads. Mental Retardation and Developmental Disabilities Research Reviews, 2004;10(4):292–302.

48. Daniels JL, Forssen U, Hultman CM, Cnattingius S, Savitz DA, Feychting M, Sparen P. Parental psychiatric disorders associated with autism spectrum disorders in the offspring. Pediatrics, 2008 May;121(5):e1357–62.

49. Immunization Safety Review Committee. Immunization Safety Review: Vaccines and Autism. Washington, DC: The National Academies Press; 2004.

50. Interagency Autism Coordinating Committee. Question 3: what caused this to happen and can this be prevented? The 2010 Interagency Autism Coordinating Committee Strategic Plan for Autism Spectrum Disorders Research – January, 19, 2010. Washington, DC: Interagency Autism Coordinating Committee, U.S. Department of Health and Human Services, 2010.

51. Courchesne E, Carper R, Akshoomoff N. Evidence of brain overgrowth in the first year of life in autism. JAMA. 2003 Jul 16;290(3):337–44.

52. National Institute of Mental Health. Recovery act grant aims to teach kids with autism how to better express themselves. http://www.nimh.nih.gov/science-news/2009/recovery-act-grant-aims-to-teach-kids-with-autism-how-to-better-express-themselves.shtml. Accessed on March 23, 2010.

53. National Institute of Mental Health. Clinical tests begin on medication to correct Fragile X defect. http://www.nimh.nih.gov/science-news/2009/clinical-tests-begin-on-medication-to-correct-fragile-x-defect.shtml. Accessed on March 23, 2010.

54. National Institute of Mental Health. NIH awards more than 50 grants to boost search for causes, improve treatments for autism. http://www.nimh.nih.gov/science-news/2009/nih-awards-more-than-50-grants-to-boost-search-for-causes-improve-treatments-for-autism.shtml. Accessed on March 23, 2010.

National Institutes of Health
NIH Publication No. 11-5511
Revised 2011

Page last modified or reviewed by athealth on January 29, 2014

Autistic Spectrum Disorders: Best Practice Guidelines for Screening, Diagnosis and Assessment

Section I - Core Concepts That Guide Screening, Diagnosis and Assessment

Major advancements in the sciences of early identification and treatment of ASD have increased public awareness and focused more attention on this class of neurodevelopmental disorders. The core concepts that follow provide guidance for all professionals in the state of California who are responsible for the screening, diagnostic evaluation and/or assessment for intervention planning for persons with ASD. These core concepts suggest a common language by which both professionals and parents can communicate with each other. Importantly, they also provide referring parties with information about what they can expect from well-informed diagnostic and treatment planning teams.

These Guidelines represent wide collaboration and consensus from expert panels across the state of California regarding screening, evaluation and interdisciplinary assessment for individuals who may meet diagnostic criteria for autistic spectrum disorder. Variables considered by the panels in developing these Guidelines included current scientific knowledge, level of expertise needed to execute a particular function, pragmatics of clinical practice and respect for the family ecology.

The DSM-IV is the current classification standard for establishing a diagnosis of ASD.

The Diagnostic and Statistical Manual, 4th edition (DSM-IV) and the Diagnostic and Statistical Manual, 4th edition, Text Revision (DSM-IV, TR) published by the American Psychiatric Association (1994 and 2000) are the current standards for the diagnosis and classification of ASD. In clinical practice, the DSM-IV is a tool to inform clinical judgment. Its use requires specialized training that provides a body of knowledge and clinical skills (American Psychiatric Association, 1994). Derivation of a differential diagnosis between the ASD and other alternative psychiatric or developmental disorders should employ the DSM-IV criteria for analysis and clarification of diagnostic impressions.

Early identification is essential for early therapeutic intervention and leads to a higher quality of life for the child and family.

Numerous studies on early intervention outcome have delineated the benefits of early identification and intervention for children with developmental disabilities and, particularly, for those with difficulties on the autistic spectrum (Dawson & Osterling, 1997; Harris & Delmolino, 2002; Smith, 1999; Committee on Educational Interventions for Children with Autism, 2001). Strong empirical support exists for the benefits of intensive behavioral programs for young children with autistic spectrum disorders, although the precise teaching strategies and curricula content are often a topic of debate (Dawson & Osterling, 1997; Gresham & MacMillan, 1998; Lovaas, 1987; Ozonoff & Cathcart, 1998; Rogers, 1998; Sheinkopf & Siegel, 1998). While the components of intervention programs are often a source of controversy, it is generally agreed that program intensity combined with early diagnosis and intervention can lead to substantial improvement in child functioning (Harris, 1994b; Sheinkopf & Siegel, 1998).

A substantial benefit of early intervention is the positive impact on the family's ability to interact in a developmentally appropriate manner with their child and to have a greater understanding of the disability and how it interacts with family life (Committee on Children with Disabilities, 1994). Early identification and diagnosis enhances the opportunity for effective educational and behavioral intervention; reduction of family stress by giving the family specific techniques and direction; and access to medical and other supports (Cox, Klein & Charman, 1999). In the end, early intervention improves the quality of life for the individual and his/her family, and is cost efficient for the human service delivery system (Jacobson, Mulick & Green, 1998).

Informed clinical judgment is a required element of a screening, diagnostic and assessment process that leads to accurate identification of and intervention planning for ASD.

In the absence of a single biomedical marker, simple laboratory test or procedure for identifying children who meet the diagnostic criteria for one of the ASD, accurate identification of individuals with ASD is entirely dependent on clinical competencies. For the diagnosis of ASD, the knowledge base must include familiarity and experience with the research literature and with children with ASD. Clinical judgment, based upon knowledge and experience with this population, is critical to the interpretation of DSM-IV criteria for ASD. Access to professionals who possess the necessary levels of clinical competency, such as pediatricians and psychologists, can be found in private health systems, state funded regional centers, and university medical centers.

The screening, diagnosis and assessment of ASD presents different challenges through the individual's life span.

