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COMMENTS & QUESTIONS [for Oct., 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.

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Dear Mr. Hutten,

I have a son who is 7 years old and was diagnosed ADHD Asperger when he was 4. Me and my husband have watched your film The Asperbergs-ADHD overlap this weekend and believe it’s a really great summery of the similarities and differences. Thank you!

I have one question though: when a person have double diagnose can the person show totally different sides because of the different diagnoses are shown randomly? We have a hard time understand what is what, what is diagnoses, personality and age. Our biggest problem is that we can’t see a clear pattern in our son. What he liked yesterday he rates today, the way he acted yesterday is different from the reaction we see today etc.

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Hi Mark,

I'm an LFMT and mom of an Asperger's (HFA) teen.  My son is almost 17 now and in 11th grade.  He's very bright, and recently quite social (although lacking in social skills of course).  He was diagnosed with ADHD as a young child but we didn't understood his defiance, extreme inflexibility and lack of frustration tolerance as placing him on the spectrum until his teen years.   I'm thinking of purchasing your ebook and would like to know when it was written.  I'm in the Los Angeles area and wondering if you've worked with any clinicians or know of any that you would consider experts in working with HFA kids in our area?  It's been a difficult year.  My ex and I are scared by our son's anger
and his impending adulthood which is just around the corner.

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Hello Mr. Hutten,

I was looking online to get some help for my Aspergers 18 yo who is a first year engineering student at Purdue. He is having a difficult time adjusting to campus life and just wants to quit and come home. I am trying to get him appropriate immediate help at the University which has proven a little difficult. His counselor is scheduled to see him on Friday. I am trying to get him into a clinic and into the academic success center, but he is not willing to take the necessary steps to help himself. He claims he wants help but cant get motivated enough to get the help. When things get rough, he avoids. He has missed a number of classes and his first Honors Engineering test on Monday (which he studied for until 2:30am) because he was too paralyzed with fear to take it. He scheduled himself to meet with his academic adviser yesterday and then he cancelled it. How do I get him the help he needs if he refuses to help himself? Do I just allow him to avoid and come home? Then what? BTW, up until missing his test on Monday he was getting all A's and B's in all of his classes. So, as he put it, it is not that he can't do it academically, it is that he is not emotionally prepared to be in college. How do I get him emotionally prepared?

To further complicate matters, the University will give us a 40% refund on tuition if he decides to withdraw this week. After that, it will be 0. Please HELP.

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Hi Mark,

I think my partner may have Aspergers’.  He brought it up once when we were having a difficult conversation, but said he’d never been diagnosed with it and didn’t want me to tell anyone.  At the time I didn’t know anything about Asperger’s- now I’ve read several articles and fear that he is though I’m not sure.  I doubt he’ll go to get a diagnosis. 

Here’s what’s crazy making for me…  We’ve only been dating 6 months but have had wonderful times together when we spend weekends together which we usually do as he lives over an hour’s drive away and can’t visit during the week.. When we’re together I feel like I’ve been falling in love with him, but then when we’re apart during the week it’s like I fall out of love with him as our phone calls are so dissatisfying for me.  It’s like he’s a different person- and since there’s no physical touching, intimacy or eye gazing, etc on the phone, I feel like he treats me as a distant acquaintance… I don’t feel much caring, empathy or warmth from him. 

He says he’s a romantic yet I rarely feel seen, valued, affirmed, complimented, appreciated or known by him.  I think he does really care for me and is consistent and loyal but I rarely get compliments  (he says it’s very hard for him to compliment- he feels it’s dangerous- same with saying I love you and all kinds of loving, empathetic affirming statements.)  Since my love language is Words of Affirmation, I feel like I’m dying on the vine. 

Also, I find our phone conversations separating as they seem so boring and just talking about surface stuff- he’s extremely smart but says himself he has a very low Emotional IQ- so he doesn’t like to talk about feelings, etc.  We seem very intimate when we’re together, but hardly at all over the phone, or in any kind of deeper conversations… And I LOVE having deep, emotionally based conversations. He has a very hard time with these kind of conversations which is frustrating for us both.  I really care for him and even love him, but sometimes, like when we’re on the phone I wonder if I even like him, or if I’ll ever really feel seen and loved by him.  I’ve communicated my desire for compliments on several occasions and he is doing a little better but it’s so far from what I would find satisfying I wonder how much better it will ever be.  Any suggestions?

