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Fight, Flight or Pretend: The 3 Anger Styles in High-Functioning Autistic Kids

“My 8 y.o. son Cory has a diagnosis of autism (high functioning) and has uncontrollable outbursts and aggression when things don’t go his way. He often becomes so distraught that his suffering is palpable. The emotions vivid on his face. His little body tense with distress. Sometimes he will meltdown, at other times he shuts down. Is this just par for the course with autism? Is there anything that can help reduce the intensity, duration and frequency of these behaviors?”

RE: “Is this just par for the course with autism?”

Yes! Many moms and dads recognize that their high-functioning autistic (Asperger’s) youngster has a problem with anger-control. Many feel that their youngster needs to develop some anger-control skills, or needs to find some kind of counseling that will help him get along better in life (e.g., at school, with a parent, with siblings and classmates, etc.). In some cases, professionals have diagnosed a highly-aggressive youngster on the spectrum with Oppositional Defiant Disorder.

Generally, anger falls into three main categories: 1) Fight, 2) Flight, or 3) Pretend to be “Flighting” (while finding indirect ways to Fight). Most high-functioning autistic kids with anger-control problems will go to either extreme of fight or flight. They tend to become aggressive and hostile, or they withdraw into themselves and become extremely quiet, silently stubborn, and depressed (i.e., a shutdown).

“The Fighters”: Child Anger Turned to Aggression—



The Fighters are pretty simple to recognize. They are aggressive. Many times, the characteristics of high-functioning autistic kids with severe anger-control problems are included in the professional diagnosis for Oppositional Defiant Disorder (ODD). Some of the warning signs in the following list are taken from the criteria for professional diagnosis. Others are additional common signs of anger-control problems for kids that are Fighters.
  • Uncontrollable fits of rage (usually these tantrums are used as threats to get their way)
  • Seriously violates rules (e.g., at home, in school, or society in general)
  • Seems to have “emotional diarrhea” and “lets it all out - all the time”
  • Physically disruptive (e.g., hitting the parent)
  • Openly and often defiant of requests
  • Often feels rules are “stupid” or don’t apply to them
  • Often demeans or swears directly to parent or others in authority positions
  • Makes threats
  • Loud voice and yelling
  • Initiates fights with others
  • Has left holes in walls and doors from violent outbursts
  • Furious temper
  • Frequently vocalizes anger
  • Does not follow rules
  • Difficulty accepting a “no” answer
  • Destroys property

The “Fighters” have anger-control problems when the problems are creating an unsafe situation for themselves, for others, or for property around them. If parents or siblings are the focus of physical aggression, the problem is extremely critical to address. High-functioning autistic teens who have abused others as kids are at a higher risk of becoming a threat to society than those who have not. Where these warning signs seem to be a part of daily life, intervention is strongly suggested. Intervention can be through anger-control counseling, or through a program dedicated and experienced in working with autistic kids with emotional regulation difficulties.
 

“The Flighters”: Child Anger Turned to Passive Responses—

The Flighters can also be fairly simple to recognize. They are passive. They do not fight back when confronted. Many of their traits may coincide with the diagnosis of depression. Some of the warning signs below are taken from the professional diagnosis for depression, and others are additional common signs of “shutdowns” for Flighters.
  • Tends to spend a lot of time alone
  • Seems withdrawn
  • Seems to hold anger in
  • Seems to have very little emotion
  • Seems depressed
  • Seems “emotionally constipated”
  • Physical problems may include upset stomach, muscle aches, backaches, frequent headaches, or other physical symptoms from “holding it in”
  • May simply “go along” with whatever - even when it is a poor decision
  • May punch holes in walls or kick doors when “the last straw drops”
  • May have few friends
  • May blame self unnecessarily
  • May be seen as a “loner”
  • Holds anger in, then “blows up” suddenly and violently
  • Has difficulty expressing emotions
  • Extremely passive to the point of getting “walked over” by others
  • Does not engage in much conversation
  • Deals with difficult emotions by “cutting” the emotions off

The “Flighters” are in danger of destroying themselves emotionally from within. They are like a balloon being constantly blown into with no release valve. When they explode, their anger may be violent, and may lead to harming themselves, harming others, or destroying property. Internalized anger is potentially as destructive to a youngster as aggressive anger.

==> How to Prevent Meltdowns and Tantrums in Children with Autism Spectrum Disorder
 
“The Pretenders”: Child Anger Silently Planning Revenge—

Perhaps the most difficult to detect, the Pretenders follow an anger style that seems to be calm on the surface, but is raging, scheming, and planning underneath. They are passive-aggressive. These kids do not directly confront the anger as a Fighter would do. They will be passive and appear to accept what is said, and then will disregard what is said to do their own thing. They are sneaky. Often, they may be unnoticed. While they are giving a person a hug, they are also stabbing them in the back (so to speak). They lack the courage to be direct, and perfect the skills to be deceitful. They know where the “back door” to revenge is, and will use it often. They will give the appearance of a Flighter. The list of Flighter traits also applies to them. Some additional traits to look for with Pretenders are as follows:
  • Tends to sabotage
  • Tends to avoid direct conflict while creating problems in other areas
  • Sneaky behaviors
  • Often gets caught in lies
  • May not admit mistakes
  • May be very good at blaming others
  • Inconsistency between what is said and what is done

High-functioning autistic kids who try to manage their anger through the Pretender style are as potentially dangerous to others and themselves as the other styles. Moms and dads tend to underestimate the Pretender style, because the danger does not seem to be as bad as the aggressive Fighter.

The Hostility Cycle—

From an anger-control perspective, an episode of anger can be viewed as consisting of three phases: escalation, explosion, and post-explosion. Together, they make up the hostility cycle. In this process, the escalation phase is characterized by cues that indicate anger is building. These cues can be physical, behavioral, emotional, or cognitive (thoughts). If the escalation phase is allowed to continue, the explosion phase will follow. The explosion phase is marked by uncontrollable anger displayed as verbal or physical aggressiveness. The final stage of the hostility cycle is the post-explosion phase, which is characterized by negative consequences resulting from the verbal or physical aggression displayed during the explosion phase.

The intensity, frequency, and duration of anger in the hostility cycle varies among children. For example, one high-functioning autistic youngster’s anger may escalate rapidly after a provocative event and, within just a few minutes, reach the explosion phase. Another youngster’s anger may escalate slowly but steadily over several hours before reaching the explosion phase. Similarly, one child may experience more episodes of anger and progress through the hostility cycle more often than the other. Despite differences in how quickly the anger escalates and how frequently anger is expressed, the child will undergo all three phases of the hostility cycle.
 

The intensity of the high-functioning autistic youngster’s anger also may differ. One child may engage in more violent behavior than the other in the explosion phase (e.g., he may assault someone). Another child may express his anger during the explosion phase by shouting at or threatening parents. Regardless of these individual differences, the explosion phase is synonymous with losing control and becoming verbally or physically aggressive.




RE: “Is there anything that can help reduce the intensity, duration and frequency of these behaviors?”

Absolutely! Here are some crucial strategies to help teach your son more constructive ways to deal with anger and frustration:

1. When Cory becomes frustrated, use those incidents as "on-the-spot lessons" to help him learn to calm himself down (rather than always relying on you to calm him down). Every time he acts-out due to low-frustration tolerance, ALWAYS use that moment as a teaching moment. For example, explain to him that we all have little signs that warn us when we’re getting frustrated. We should listen to these signs, because they can help us stay out of trouble. Next, help Cory recognize what specific warning signs he may have that tells him he is starting to get angry (e.g., I talk louder, my cheeks get hot, I clench my fists, my heart starts pounding, my mouth gets dry, I breathe faster, etc.).

2. Use books and social stories about anger to help your son understand and manage it. Well-presented stories about anger and other emotions validate a youngster's feelings and give information about anger. It is important to preview all books about anger, because some stories teach irresponsible anger-control.

3. Use role-playing, puppets, or videos to teach social skills (e.g., how to treat each other, how to work out disagreements, etc.).

4. Use feeling words to help Cory understand the emotions of others (e.g., “Robbie is sitting alone and looks very sad; he may be lonely” …or “When Michael tripped, he looked embarrassed”).

5. Train your son to respond to your "signal" (e.g., a hand motion) to stay calm. Give that signal as soon as he starts "stewing" about something. Alternatively, you can use distraction as soon as you notice him exhibiting an anger sign. If he refuses to be distracted or engaged in dialoguing about his anger and starts yelling, stomping or breaking an object, impose appropriate consequences. But, have these consequences in place ahead of time to serve as a guideline. That means that you have discussed them beforehand and written them out for future reference. Armed with a list of consequences (which preferably consist of withdrawing privileges or charging your son a "penalty"), encourage him to choose such alternatives as doing something else, walking away, or talking about the anger rather than acting it out.
 

6. Try a "time-in" rather than a "time-out." As a parent, you are Cory's main guide in life. He relies on you to be there with him through his difficult emotional experiences, whatever that may be. Thus, no time-out and no isolation may be the best option on occasion. Instead, try a "time-in." Sit with Cory and incorporate other methods mentioned in this post (e.g., work on breathing with him, ask him questions about his feelings, etc.). The important thing is to be fully present with Cory to help him through his emotions. Remember, you are teaching him social skills to be in relationships with others, rather than acting out alone. When some autistic kids are isolated, they often ruminate and feel guilty for their behavior. This only serves to create low self-esteem, which often cycles back to creating behavioral problems.

7. The thought "It's not fair" is a big anger-arouser for many high-functioning autistic kids. If that is the case, ask your son, "Do you feel you are being treated unfairly?" When he answers the question, listen and don't rush to negate his feelings.

8. Teach Cory to take a time-out from the difficult situation and have some “alone-time” for a few minutes. During the time-out, he can rethink the situation, calm down, and determine what to do next. The length of the time-out is determined by the intensity of the emotion. An autistic youngster who is simply frustrated may just need to take a deep breath. The youngster who is infuriated probably needs to leave the room and settle down. After Cory has calmed down, it’s time to decide on a more appropriate response to the situation. There are at least 3 positive choices: talk about it, get help, or slow down. Simplifying the choices makes the decision process easier. Even autistic kids can learn to respond constructively to frustration when they know there are just a few choices.  These choices are skills to be learned. Take time to teach Cory these skills, and practice them as responses to mad feelings.

9. Teach your son to talk about how he feels. Give him a language to express his feelings. If he is too angry to talk or doesn't have the words to express his feelings, ask about the feelings relevant to the specific situation. For example, "Do you feel rejected?" "Hurt?" "Let down?" …etc. When your son expresses the feeling behind his anger (e.g., embarrassment or rejection), suggest some other ways to look at the same event that might not be embarrassing or humiliating.

10. Some high-functioning autistic kids get upset when they know they made a mistake. Instead of admitting their mistake, they act out in anger to deflect the attention off of them. If you realize that this might be the case, it's helpful to say to your son, "Everyone makes mistakes. I am okay with it. Don't feel so bad about it."

==> How To Prevent Meltdowns and Tantrums In Children With High-Functioning Autism and Asperger's
 

11. Stop any and all physically aggressive behaviors! Say something like, "I can't let you hurt each other," or "I can't let you hurt me." Then remove Cory as gently as possible.

12. Sometimes an autistic child’s anger and frustration are caused by very real and inescapable problems in his life. Not all anger is misplaced. Occasionally it's a healthy, natural response to the difficulties that the “special needs” child faces. There is a common belief that every problem has a solution, and it adds to the parent’s frustration to find out that this isn't always the case. Thus, the best attitude to bring to such a circumstance is not to focus on finding the solution, but rather on how you handle the problem as painlessly as possible.