While the core impairments in individuals with autistic disorder are commonly identified in early childhood, other spectrum disorders (PDD-NOS, Asperger's disorder) may be identified much later. Although identification of an ASD is usually made during childhood, it is important to recognize that ASD is a lifelong disability that compromises the individual's adaptive functioning from childhood through adulthood to variable extents, and requires different forms of intervention throughout the lifespan. Assessment should never be viewed as a discrete process, but rather as ongoing, flexible and responsive to changes in the individual's profile caused by intervention effects, maturation, family dynamics and other factors.

Practitioners must be aware of and understand confidentiality issues and honor the need for shared information.

Th[e] Guidelines encourage the use of interdisciplinary teams and interagency collaboration in the screening/early identification, diagnostic evaluation and assessment of individuals suspected of having an ASD. Th[e] Guidelines also recognize that "open" oral and written exchange of information among clinicians and agencies places a grave ethical and legal responsibility on those professionals to share only personal information that is clinically pertinent to the purposes of the intervention. A fully informed written consent at each step in the process is not only an ethical responsibility but a legal one as well. The scope of information shared should be decided on a "need to know" basis. For example, the education system might need specific information from the diagnostic and assessment team about a child's learning strengths and challenges. However, family history regarding psychiatric or other health illness that may be important to the diagnostic process should be held in confidence and not automatically shared with the educational planning team without specific consent. Such discretion can be difficult to manage when parents, for example, are asked to sign multiple releases of confidential information with many providers.

Accurate diagnostic evaluation and assessment requires collaboration and problem solving among professionals, service agencies and families.

Th[e] Guidelines promote interdisciplinary, interagency collaboration and partnership between the referred individual, their family and the service delivery system. It is critical that service providers promote collaboration across disciplines, agencies and programs to resolve conflicts of legal mandates.

Collaborative efforts should be made to avoid duplication of effort and maximize efficient use of time in pursuit of the desired outcomes for the individual and his/her family. Respect for divergent perspectives is necessary to delineate a comprehensive diagnostic profile of children, adolescents and adults with autistic spectrum disorders. Rather than viewing each component of the process as separate, these Guidelines stress establishing linkages among, for example, the primary care provider (PCP), the diagnostic and assessment team and educational planning teams. The diagnostic team, in turn, needs to keep the PCP informed by providing feedback and assisting the PCP in working with the family to ensure appropriate referrals for intervention services, transition planning and family support.

An interdisciplinary process is the recommended means for developing a coherent and inclusive profile of the individual with ASD.

Autistic spectrum disorders affect multiple developmental domains. Therefore, utilizing an interdisciplinary team constitutes best practice for a diagnosis of ASD and is an essential component of the assessment process. An interdisciplinary team is essential for establishing a developmental and psychosocial profile of the child and family to guide intervention planning. Such an approach promotes seamless communication among team members and leads to a more integrated, cohesive translation of findings. The interdisciplinary team creates a view of the individual that is detailed, concrete, easily understood and offers realistic recommendations (Klin, Sparrow, Marans, et al., 2000). A quality interdisciplinary process involves shared leadership, respect, integration and coordination among professionals. Team members recognize that their individual contributions inform construction of the overall picture of the child and that their individual interpretations enable formulation of conclusions and recommendations based upon the combined efforts of the team.

From screening through intervention planning, the evaluation process must be family-centered and culturally sensitive.

A family-centered frame of reference reinforces the concept of parents and caregivers as the most knowledgeable source of information about the child, acknowledges that the child is part of a larger family system and sets the stage for ongoing collaboration and communication between professionals and family members. The needs, priorities and resources of the family should be the primary focus and be respectfully considered during each step of screening, diagnostic evaluation and assessment for intervention planning.

A family-centered frame of reference includes cultural sensitivity and regard for family and community diversity of cultural values, language, religion, education, socio-economic and social-emotional factors that influence coping and conceptualization of the individual with ASD. Maintenance of family involvement should remain at the forefront of interactions in keeping with the concept of family as an equal partner in the diagnostic, assessment and intervention processes.

Timely referral and coordination of evaluation and ongoing assessment enhances outcome.

The diagnostic and assessment process should proceed in a timely manner to expedite the provision of services to the individual and family. Referring professionals should be familiar with options within the individual's geographic area and serve as the communication bridge with service providers to minimize service delays and duplicative efforts. While a child may receive a diagnosis at a young age, a comprehensive profile of skills and deficits is often not obtained for months (and sometimes years) after diagnosis. This incomplete or absent documentation of skills is problematic for the child, family and community service providers. Parental stress is heightened as parents worry about their child while also spending time and energy trying to arrange for needed intervention services. Timely referral, integration, and coordination of clinical teams and service providers lessens family stress and leads to more streamlined and efficient service delivery.

Rapid developments in the field require regular review of current best practice procedures and up-to-date training.

Rapid developments in conceptualization, measurement and basic research on ASD require a commitment to periodic review of current best practices. The heterogeneity of behavioral expression in ASD across age and developmental status, combined with rapid increases in clinical research and knowledge about the core features of the disorder, necessitate ongoing education and training opportunities for participating clinicians. Major shifts have occurred in scientific thinking about ASD. The knowledge base in ASD is changing so rapidly that parents and professionals face a daily challenge of keeping abreast of new developments. The challenge is to stay current with new methods of evaluation and treatment, learn about and obtain the latest screening tools, and maintain an awareness of local and regional community resources.

Source:

Autistic Spectrum Disorders: Best Practice Guidelines for Screening, Diagnosis and Assessment

California Department of Developmental Services: 2002
The Guidelines, a publication of the California Department of Developmental Services, are intended to provide professionals, policymakers, parents and other stakeholders with recommendations based on published research, clinical experience and judgment available about "best practice" for screening, evaluating and assessing persons suspected of having ASD. Complete Guidelines can be found at Autistic Spectrum Disorders: Best Practice Guidelines for Screening, Diagnosis and Assessment

Reviewed by athealth on January 29, 2013

Bariatric Surgery for Severe Obesity

Severe obesity is a chronic condition that is hard to treat with diet and exercise alone. Bariatric surgery is an operation on the stomach and/or intestines that helps patients with extreme obesity to lose weight. This surgery is an option for people who cannot lose weight by other means or who suffer from serious health problems related to obesity. The surgery restricts food intake, which promotes weight loss and reduces the risk of type 2 diabetes. Some surgeries also interrupt how food is digested, preventing some calories and nutrients, such as vitamins, from being absorbed. Recent studies suggest that bariatric surgery may even lower death rates for patients with severe obesity. The best results occur when patients follow surgery with healthy eating patterns and regular exercise.