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Mark,

Good Morning.  Thank you for your thoughts.  We have re established contact with our son and yes he is taking his meds and seeing doctors in Austin for his various medical issues.  All those are good things.  Once upon a time when he was 18 months old, (more or less) he had an encounter with a bicycle gear.  In other words he lost part of his finger in that gear.  His 3 year old brother was riding the bike.  There was a product liability lawsuit and he and his brother won.  They got between them around $100,000.  That’s good.  The court allowed us to use some of the money to pay for parts of his psych treatments and pay taxes and other expenses. 

We never put the $ in trust so when he turned 18 the money became his.  Yes i took the cowards way out and never set up a trust as i didn’t know who could be the trustee for a reasonable fee.  Now i am paying the price for my cowardice.  The money he had is down to about $7000.  He spent the money on a new Fiat 5000 all kinds of tech gear and furnished his apt in Austin.  My wife and I can’t afford to support him in his new life in Austin.  Help yes, a little yes.  His entire rent which is about $1100 no.  We also got use to him not living with us and both feel so much better about hime being out of the house.  I feel free again and not like i’m walking on egg shells.  I really can’t take it when he gets verbally abusive to his mother, ( my wife), so we would prefer that he stay out of our house as a resident.  Visit yes.  Stay no.

Im not sure how to get him to slow down his spending,  .  Maybe if we are lucky he will start a job at Chipote which he has applied to and hired, but not yet started.  I am hoping that there is something we can say to our son that makes him stop spending like a drunk salior or ( the federal government.  I really don’t know if we can do this the “hard way”,  meaning let him live on the streets or out of his car.  He really can be a great person, just not necessarily to his parents.  He has great talents but how to monetize them is a different question.  He is great with technology and cooking.  But somebody has to hire him and pay him.  He tried working for Postdates, which is a food delivery service.  Great idea, except for the accident, he ran into a curb and 3 flat tires.  So he didn’t actually net out any money.  At least he realized it was to expensive to continue.  Any thoughts or suggestions would be appreciated.

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Hello, I am in the UK and struggling with my high functioning autistic teenager. He is very close to Asperger and lacks the diagnosis as he was non-verbal until 10. He is very intelligent, a talented pianist and successful artist. His spoken language is still limited but he writes well with great expression and his comprehension is good.
Over the past year his meltdowns have intensified become increasingly destructive, aggressive with self harm and a total loss of control. He tries so hard to calm himself it is painful to watch. He will cry afterwards for at least an hour.
To answer the problem his doctor has put him on antipsycotic medication but it usefulness is limited and the dose has been increased and increased to the point where he is a wiped out zombie. It is spoiling his life and taken the fun and good times.I want to reduce the medication, stop it and have my lively, funny, talented son back.

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I have 17 year old daughter that I sadly fear will either end up dead or incarcerated in next 10 years.  This all started 3 years ago with inappropriate behavior with boys.  We sent her to boarding school in mississippi that worked with kids like Emma.  She got kicked out after 8 months for sex with student.  Then, used our last bit of money to send her to Outward Bound.  Great program, we were very hopeful.  Since getting home I got a call from principal she cyberharrased a fellow student and was on verge of being expelled from public school.  Yesterday, I learned over last couple months she stole about $500 from her grandmother who has been very loving and generous with her.

I am reluctant to spend any more money on her and was going to call the tenneesee women's prison for tour for her.

Thank you for letting me vent.  I just don't have much hope anymore.

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Hi Mark:

I have a quick question-parent to parent! My son is in middle school (7th grade)-on the spectrum. They are assigning a book to read called, "The Boy in Striped Pajamas".  It is about two little boys who meet in a concentration camp. In the end, they die in a gas chamber together.  The reading is required, and then they watch the movie over the book.  Due to the contents of the movie, parental consent is required.  However, the book is not an option.  

I know that the book will affect my son deeply in ways I am not even certain of yet.  But he is very sensitive...and so I spoke with the Language and Literature teacher in a meeting about seeking an alternative.  She said there was nothing that could be done, but that she would speak to the Dept. Chair, as the students would not be studying the book until after Fall Break.  (Note-they finish with the book just before Christmas Break and watch the movie.)

I followed up today with the teacher to find out what had been determined, and her reply was, "unfortunately, the Dept. Chair didn't come up with anything, so I and your son's Resource teacher will be as supportive as we can be." 

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First of all I want to say a resounding thank you. Your youtube video on obsessive thinking was spot on and I have honestly never heard someone describe it as well as you did. Thank you so much for that. Second, I am wondering if you do Skype sessions or even phone sessions. I am an adult with Aspergers syndrome who is married to my partner. How long would the session be and for how much?