13. Try to establish a home environment that reduces anger and teaches tolerance. For example, you can set a personal example for your son that "big people apologize when they hurt someone” and “it's o.k. to loose and try again.”

14. Simple relaxation tools can help Cory calm down. For example, he can (a) use imagery and visualize a relaxing experience from either his memory or his imagination; (b) slowly repeat a calm word or phrase (e.g., “relax” or “take it easy”) and repeat it to himself; (c) breathe deeply from his diaphragm (however, breathing from the chest won't relax him, so he should picture his breath coming up from the belly).

15. Resist taking Cory’s angry outbursts personally. His motives have more to do with alleviating uncomfortable emotions than with deliberately trying to be “nasty.”

16. One thing that makes many moms and dads angry is to see their youngster challenging their authority and defying them. Sometimes it may appear so, but that may not be the intention of the high-functioning autistic youngster. For example, the child may be too unhappy to be told ‘no’ because he wants something so badly. Of course, you shouldn't give in to your son’s demands, but try to understand what might really be his intention.

17. Many children on the autism spectrum act-out because they simply don’t know how to express their anger any other way. Kicking, screaming, swearing, hitting or throwing things may be the only way they know how to express their emotions. To help Cory express his frustrations appropriately, create an “emotion words” poster together (e.g., "Let’s think of all the words we could use that tell others we’re really frustrated"). Then list his ideas (e.g., angry, mad, annoyed, furious, irritated, etc.). Write them on a chart, hang it up, and practice using them often. When Cory is upset, use the words so he can apply them to real life (e.g., "Looks like you’re really frustrated. Want to talk about it?" …or "You seem really annoyed. Do you need to walk it off?"). Then keep adding new feeling words to the list whenever new ones come up in those "teachable moments" throughout the day.

18. Listen, reflect and validate (without judgment) the feelings Cory expresses. After listening, help him identify the true feeling underlying the anger (e.g., hurt, frustration, sadness, disappointment, fear, etc.). Say something like, "That hurt when your friend was mean to you," or “It was scary to have those boys bully you.”

19. Involve Cory in making a small list of “house rules” (e.g., we work out differences peacefully, we use self-control, we listen to others, we are kind to each other, etc.). Write them down and post them on the refrigerator. Make the rules clear, and follow through with meaningful consequences that are appropriate for Cory’s age when the rules are ignored.

20. Model responsible anger-control yourself. High-functioning autistic kids have an impaired ability to understand emotion when their parents show a lot of anger. Parents who are most effective in helping their kids manage anger model responsible management by acknowledging, accepting, and taking responsibility for their own angry feelings, and by expressing anger in direct and non-aggressive ways.
 

21. Help Cory to understand that anger is a natural emotion that everyone has. Say something like, "It's normal to feel angry. Everyone feels angry from time to time, but it is not O.K. to hurt others."

22. Help your son develop self-regulatory skills. Parents of kids on the spectrum do a lot of “child-regulation work" (i.e., doing things ‘for’ their child rather than ‘with’ their child). This is because parents know that their child has a very limited ability to regulate emotions. As the high-functioning autistic child gets older, parents can gradually transfer control to their child so that he can develop self-regulatory skills.

23. Facilitate communication and problem solving with Cory by asking questions (e.g., How can I help you? What can you do to help yourself? What do you need? Is your behavior helping you solve your problem? …and so on).

24. Encourage Cory to accept responsibility for his anger and to gain control by asking himself the following questions: Did I do or say anything to create the problem? If so, how can I make things better? How can I keep this issue from happening again?

25. Create a “ways to relax” poster. There are dozens of ways to help autistic kids calm down when they first start to get bent out of shape. Unfortunately, most of these “special needs” children have never been given the opportunity to think of those other possibilities. Thus, they keep getting into trouble because the only behavior they know is inappropriate ways to express their frustration. So, talk with Cory about more acceptable "replacement behaviors.” Make a big poster listing them (e.g., draw pictures, hit a pillow, listen to music, run a lap, shoot baskets, sing a song, talk to someone, think of a peaceful place, walk away, etc.). Once he chooses a replacement behavior, encourage him to use the same strategy each time he starts to get upset.

26. Encourage your son to “label” his emotions. For example, a permanent record (book or chart) can be made of lists of labels for “anger” (furious, mad, hot, irritated, annoyed), and he can refer to it when discussing angry feelings.

27. Be sure to VALUE what Cory is experiencing. For example, if he is hurt and crying, never say, "Stop crying." Instead, validate his experience by saying something like, "I’m sure that hurts. That would make me cry too." This makes an ally out of you, rather than a target for free-floating anger. As an ally, Cory learns to trust you, realizing you are there for him no matter what. If he can trust you, he can learn to trust himself and the outer world.

28. Acknowledge strong emotions, helping Cory to save face (e.g., say, "It must be hard to get a low score after you tried so hard").

29. All of us exhibit some "signs" just as we begin to get angry. So, it’s actually fairly easy to identify the “anger signs” in a youngster with high-Functioning Autism. For example, you may detect a certain look in the eye, a tone of voice, or a tightness in your child’s body. Thus, your first course of action is to help him observe these signs right at the onset of anger. Once he can identify the early signs of his anger, he can also learn to diffuse it by self-soothing techniques (e.g., walking away, taking full and vigorous breaths, etc.).

30. Lastly, help Cory understand that he can “choose” how to react when he feels angry or frustrated. Teach him self-control and positive ways to cope with negative impulses (e.g., write about feelings, tense body and then relax, tell someone how you feel, play music or sing, look at books or read, hug a pet or a stuffed animal, find a quiet place or sit alone, exercise, draw or play with clay, count slowly, calm self by breathing deeply, etc.).

By using a few of the ideas listed above, you can help strengthen your relationship with your high-functioning autistic youngster and give him the tools he needs to cope effectively with frustration and anger.

Resources for parents of children and teens on the autism spectrum:
 
 
 
More articles for parents of children and teens on the autism spectrum:
 
Social rejection has devastating effects in many areas of functioning. Because the ASD child tends to internalize how others treat him, rejection damages self-esteem and often causes anxiety and depression. As the child feels worse about himself and becomes more anxious and depressed – he performs worse, socially and intellectually.

Click here to read the full article…

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Meltdowns are not a pretty sight. They are somewhat like overblown temper tantrums, but unlike tantrums, meltdowns can last anywhere from ten minutes to over an hour. When it starts, the Asperger's or HFA child is totally out-of-control. When it ends, both you and your child are totally exhausted. But... don’t breathe a sigh of relief yet. At the least provocation, for the remainder of that day -- and sometimes into the next - the meltdown can return in full force.

Click here for the full article...

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Although Aspergers [high-functioning autism] is at the milder end of the autism spectrum, the challenges parents face when disciplining a teenager on the spectrum are more difficult than they would be with an average teen. Complicated by defiant behavior, the teen is at risk for even greater difficulties on multiple levels – unless the parents’ disciplinary techniques are tailored to their child's special needs.

Click here to read the full article…

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Your older teenager or young “adult child” isn’t sure what to do, and he is asking you for money every few days. How do you cut the purse strings and teach him to be independent? Parents of teens with ASD face many problems that other parents do not. Time is running out for teaching their adolescent how to become an independent adult. As one mother put it, "There's so little time, yet so much left to do."

Click here to read the full article…

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Two traits often found in kids with High-Functioning Autism are “mind-blindness” (i.e., the inability to predict the beliefs and intentions of others) and “alexithymia” (i.e., the inability to identify and interpret emotional signals in others). These two traits reduce the youngster’s ability to empathize with peers. As a result, he or she may be perceived by adults and other children as selfish, insensitive and uncaring.

Click here
to read the full article...

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Become an expert in helping your child cope with his or her “out-of-control” emotions, inability to make and keep friends, stress, anger, thinking errors, and resistance to change.

Click here for the full article...
 
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A child with High-Functioning Autism (HFA) can have difficulty in school because, since he fits in so well, many adults may miss the fact that he has a diagnosis. When these children display symptoms of their disorder, they may be seen as defiant or disruptive.

Click here for the full article...

The Role of Environment in the Psychiatric Difficulties of Kids on the Spectrum

In a multitude of ways, the environment affects children with Asperger’s and high-functioning autism (HFA), and is a major factor that influences the severity of comorbid psychiatric disorders (e.g., anxiety, depression, OCD, bipolar disorder, ADHD, Tourette Syndrome, personality disorders, ODD, etc.).

Undeniably, the varied expression of psychiatric problems in kids with Asperger’s and HFA is directly related to environmental factors, which suggests the opportunity for planning various interventions. For example, family and daily routines should be considered as environmental factors that can lead to exacerbation (i.e., an increase in severity) or amelioration (i.e., a decrease in severity) of comorbid disorders.



The challenge of understanding the special needs of Asperger’s and HFA kids, and the problems associated with building a close relationship with them, often contributes to increased stress in their moms and dads. Parents of kids on the autism spectrum have been shown to have a reduced sense of happiness and security, and tend to display a general lower quality of life – even in comparison with parents of kids with other disorders (e.g., cerebral palsy or mental retardation). Furthermore, moms were found to experience a higher level of stress than dads, and this higher stress is often related to unusual behavioral traits of the youngster (e.g., hyperactivity, conduct problems, etc.).

==> Parenting System that Significantly Reduces Defiant Behavior in Teens with Aspergers and High-Functioning Autism


Other research reports elevated rates of anxiety-related personality traits among the relatives (e.g., siblings, grandparents, etc.) of kids on the spectrum. Moreover, elevated anxiety levels in the moms and dads of these young people can be considered an important environmental factor that can trigger genetically-determined personality traits that are eventually shared with other family members and constitute a genetic family-loading for psychiatric disorders.

The importance of environmental factors in the expression of psychiatric symptoms was investigated in a sample of young people with Autism Spectrum Disorders (ASD), including children with Asperger’s and their siblings, with an evaluation reported independently by parents and educators. Reports by educators showed a much lower prevalence of comorbidity in these children (in particular for somatic, oppositional, conduct, attention, anxiety, and affective problems) as compared to the reports by their moms and dads. These results support the idea that the expression of psychiatric problems in kids with Asperger’s varies depending on the environmental context, and that their identification depends on the type of observer (in this case, teacher versus parent).

There is often a lack of consensus between the reports of parents and educators regarding the behavioral characteristics of kids with Asperger’s and HFA, hence suggesting that caution should be used when making conclusions about the presence of comorbid psychiatric difficulties based simply on the environmental context or a single informant source. Instead, information should be gathered from multiple sources and settings, including direct observation by therapists.

The problems that the youngster experiences in terms of social relationships are even greater outside of the home environment (e.g., school, church, scouts, etc.). The lack of adequate teacher-parent communication, coordination among social service providers, and social support often leaves the parents alone with the burden of providing a more intensive level of care and any additional support.

Unfortunately, schools are not always equipped to deal with the unique needs of the Asperger’s or HFA student, and this often drives him or her to develop feelings of low self-esteem, sadness, and self-blame, which often leads to other problems (e.g., meltdowns, depression, hyperactivity, conduct problems, etc.).

Research has also reported that negative events (e.g., parental discord, frequent changes of own residence, death of a family member, etc.) have significant influence on the youngster’s mood and functioning – and have been associated with clinical depression. These children tend to react to negative life events more severely (and in a different way) than “typical” children do. HFA students are also more vulnerable to developing mood disorders and depressive symptoms than other children (which may be correlated to a genetic predisposition).

Since environmental factors appear to substantially influence the expression of psychiatric comorbidities in children on the spectrum, more attention should be focused on the interactions between these children and their diverse everyday life events. Parents, teachers, and professionals can develop coping strategies and provide a better social support that may contribute to a decrease in the incidence of psychiatric disorders in Asperger’s children.