Bariatric Surgery for Adults

Currently, bariatric surgery may be an option for adults with severe obesity. Body mass index (BMI), a measure of height in relation to weight, is used to define levels of obesity. Clinically severe obesity is a BMI > 40 or a BMI > 35 with a serious health problem linked to obesity. Such health problems could be type 2 diabetes, heart disease, or severe sleep apnea (when breathing stops for short periods during sleep).

Recent Development

The Food and Drug Administration (FDA) has approved use of an adjustable gastric band (or AGB) for patients with BMI > 30 who also have at least one condition linked to obesity, such as heart disease or diabetes.

Who is a good adult candidate for surgery?

Having surgery to produce weight loss is a serious decision. Anyone thinking about having this surgery should know what it involves. Answers to the following questions may help patients decide whether weight-loss surgery is right for them.

Is the patient:

  • Unlikely to lose weight or keep it off over the long term using other methods?
  • Well informed about the surgery and treatment effects?
  • Aware of the risks and benefits of surgery?
  • Ready to lose weight and improve his or her health?
  • Aware of how life may change after the surgery? (For example, patients need to adjust to side effects, such as the need to chew food well and the loss of ability to eat large meals.)
  • Aware of the limits on food choices, and occasional failures?
  • Committed to lifelong healthy eating and physical activity, medical follow-up, and the need to take extra vitamins and minerals?

There is no sure method, including surgery, to produce and maintain weight loss. Some patients who have bariatric surgery may have weight loss that does not meet their goals. Research also suggests that many patients regain some of the lost weight over time. The amount of weight regain may vary by extent of obesity and type of surgery. Habits such as snacking often on foods high in calories or not exercising can affect the amount of weight loss and weight regain. Problems that may occur with the surgery, like a stretched pouch or separated stitches, may also affect the amount of weight loss.

Success is possible. Patients must commit to changing habits and having medical follow-up for the rest of their lives.

Bariatric Surgery for Youth

Rates of obesity among youth are high. Bariatric surgery is sometimes used to treat youth with extreme obesity. Although it is becoming clear that teens can lose weight after bariatric surgery, many questions still exist about the long-term effects on teens' developing bodies and minds.

Who is a good youth candidate for surgery?

Experts in childhood obesity and bariatric surgery suggest that families consider surgery only after youth have tried for at least 6 months to lose weight and have not had success.[1] Candidates should meet the following criteria:

  • Have extreme obesity (BMI > 40 )
  • Be their adult height (usually at age 13 or older for girls and 15 or older for boys)
  • Have serious health problems linked to weight, such as type 2 diabetes or sleep apnea, that may improve with bariatric surgery

In addition, health care providers should assess potential patients and their parents to see how emotionally prepared they are for the surgery and the lifestyle changes they will need to make. Health care providers should also refer young patients to special youth bariatric surgery centers that focus on meeting the unique needs of youth.

Mounting evidence suggests that bariatric surgery can favorably change both the weight and health of youth with extreme obesity. Over the years' gastric bypass surgery has been the main operation used to treat extreme obesity in youth. An estimated 2,700 youth bariatric surgeries were performed between 1996 and 2003.[2] A review of short-term data from the largest inpatient database in the United States suggests that these surgeries are at least as safe for youth as adults. As yet, AGB has not been approved for use in the United States for people younger than age 18. However, favorable weight-loss outcomes after AGB for youth have been reported abroad.

The Normal Digestive Process

Normally, as food moves along the digestive tract, digestive juices and enzymes digest and absorb calories and nutrients. After we chew and swallow our food, it moves down the esophagus to the stomach, where a strong acid continues the digestive process. The stomach can hold about 3 pints of food at one time. When the stomach contents move to the duodenum (the first part of the small intestine), bile and pancreatic juice speed up digestion. Most of the iron and calcium in the food we eat is absorbed there. The other two parts of the nearly 20 feet of small intestine absorb nearly all of the remaining calories and nutrients. The food particles that cannot be digested in the small intestine reside in the large intestine until eliminated.

How does surgery promote weight loss?

Bariatric surgery restricts food intake, which leads to weight loss. Patients who have bariatric surgery must commit to a lifetime of healthy eating and regular exercise. These healthy habits may help patients maintain weight loss after surgery.

Types of Bariatric Surgery

The type of surgery that may help an adult or youth depends on a number of factors. Patients should discuss with their health care providers what kind of surgery is suitable for them.

For additional information, go to http://win.niddk.nih.gov/publications/gastric.htm

The Weight-control Information Network (WIN) is a national information service of the National Institute of Diabetes and Digestive and Kidney Diseases of the National Institutes of Health, which is the Federal Government's lead agency responsible for biomedical research on nutrition and obesity. Authorized by Congress (Public Law 103-43), WIN provides the general public, health professionals, the media, and Congress with up-to-date, science-based health information on weight control, obesity, physical activity, and related nutritional issues.

U.S. DEPARTMENT OF HEALTH AND HUMAN SERVICES
National Institutes of Health
Adapted from NIH Publication No. 08-4006
Updated June 2011

Reviewed by athealth on January 29, 2014

Battling an Eating Disorder: When Bulimia Becomes a True American Idol Sized Problem

By Abigail Natenshon, MA, LCSW, GCFP

In a People Magazine article, American Idol contestant, Katherine McPhee disclosed that she has secretly suffered from bulimia for the past five years. It was her success in television's American Idol competition that inspired her to come forward and get help to recover from her life-threatening eating disorder. Katherine, a vocalist who at her worst point was self-inducing vomiting up to seven times a day, claimed that she realized her bulimic behaviors were "equivalent to taking a sledgehammer to her throat" and brought herself to treatment.