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  I could really do with this at the moment, my marriage is hanging by a thread and we're now waiting for a mediation appointment.  My husband ABSOLUTLEY REFUSES to acknowledge that he has aspergers.  Instead I am the persecutor, a liar and not to be trusted.  This has not been help by a lovely psychiatrist who would not diagnose because she said he didn't meet the current criteria and didn't have impairments in all categories of the DSM, namely he told her he played team sports when he was younger and she told me that people with aspergers cannot play team sports??

Sorry for the ranting.  By the way, I am in Ireland and a therapist myself!?? makes me feel even more awful to be honest.  

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Hello Mr. Hutten,

My name is Laurie Cummings and I am the mother of a 23 yr old adult son on the spectrum, Dylan, and would like to inquire if you are accepting new Skype clients.  We are in Oklahoma.  I ran across your website when researching online counseling options for Dylan.

Dylan has struggled for years and has multiple DXs, including severe ADHD/Executive Function deficits, Anxiety, And auditory processing deficits…along with social anxiety.  In addition, he has struggled with compulsive self harm behaviors such as skin picking and pricking.  He is under the care of a psychiatrist AND pain management physician, however, we are looking for a psychologist for CBT to help Dylan with his struggles…. from the privacy and convenience of home.   Dylan additionally has had struggles with substance abuse (painkillers), however, is stable and in treatment separately for that.  We are looking for the “Third leg” of his treatment team…. a great therapist he can connect with.

Dylan is currently on SSI Disability due to these conditions, having been approved in 2015, without appeal, due to his extensive medical documentation over the years.  In short, he is a complex young man, but super sensitive, loving and smart.

Dylan agrees with the idea of additional therapy.

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Hello,
Just briefly:
1) What do I do to try to get my son to talk about things?
2) Respect household rules/curfews?

Anytime I try to talk to him he calls me a “helicopter” parent…regardless of what the topic is.

He recently had homecoming dance.  I said after the dance he needed to come home (he wanted to stay the night at his girlfriends house- Her Dad was there - we don’t know him and the girlfriend said it would be ok!)  Regardless we stated that it would not be appropriate and that he needed to be home when the party was breaking up. He stayed out (we didn’t have her address or phone # and his phone “died” with no charger (they are all generic chargers).

I was trying to come up with a consequence, keeping in line with the consequence should match the rule broken.  However he has his own pick up that he pays for himself (plus taxes, license, insurance, gas, and repairs).  I thought about using his spare key to “take” the pick up away from him, but could he then file a police report of theft?

There is no “grounding” him as he just refuses to listen.  So we ground him with other consequences:  Ex: Brother and sister get lunch bought for them because they are obeying the house rules.  You get to miss out on this lunch.

His girlfriend (really nice good natured young lady, with a kind heart) had a curfew with her Dad as did the other kids in the group.  I asked him about that.  I also asked if the Dad had any house rules for his daughter having her boyfriend stay over and he said “I had to sleep in the basement and she had to stay upstairs.  He has x,y,and z types of guns, knows how to use them, and told me of some land he owns?”  I think the Dad is military (which my son respects and is planning on joining himself. )

So basically, he understands and follows other peoples house rules, curfews, and treats them with respect but we get the opposite.
I have tried to encourage my husband to take him out, spend time hunting, fishing and talking with him.  It also opens up a pathway of two way male conversations.  They do go, spend time bonding, but it doesn’t seem to help when the chips are down.  It’s simply our sons way or no way!

How do we get him to understand that “parenting” is something all parents do!  Rules need to be followed at home, in school, at church, in the community, at his job, in traffic and online!  The only rules he has a problem with are home and school.  He sometimes leaves school during lunch but he doesn’t have the schools permission (due to failing grades, or time owed), but he wants to “go out” to lunch!
He won’t use notes for tests and sometimes (not always, as we have seen improvement) refuses to meet with teachers (as per his IEP) to get help from them.

I am going to stop here, as it’s already too long!  Sorry.
Any advice?   He just shouts, gets angry, and gets up and leaves.
I am reaching out for help and hope you respect that by passing on some info. you think might help us.

Sorry to be blunt, but I need help, solutions, advice, and guidence …our son is a good kid but I don’t know what to do to help him understand, cope, problem solve and remain calm in stressful situations.

We have tried various things, some work, some don’t.  Just looking for something new.
Thank you for your time.

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Hello-

Our 17 year old, 12th grade son was diagnosed at the age of 13. He has a difficult case according to the three doctors, school district testing, etc.   He had a medical reaction to the two different ssri administered at the age of 13.  It was so bad (every black box) description. We almost lost him. It took a year for him to recover from not knowing his name, violence against walls, and hit me once one time,  etc. during this time, cops were called twice by my husband.