==> Parenting System that Significantly Reduces Defiant Behavior in Teens with Aspergers and High-Functioning Autism


There are numerous accommodations that parents can make to help their child cope effectively with his or her environment. Here are just a few:
  1. Allow more time to complete chores, homework, etc.
  2. Avoid being critical and negative toward your youngster.
  3. Avoid over-scheduling him and allow him free time to play, read, listen to music, or just relax.
  4. Avoid placing unrealistic expectations on your child.
  5. Break tasks down into a few small steps (no more than 5) that can be completed one at a time so that your youngster does not feel overwhelmed with the task. For example, “It’s time to clean your room. So, put your clean clothes in this drawer. Pick up your dirty clothes off the floor and put them in this laundry basket. Then take the basket to the laundry room.”
  6. Create a special signal (e.g., tapping the tip of your nose) that you can use with your youngster to redirect his attention back to what you are saying whenever necessary.
  7. Demonstrate active interest in your youngster’s school progress and support her with her learning and homework.
  8. Encourage physical activity and healthy eating habits.
  9. Have a crisis plan in place in the case of meltdowns (e.g., due to your child’s sensory sensitivities, due to his inability to cope or interact with siblings, etc.). This plan may include providing a quiet place for your youngster to go when needed.
  10. Help build your youngster’s sense of self-worth by recognizing his achievements.
  11. Listen to your youngster and encourage him to talk about his feelings and worries.           
  12. Manage your own stress, and be a positive role model.
  13. Monitor their youngster’s access to media and ensure she is aware of safe online practices.
  14. Prepare your child in advance for any changes in routine or other unexpected activities. For example, use this 3-stage warning: “In 15 minutes, we are going to the grocery store.” Then after 5 minutes have passed, repeat your instruction and say “In 10 minutes, we are going to the store.” Then after 5 minutes, say “We are leaving in 5 minutes.”
  15. Provide a written, predictable schedule of events (e.g., “On school days, you get dressed, brush your teeth, eat some breakfast, get your school bag, and then get on the bus”). Remember, Asperger’s kids thrive on routine.
  16. Regularly spend calm and relaxing time with your youngster.
  17. Set firm expectations regarding house rules. In many cases, Asperger’s kids may not want to follow a rule that holds no interest for them (e.g., “Be sure to wash your hands before you come to the dinner table”). It is important for parents to establish and maintain control – even when their child has an Autism Spectrum Disorder.
  18. Show active interest in your youngster’s activities and hobbies, and participate when possible.
  19. Support your youngster if he is exposed to bullying.
  20. Use less verbal instruction, and replace it with visual instruction. For example, use drawings, pictures, or other images to create a “chores chart” or a “house-rules chart.”
  21. Use positive reinforcement for good behavior as often as possible!

When environmental stress becomes too much to handle, the youngster can develop a range of physical, emotional or behavioral symptoms, and can even be at risk of developing other mental health problems. Also, he may find it difficult to recognize and verbalize when he is experiencing stress. Thus, it is important for moms and dads to teach their “special needs” child to recognize and express his emotions, and to use healthy ways to cope effectively with the environment.

More resources for parents of children and teens with High-Functioning Autism and Asperger's:

==> How To Prevent Meltdowns and Tantrums In Children With High-Functioning Autism and Asperger's

==> Launching Adult Children with Asperger's and High-Functioning Autism: Guide for Parents Who Want to Promote Self-Reliance

==> Teaching Social Skills and Emotion Management to Children and Teens with Asperger's and High-Functioning Autism

==> Parenting Children and Teens with High-Functioning Autism: Comprehensive Handbook



==> Parenting System that Significantly Reduces Defiant Behavior in Teens with Aspergers and High-Functioning Autism

Six Symptom Clusters of ASD [level 1] that May Warrant Medication

"We have generally been against trying medication, even to treat the worst symptoms of our autistic child, but is there a point at which the advantages of some form of drug treatment outweigh the disadvantages?"

To answer this question, we will need to look at six clusters of symptoms. They are a convenient way of talking about drug treatments for the common kinds of behaviors that hinder the lives of children and teens who have Asperger’s (AS) and High-Functioning Autism (HFA).

These clusters are not comprehensive, but were chosen because they are common reasons to seek drug treatment for HFA:

1. Inflexibility and Behavioral Rigidity: Symptoms of inflexibility or behavioral rigidity are often difficult to quantify, and yet often introduce some of the most disruptive chronic behaviors exhibited by children with HFA. These can be manifest by minor differences in the environment (e.g., changes in location for certain activities), difficulties tolerating changes in routine, and changes to plans that have been previously laid out.

For some of these “special needs” kids, this inflexibility can lead to aggression, or to extremes of frustration and anxiety that thwart activities. Parents may find themselves “walking on eggshells” in an effort to circumvent any extreme reaction from their “fragile” child. Also, theHFA child himself may articulate his anxiety over fears that things will not go according to plan, or that he will be forced to make changes that he can’t handle. Sometimes these behaviors are identified as “obsessive-compulsive” because of the child’s need for ritualized order or nonfunctional routine.



It is not known whether these symptoms are produced by disturbances in the same cortico-striatal-thalamo-cortical circuitry that is believed to produce OCD. However, the model of obsessive-compulsive disorder has suggested that use of SRI agents can be useful in ameliorating this problem. Whether the effect of SRI medications on this symptom cluster is mediated by a general reduction in anxiety, or is specific for “needs for sameness” is not known. Reports from studies of alpha-adrenergic medications (e.g., clonidine, guanfacine) also suggest a decrease in these rigid behaviors.

==> Unraveling The Mystery Behind Asperger's and High-Functioning Autism

2. Stereotypies and Perseveration: Stereotyped movements and repetitive behaviors are a common feature of HFA. As with behavioral rigidity and inflexibility, similar models for stereotypy and obsessive-compulsive disorder have been proposed. Stereotypy also may be closely related to tic disorders in which repetitive behaviors emerge from impairment in dopaminergic and glutamaturgic systems.

The treatments for stereotyped movements and perseveration closely parallel those for behavioral inflexibility, and the two clusters are often grouped together in studies of treatment effectiveness. Thus, serotonin reuptake inhibitors and alpha-adrenergic agonists may be helpful. Also, the hypothesis that dopamine may play a role suggests that dopaminergic blocking agents should be added to the possibilities. Reports from studies of olanzapine, risperidone, and ziprasidone suggest this is warranted.

3. Hyperactivity and Inattention: Hyperactivity and inattention are common in HFA kids, particularly in early childhood. Differential diagnostic considerations are vital, particularly in the context of AS and HFA. Hyperactivity and inattention are seen in a variety of other disorders (e.g., developmental receptive language disorders, anxiety, and depression). Therefore, the appearance of inattention or hyperactivity does not point exclusively to ADHD. The compatibility of the child and her school curriculum is particularly important when evaluating symptoms of hyperactivity and inattention. There is a risk that a school program that is poorly matched to the child's needs (e.g., by over-estimating or under-estimating her abilities) may be frustrating, boring, or unrewarding. If the verbal or social demands exceed what she can manage, they may produce anxiety or other problems that mimic inattention or induce hyperactivity.

Virtually every variety of medication has been tried to reduce hyperactive behavior and increase attention. The best evidence at this point supports dopamine blocking agents, stimulants, alpha-adrenergic agonists, and naltrexone.

4. Anxiety: Young people with HFA are particularly vulnerable to anxiety. This vulnerability may be an intrinsic feature of ASD through a breakdown in circuitry related to extinguishing fear responses, a secondary consequence of their inability to make social judgments, or specific neurotransmitter system defects.

The social limitations of HFA make it difficult for these “special needs” children to develop coping strategies for soothing themselves and containing difficult emotions. Limitations in their ability to grasp social cues and their highly rigid style act in concert to create repeated social errors. They are frequently victimized and teased by their peers and can’t mount effective socially adaptive responses.

Limitations in generalizing from one situation to another also contributes to repeating the same social mistakes. In addition, the lack of empathy severely limits skills for autonomous social problem-solving. For higher functioning kids on the autism spectrum, there is sufficient grasp of situations to recognize that others “get it” when they do not. For others, there is only the discomfort that comes from somatic responses that are disconnected from events and experience.

Several agents have been tried for treatment of anxiety. There is no reason to suspect that children with autism are less likely to respond to the medications used for anxiety in children without autism. Therefore, SRIs, buspirone, and alpha-adrenergic agonist medications (e.g., clonidine, guanfacine) all have been tried. The best evidence to date supports use of selective serotonin reuptake inhibitors. (Note: Kids with HFA may be more vulnerable to side effects and to exhibit unusual side effects.)

5. Depression: Depression seems to be common among teens and young adults with HFA. Many of the same deficits that produce anxiety may conspire to generate depression. There is also good evidence that serotonin functions may be impaired in young people with autism. The basic circuitry related to frontal lobe functions in depression may be affected. In addition, deficits in social relationships and responses that permit one to compensate for disappointment and frustration may fuel a vulnerability to depression. There is some genetic evidence suggesting that depression and social anxiety are more common among first-degree relatives of autistic kids, even when accounting for the subsequent effects of stress.

==> Unraveling The Mystery Behind Asperger's and High-Functioning Autism

The medications that are useful for depression in “typical” kids and teens should be considered for those with HFA who display symptoms of depression. Since some features of depression and autism overlap, it is important to track that the changes in mood are a departure from baseline functioning. Therefore, the presence of social withdrawal in a child with HFA should not be considered a symptom of depression unless there is an acute decline from that child's baseline level of functioning.

The core symptoms of depression should arise together. Therefore, the simultaneous appearance of symptoms (e.g., decreased energy, further withdrawal from interactions, irritability, loss of pleasure in activities, sadness, self-deprecating statements, sleep and appetite changes, etc.) would point to depression.

Children and teens on the autism spectrum who display affective and vocal monotony are at higher risk for having their remarks minimized. They can make suicidal statements in a manner that suggests an off-hand remark without emotional impact. When comments are made this way, parents may underestimate them. In young people with HFA, the content of such comments may be more crucial than the emotional emphasis with which they are delivered.

Drugs that are useful for treatment of depression in children with HFA are serotonin reuptake inhibitors. There also may be indications for considering tricyclic agents with appropriate monitoring of ECG, pulse, and blood pressure. There are no medications that have been shown to be particularly more beneficial for depressive symptoms in children on the spectrum. Therefore, the decision as to which ones to use is determined by side effect profiles, previous experience, and responses to these medications in other family members.




6. Aggression: Aggression is seldom an isolated problem and is particularly complex in children with AS and HFA. It is important to understand that aggressive behavior is not always associated with just one condition and can have highly varied sources. An array of theoretic models has been proposed to understand aggressive behavior in kids on the spectrum. There are promising biologic models that suggest the behavior arises from alterations in dopaminergic reward mechanisms, and cognitive models suggesting that such acts are an outcome of conditioned learning. Tantrums and physical aggression are often responses to a variety of circumstances and occur in the context of diverse emotions.

==> Unraveling The Mystery Behind Asperger's and High-Functioning Autism

It is useful to know the circumstances preceding and following aggressive outbursts before selecting a particular medication. For instance, when aggression is a response to anxiety or frustration, the most helpful interventions target those symptoms and the circumstances that produce them rather than exclusively focusing on aggressive behavior.

Unfortunately, the request for drug treatment typically follows a crisis, and the press for a rapid, effective end to the behavior problems may not permit the gathering of much data or discussion. Nonetheless, it is NOT appropriate to “always” begin with one agent or another. Moving to a more “reliable” medication too quickly may mean that the child takes on cardiovascular, endocrinologic, and/or cognitive risks that may be otherwise avoided.