Glamorizing Eating Disorder Illnesses? Or Becoming an Invaluable Role Model?

Some may think when celebrities like Katherine come forward with such problems it only "glamorizes" the illness and encourages dysfunction in impressionable young people. In reality, some impressionable youngsters may respond by engaging in self-destructive experimentation, but for the most part, the responses of people like Katherine McPhee provide invaluable role modeling for fans.

Though statistics show that 1 percent of young females in this country suffer with bulimia, the numbers most likely do not reflect the enormity of the problem, as bulimia is among the most frequently missed diagnoses, and only a minority of people with eating disorders, especially with bulimia nervosa, are treated in mental healthcare. A problem cannot be solved until it is defined. In coming forward as she has, McPhee has displayed the courage and intention to achieve her dreams, to become proactive in making her life as healthy, gratified and fulfilled as it can be. Despite the widely held misconception that "once eating disordered, always eating disordered," eating disorders are fully curable in 80 percent of cases where recognized early and treated effectively. In her forthright and courageous stand, this American Idol contestant has become a true American idol.

Uncovering the Secrets of Bulimia Nervosa and Anorexia Nervosa: The Most Lethal Mental Health Disorders

The most lethal of all the metal health disorders, bulimia nervosa and anorexia nervosa are extremely hard to recognize. Highly secretive diseases, they rarely show up in doctors' offices during physical or functional assessments; even laboratory tests do not show evidence of eating disorders until they are in their most advanced stages. By their nature counterintuitive, eating disorders typically give victims a pseudo-sense of power and control, creating the illusion of feeling and becoming "better than ever." In actual fact, certain stages of recovery feel more precarious and painful than does the disease itself. Making matters even more confusing, many of the symptoms of these lethal disorders lay somewhere along the continuum of normal human behaviors. Who doesn't overeat, under-eat or engage in emotional or social eating at times?

Eating disorders, which essentially represent an abuse of food in an effort to resolve emotional problems, transcend a dysfunctional relationship with food to represent the tip of a physical, emotional, cognitive, behavioral and social iceberg, with early signs of clinical eating disorders typically evident in diverse life spheres.

Eight signs that parents and families may see at home, around the dinner table, in the family bathroom, or the child's bedroom:

  1. Erratic eating, eating too much or too little, too frequently or too seldom.
  2. Dieting and other restrictive eating behaviors (in some instances vegetarianism or skipping meals) that can result in extreme hunger and gorging, irregular menstrual periods.
  3. Fear of putting on weight, with an all-encompassing preoccupation with food and eating that can account for as much as 80 percent of an individual's thoughts.
  4. Hiding food, and feeling shame and guilt after eating it. The refusal to eat in the company of others.
  5. Depressive moods
  6. Various forms of purging, including self-induced vomiting, excessive exercising, laxative, diuretic, or Ipecac abuse.
  7. Disappearances into the bathroom during or following meals.
  8. Impulsive, immoderate and out of control behaviors beyond the realm of eating, that might include shop lifting, promiscuity, cutting, engaging in chaotic relationships, abuse of substances such as drugs, alcohol, nicotine, diet pills, etc.

There is nothing passive about eating disorders. Always on the move, they are either getting better or you can be certain they are getting worse. Eating disorder recovery can be a long-term process, requiring input from a diverse team of professionals including physicians, psychotherapists, family therapists, nutritionists, psycho pharmacologists and school counselors. The course of recovery will be as variable, must be as comprehensive, and in many ways will feel as convoluted as the course of disease, typically combining outpatient and inpatient treatment milieus and diverse treatment modes. Victims of eating disorders, as young as age 5 or as old as 60, male or female, individuals alone or living within the context of a supportive or not so supportive family system need help to recognize, accept and conquer these diseases...to become capable of reclaiming their lives, proactively, with steadfast commitment... to fight the good fight for life and life quality.

About the Author:

Having specialized in the treatment of eating disorders for the past 36 years, Abigail Natenshon, MA, LCSW, GCFP, psychotherapist, author of When Your Child Has An Eating Disorder, A Step-by-Step Workbook For Parents And Other Caregivers (Jossey Bass Publishers) and director of Eating Disorder Specialists of Illinois is available to support the role of parents and family as advocates for recovery and to answer all of your questions about eating disorders, their prevention and treatment. As a Guild Certified Feldenkrais Practitioner, Abigail is on the cutting edge of combining traditional psychotherapy with this potent holistic adjunct body technique to enhance body-and self-image healing. For more free resources and information, or to have Abigail speak at your next parental or professional group go to http://www.empoweredparents.com

Page last modified or reviewed by athealth on January 30, 2014

Behavioral Treatment for ADHD

by David Rabiner, PhD

ADHD Introduction

The information presented below is intended to provide a general overview of a behavioral approach to improving children's behavior. Designing and implementing an effective behavioral plan will vary from one child to the next, however, and consultation with an experienced child mental health professional is recommended.

Despite the well documented benefits of stimulant medication for treating ADHD, medication is no panacea, and some children with ADHD should not receive it. There are several reasons for this. First, although medication helps the majority of children with ADHD, as many as 20% derive no real benefit from medication. Second, some children experience side effects that prevent them from receiving medication on an extended basis. Third, many children who benefit from medication still have difficulties with primary ADHD symptoms or associated problems which must be targeted via other means. Fourth, some children with ADHD can have their symptoms managed effectively without medication (this is most likely to be true, however, when symptoms are relatively mild.) In addition to these reasons, some children have extremely strong objections to taking medication - this may be more likely to occur with teenagers. In these circumstances, trying to force medication on a child can create more problems than it solves. For all these reasons, other treatments are often necessary - and some would say, always necessary - to effectively treat ADHD.