At the age of 14 he went to high school. Recovered more and by junior year thriving with basketball, chess club, drama, musicals, grades etc.. to a point the doctor thought we were doing well and we kept in contact. School officials and teachers also saw the phenomenal growth and trajectory.

Then in second semester junior year, he regressed to not showing up on time (hour late). Feeling like he was not doing well. Was bullied at school. We worked with school. During this time his OCD germ phobia that he has kicked in higher.

Now it's senior year. His first week started on time. Then bully spit on him and school told him something that was unprofessional (they did charades of students to orient new teachers and he was told). Now He's showing up later and later (meaning I'm late to work as well) because his OCD has kicked into high gear from spraying nothing to spraying everything with either febreeze or soap and water. I mean everything (floors car handles and seats books papers etc).  Hes also hoarding the soap bottles, cans, etc. we can't touch the items. We have tried. When do, he melts down  and doesn't move forward. He is processing everything, the ritual of what moved when, how,,etc. until it's put back. The cops were recently called by our neighbors because they heard my son saying you're hurting me, which was actually the other way around. Since then, he saw a cop drive by our house and he literally comes running to me and says "mommy mommy please protect me. You didn't call them did you. Please protect me." I hadn't called. The cop was just driving by.

Our son is also controlling when we/I leave our room and where we/I can walk through house.

My husband and I have temporarily separated about August 13, at my son request, because my husband had so many disagreements and such poor communication between us two. As our doctor said three years ago, we need to get on same page, but we couldn't. So, thinking it would help us and help him, my husband and I agreed to temporarily separate with the intent to get back together.

At the end of August our son started to slap me when routine was disrupted. He's not done this multiple slapping thing before, even at worse time when he was 13. Since august 13, he has slapped me four different times for lengthy periods. He blocks me from moving or retreating.  I bruise easy. They were slaps. I understand  it's bad, and son started to see that not good and started to self regulate by saying I need to go for a run, I'm upset. Because of this self correct  and because he is fine in all other places including mainstream school, I don't want to call the cops.

But the last time (oct 14) he changed. It's now kicking and slapping harder. I told him to stop. Its inappropriate. He said stop talking and reacting or I will hit you more. I stopped. He stopped. It's now been two days of processing how bad he feels for doing what he did, etc.

My husband and I are back seeing the psychiatrist  and seeing a marital counselor in the next week. Our psychiatrist has referred us to marital counseling so that we can decrease the stress and thereby decrease the OCD etc.  the doctor also notes our son appears at times to runs roughshod over us. I stand up as much as I can, correct him in loving manner when in error (and he is receptive when not in meltdown), and when it's the right battle to choose...Like getting to school, etc. but lately  when I state we must leave At such and such time and give warnings, he regresses into further processing everything. Then when he is late, he regresses because now he's late to school. The desire is there, its implementation.

My son is sleeping normal hours for a teen.  He's not in drugs or alcohol. During meltdowns or processing, he can't eat, but otherwise eats well. I know because I'm with him.

Also, my son refuses medicines of any kind, refuses to see doctors, etc because of everything that went on before. It actually causes horrendous issues just seeing his orthodontist.

 I am supported by people like you, our psychiatrist who has said I'm doing the right things, the aspergers experts, the aspergers parenting community, several friends, and my faith. But, I am honestly getting tired from doing all the work physically and basically emotionally alone (I.e. No one is with me when a melt down occurs); being the primary bread winner throughout our marriage; dealing with my temporary separation; and my husband's recent unemployment. I'm looking for tools to help me help my son.

My son refuses to let anyone else help. When I say I need to have someone else drive him to school or that I need a few minutes to take a rest because I've got a cold,  he melts down and says I'm not there for him and I'm his rock I need to be there. 