There are reports in support of using serotonin reuptake inhibitors, alpha-adrenergic agonists, beta-blocking agents, mood stabilizers, and neuroleptics for aggressive behavior. When a doctor has the luxury of time, the support of family, and collaboration with staff where the child is attending school, then a drug that is safer, but perhaps takes a longer time to work or is a little less likely to help, can be tried.

In addition to cognitive and behavioral interventions, many children and teens on the autism spectrum are helped by medications (e.g., selective serotonin reuptake inhibitors, antipsychotics, stimulants, etc.) to treat the associated problems listed above. Experts agree that the earlier interventions are started, the better the outcome. With increased self-awareness and therapy, most kids and teens learn to cope with the challenges of AS and HFA.

 
 
More articles for parents of children and teens on the autism spectrum:
 
Social rejection has devastating effects in many areas of functioning. Because the ASD child tends to internalize how others treat him, rejection damages self-esteem and often causes anxiety and depression. As the child feels worse about himself and becomes more anxious and depressed – he performs worse, socially and intellectually.

Click here to read the full article…

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Meltdowns are not a pretty sight. They are somewhat like overblown temper tantrums, but unlike tantrums, meltdowns can last anywhere from ten minutes to over an hour. When it starts, the Asperger's or HFA child is totally out-of-control. When it ends, both you and your child are totally exhausted. But... don’t breathe a sigh of relief yet. At the least provocation, for the remainder of that day -- and sometimes into the next - the meltdown can return in full force.

Click here for the full article...

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Although Aspergers [high-functioning autism] is at the milder end of the autism spectrum, the challenges parents face when disciplining a teenager on the spectrum are more difficult than they would be with an average teen. Complicated by defiant behavior, the teen is at risk for even greater difficulties on multiple levels – unless the parents’ disciplinary techniques are tailored to their child's special needs.

Click here to read the full article…

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Your older teenager or young “adult child” isn’t sure what to do, and he is asking you for money every few days. How do you cut the purse strings and teach him to be independent? Parents of teens with ASD face many problems that other parents do not. Time is running out for teaching their adolescent how to become an independent adult. As one mother put it, "There's so little time, yet so much left to do."

Click here to read the full article…

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Two traits often found in kids with High-Functioning Autism are “mind-blindness” (i.e., the inability to predict the beliefs and intentions of others) and “alexithymia” (i.e., the inability to identify and interpret emotional signals in others). These two traits reduce the youngster’s ability to empathize with peers. As a result, he or she may be perceived by adults and other children as selfish, insensitive and uncaring.

Click here
to read the full article...

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Become an expert in helping your child cope with his or her “out-of-control” emotions, inability to make and keep friends, stress, anger, thinking errors, and resistance to change.

Click here for the full article...
 
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A child with High-Functioning Autism (HFA) can have difficulty in school because, since he fits in so well, many adults may miss the fact that he has a diagnosis. When these children display symptoms of their disorder, they may be seen as defiant or disruptive.

Click here for the full article...

Children on the Autism Spectrum and "Medication Phobia"

"Our daughter (autistic) is suppose to take 2 meds everyday, but always has a meltdown whenever we try to give them to her. She is so afraid of the side effects that she can’t put her anxiety aside long enough to take them. Is this common? What can we do? She has to take these two prescriptions according to the doc."

While lack of awareness by parents and their Asperger’s (high-functioning autistic) child of adverse drug reactions can have serious consequences, having a phobia of medications can also have serious harmful effects on the child’s health (e.g., problems with medication compliance, refusal of necessary drug intervention, etc.).

Medication phobia can also present in moms and dads who are concerned about giving medications to their youngster, fearing that the medications will do more harm than good.

Fears of taking medication is prevalent in children who have experienced unpleasant withdrawal effects from psychotropic drugs. Also, medication phobia can be triggered by unpleasant adverse reactions to drugs that are prescribed inappropriately or at excessive doses. Furthermore, due to sensory sensitivities, many children on the autism spectrum have great difficulty with – and a fear of – swallowing pills.



The nature of Asperger’s and high-functioning autism (HFA) introduces significant challenges, particularly when using drug treatments. Building a relationship and gaining the child's trust can be hard to accomplish. Many young people on the autism spectrum feel forced to take medication and commonly recoil from the idea of drug treatment. Some are so frightened of the effects of medications that they can’t put those fears aside long enough to try one.

 A real paradox occurs in the area of anxiety. Many, if not most, children on the spectrum experience anxiety. However, the degree of anxiety that makes it appropriate to consider medication for it can also interfere with the child adhering to a prescription. Despite the enormous distress the child’s anxiety symptoms generate, he or she may not be able to put aside worries about the medication. Parents may be the only people the child will allow to counter these fears.

==> How To Prevent Meltdowns and Tantrums In Children With High-Functioning Autism and Asperger's

Many of the difficulties associated with anxiety (e.g., behavioral problems) are more distressing to those around the child (e.g., parents, siblings, teachers, etc.) than to the child herself. Children with Asperger’s and HFA commonly lack the ability to perceive the signals of comfort or pleasure of others or, once acquired, to use others' emotions to guide their behaviors. Lacking this ability, these children struggle with the initial fears related to taking medication or entering into other therapy that can help them get along with others. Often they can’t see why they should be required to take a particular drug simply because others are upset. Threatening an unpleasant consequence is usually ineffective. These “special needs” kids are often willing to accept dreadful consequences rather than compromise a rigidly held rule, contain a pressing urge, tackle managing an anxious feeling, or yield control to someone else.

Another hurdle is the limitations children with Asperger’s and HFA have in identifying their own internal mood states and emotions. As a result, parents, teachers and other adults may be unable to gauge whether the child experiences less subjective anxiety, anger, or sadness. The child's emotional “comfort” may not be available to the therapist for rating improvement. To monitor progress, the therapist may have to draw on multiple observations, rely more or less exclusively on the child's somatic experience, and to use highly concrete measures.

An associated obstacle is the deficits children on the autism spectrum have perceiving and understanding other's intentions, wishes, or needs. This blindness to others often contributes to the child’s inability to grasp how his reactions contribute to a bad result. More often, the child believes he is being victimized. The teasing and bullying that the Asperger’s or HFA child often has to endure at school only adds to this. For this child, it may be impossible to tell the difference between (a) the natural consequences associated with his choices and (b) mistreatment by others. Nonetheless, the child is likely to be oblivious to how his actions contribute to a chain of events that end in a meltdown, outburst or aggression – or even to believe that the outcome should be prevented in the future. This blindness also produces a tendency for the child to accuse those around him of causing problems. Faulting others is highly characteristic and is a direct result of the disorder.

Many children with Asperger’s and HFA display profound weaknesses in the ability to observe sequences of events and transactions accurately, and in understanding the “logical” responses of those around them. These kids can be highly concrete. The “big picture” of behaviors and emotions is often lost to an excessive attention to small changes in circumstances or minor details. They often have a flawed sense of proportion (e.g., premeditated, forceful retaliation may be viewed as a justified response to someone else's small gaffe).

In addition, kids on the autism spectrum often are rigid in their behaviors with inflexible routines, dedication to unnecessary rules, or ritualized behaviors. Sometimes these may be no more than a minor irritation to others, but when severe, they can obstruct action and exasperate those around them. Severe rigidity can be highly frustrating to others, and attempts to counter it may produce aggressive reactions from the child. She may perceive that “if only my parents would let me do what I want,” there would be no problems at all.




==> How To Prevent Meltdowns and Tantrums In Children With High-Functioning Autism and Asperger's

Several other obstacles are related to the issue of medication:


1. No drug influences the core pragmatic social deficits (e.g., misinterpreting cues, failure to appreciate social cues and nuances, etc.). As a result, there is no one algorithm to follow that targets the primary source of impairment or the greatest source of difficulty for the Asperger’s child.

2. There is an absence of high quality, valid studies of the efficacy of different drugs for specific symptoms in this population. Most of the studies are case reports or small-scale, open, unblinded trials. This requires the clinician to take findings from studies of other disorders in the hope that the results translate to Asperger’s. This presumption is entirely theoretic at this point. Much of the time, a clinician has no way to gauge the child’s response in comparison with others with this disorder. Global functioning may or may not be meaningfully improved.

3. A third obstacle is the absence of treatment and outcome studies of Asperger’s with comorbid conditions. For instance, it may be erroneous to presume that mood dysregulation and the response to mood stabilizers in the context of Asperger’s is identical to bipolar disorder in an otherwise ordinary teenager. Nearly all treatment studies of other childhood disorders exclude children with PDD spectrum disorders. As a result, when an Asperger’s child appears in the clinician's consulting room, unless one has the luxury of a previous relationship and a sense of that child's baseline functioning, one can’t know what the child looks like when the comorbid condition is “resolved.” Most of the core social impairments are likely to remain, although functional gains are possible.

Treatment of Medication Phobia—

Treatments for medication phobia can be approached from several different angles. For example:
  • Practicing relaxation techniques (e.g., deep breathing, yoga, muscle relaxation, etc.) can help the Asperger’s child deal with the emotional and physical symptoms of medication phobia.
  • Learning to keep negative thoughts at bay is helpful, because a negative train of thought can initiate the medication phobia. 
  • If choking while taking medicine is the child’s fear, then the physician can give options for liquid or crushed medicines. 
  • Children with medication phobias can learn self-help methods to deal with the worst of the symptoms. Getting informed about the phobia is the first step in overcoming the fear.
  • Cognitive-behavioral therapy, more commonly known as exposure therapy, may be the best approach for dealing with medication phobia. Using the exposure therapy method slowly exposes the child with his phobia first through the mind in therapy sessions, and then in real life situations. Depending on the severity of the case, therapy can help the child cope with his fear and get his health back on track.

Being afraid of taking medicine - or of suffering adverse reactions - is not uncommon for children on the autism spectrum. However, by utilizing the treatment methods listed above, parents can help their child gain a comfort level such that taking prescribed medication is perceived as a rather harmless endeavor.

More resources for parents of children and teens with High-Functioning Autism and Asperger's:

==> Parenting System that Significantly Reduces Defiant Behavior in Teens with Aspergers and High-Functioning Autism

==> Launching Adult Children with Asperger's and High-Functioning Autism: Guide for Parents Who Want to Promote Self-Reliance

==> Teaching Social Skills and Emotion Management to Children and Teens with Asperger's and High-Functioning Autism

==> Parenting Children and Teens with High-Functioning Autism: Comprehensive Handbook

==> Unraveling The Mystery Behind Asperger's and High-Functioning Autism: Audio Book

==> Parenting System that Reduces Problematic Behavior in Children with Asperger's and High-Functioning Autism


COMMENTS:

•    Anonymous said…  I have a 7 year old who won't take medicine. I hope he can learn over the years ✨🙏🏼✨
•    Anonymous said…  Mine wouldn't take any meds until he could take a pill (this included antibiotics). He would actually throw up on me if I forced them. I had to be really creative in hiding the meds in foods and drinks. I taught him to swallow pills using mini m&m's when he was 4. Now he takes a daily medication with ease.
•    Anonymous said…  My daughter is 15 and takes meds really well now. She knows if she doesn't take those meds her actions are bad and she has withdrawals. I would talk to a doc and see if anything liquid or other possibilities are available
•    Anonymous said… Carbonation helps to float the tablet in their mouth. It is how I had to teach one of my kids to swallow a pill. She could not do it with regular water and still cannot. We practiced with Tic Tac's a lot.
•    Anonymous said… Dispersible tabs here and a capsule emptied into water every single morning. No way he'd ever swallow tablets. And his melatonin drops have to be made up without flavouring......
•    Anonymous said… Fascinating reading everybody's comments about swallowing. My son cannot swallow any form of tablet. Puts it on his tongue and then just freezes and panics. Interesting that so many of you have the same issue. Another thing I have learnt today.
•    Anonymous said… His OT worked with him on swallowing 'pills', mini MM's and regular size cut in half. Now he Can swallow the small gel oval shaped laxatives, but doesn't want to. Currently he is applying DoTerra Oils himself.
•    Anonymous said… I can't even get my son to take melatonin. I hide it in chocolate milk. He had eye surgery and it took 3 of us to hold him down just to get the woozy meds in to him, which he then spit half of it out and in to the nurse. He was 5 then, he's 8 now.
•    Anonymous said… I have a 12 year old who won't take medicine.
•    Anonymous said… Mine doesn't take medication. I think it's only kids with Adhd that are medicated isn't it? Or kids with excessive stimming?
•    Anonymous said… Mine is afraid to swallow the capsules. I break them open over a spoon of yogurt and he eagerky takes them. He says they allow him to stop and think.
•    Anonymous said… My 16 year old Aspie takes only brufen willingly. No tablets . Antibiotics only yellow one for kids. Thank God she hasn`t needed anything else so far.
•    Anonymous said… My daughter (8 1/2 yrs old ) refuses to take tablet form she thinks she going to choke and will not let u put it in her mouth so we always get liquid which she takes no problem.
•    Anonymous said… My daughter is the absolute worse at taking medicine. I am very thankful we do not have daily meds and that she is very healthy.
•    Anonymous said… My son (7.5 YO) has epilepsy medicine, and he hated the liquid form, but we slowly introduced the pill form instead. It was by a process of putting pill taking in the daily routine, and making sure it was accompanied with a nice drink, i.e. apple juice or milkshake, and occasionally some bribery, i.e. a toy car, a Lego figure, that he now takes it with very little fuss. Routine and patience were rewarded.
•    Anonymous said… My son hates taking his- luckily we get capsules and can mix it into his breakfast drink. He hates taking it but he told me as long as I don't see you putting it into my drink it's fine.
•    Anonymous said… My son is afraid of gagging. We have to break open the capsule and he swallows the beads, but occasionally he will gag and throw up all the medicine. That's his Ritalin. He doesn't have an issue with his seizure medicine that is an orally disintegrating tablet. He likes the minty flavor also.
•    Anonymous said… My son isn't afraid to take his but he doesn't like it. And he will occasionally refuse to take it when he's mad at me, as though he's punishing me. But he's been pretty good about it the last few years.
•    Anonymous said… My son refuses to take medication- terrified what it might to him
•    Anonymous said… My two aspie kids will NOT take meds. They are both horrible with meds. We have to hold them down to give them anything
•    Anonymous said… No afraid to take it but complained because he only liked the circle ones not the oval ones. Something about the circle ones go down better than the oval ones. I had his doctor explain to him that he needed to take them regardless off shape or color and that seemed to work.
•    Anonymous said… Oh wow!! Our very recently diagnosed 6 year had his tonsils out a fortnight ago. We had medication battles every two hours!! Thankfully he is better today and it's all over. We had no idea that this was common to HFA kids!!!
•    Anonymous said… Terrified of any and all meds - yes yes yes - so is his dad.
•    Anonymous said… Will not swallow a pill. Chews his Guanfacine. My friend is a pharmacist and is looking into compounding for him
•    Anonymous said… Yep! It's a nightly battle. This week the doctor told us to just hide it.
•    Anonymous said… Yes he is very dubious. Its quite a process. It takes lots if talking. Spoon was best we found, syringe a bit scary. And we just give it in small amounts with sips of water in between until dose taken.
•    Anonymous said… Yes my son would try really hard to take it. He found it very difficult. When he was about 9 I put $2 on the container which he could have if he got a tablet down. He did it for the first time with food and since then it's been a lot easier
•    Anonymous said… YES! We have tried EVERYTHING to mix it with. The only thing that sometimes works is offering Pokemon cards (it's his thing right now). We put them in sealed envelopes which he has decorated. Then we make it a big deal "Which one will you choose?" thing. Sometimes we just can't get him to take it. We used to have two of us hold him down but then when he was willing to take it, he would want to "play" that he wouldn't and ask us to hold him down.
•    Anonymous said… Yes, he refuses all medications.
•    Anonymous said… Yes, I have struggled the past 3 years for my now 17 year old to take his required Thyroid medication. He claims he has a fear of swallowing and chocking on it. Even if we crush it. Very frustrating. I have tried mixing it in food, but he always knows, he is 17 after all.;-) We have therpists coming twice a week to work with him on this, and he does great for about a month, than he stops taking it again. Trying to figure out what more he fears about this medication, sadly, he can't function without it as he sleeps 24/7 when he doesn't take the meds. And yes, he flat out refuses it. He has learned over the years to just answer "I will take it later on my time" to get us off of his back. And later never happens.
•    Anonymous said… Yes. My 8 yr old boy was scared to take anxiety meds. Luckily it came in a liquid (and he didn't mind the taste) and I explained that I take meds too. So we take them together. That seemed to get him past it.

Please post your comment below…

COMMENTS & QUESTIONS [for May, 2016]

 Do you need some assistance in parenting your Aspergers or HFA child? Click here to use Mark Hutten, M.A. as your personal parent coach.

~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~

Mark,
You are a clever man. You're saving thousands of parents and their children. I just want you to know you're immensely humanitarian and I'm so very grateful to you and the Internet for finding you. After all these years I've only just discovered my son is probably Aspergers but have just thought he's always been a bit awkward and contrary. I never considered he might be wired differently to other children (though he's certainly different to my younger sons). He would hate labels in his clothes as a toddler, would fight other children causing me to avoid socialising with him, going in car seats, getting his hair cut at the barbers etc but he got through school and worked hard despite OCD tendencies and never had behavioural problems at school. He just seemed to lose all motivation after his A Level mock exams in February and wants to hide away and play on his games all day.
It's going to be a struggle but with your help I  hope to get him through before he ends up on the wrong side of the law.
Seeing his counsellor still as he likes him and also trying hypnotherapy for his anxiety. Do you think he will need additional specialist support as he needs to somehow motivate himself to get back to his studies and the outside world? His doctor has prescribed IBS medicine and told him to carry on seeing his counsellor but Aspergers has never been discussed. Do you think I should see him again and ask what support he can obtain with regards to his further education now?

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Hi Mark,
I just purchased the book. The program help parent with defiant asperger teen we purchased a few weeks ago really works. My son has not argued with me about two weeks.He is very mild asperger kid, I feel sorry I have not  looked for help earlier since he gets along with my husband very well. He only likes to control me and pick his younger sister. My husband tries his best to help us get along with each other until I change my parent style after I read your book and listened to your vedio.
Again, thank you very much for your help.
Regards,
Cathy

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Dear Mark,
I have been writing to you on and off about my son Aditya. His main problem is depression. This has been under pharmacological  treatment for the last three and a half years. He also has frequent mood swings between being ok and very depressed.

We  have been telling him about his Asperger personality traits and how the social experiences may contribute to depression and that social skill development is doable and will help him get over his sadness and social inhibition . However he has not really taken this very seriously.
 His main problem used to be about his lack of success with having a girlfriend. However now his depression has made him disinterested in everything and he says he doesn't even want a girlfriend any more. Many changes of antidepressants seem to help only marginally. He seems to have given up on having a happy life. Also he has been reading up on spirituality and it seems to have made him even more detached. He probably has taken it all too literally...
You had once said that you do 'life coaching ' of Asperger Synd people. Is this something you still do? Would you be willing to help Aditya rediscover his joy of living , which he did once have in his younger days? He is 29 years old now.
Please do let me know the details about this,  and also how much you charge for your help.

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Thank you for providing this resource for us. A little background: My daughter, Josie, is 12 yrs old and in 6th grade. Since she was 4 yrs old she has had assessments done by pediatricians, psychologists, physical therapists, neuro-psychs, and speech therapists. Lots of things were ruled out but until she was 7 yrs old she did not recieve a diagnosis from anyone. A psychologist finally gave her a PDD-NOS diagnosis. She started got her an IEP at school and she started physical therapy and ADHD meds (the meds did not do anything but ramp up her anxiety) she was generally doing quite well at the time, but struggled with impulsivity and self care skills, it was managable for us at the time. She is creative and sings, plays piano and is a great artist. These skills have kept her happy and occupied while she was younger.

Now she is 12 and in 6th grade, and her deficits with executive function and social skills are starting to affect her emotionally. It is no longer enough for her to draw and play music, she desperately wants friends. Resources for tween/teen girls have been difficult for us to find even though we live in Los Angeles. The good programs are out of our reach financially and our insurance won't cover. She has done some talk therapy but that did not seem to help. So we are really struggling with how to help her.  Her main issues are:

1. Self care (she has poor personal hygiene and she will shower everyday but forget to use soap, she doesnt brush her teeth properly but refuses to let us help her, she won't wash her hands and has trouble taking care of her hair etc) This has become more much challenging as she wants and needs independence and gets very upset if we try to help her in these areas. I don't want to have her feel humiliated- so we have made a list that hangs in the bathroom, we give her gentle reminders, send her back in the shower etc. This has been going on for about a year and with our way of doing this she still has not been able to make it routine.  This issue affects the next area she struggles with.

2. Friendship/social skills: She is friendly and fun and initially seems to be able to make friends. These friendships don't last very long though. And she has never really had a true friend. No hanging out with friends after shool, sleep overs etc. She is lonely. She is not very open with us so we do not know what exactly ends these short term friendships, but we are assuming that she behaves in a way that makes the friend distance themselves from her. She tends to obsess over the friend and contacts them too much, her humor is a bit off and she can be very blunt. She also does not understand the give and take needed to establish close relationships and is not very interested in the other childs point of view or interests and mostly talks about herself. We do try to model this for her as well as talk to her about the importance of asking questions, showing interest and not overwhelming a friend. But with this we also are not making much progress.

3. Computer/online use: She is completely obsessed with being on the computer. She loves games like Movie star planet and IMVU. These games have chat rooms and lots of on line social interaction Ironically we have found that she has learned a lot from these games in terms of how to socially interact, music, fashion and other things that girls her age are interested in. So initially we thought it was a good outlet for her to have a quasi social life. The characters the kids create interact etc. And it makes her extremely happy when she is playing these games. At the same time she is not always safe and gives out personal info or gets sucked into drama that is above her maturity level. She creates dramatic alter egos for attention  and we had to shut it down. She was very depressed about this for a very long time and began self harming by cutting her upper arms. Her psychiatrist told us that this is not uncommon for teen girls with ASD and is a form of self stimulation. She ha!
 s not attempted this in along time and we now let her use the computer for very short supervised periods of time. But she is sneaky and will take my phone or use a siblings tablet.

I know that it is best to focus on one issue at a time. These are our main issues currently and we are not sure where to start and which issue to focus on. Her moods are very dependent upon access to being on-line (we use it as a rewards system and that seems to work) We dont know if we should completely take computer/tablet/phone privileges away from her until we have a handle on her behaviors and have built trust, and at the same time she almost becomes depressed if she does not have access because this is her only social connectivity and she really needs that at her age. We hope that you can help guide us on where to start.

We are enrolling her in a once weekly social skills group and she does have a psychiatrist that she sees for anxiety meds and ADHD management but he does not believe that she has ADHD. He tells her that she is immature for her age and that she will grow out of it. What else should we be doing? Are there any skills groups for teens re executive function? We have searched everywhere and cannot seem to find anything for girls her age. Most services seem to be for younger kids. Even social skills groups are mostly for boys.