An important, non-medical approach used in treating children with ADHD is known as behavior therapy or behavior management. Behavior therapy is based on several simple and sensible notions about what leads children to behave in socially appropriate ways. One reason is that children generally want to please their parents and feel good about themselves when their parent is proud of them. When the relationship between parent and child is basically positive, this is a very important source of motivation. A second reason that children behave appropriately is to obtain positive consequences for doing so (i.e. privileges or rewards). Finally, children will behave appropriately to avoid the negative consequences that follow inappropriate behavior.

The goal of behavior therapy, therefore, is to increase the frequency of desirable behavior by increasing the child's interest in pleasing parents and by providing positive consequences when the child behaves. Inappropriate behavior is reduced by consistently providing negative consequences when such behavior occurs. This is a simplified, but not unreasonable view, of what behavior therapy is all about.

Parent-Child Conflict

My child and I seem to be in conflict almost all the time, and I don't think he cares about pleasing me at all. How can I change this?
Let's begin by focusing on children's desire to please their parents. Often times, relationships between parents and children become fraught with conflict and angry feelings in response to the frustration caused by ADHD symptoms. Good times between parent and child can dwindle to almost nothing, and the child's desire to please his or her parent can evaporate. After all, most of us are not interested in pleasing someone that we constantly argue with. Unfortunately, when this important positive source of motivation for good behavior disappears, parents have to rely more exclusively on the threat of punishment to induce compliance. This generally makes for ongoing conflict and struggle.

Therefore, in many situations the first step in behavioral treatment is to enhance the amount of positive feelings between parent and child. One helpful way to do this is to set aside a certain amount of time each day (30 minutes is certainly sufficient) that is designated as the child's "special time." During this time, the child gets to choose the activity (it must be within reason, of course), and the parent's sole focus is on trying to have a good time with his or her child. During this time, it is important to avoid asking too many questions or giving commands. Instead simply tune in to what your child is doing in an interested and complimentary way. For example, if your child is building a tower with blocks, the comment, "Don't you think it would be better if you used these bigger blocks first?", will be less helpful than a comment like, "Boy, the tower your building is really getting tall!"

The goal of this time is build up good feelings between your child and you so that your child will become more invested in wanting to please you. When this occurs, discipline and limit setting generally go much smoother. When parents first begin to try this, they are often surprised when the child responds by getting chores, homework, or errands done. The absence of this special time can be a real loss for both parents and children, and working to make it part of your routine can yield substantial benefits in parents' relationship with their children.

Using Positive Reinforcement

The second focus of behavioral treatment involves providing your child with positive consequences for behaving in appropriate ways. The simple logic is that you can increase the frequency of desired behavior (e.g. putting away toys) by providing rewards when such behavior occurs. At the simplest level, this requires nothing more than noticing when your child is doing something you want to encourage (e.g. playing quietly) and making sure to comment on it ("Your doing such a nice job of playing quietly. I really appreciate that."). Think about the kinds of behavior you want to encourage, make sure your child understands what you want him or her to do, and then be sure to praise your child whenever you happen to observe it occurring. This simple technique of noticing good behavior is easy to overlook and can be quite helpful. I often recommend to parents that they make a conscious effort to catch their child doing something good at least 5 times a day and to point it out. When children are convinced that their parents notice and appreciate their efforts at behaving well, it frequently increases their desire to do so.

In addition to these "social rewards", behavioral treatment also involves providing your child with concrete rewards and/or privileges for appropriate behavior. As an example, suppose your child has developed the problematic habit of talking back. You tell him to put away his toys, and he tells you "not now, later". One way to increase your child's compliance is to make a tangible reward or privilege contingent on his following your request. For example, you could explain that each time he does what he is told he will earn a point. These points can then be used to "purchase" a privilege such as access to TV, computer time, etc.

Design a Good Behavior Plan

Designing a good behavior plan and implementing it effectively is not easy, and parents may require professional assistance to do this successfully. Although the specifics of a good plan will vary from child to child and from parent to parent, there are several general principles that are important to keep in mind:

  • Be very clear about what behavior is expected of your child in order to earn the reward and make sure your child's understands this.
    For example, "Listening to what I say" would be too vague; "Picking up your toys and putting them away the first time I ask" is more specific.
  • Make sure that the expectation you have for your child is reasonable.
    Do not set you and your child up for failure by having expectations that are not appropriate for your child's age.It is always a good idea to reflect on what you expect from your child and consider whether your expectations are reasonable. For example, punishing a 5 year old for being unable to sit quietly at the dinner table for an hour will generally create problems because most 5 year olds simply cannot do this. For children with ADHD, behavioral expectations need to take this into account, in addition to the child's age.
  • Don't try to work on too many different things at one time.
    It is generally better to focus on a couple of things that are really important rather than taking on everything at once. Choose your battles carefully and selectively!
  • Let your child participate in choosing the types of rewards he or she can earn.
    Children are generally more invested in this type of program when they have some input in it's design. Try to create the feeling that this is something that you are doing with your child rather than something you are doing to your child.
  • Design the program so your child has a good chance to experience some initial success.
    It is important that the child experience some initial success in order to maintain and enhance their motivation. As their behavior improves, you can gradually raise the criterion required to earn rewards.
  • Be sure to provide lots of social rewards (e.g. praise) in addition to the more tangible rewards that can be earned.
    This is a great way to increase your child's desire to please you and to increase the amount of positive feelings between you and your child.
  • Be consistent.
    For this approach to succeed you have to apply it consistently. Using the program one day but not the next, or failing to provide rewards when they are earned, is a sure fire way to keep this from being helpful.

Isn't this bribing my child? Why should he be rewarded for things he should do anyway?

Parents are often concerned that providing their child with rewards for behaving appropriately is nothing more than bribery. The way I prefer to look at this, however, is that you are providing your child with the opportunity to earn extra privileges for behaving in a more mature and cooperative manner. An analogy to the adult workplace may be useful here. If your boss promises a promotion and raise for a specified level of productivity, are you being bribed, or are you being given the chance to earn a deserved reward for a job well done? If your child's behavior improves, shouldn't he or she have access to more privileges than when the child was behaving poorly? That is really all that is being talked about here - the main difference with what most parents already try to do is that the expectations and rewards for meeting those expectations are made more explicit.