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Dear Mark

 Two months ago my adored Aspie/HFA partner of 23 years announced he was leaving and never coming back. He has bought a motor home and plans to live in it, go to music festivals and ‘explore other relationships’. I know our relationship was struggling, I have had such huge pressures over the last few years (being sole breadwinner and homemaker, redundancy from a well paying job I enjoyed, having to take a lower paid new job I do not enjoy, menopause, overweight, two teenage boys to raise, one of whom also has had an autistic spectrum diagnosis) I could no longer meet his needs or deal with his ‘idiosyncrasies’. He had his diagnosis in his late 30’s, shortly after his nephew was diagnosed. It gave him some explanation of why he is how he is but there was little support or information available at the time. How I wish I had you then! I could have done so much more. Your book has gone a long way to help me understand, I resonate so much with many of your correspondents. I am at such a low ebb myself, with having to maintain domestic normality as he has not yet told our sons of his plans, I am at a loss as to how to proceed. He is adamant that our relationship is over (in his words) ” I respect you as a friend but I don’t see you as a lover anymore”. How wounding is that to a 55 year old overweight NT woman who feels she has given him everything and how typically AS? I would be very appreciative of any advice you could give me that would help our partnership as I feel it can be salvaged. I know he would not consider relationship counselling, he does not appear to want to save ‘us’ and would view it as ‘someone else always telling me what to do’ –one of his main gripes with me was that I always made decisions for him = me not believing him capable of decision making. He is capable, but so careful and so considered in his decision making that it invariably overruns the timescale within which the decision has to be made! I am trying to be strong and considerate to him through this but I am really cracking now and don’t know where to turn, please help!

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Hi,
I am wondering whether you could help me.  Let me describe my situation.
My son is 19.  He is difficult and manipulative with me but well behaved in the outside world and an excellent student.  He has a twin sister.  He played with her a lot when they were little but never had much of an interest in outside friendships.  By high school, he avoided being with friends if he could.  All he cared about was school work and getting into a top college.  He stressed himself out trying to be a perfect student.  He didn't get into any schools close to home that he wanted, so he went to a top school that is a plane ride away even though he had never been away from home and was very nervous.
He hated it from the start, always thought he was failing even though he ended the year with a 3.85 gpa.  He lost twenty pounds from stress, anxiety, and depression.  He developed an intestinal blockage from the weight loss and was hospitalized this summer and needed a feeding tube.
He did not go back to this college.  He is currently on leave.  He is home recovering and taking classes at a local school and doing an internship.
He's upset and stressed and feels like a failure.  He also has sensory hypersensitivity to light, sounds, and clothing seams and tags.
I'm really the only person he enjoys spending time with.  However, if I say something that annoys him (like if I tell him that he doesn't have to go to a top college to be successful), he starts insulting me and telling me I don't know what I'm talking about, and it just goes on and on.
He doesn't want to see a therapist, but I told him he had to go a few times.  The therapist he saw of course said he's extremely anxious about school, and this makes him controlling.  The therapist says he has sensory integration disorder and possibly Asperger's, and that the Asperger's could be causing his rigid thinking and perfectionism.
However, he understands jokes and sarcasm and doesn't take thinks literally and easily manipulates me (he knows how to push my buttons).  His speech is excellent and normal, and his coordination is normal.  The therapist says autism is a spectrum, so my son could just be very high functioning.
What do you think?  I found you by googling whether kids with Asperger's are manipulative or defiant with parents.  It seems like they can be defiant.  But can they manipulate, or does that require theory of mind?
He's also worried about being late, and he is just perfectionistic all around.  He could also have obsessive compulsive personality disorder and not Asperger's, but the therapist says that since he has always been this way and has tantrums starting at seventeen months and has sensory issues, it seems like Asperger's.
I can't get my son to keep seeing a therapist, and the therapist said not to force him because he will see it as an insult.  It will also just anger him.


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Dear Mark,

My husband and I are in Toronto.  

Our 21 year old son has recently been diagnosed with ADHD.  He is "addicted" to gaming and rarely leaves his room for anything or anyone other than his girlfriend, a bit of food at night, and occasional night wanderings in the city.  He does not like to work and is having trouble finishing high-school although he has a very high IQ.  We are currently in our 4rth year of trying to support him finishing high-school since he crashed his 86% average and scholarship in 2013 - failing in the last two months of Grade 12.

For years I have been saying, we must remove the computer from his room.  He built himself a mega-gaming computer last year after burning out his laptop.  Recently we bought him a laptop for his school work with the plan of removing the gaming computer which is so much faster - but it has remained in his room, pending all sorts of promises and assurances and we have repeatedly bought into the concept of "harm reduction" rather than "cold turkey".

We have consulted numerous professionals who never seem to get the seriousness of the gaming addiction.  They dismiss the games and look for the underlying problem - as if leaving the bottle of vodka on the table helps an alcoholic explore their deeper emotional issues.  Imagine what would happen to anyone spending 1,000's of hours on those repetitive sniper attacks!  He sits for hours at a time.  While his mind and body have gone into decline over the last 5 years (really since Grade 11), we have not gotten the moral support/professional help we need to take what feels like a risky step.  He has scared us; he has made threats.