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            I'm sure this is not the first letter you have received from a grandparent asking for your help or if the program can help,so I'm hoping the answer is yes it can. Our grandson is turning 9 in a few weeks was diagnosed with Aspergers in first grade I have noticed he is becoming more aggressive toward his sister and two cousins whom are both girls and younger than him, and not just verbally abusive but also physically. His parents of course are embarrassed and frustrated and his Aunts and Uncles are starting to avoid including him in family functions for fear he will hurt one of the girls, at our last family gathering there were friends over with boys about the same age as him and he punched one in the face and threatened to saw him in half  (I'm hoping he had watched a circus act and meant this in a comedic way but how do you explain that to a parent as they are rushing out the door in horror with their boys). We live about two hours away from them and don't see them as often as we would like but I would love to be able to share this with our daughter so she, our grandson and granddaughters can enjoy family time again.......help?

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 I have this immensely stressful situation with our son and in all honesty, I am alone in parenting and managing the chaos because my husband is holding on to so much resentment that he is unwilling to address it or let go of it.  I just don't know how to be the anchor in my family.  I am completely depleted by my sons behavior, but also very much depleted with my husbands reactions, resentment and anxiety.  He also has, all or nothing type of the thinking and an intense level of going through the anxiety cycle that is provoked by my sons behavior.  I feel ungrounded and anxious myself.  I am having a hard time putting one foot in front of the other this week.

My son has refused to come home because he does not want his car taken from him.  We know he is town because I have seen his car in passing and he has texted once.  He has been gone for 2 days and this creates much anxiety in the sense that he has been chemically imbalanced for days now, not taking his meds.  His impulsivity is off the charts and with this imbalance it makes things very nerve wracking on our end because anything can happen.  Our own anxiety kicks in because it's now a safety issue where if he hurts someone we are liable and responsible.  Realistically, what are our options here? 

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I've downloaded your very encouraging and extensively-equipped e-book and begun to implement better discipline techniques with our almost 17-year old son.
He has crippling social anxiety which has prevented him from continuing with his studies since February and we're trying all manner of therapy to help him with those issues but he is the most obnoxious, spoilt lad and fits the profile of your example aspergers teen very much although he has got through school all these years with no problems if he has had problems mixing with others but only to a degree until recently.

He has a small group of friends but has totally isolated himself to mainly communicating online so is only reinforcing his social phobia by avoiding going out.

Coupled with these problems he blames us for everything and refuses to seek help or discuss what he wants to do which gets very frustrating.
Today my husband demanded he discusses things with us and it resulted in a huge rage incident where both myself and my husband tried to physically throw him out of the house but were unable to. He's very strong and tall with the mind of a 9 year old like you say.

Anyway we told him to give us his laptop after we confiscated the Xbox and was met with more foul language but he eventually gave it to us after we said he can have his stuff back after 3 days if he doesn't abuse us any more.

He is still being abusive and I guess I'm to tell him he will lose an extra day? The trouble is he will still ignore that and carry on being abusive. Whenever we confiscate his stuff he immediately reacts with abuse. He still has his phone but I've put a timer on the wifi now so nobody can use it after 11pm.
What has prevented us tackling it previously is because giving in I guess has prevented these raging tantrums which his younger brothers have had to witness numerous times.

I'd just like some further clarification on the abuse-after-consequence is enforced as I want to avoid piling up never-ending consequences  but the profanity is simply demonic towards us.

Any advice gratefully received as you seem to know exactly what we're dealing with.

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Last night I was hurt by my 13 year old daughter . She didn't want to leave a party ("I was finally having fun mom ") and hit me in the driveway with
Her coat in the face . She didn't realize her phone was in there and it caused a huge welt above my eye immediately and I am still
In pain .

I want to make sure my reaction sends the right message to this serious issue . I am more than hurt. Of course
I am worried someone saw from the front window and our friendship with the hosts and guests will
Be impacted .   I know my daughter is most likely an aspergers teen and was struggling all day . ( a stressful
Private school Spanish exam that cause tons of anxiety that morning, a cake that didn't turn out right and she
Abandoned her friends and the project and the mess at my house that afternoon .  I know she was reluctant to come to the party and I struggle with
Leaving her home because once I do she tries to skip/avoid that social event each time . It seems important to bring her the few places we r still invited and welcome. These families have nice daughters her age that are really tolerant and nice to her.

What would u do ? For how long ? Who what where when????  I know the why .

Please help me . Our therapist sees us every other week and downplays most of my concerns.

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Hi There,

I am really concerned about my 9 -year old, he's adjust about 3 years.  My
son has a multitude of complex medical issues. He was recently
re-evaluated for his special ed eligibility.  We found out that he has
receptive language disorder and most likely from the OT eval central
auditory. He's been through OT and speech when he was younger and some
early intervention. I have been told he's been cleared of being on the
spectrum and that was through several speech therapist.

Here is what Joel is doing. His expressive language is o.k., but when he
speaks, usually excited about something he will repeat the sequence of
something he did or something he gets to do. Its almost like the brain
gets stuck or a continuous loop, I try to redirect , but he still stays
fixated.

I live in a small town, so not allot of services, would like some input.

Here is what he does:  "So for example his dad will take him to turn in
cans and then to get a video after he has save his money."

So this is Joel's conversation: Daddy going to take me to get cans , turn
in, go to game stop and he will repeat that for several hours, some times
a pause, until it happens.  plus excessive talking and interruptions. Dad
and I both try to redirect, but it does wear on us.

I have been doing research, and I wasn't sure if this would fall under
Asperger's or not. I know that Echolalia term has been used ..

Any input would be helpful...

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Dear Mr. Hutten,
I am a mom of a 17 years old boy. It was only last year I brought him to see a psychiatrist after he broke down and refused to attend public school.  The psychiatric just said that he has asperger syndrome after seeing my son body language. He was unable to make him talk after 4 session with him. He told me it would be fruitless if my son refuse to talk to him. It was best for us as parents to guide him at home.
My son was a normal kid until we sent him to Chinese speaking school which he did not master. It was fine for the 1st year, for the 2nd year results was not good. I spent time to coach him Malay language and sent him Chinese tuition. His grade getting better for Malay but not Chinese. He never fail the Chinese subject, though. By the way, all subjects were in chinese. He excelled in his chinese maths. Maths is his favourite subject.
It was until when he was in year 3, i believe one of the teachers made fun of him or scolded him in front of the class that cause him refusing to speak to teachers until now. He is a very prideful child and smart kid. He knows he was rude for not speaking or not looking at teachers when spoken with. He would speak to his friend and the friend would answer to the teacher.
My son told me he has social anxiety and didn't know why he was reacting that way. He was very frustrated that was when he accepted psychiatric help. But when psychiatric waz unable to help, he felt hopeless for a while and refuse seeing other psychiatric. I could not even mention it, he would shut himself out.
Since the day he broken down, I hv pulled him out of public school and let him studying ICGSE O-level on line. He is coping very well with his studies and less depressing now. 

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At school, if he gets yellow or orange behavior card, he is grounded for 2 days and no privileges to use his toy and free time. (he needs to get green or blue behavior color to receive all of his privileges)
We have noticed that he sometimes change the color of the behavior card he receives (he erase yellow color, and change to green before come back home), and we have decided to ground him for 3 days if he lie or cheating. (2 days grounding for normal violation and 3 days of grounding for cheating or lie)

Problem is he violates(cheating, do not follow grounding direction) for almost everyday since middle of the April, and we reset grounding for almost 3 weeks. So, he has no use of anything for 3 weeks!  Incident happened yesterday was, he stole small accessary (lock and keys) at school book fair, and teacher noticed him, and consequently got a office visit.  Me and my husband also brought him to local police station last night to teach him a lesson.  However, he brings his wallet to school today to buy the small accessary without our permission.

I know 3 weeks of grounding is really too harsh to him, and he seems frustrated everyday.
I wonder we are really in the right track...to keep this program is worthy for him.
Actually his first IEP meeting is 2 days ahead, we don't have much strategies for the meeting.
He has diagnosed as ADHD in 2015 and additionally diagnosed as mild ASD & Asperger's syndrome in April 2016 from private doctor. (he is 7 years old and 2nd grade)
School district has also assessed him during 1 month, and I have received evaluation report yesterday. For your reference, I am attaching APPENDIX part of school evaluation report.

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Hi, I adopted my granddaughter at age 6, she is 11 now.  She was taken away from her mom at age 3 and placed in foster care.  She lived out of state so I did not have much of a connection until she came to live with me.  She has been diagnosed with RAD and ODD.  She was in counseling the first 3 years she lived with me, and the counselor felt she was no longer in need of his services.  I just had a incident at school where she lied and said another student hit her, but found out she had not and that the student had accused my granddaughter of stealing one of her pencils.  She went do far with this lie that she told 2 teachers and the principle about it.  I have seen more anger issues lately, she has stolen things off and on, and much lying.  My question is what can I do to help her?  Is there a special kind of therapist or counselor I need her to see, and what approach should I be taking with her?  Thank you for your time

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My 10 year old son has ODD. He gets sent home from school early everyday & his schedule is only 3 & a half hours daily already. The school has called DFS in the past for my “inability to parent” . He did great for a few months but like everything else it worked for awhile then it no longer did with no apparent reason for the change. Everything I try takes so long to work the school assumes I’m doing nothing at all. Explaining what I’m doing also does no good because they assume I’m either making excuses for my son or myself. The last time we spoke about his behavior they were vague & mentioned ‘outside agencies’ might be necessary. I’m at the end of my rope with no end in sight. HELP!

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Hello, I am seeking answers for a situation I have with my son who has Asperger's/ADHD/etc. The situation is so multi-layered, I don't know where to begin. I will try to condense. My son has Asperger's/high-functioning autism, and he is so intelligent in some areas that it is really hard to tell for some people. If you don't live with him, people just think he is a selfish jerk. At age 19, he decided to exclude himself from family holiday gatherings that have always been dysfunctional and torturous for us to make our obligatory attendance every year. He told me to tell everyone that if they wanted to see him, they were welcome to come by and visit as he would be celebrating comfortably and happy at home. I commend him for his independence and logic, but they call him selfish and rude. Anyways, this is just a little insight about his nature. The problem I seek answers to at the moment is this: Almost a year ago, his girlfriend moved in with us (my son and I) the day she turned 18, to get away from her “controlling” parents. Last night, I was in the kitchen cooking and they came in to make their dinner. My son was apparently trying to teach her how to cook. This is when I noticed what other people have recently noticed. He is very controlling of her. He was telling her very detailed instructions in a very rigid manner, and she had no room for error. I had to step in and comment when I saw her body language and facial expressions, which reminded me of my own past abuse issues from bad relationships. I told him to let her do it the way she wanted, more or less. She then looked mortified at what his next reaction would be. He became very silent and I knew a storm was brewing. In a nutshell, I have many of my own issues, my son has many of his own issues, and his girlfriend has hers. We are oozing issues all over each other and I don’t know where to begin, as we all need help. My son won’t do anything to seek help. Any suggestions? Thanks so much!

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Dr. Hutten
I am a speech pathologist working in a private school for children with learning differences and high functioning autism or asp in high school.  I have experience with younger children but need more information regarding teenagers.  I would like some suggestions for my program and especially would like information I can give to my parents.  Thank you for your support. 

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My daughter is 15 now and  was diagnosed at an early age.  She has had early intervention, sporadic therapy , and medication.  We recently changed her meds as abilify was way too expensive and it was not a perfect fit either, she is now on Lexapro.  Currently she is having many rage issues, anxiety, meltdowns and has described herself as scratching herself on her bus ride home due to over stimulation around her.  She does see a therapist and a psychiatrist, although my husband and I are seeking additional resources to help with her behavior. Will this program be helpful for her and us? When her therapist sees her my daughter presents as a normal adolescent , not like the individual we experience daily for this reason I don't feel the therapy she is receiving is very helpful .