Using Negative Consequences to Reduce Misbehavior

In addition to using positive reinforcement to encourage good behavior, behavioral treatment also relies on negative consequences or punishment to reduce undesirable behavior. Simply stated, when a particular behavior is consistently followed by negative consequences for a child, it should diminish in frequency and intensity.

For example, suppose you are trying to reduce your child's tendency to "talk back," and this is being targeted in your behavioral treatment plan. Here is a general approach one might take.

  • First, your child would need to understand exactly what you mean by "talking back" so it is clear what should not be done.
  • Second, you would want to teach your child an acceptable way to disagree with you - how he or she is allowed to express disagreement and how the child can not.
  • Third, as discussed above, you would review with your child the rewards they will earn for not talking back and for expressing disagreements in an acceptable way.
  • Finally, you would discuss with your child what privileges he/she will lose each time the child "talks back". For example, talking back could result in their having to take a "time out", losing TV time, having to go to bed early, etc. If you are using a token system where your child is accumulating tokens that can be used to purchase rewards, talking back can result in the loss of a pre-specified number of tokens.

By setting things up this way, what you are trying to do is to make sure your child understands that there is simply no pay-off for bad behavior. Instead, when he or she acts appropriately, it will always result in good things coming their way. In contrast, when behavioral expectations are not met, the consequences are always negative.

Important: Try hard not to overdo the negative consequences. Children tend to get discouraged if negative consequences are used too frequently, and the child can lose interest in the program as a result. If you find yourself having to resort to negative consequences too frequently, it's important to take a careful look at what may be going wrong - with an eye towards redesigning the program.

Have a Game Plan

Now, it would be wonderful if the first time you used a negative consequence as discussed above, it effectively ended your child's misbehavior. As we all know, however, this is often not the case. Instead, you may take away TV time because of some misbehavior, and your child either ignores you or says he "doesn't care" and continues with the problematic behavior.

It is easy to become frustrated and angry in situations like this. At such times it is easy (I know from experience because this is a mistake I make myself) to blurt out a punishment that is born of frustration and will be difficult if not impossible to enforce:

  • "Your grounded for the next 2 weeks!"
  • "That's it! No more birthday party for you!"

I know that I've had the experience of shouting out something like this and realizing right away that it wasn't something I would stick with. In fact, it wasn't even something I should stick with because it was excessive and unreasonable. As a parent, you are then left with the uncomfortable choice of enforcing something unreasonable to show your child that you mean business or backing down. Choose the former and your child is justifiably upset, and you wind up feeling guilty. Choose the latter, and your child gets the idea that punishments don't matter because you don't stick with them anyway.

One helpful way to avoid this dilemma is to plan out, in advance, a graded series of punishments for persistent misbehavior. For example, when your child initially fails to comply, you could impose a 5 minute time-out. If the non-compliance continues, you could say "If you don't do what your told now, the time out will increase to 10 minutes." Continued non-compliance results in loss of TV in addition to the time out. After that, an earlier bed time could be imposed. You have to decide what specifics make sense, of course, but the general point is to have an escalating series of consequences that you can calmly but firmly announce and calmly but firmly enforce. (It is best that these consequences do not extend into the following day so the new day can get off to a fresh start.) Having this plan in mind can help you to keep your cool and prevent you from blurting out a punishment that is not going to be helpful. If you can stick with this, your child should learn that there is nothing to be gained by persistent disobedience.

Don't Teach Your Child To Misbehave

Here is a pattern that is easy to fall into and which is associated with increasing misbehavior and non-compliance. You ask or tell your child to do something like pick up his toys. Your child ignores you and keeps on playing. You repeat your request, and your child ignores you again. You get angry and intensify your demand; your child gets angry in response and starts to tantrum. After a few more cycles of this, you are both angry. To keep things from exploding, you drop your demand, send your child away, and pick up the toys yourself because "it's not worth all the hassle and aggravation" trying to make your child do it.

Most parents have been through something like this, and with children who have ADHD and who are also oppositional, this is a distressingly frequent occurrence. Unfortunately, what a child learns from this type of exchange is that if he/she just hangs in there and persists in being defiant, the child will eventually get his/her way. What happens, therefore, is that your child's disobedience is actually being rewarded. This can really result in things going downhill because your child is being taught that defiance actually pays off.

This is why it is important to chose your battles carefully. Once you demand something of your child, be sure to follow through with it. If your child persists in being defiant, try using the graded series of consequences as discussed above. Your child needs to see that you mean business, and that there is absolutely no payoff for being disobedient.

Factors Specific to ADHD Child

This type of behavioral approach sounds like something that would be useful with all children. Is there anything different about using this approach with a child who has ADHD?

Using a combination of special time, positive reinforcement, and negative consequences to encourage good behavior is, of course, a technique that can be useful with all children. Although the basic principles are similar for children with and without ADHD, factors specific to ADHD generally require certain modifications to be made. Several of these important modifications are:

  • Children with ADHD generally require more frequent feedback about how they are doing in meeting the parent (or teacher's) expectations.

Research has consistently demonstrated that children with ADHD perform better when they are given frequent feedback about their performance. Thus, if the behavior you are targeting is "following directions", it is better to provide your child with feedback about how well they are following directions every hour, rather than doing this once at the end of the day. The actual time interval is something to experiment with; the important point is that a child with ADHD needs frequent feedback for behavioral programs to be effective.

  • Children with ADHD do better with short term goals than long term goals.

This follows from the above. Along with more frequent feedback, children with ADHD generally require shorter intervals between the opportunity to earn rewards. For example, promising a weekend reward for good behavior during the week may be too far in the future to function as an effective motivator for a child with ADHD. Daily rewards, or even more frequent opportunity to earn privileges, will often be necessary. Providing a child with points or "tokens" for good behavior that can be used to purchase more tangible rewards (e.g. TV time; Nintendo time; getting to rent a video) can be useful because they can be frequently and easily dispensed, and have value because of their connection to desired activities and objects.

  • Children with ADHD require more frequent reminders about what is expected of them and what they can earn for meeting those expectations.