However, I feel like I can't sustain this any longer...we are now paying for private school, gym membership, cell phone, therapy, medications, and visits to his girlfriend in another town - and we get nothing in return.  He is still skipping school and the gym; he has no outside job, dreadful sleeping and health habits, a regular diet of hostility towards us and he is spewing conspiracy theories while reading all sorts of things on-line.  I fear we are training him into mental illness by supporting his on-line life.  
 
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Hi Mark,


My son (JT) has been diagnosed by a respected psychiatrist in the Salem, OR area about 3 - 4 years ago with Asperger's Syndrome (HFA).  Over the last 18 months, my 17 year old son's OCD has been getting worse & my wife & I are often at wits end & are very frustrated on how to deal with this.  Here's are some of the aspects of his behavior which are of concern:


1)  Fear of germs:  We are not allowed out of our room in the morning to go to work unless (JT) has done is ritualistic cleaning which includes spraying (usually with Febrees) one or both of our cars, hallway, kitchen, sometimes the door handles and sometimes new things we have bought.  He also uses soap or Febrees on his hands without washing the soap off which makes his hands red & knuckles split open.  Also, he has a ritual of vacuuming a certain part of the family room carpet before we can leave our room..  He sprays so much liquid from the chemical every day that the laminate flooring in our hallway is starting to buckle.  My wife is concerned the carpet in her car is getting moldy.  Also, every area where we step including the garage floor is sprayed.  The only exception is the carpet inside our house.


2)  Hoarding Objects:  He will not throw away empty hand soap, laundry soap, Febrees bottles, or drink cans.  All rooms in our house my son feels comfortable in have his clothes, food, objects I have touched he thinks are contaminated, etc. spread out on the counters and floor.  Apparently, not throwing away stuff is tied to good or bad memories he is not ready to release yet.  Or it may be he must accomplish a certain goal before he can clean.  Problem is, he doesn't always tell us what his goal(s) are.  If we as parents try to help him clean or touch objects which should be thrown away, this causes my son to freak out.


3) Excessive tardiness, absences from his first period:  Naturally, this is a byproduct of his OCD and stress he goes through every morning causes JT and my wife and I to be late to work.


4) Discipline:  When we as parents try to use various types of discipline or correction such as, Please don't spray the floor, it is damaging the wood, etc., he will usually respond with, "Stop, you are causing me more stress"  Or if I say, JT let's go now, he responds with something like, Dad, you are causing me more stress, stop talking or we are going to be later.


Do you have tools to help our son with these specific issues?  We believe getting him to see a counselor would cause more stress so this is not an option at this time.  Is there a online blog or support group to understand what other parents have done in similar circumstances with successful outcomes?


Your suggestions are greatly appreciated!

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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.

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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.

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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.

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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.

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COMMENTS:

Jane said: You learn more from them than you teach. You will grieve the loss of the So called perfect child you thought you would have many times, but once you know and accept that you were never entitled to a perfect child in the first place, you love them for who they are. They've got you, and who's to say they aren't asking God, "Why did you give me these parents?"😉

Kari said: I agree 100%. I have no patience for people who are insensitive to people with special needs and I would rather have my unique and kind child rather than a perfectly functioning bully. That is what I always came back to when I would worry for her.I would like her life to be perfect but if I have learned one thing through all of teach successes and fails we have as parents, it is that life isn'the perfect and we just have to keep moving forward.

Children on the Autism Spectrum Who Wander Off

“I have pulled my son back from walking into the road numerous times. He is aware of the danger but he shuts off and hyper focus's on his thoughts to block out sensory stuff which makes him oblivious to his surroundings. Also, he will disappear from our fenced in backyard [thru the gate] and wonder down the street on those rare occasions that I go in the house for literally a minute or two. I CANNOT take my eyes off of him for a second! How can one keep this child from wondering off like this? Suggestions?”

Research reveals that about 50% of kids on the autism spectrum run off at least once. Many have been gone long enough to cause parents to report their child missing to authorities, and some have tried to wander off multiple times. The most common places these kids wander from are their homes, schools, or a store. 

There are several reasons why kids on the spectrum wander off (e.g., seeking a place they enjoy, trying to find a place they can go to avoid an uncomfortable situation, impulsivity, feeling stress or sensory overload, anxiety, etc.). It has been suggested that wandering off may be the leading cause of death among these young people. Drowning appears to be the most common among these casualties.



For moms and dads who have a “wandering” youngster on the autism spectrum, here are a few precautions to ensure his or her safety: 

1. DNA registration can be a useful tool for identification. Some companies will store your youngster’s DNA for up to 18 years.