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Dear Mark,
I just came across your website while searching in desperation for advice on what to do with my 13 year old stepson. I'm not sure if you offer advice over email, but I thought I'd try. 

My stepson (we'll call him Alex) has always been hard to discipline because he has absolute to response to consequences - good or bad. You can offer the exact thing he's been wanted and he's willing to throw it out the window in favor of acting out or not listening or you can take away absolutely everything and he doesn't care. I have often wondered if he has separation anxiety disorder or depression (as I tend be a bit of an armchair psychologist). 

His mom lacks basic parental instincts or behavior and will often say the most awful things you've heard a mom say to a kid. She left him to be with another man in the middle of the night and that's part of why I wonder about the separation anxiety disorder (not getting attached to things that can be taken away). Alex is with us Friday PM-Tuesay AM which means every weekend is awful - his defiance completely ruins every weekend.

After 5 years of me pushing for a conversation with the school and the doctor, my husband finally pursued an ADD/ADHD evaluation because Alex was clearly off-the-charts ADD and we received the diagnosis in March. Instantly, on adderol, Alex was a different kid - handwriting changes, he was thinking critically, writing in complete sentences, clearly articulating what's happening in school, remembering things etc. His grades went from Fs to Bs in a matter of weeks.

BUT, getting him out of bed has always been a challenge and we've seem to run head on into teenage defiance meeting a body that needs rest from both puberty and the meds. He absolutely refuses to get out of bed for school, and because he doesn't care about consequences, your suggestions from this post aren't working. We fought super hard to get him onto the baseball team through his new 504 and despite of his bad grades. He's thriving, but willing to throw it away because he won't get out of bed. He doesn't care about make-up homework or grades and will just flat out refuse to do anything my husband tells him to do. He was always nice to me, but has become flat-out defiant and nasty to me and won't do anything. Just yesterday, one of our chickens had been attacked and had no skin on his head; I was only home with Alex (who was sleeping) and ran into his room with a bloody chicken in my hands asking for help saving it's life and he just rolled over, told me to get a towel and deal with it myself, and went back to sleep. I no longer choose to engage with him (which is probably the opposite of what I should do, but I can't take the abuse being hurled at me, and as the stepparent, I'm backing away).

My husband is at a complete loss of what to do and feels helpless. I'm newly pregnant and need to focus on minimizing my stress. 

Any help you can offer would be appreciated more than you could know.
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I read online this program might work for adults.  My son became a diabetic at age 23-diabetes type one. He now was living out of state. His job moved him there. Alcohol wa a problem in college but once diabetic he quit drinking.  He was in hospital frequently with keto acidosis. A pump helped wonderfully for 5 years but with insurance changes could no longer afford supplies.  Now he is on dialysis and has gastroparesis.  Why am I asking niw you say "he purposely shoots himself in foot all the time"  he much if the time has vomiting diarrhea or both.  He did not like last endocrinologist and didn'go until had to. Wouldn't change either.  I think he could help some with gastroparesis . After about 10 days of Gi issues wanted to go out to eat after studying menu ordered fajitas with chorizo. Eric I said to him chorizo?  We hadn't been home an hour until all came up? Why he knew better.

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Good Morning!
I am back to scouring the internet for solutions on what to do with my son, when I came across your website.  I am considering trying your OPS, but I have a couple of questions for you. This system seems to be tailored more towards defiant, oppositional children, and my son doesn't really fall into that category.  (My son just turned 15 this month and is on medication for ADHD.) 
However, he has been sneaking out of the house repeatedly, despite our efforts to keep him from it.  A few of the nights he snuck out he and some friends stole the school's driver's ed car and the police brought him home.  So he has been in trouble with the law, which as it turns out was very lenient with him and only gave him community service, took his license, and gave him a curfew.  I thought the curfew would deter him from sneaking out but it hasn't. We have taken all of his electronics to deter communication with these "friends", however he keeps finding ways to get iPods, he stole his sisters, and his friends keep providing him with them. 
We also grounded him from doing anything outside of the house, no friends ect.  We started a reward/punishment system with him where if he does certain things like sneaking out for example he gets another month of grounding; picks on his brother or sister, an additional day; and if he does certain positive things he can reduce his grounding.  We thought putting this in his hands would help give him control over the situation and realize his actions have consequences.  It has been going great during the day, he has been more responsible and doing what we ask around the house, earning back some days from his grounding, then we find out he snuck out 3 more times earlier this month and had one of his friends Ipods, which is how we found out he had snuck out!
I don't know what more to do.  We have tried counseling (which didn't help at all) and even tried to get him in to a boys home for help, but that isn't going to work either unless we want to be bankrupt!  Will your system help us too? 
He is a good kid, loving, in fact he acts immature for his age.  The problem is he has this other side to him that he continues to sneak out to hang out with his friends despite all we have tried, or even the fact that he could get in trouble with the law being out after curfew.  He claims he meets with his friends because he and his friends confide in each other, his friends need someone to talk to. I believe there has been some drinking involved initially.  And he was messing with making cigarettes before as well.  I have no idea if that has stopped.  Oh, and did I mention the lying?  He is a very good liar. 
No one seems to have any answers for us, not the counselor, the states attorney, his doctor.  I don't know what else to do aside from having a security system installed on our house and hire a babysitter to watch him all day! We cannot trust him at all.

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Hi there

I'm a mum from Scotland is despair. My son is having several problems at school and unfortunately I'm not receiving much help from his teachers or the school itself.

How do I know if my son has Asperges. I've been through many websites and he does follow some of the patterns, but by no means all.

He struggles to get involved in teams and often prefers to play his own game, he's happy for others to get involved but he struggles to involve himself in their games.

He lacks empathy and resilience, things we are working on. His teacher recently suggested he receive support with his spelling and social stories for his inability to get involved with his peers. Does this mean she suspects Asperges?

I am very lost and need help. Any suggestions would be gladly received.

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Hi Mark,

Thanks for your follow up email. 

Currently encountering cross road about my marriage and we just got married last year October.  Its our second marriage!  When he told me after we got married that he is Aspie which I've no cue what is that about.  He seems to be fairly normal and smart but he does have some issues which I thought it was related to his family upbring.

I have been reading about Asperger and does helped me to understand certain behaviours of his.  The point is I am not sure he is aware of his aspie issue can destroy the relationship?  It has been challenging to deal with his disrespectful name calling towards me?  Not feeling remorseful nor sorry.

We have not been talking for a week now, emailed him (he said communicated via email) to ask for a proper discussion on how are we going to move forward. His replied was he is not ready and he is shutting down. He just returned from US ( we living in Asia) and he had an back operation few weeks ago.

Anyway, I am ready to give up now. 

Cheers
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Hi Mark,

I came across your interesting website and decided to write to you. I have a 27 year old son with Asperger’s Syndrome who has refused to communicate with me for 10 years. I love him and was his advocate all his life. His behavior towards me became violent at around age 13-14 and then, at 17, his father was forced to let him live with him. His father and step mother did not want him but coped with the situation. My son turned against me and they allowed it. My AS son lives with his girlfriend and doesn’t even communicate with my younger son anymore. I have reached out and searched for an answer to this sad situation for years. My AS son needs social skills help (he is gifted and bright, drives, takes care of himself and girlfriend but doesn’t work or go to college). I am wishing for an intervention of some kind. 

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We have an almost 24 yr old son, Andrew, with Aspergers’ (though he denies it).  We also have a 20 year old daughter, Alison, with Rett Syndrome.  Andrew blames Alison for ruining his life.  He claims he was traumatized at an early age by her because he didn’t understand what was going on with her.  We tried desperately to help him to understand her condition as will as try to provide equal time between the two of them.  He now claims that he was totally paralyzed with fear and afraid to ask for help.  He is now mad that we never realized it.  We’ve had him in therapy on and off for years trying to help him deal with our family situation; nothing seemed to provide relief.  It wasn’t until three years ago that we told him of his diagnosis and, if hind sight is 20-20, we probably should have told him from the beginning.  Both kids were diagnosed around the same time and we didn’t want him to feel that something was “wrong” with him like there was with his sister.  Anyway, for the past three years he’s been in therapy and has been seen by numerous Psychiatrists (he hates them all because he feels the profession is BS).  He says he doesn’t consider his sister to be human and we need to put her away so he can get on with his life.  That is not an option for us for various reasons.  The bottom fell out a few weeks ago and we’ve had several family sessions with his Psychologist.  Unfortunately we haven’t really gotten anywhere.  Andrew has his own apartment, drives for Uber, and can, for the most part, live on his own but he comes and stays at our house quite frequently because he says he keeps having relapses because “of her” and can’t get on with his life. The stress of him being here is insurmountable.  We in no way minimize how he felt as a little kid, but we do see a pattern here.  He has always done the classic obsessing  over things which have lasted for months at a time and we think he is doing it again with this, only this has manifested into something very damaging.  It is almost like he enjoys being the victim, the comfort of the attention from his dad myself, and his psychologist, and the excuse to not have to become responsible.  We are at our wits end.  We think his Psychologist is too passive and basically lets him vent without giving him concrete skills to overcome this.  It’s so frustrating because he would rather blame everyone for his woes.  There has to be a way of getting him unstuck from his past and take responsibility for his thoughts, feelings, etc.  How do we do this?   Your help would be greatly appreciated.

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Hey Mark!
I'd like to pick your brain on something.
I work at a company that trains individuals with AS and HFA how to develop apps, games via technology. 
There is an individual I will refer to as Nick (that's my son's name) with AS.  Nick has had a crush on two different neurotypical young female staff members.  The first crush was handled by one of the (male) directors.  This director talked to Nick about his apparent 'crush' on female #1 was not appropriate since she was staff, etc. 
Now when Nick sees female #1 he literally runs in order to avoid/escape her presence.
Last week Nick tried to kiss Female #2 by telling her he wanted to show her something.  He had her seat in front of a computer and when she sat, he put his hand softly around the back of her neck and reached down and tried to kiss her.  She rejected his attempt.  Female #2 told him no and held her hands up to block his kiss.  He voiced that she was giving him all of the signals that she was interested in having a relationship. 
Female #2 feels awful that Nick was under the wrong impression.  The director called him into the office and explained that it is inappropriate for Nick to have a relationship with staff. 
Female #2 also feels awful that her 'actions' may have gotten Nick in trouble. 
I told her to be prepared for his escape/avoidance behavior next week. 
She told him last week that they would talk  about the scenario and he said don't come near me.
Do you have some helpful advice for her?  And for him?
Thanks.  Interested in your thoughts!

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My son was recently diagnosed, because I noticed his increased difficulty to keep friends, he's 8 years old, and nobody ever gave us an indication of his situation. I always had to ask him about his social time at school and last year wasn't that bad, he had a best friend, but this year little by little he's become isolated, even kids who were friendly to him, now are rejecting him. How can I help him? It breaks my heart to see that he used to be a lively and happy kid and now he's not like that.