For this approach to be effective, it needs to occupy a prominent place in a child's mind. Children who forget what their behavior goals are and what they are trying to earn by achieving those goals are unlikely to be successful. For a child with ADHD, frequent reminders about the goals and rewards are important. This can be done in the context of providing feedback on how the child is doing.

  • Children with ADHD often require frequent changes in the program to remain interested in it.

Those of you who have already tried various behavior plans may be well aware of this. It is not uncommon for a child to get off to a great start and then lose interest in earning any rewards. The best way to combat this is to try change the program to keep it feeling "new". This can be done by changing the rewards (e.g. one day the reward to be earned in TV time, the next day it is getting to stay up an extra half hour, etc.) If you're using tokens, changing the actual token can also be helpful. For example, one week pennies might be used, the next week marbles, the next week stickers, etc. Obviously, this all depends on the age of the child and what his or her interests happen to be. It certainly takes plenty of hard work and creativity on parents' part.

What kinds of behaviors can be addressed with this type of approach?

In theory, virtually any type of behavior can be targeted using a behavioral treatment approach. For example, primary ADHD symptoms such as not completing tasks can be targeted by providing rewards for task completion. Symptoms such as interrupting and talking out of turn can be targeted in similar ways. Associated difficulties such as deliberate non-compliance, aggression, etc. can also be targeted in a behavioral treatment plan. Regardless of what behavior is being targeted it is essential to be sure that:

  • the child understands what is being expect of him or her;
  • the expectation is reasonable and something the child is capable of doing;
  • the child understands what rewards can be earned by meeting the expectation;
  • the child understands what the negative consequences will be for not meeting the expectation;
  • you follow through with what you say you are going to do

Remember, don't take on to many things at once. Try to set things up so the child has a good chance to experience some early success. Don't expect or require perfection. Even a small improvement is still an improvement.

I don't think this will work because it's impossible to enforce consequences with my child. Trying to enforce a punishment just makes him angrier.

Unfortunately, things can get to this point. Even in these situations, however, sometimes one parent has more success than the other. For children with ADHD who are also oppositional, fathers often seem to have greater success than mothers.

If this is the case, one approach is for mom to calmly and firmly attempt to induce compliance from the child and to be clear about what the consequences for continued non-compliance will be. If the child refuses to comply, make it clear that when dad gets home the child will need to do what is being demanded and that the consequences will be enforced at that time. Plus, an additional negative consequence will also be administered. By refusing to listen to mom, therefore, the child is not getting out of what he or she doesn't want to do, but only delaying the inevitable. In fact, by not listening to mom, the child will actually be making things worse. The intent here is to keep mom from getting into an unsuccessful and escalating battle with the child while making it clear to the child that there is no pay off for not listening to mom. For this approach to work, cooperation between parents and support for each other's efforts is essential.

What if neither parent can get their child to comply?

This is sometimes the case. If both parents are unable to induce compliance from their child, and their best efforts are not successful, consultation with an experienced child mental health professional is essential. The longer behavioral difficulties persist the harder they are to change, and it is critical to stop an escalating cycle of misbehavior as quickly as possible.

The ideas discussed above are intended to provide parents with a general overview of a behavioral approach to improving children's behavior. In many cases, consultation with an experienced child mental health professional will increase the success that parents experience with this approach.

Dr. David Rabiner is a clinical child psychologist who specializes in the evaluation and treatment of children with ADHD. He teaches and conducts research at Duke University. Dr. Rabiner's research on children's social development has appeared in leading national and international journals and has been presented at numerous conferences. He has also served as a consultant on two federally funded grants involving ADHD. His website is at Attention Research Update

Page last modified or reviewed by athealth on January 30, 2014

Being an Effective Parent - Helping Your Child Through Early Adolescence

What can I do to be a good parent for my early adolescent child?

Parents often become less involved in the lives of their children as they enter the middle grades. But your young adolescent needs as much attention and love from you as he needed when he was younger and maybe more. A good relationship with you or with other adults is the best safeguard your child has as he grows and explores. By the time he reaches adolescence, you and he will have had years of experience with each other; the parent of today's toddler is parent to tomorrow's teenager.

Your relationship with your child may change. In fact, it almost certainly must change; however, as she develops the skills required to be a successful adult. These changes can be rewarding and welcome. As your middle school child makes mental and emotional leaps, your conversations will grow richer. As her interests develop and deepen, she may begin to teach you how to slug a baseball, what is happening with the city council or county board or why a new book is worth reading.

America is home to people with a great variety of attitudes, opinions and values. Americans have different ideas and priorities, which can affect how we choose to raise our children. Across these differences, however, research has shown that being effective parents involves the following qualities:

Showing love.

When our children behave badly, we may become angry or upset with them. We may also feel miserable because we become angry or upset. But these feelings are different from not loving our children. Young adolescents need adults who are there for them - people who connect with them, communicate with them, spend time with them and show a genuine interest in them. This is how they learn to care for and love others. According to school counselor Carol Bleifield, "Parents can love their children but not necessarily love what they do, and children need to trust that this is true."

Providing support.

Young adolescents need support as they struggle with problems that may seem unimportant to their parents and families. They need praise when they've done their best. They need encouragement to develop interests and personal characteristics.
Sidebar: Children with ADHD and other behavioral disorders are particularly vulnerable to low self-esteem. They frequently experience school problems, have difficulty making friends, and lag behind their peers in psychosocial development. They are more likely than other children to bully and to be bullied. It is important that parents make themselves aware of their children's concerns and respond to them in positive, consistent, and supportive ways.

Setting limits.

Young adolescents need parents or other adults who consistently provide structure and supervision that is firm and appropriate for age and development. Limits keep all children, including young teens, physically and emotionally safe. Carole Kennedy is a former middle school principal, U.S. Department of Education's Principal-in-Residence (2000) and president of the National Association of Elementary School Principals. She puts it this way, "They need parents who can say, 'No, you cannot go to the mall all day or to movies with that group of kids."

Psychologist Diana Baumrind identifies three types of parents: authoritarian, permissive and authoritative. By studying about findings from more than 20 years of research, she and her colleagues have found that to be effective parents, it's best to avoid extremes. Authoritarian parents who lay down hard-and-fast rules and expect their children to always do as they are told or permissive parents who have very few rules or regulations and give their children too much freedom are most likely to have the most difficult time as parents. Their children are at risk for a range of negative behavioral and emotional consequences. However, authoritative parents, who set limits that are clear and come with explanations, tend to struggle less with their adolescents. "Do it because I said so" probably didn't work for your son when he was 6 and it's even less likely to work now that he's an adolescent.

Being a role model

Young adolescents need strong role models. Try to live the behavior and values that you hope your child will develop. Your actions speak louder than words. If you set high standards for yourself and treat others with kindness and respect, your child stands a better chance of following your example. As adolescents explore possibilities of who they may become, they look to their parents, peers, well-known personalities and others to define who they may become.

Teaching responsibility

We are not born knowing how to act responsibly. A sense of responsibility is formed over time. As children grow up, they need to learn to take more and more responsibility for such things as:

  • completing chores, such as doing yard work, cleaning their rooms or helping to prepare meals, that contribute to the family's well being;
  • completing homework assignments without being nagged;
  • taking on community activities;
  • finding ways to be useful to others; and
  • admitting to both the good and bad choices that they make.

Providing a range of experiences

Adolescence is a time for exploring many areas and doing new things. Your child may try new sports and new academic pursuits and read new books. He may experiment with different forms of art, learn about different cultures and careers and take part in community or religious activities. Within your means, you can open doors for your child. You can introduce him to new people and to new worlds. In doing so, you may renew in yourself long-ignored interests and talents, which also can set a good example for your child. Don't be discouraged when his interests change.

Showing respect

It is tempting to label all young adolescents as being difficult and rebellious. But these youngsters vary as much as do children in any other age group. Your child needs to be treated with respect, which requires you to recognize and appreciate her differences and to treat her as an individual. Respect also requires you to show compassion by trying to see things from your child's point of view and to consider her needs and feelings. By treating your young adolescent with respect, you help her to take pleasure in good behavior.

There are no perfect parents. However, a bad decision or an "off" day (or week or month) isn't likely to have any lasting impact on your child. What's most important in being an effective parent is what you do over time.

Source: US Department of Education
Last Modified: 09/11/2003

Page last modified or reviewed by athealth on January 30, 2014

Bereavement and Grief

What is bereavement and what is grief?

Bereavement is defined as a state of sadness or loneliness. Grief is the collection of feelings and behaviors associated with the loss of a person. The loss is commonly caused by death of a friend or family member. However, the loss can also be caused by such events as someone moving away or by a divorce.

What feelings and behaviors are associated with bereavement and grief?

Some feelings associated with bereavement and grief are numbness, loneliness, sadness, guilt, shock, anxiety, depression, anger, and agitation.

Some behaviors associated with bereavement and grief are crying, insomnia, restlessness, and withdrawal.

What are some of the characteristics associated with grief?

It is extremely common for the person who is grieving to be critical of himself/herself for either doing something to or not doing something for the person who has died or left. It is also common for the grieving person to think that he/she should have died instead of the loved one. It is not unusual for the grieving person to be angry toward others, especially other family members or God.

During the grief process many people are surprised to feel the strongest feelings they have ever felt in their lives. Having a depressed mood during grief is quite normal. Insomnia, crying spells and social withdrawal are common. However, a sense of worthlessness, severe guilt, or thoughts of suicide can signal a problem with the grief process. An evaluation and treatment by a professional can often help the person deal with both normal and abnormal feelings of grief.

What is anticipatory grief?

Anticipatory grief is usually experienced by someone who is observing a loved one die slowly from a terminal illness or an unexpected injury. During this period some people prematurely separate and withdraw from their dying loved one, and therefore, anticipatory grief can sometimes lessen the impact of the loss at the time of death. At other times, however, the person feels a strong sense of closeness to the loved one during the anticipatory grief period, and this leads to a greater sense of loss at the time of death.

How often is grief seen in our society?

Grief is universal for people with close emotional bonds to their friends and families. Since loss is a part of life, grief is extremely common.

How is grief treated?

Although most people recover from their grief, there are those who get stuck in the grieving process. Frequently, brief supportive therapy can be helpful. Support groups can also be quite helpful because a group provides the grieving person with mutual support, empathy, and understanding. Sometimes the grieving person may need medications for depression if the depression becomes severe or if it lasts for more than a couple of months. Also, medications are helpful to the person suffering from prolonged insomnia or excessive anxiety associated with grief.

What happens to someone with grief?

There are usually three overlapping phases of grief:

    • Shock and denial
    • Anguish
    • Resolution

First, a person experiences feelings of disbelief and numbness upon the loss of someone close. The person often describes "being in shock" or "in denial." This period might last just a few minutes, but it can also persist for weeks.

Next, a person in grief goes through a time of acute anguish. During this period he/she experiences waves of distress lasting from a few minutes to an hour or more. Emptiness, weakness, and mental pain are common feelings. The person might believe that he/she can actually see, hear, or communicate with the deceased person.

During the third phase, which can last many months, resolution of the loss takes place, and the grieving person returns to his/her usual activities.

People in grief often experience the same symptoms as those associated with depression. Depressive symptoms such as poor appetite, insomnia, and weight loss are frequently present.

While some people experience unusually intense and disruptive feelings of grief, still others do not express the feelings that are expected or that are considered usual, normal, or healthy during the grieving period. Rather, these people encounter a muted, delayed, or inhibited reaction to the loss of their loved one.

Although most people normally recover from their grief, some people do not, and they experience an intense, prolonged, or chronic grief. If the grief period is too intense, too long, or too inhibited an evaluation and treatment by a professional is recommended.

What can people do if they need help?

If you, a friend, or a family member would like more information and you have a therapist or a physician, please discuss your concerns with that person.

Page last modified or reviewed by athealth on January 30, 2014