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Hi Mark,
First off, I wanted to compliment you on the page you have created at http://www.myaspergerschild.com/2010/09/aspergersautism-online-resources.html. While I was on the page for work, I noticed you featured FamilyEducation's homepage:
FamilyEducation is a great resource for teachers, but what if you want to easily create and customize a free lesson plan for a math, science and language arts class? Well, our startup, FormSwift, has a solution.
We thought that we could create better-looking, more efficient lesson plan templates, which could help teachers and educators expedite the process of writing a lesson plan at absolutely no cost. Here is our finished work:
In my opinion, our Lesson Plans Hub is more thorough, up-to-date, and user-friendly than any other existing online lesson plan template resource, not to mention it is completely free for anyone to use. So, considering you have previously shared FamilyEducation's website, I think it would be great if you could add our Lesson Plans Hub as a companion tool for your readers.
I hope to hear from you soon. Thank you for your time and consideration!
Cheers,
Jamie

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We have seen 4 therapists, 2 pediatricians, an internal medicine doctor, a sleep study doctor, taken a 15 minute test for ADD from licensed psychologist, consulted psychiatrists, been in an inpatient behavioral health center for a little over 2 weeks. I have had conflicting advice and diagnoses. One therapist said no to Borderline Personality or Aspergers. One therapist said he may possibly be on the spectrum. Another had a diagnosis of Oppositional Defiant Disorder. Psychiatrists one said he was depressed and put him on Prozac. Which seemed to help, but the son quit taking when he goggled what it was for. Another psychiatrist prescribed Adderal which seemed to help one day but he stayed up all night playing video games and blamed the medicine. He quit taking. The latest therapist is seeing obvious signs of video game addiction. He has stayed up 24 hours playing when allowed by therapist advice. (Awake for 36 hours with 1 1/2 nap.) Refusing to do school and stay in bed all day when gaming taken away. Currently 6 months behind in school. Current therapist sees possible personality disorders including borderline and narcissism. Son will be 17 in a month. We have not had autism tested, but therapist suggested. Our teen is non-compliant concerning medicines, therapy appointments, and doctor's appointments. We have made and missed multiple appointments. No guarantees to get compliance on anything. He is a picky eater. 6'2 and 145 lbs. Only wants certain foods at home or eat out daily. Very difficult child. Lazy, not motivated. Doesn't care if he is a high school drop-out. His plan is to live at home with parents, play video games and spend his car fund savings account on gun graphics for his game. Need help.

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Hi Mark:
My son threatened suicide and is now in  a treatment center.
We have struggled all of his life . However, now that all the
stress of school is gone and the pressure is off I can see
the mental component much more clearly.
It gets lost in public school and in daily life.
Now placing him in an alternative school for High Functioning Autism.
is extremely difficult .
I have my work cut out for me . Matthew , has an I.e.p, but the school
thinks they can handle it . They cant I am seeking counsel in my area.
This book is going to help us further parent Matthew, my son .Thanks.

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Hi,

I think I have a brother with ASD, it's causing my mother and I a great deal of emotional problems. Can you help me to understand if he does actually have this, or just a total asshole or psychopath. It would really help us to deal with him. 

I can chat via skype, and send you a very long email thread that will show you everything about our relationship. 

Please get back to me. My skype is: olli
I get a lot of spam, so please include a message saying it's about this with your request. 

Thanks.

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Hello,
We have a son with high functioning aspergers. We live in California. He was adopted at birth as well. He is a great kid but has always been difficult. He is being a bit rebellious and has trouble with disrespect to us and anger. He is pretty social but sabotages any friendships even though he is liked. He suffers from low self esteem and wrong perspectives. We are not doing well as a family here and are seeking help. Maybe in depth therapy somewhere to help him and us with our relationship. He is not violent or a drug user and we are a Christian family. Do you know of any place he can go for some therapy that would be safe and helpful with the knowledge or aspergers .? Appreciate any help.
Thanks

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Can you point me to links/help related to an ex-spouse who is enabling & coddling 20 yr old aspie son, specifically what WE can do to set boundaries with 1. son (who refuses to go to therapy/help) and 2. mother (who coddles like you rarely see, e.g. mom texts before he goes over there if he wants his cinnamon sugar toast ready-level of coddling, etc..)

My husband (Dad) and I (step-mom) are all on board with suggestions per Mark's launching advice, however while ex-spouse sees spectrum behavior, she has ignored Mark's info which we sent to her and seems to believe her "ways" will someday ("maybe it will take him until he's 27") finally "work" and he'll be independent.  

Her level of coddling with a NT would be dysfunctional and harmful for launching.  Add an Aspie and it's lethal.

What can we do to set healthy boundaries with son and ex-wife, so that when the next crisis happens it's on her and he can't live here unless he gets help and shows effort towards independence.

-admitted to hospital psych ward after he wigged out about a family friend (girl), who took him under her wings away at college, finally set HER boundary and said you need to figure this out by yourself..... he must have thought she liked him and then was devastated she abandoned him.

-2 horrible college semesters (away, huge state college)
-3rd semester he did nothing, literally 0.00 for 13 credits....................no care in the world when he came home and lied during semester when dad went up there many, many times to check on academic status

-flew the coop on a bus to another state bec he didn't want to watch his little sister during the summer (mom's 7 yr old daughter she had while married to dad = divorce)

So step-son is "messed up" with that too. I.E. needs therapy in many ways, social skills training, etc....

Do we tell him can't stay night here unless he agrees to therapy?  Do we say mom you're on your own with him.  Don't call us when the next crisis happens.  You made your bed with him now sleep in it, until you agree to support healthy moves to independence?

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Hello Dr. Hutten,

I have a 12 year old son who has been diagnosed with Aspergers. I knew something was wrong since he was a baby and I have been through a very rocky road with him trying to get doctors to explain to me what was going on but, they all just pushed him aside. They even said they could not really diagnose him for sure with Aspergers because he was all over the place. He had a little bit of everything. Even a so called “author of Aspergers” told me the exact same thing. I was so frustrated with the system that was suppose to be there to support us but, instead they turned their back on us. If it wasn’t for certain angels I met along the way, I don’t know that I would be where I am with him today. I have pretty much struggled on my own to be an advocate for my child and have hit quite a few bumps along the way. On top of this my daughter (my son’s twin sister) recently developed generalized anxiety. She is also on the borderline of anorexia nervosa. Why borderline? She too does not “quite meet the criteria” for a treatment program. Her BMI is barely 16 and the criteria is 15. Trying to get help for her has been a struggle too.

I often feel overwhelmed and like I am failing my children not to mention that I feel like a failure as a Parent and, I am reminded of this on a daily basis. There are times when I just feel like I can’t hang on anymore but, I know I have too. My health has taken quite a toll. Lately, I have been extremely stressed out and I am about to hit menopause. I have circulation problems along with nerve damage on the right side of my body and, arthritis in both my knees. I am always putting myself aside because I do not have time to tend to my needs with everything I have on my plate. So, I just suck it up and deal with all the pain and keep moving forward. I just learn to deal with it! But, I don’t like it. I don’t feel the happiness that other parents feel with their children. I often wonder if I am just not cut out to be a parent but, then why would God have given me 2 beautiful children? I love my children. My calendar is always full of doctors appointments. That’s all our lives seem to revolve around. I feel that it is taking a toll on the whole family. I don’t want my kids to grow up and most of their memories are doctors offices.

I feel like every time I reach out for a resource that fits the bill, my child is turned away because they just “don’t meet the criteria completely”. I hear this alot.

My son has therapy on a regular basis, but I feel that it is not really working. He has been on medication for some time now to treat his generalized anxiety, vocal ticks and ADD. He also has a little OCD.  Recently, he started middle school and that is when all hell broke loose. He gets upset easily and trying to talk to him is usually a failed attempt because of his resistance and explosive outbursts. Everytime he gets in the car with me he starts attacking me by yelling at me, calling me horrible names, and takes out his aggression on his sister which ends up in a verbal fight. I put on classical music for him after school while in the car, he has his phone in case he wants to play a game and, I try not to have conversation so it does not cause a reaction out of my son. I dread the time we spend together in the car. Never pleasant :(

Today, he took his fist and hit my dashboard inside the car as hard as he could because I told him we could not get ice cream today when he had asked me. As I started to explain why, he interrupted me and yelled at the top of his lungs. I tried to tell him we could go tomorrow and , he wasn’t having it until he calmed down an hour later. I feel he has no empathy whatsoever and now, I am getting scared that he might hit me in the near future while I am driving or I might be the story of the child who killed his parents while they were a sleep at night. My son is frustrated with me and he feels that I do not listen to him at all because he wants to yell at me when he wants me to listen to him. I always feel like I am the bad guy. I guess this is how most parents are feeling but, I feel it on a different level.

I desperately need some guidance. A support group for all of us. I don’t know if I need to do brain mapping, ABA therapy, or what.

My son plays the violin which he loves and is doing exceedingly well. He is a part of his school orchestra and a conservatory of music outside of school. My daughter is an artist and loves to sing with her school choir. My kids love to go camping which we do a lot. They both have playdates, but my son tends to want to have down time a lot which for him means, “don’t go anywhere, just stay home and play wii or watch tv”. I prefer he gets some outside activity. His Dad will take him to play basketball and I will sometimes take him to play tennis with his sister and I. He likes both of these activities.

Both of my children made Honor Roll this year on their own. No pressure from us. I don’t believe in that. I am very proud of them, but my son feels I am not always proud of him.

Any guidance you can offer would be greatly appreciated :)

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Hi Mark,

I really need someone to talk to about my 14 year old son with Aspergers and my ex-husband who I believe has Aspergers.  We also have two other children, ages 12 and 8.  We have been divorced for about 3 years but I want to reconcile, but that doesn't go over so well with someone with Aspergers (and probably most people anyway).  I am in a very, very difficult situation with my children right now and I really need someone knowledgeable about Aspergers to help me sort out some things.  I know we haven't met, but if you have any time today I would really appreciate it because this is really urgent.
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I would like to discuss with you two main things:  any experience you have with reconciliation between a couple where one partner has Aspergers, and though very difficult for anyone, how you would approach this with someone in that very rigid mindset (also, he does not know I think that he has Aspergers, but I now understand Aspergers much better and can give many reasons why I believe this is the case); second, I need help structuring a treatment plan for my 14 year old son (including my other two boys, ages 12 and 8, who have been deeply affected by this situation dealing with home life with their brother).  I want to discuss with you our current situation, what I am trying to do, and any input you may have on what I may need to include that I haven't thought of.  I realize this is a tall order, and you don't know us personally, but I want to talk with someone with your experience and just get your general opinion.  I know that there are many other people who are advocates for autism, Aspergers, etc. with a lot of knowledge, but I notice that in much of the information out there, you go in depth into the topic of marriage/living with an Aspergers partner more than most, and really advocate for that aspect of it.  You also go into a lot of depth about about dealing with defiant Aspergers kids/teens, and that understanding is very important to me as well.

There are three more things I want to mention.  First, my children's Dad does not recognize or accept that our son has Aspergers, in fact, he completely disagrees with it and believes that I am labeling our son, despite having seen certain behaviors himself and psychological assessments.  Second, he is currently trying to get full custody of the boys.  This was triggered when I started to renew efforts to get some more assessments done for our son, and our hearing is next week.  

Finally, I don't know if you are a person of faith or not, but for me, a big spiritual component has developed.  Despite all these obstacles, despite how impossible it seems, I believe God is bringing us around this mountain again.  The legal custody thing is important, but to me right now its not the biggest thing.  Its just one component of a lot of things.  I have struggled to fully get my son the help he needs over the last few years, and my other boys are at their wits end with dealing with this.  We are at a critical tipping point of either getting on the road to health--or not.  I cannot emphasize this enough.  Our home life has become so difficult that we are at a crisis level.  There is no 'win' in this custody thing either.  The only thing that is slightly better is that I will have out on the table all of the therapy and treatment that my son needs, and with me, I will pursue treatment.  If the boys go with Dad, Dad will not support treatment.  But, everyone's hurt either way.  God has put on my heart in the heaviest way the depth of what I have caused in this divorce.  It is almost unbearable to me.  But God has also placed in my heart to pray for restoration and healing of my WHOLE family, to include reconciling with Dad and facing his Aspergers, and that this situation is NOT impossible.  I believe God wants me to trust Him and pursue this.  I really hope you can help.
 
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