2. Locator technology is another useful tool. There are GPS devices that kids can wear which will help parents locate their lost youngster.  For example, the EmSeeQ locator band is a watch-like device that uses cell phone technology. Other security companies offer a variety of options to help parents keep track of their youngster.

3. Having a youngster on the autism spectrum forces parents to “think out-of-the-box.” Thus, try to understand your youngster’s motivation for wandering off, and then try to find a safer way to meet that desire. For example, many children on the spectrum have a fascination with water. So, if your child has wondered off to the pond near home, then possibly a kiddy pool in the back yard would meet his need to explore water.

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

4. Keep your house safeguarded.  For example, set up sensor motion lights around the periphery of your home, set alarms that notify you when someone opens a door or window, and make sure your child’s bedroom is close to yours.

5. Keep a diary of places that your youngster has shown an interest in. Think of specific convenience stores, neighborhood friends’ residences, parks, playgrounds, streams/ponds/lakes, and other places your youngster seems to gravitate to.

6. Use the “stay within my reach” rule. When your child prefers to walk without holding your hand in potentially unsafe zones (e.g.. in a parking lot, at the mall or grocery, on sidewalks, crossing the street, etc.), let him know that’s fine as long as he stays close enough to you such that you can reach out and grab him if needed. Also, let him know that if he violates this rule at any point, you will have to hold his hand for a count of 30, and then try again. This models how to practice self-control, which is a very important concept for children on the autism spectrum. To reinforce compliance with this rule, tap your child on the shoulder every few minutes (if he is being successful with following the rule) and say, “I can still reach you. I appreciate you staying close by my.”

7. Use the “stay within talking distance” rule. When your child prefers to walk without holding your hand in rather safe places (e.g., at the park, on hiking trails, along the beach, down long hallways, etc.), let her know that’s o.k. as long as she stays within vocal range (however, if you have to scream loudly to get her attention, that’s too far!). If she violates this rule at any point, then revert back to the “stay within my reach” rule for a period of 3-5 minutes, then try again.

8. Register the youngster for proper ID through the local police department. Some police departments are set up to receive vital information for kids on the autism spectrum in case they need to refer to it.

9. Advise your neighbors of your child’s wandering tendencies. Tell them to feel free to notify you if they see something or if they see your youngster running away.  Also, tell them not take anything for granted.

10. Advise the school, too. When teachers and other staff interact with your youngster, make sure they emphasize that wandering off is dangerous. In addition, ask your child’s teachers if they would educate him or her on some basic identification facts (e.g., his or her address, the school he or she attends, parent’s cell phone number, etc.).

Have plenty of patience on hand as your youngster learns the importance of not wandering off. No doubt, there will be times when the child with a history of wandering tests the boundaries. In those cases, remind him of the danger, as well as the punishment that will be implemented (e.g., grounding with no privileges).


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


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


COMMENTS:

•    Anonymous said…  He's 9 and has mostly stopped it. No more wandering, but he does still occasionally worry me with the bolting when he gets very overwhelmed.
•    Anonymous said… All the time!!
•    Anonymous said… As a much younger child, though, he was prone, always, when noise levels went up to just set off running in a random direction; sometimes that turned into climbing if the opportunity arose, and we'd find our three year old on top of an eight-foot stone wall.
•    Anonymous said… even now as a teenager, he'll wonder off if I'm not paying close attention.
•    Anonymous said… Functioning Labels are misleading and rigid. How a person is impacted is a more fluid, accurate representation. A person can slip into different impaction zones (mild/moderate/severe) based on mood, location, or health.
•    Anonymous said… He has stopped, probably after age 7. Wasn't necessarily bolting to, but bolting away from something with no thought of where he was headed. Any type of large group settings (school, summer day camp, Sunday School) until he got comfortable. My older, not diagnosed, son did too with things like fireworks. He bolted for the gate at Disney World when the afternoon fireworks at the castle went off.
•    Anonymous said… In autistic children it's called fight/flight and it's due to their anxiety escalating. When my son runs it can be very dangerous. We never chase him. We follow from a distance and keep him in eyesight.  The best thing to do is to watch for triggers and use calming techniques. For example if our son is adverting eye contact, rocking on his heels swaying back and forth or wringing his hands...these are all signs that he is considering to run. We will start try to decompress by talking in low calming voices. We will also use a weighted blanket. If he's resistant we stop talking altogether and try deep breathing.  If he runs out of our subdivision we call 911. What's important when calling is to identify your child is autistic to the dispatcher. We actually contacted our local sheriff department and they already have a summary profile that pulls up on their computers about our son. It provides them information about him that will help when they are handling him. Seek medical help, there are medications that can help decrease your child's anxiety.
•    Anonymous said… It seemed frequent between ages of 5-7? Not as much now. He's 9.
•    Anonymous said… It was actually a diagnostic question for admission to a specialty Aspergers school: "fight or flight?"
•    Anonymous said… My 5 year old ran out into the road, I was just behind him but a lovely woman tried to stop and help and he thought she was kidnapping him so he's never done it since but his lack of impulse control makes it a risk. Unfortunately that rules him out of school trips unless I can attend to take responsibility.
•    Anonymous said… My almost 9 yr old with recently diagnosed autism level 1, chased leaves into the road, and he also never uses a sidewalk. He is always walking in the grass between the road and sidewalk.
•    Anonymous said… my aspergers son is 15 and he has never done anything like that. I always feel for people who deal with that. The worst he has done is kicked holes in his bedroom wall when he was younger. Extremely stubborn though and the shutdown is hard but luckily nothing crazy.
•    Anonymous said… my child stays exactly where I say to. Thankful I haven't had to exp that and I'm sorry you have. My child acts like an adult who likes to stay put at home.
•    Anonymous said… My HFA Aspergers son who is 11 runs when he is scared, mad, or hears loud noises. It is scary because he just runs with no awareness of his surroundings
•    Anonymous said… my son 7 was just diagnosed aftet 3 yrs. He ran away from school when they were at recess. They caught him before he left the parking lot. At home he says hell run away and i keep an eye on our doors. When we go for walks and stuff he insist on walking in the middle of the road or in peoples yard.
•    Anonymous said… My son did when he was younger, what was worse is he wasn't scared of being hit by a car because he believed he had super powers. We locked the doors and put the key up high
•    Anonymous said… My son has yet to receive a diagnosis (red tape). He has only darted out in front of a car to escape a wasp.
•    Anonymous said… My son is (in)famous for being the first child in 33 years to "escape" from the local community art school at age 6 1/2-7. The class meant his lunch schedule was off, and he was hungry, so he decided, during a moment when the teacher was out of the room gathering materials, he was going to walk home. He walked out of the class, out of the campus gate, and was about 2/3rds of the 2-mile way home--accurately, in spite of several turns--when one of the seven staff members scrambling to look for him caught up. Everyone was terrified because the school was on the edge of a lake; except me. I knew as soon as they contacted me where he was probably going and that he was probably doing just fine, so as long as I didn't let myself imagine something actively sinister, his sense of direction was so impressive I assumed I could just head to my house and wait.
•    Anonymous said… My son is five and he threatens to walk out of school.
•    Anonymous said… My son is only 5 but yes all of the time. I'm constantly aware of what he is doing and ready to grab him because he can disappear very quickly.
•    Anonymous said… my son used to do that, apparently he is not aspergic, but suffers from sensory overload. And my stepson who is still awaiting to be statemented if the council don't lose the paperwork again.
•    Anonymous said… My son was home alone, had a meltdown and ran. I was very fortunate that only a few doors down, he got it together and came back home. I had already called the police and they checked on him. He has also tried to run from school during a meltdown but was talked down by a police officer he knew. He has a special bond with officers since both my husband and I are former officers. The school went berserk and escorted him everywhere last year. We started this year on a clean slate and so far so good.
•    Anonymous said… My son was the resident escape artist at his school when aged 5-8. I repeatedly explained to the teachers that he was a runner and they would have to learn to shut the school gates. That leaving furniture around he could climb was also a big no-no. The message didn't sink in. He found every escape route possible. Open school gates, closed farm gates, 6 foot pool gates, double locked doors (they only placed the door handles 2 foot apart so one hand on each handle and he was out). I would get phone calls to say they had to get in the car to look for him. Having a photographic memory he would run the back roads home whilst they looked for him on the main road. They would find him over 1km from school. Parents passing would find him in the local pony club and report his whereabouts to the school. BUT he did grow out of it and at 11 he is still alive having managed to not get himself run over in the process.
•    Anonymous said… My son who is non verbal autistic is known for his running. We had to fence around our whole house and we don't go anywhere unless know he is secure either with his harness or inside a buggy. We had belts that I wore and he wore that were connected as well. There have been times still that he got away from me. I have horrid nightmares about him getting away and getting hurt.
•    Anonymous said… My would just leave and when the police found her for me she would have no reason as to why she left, she just wanted to leave but would eventually come back.
•    Anonymous said… No but in a public place he will wonder off to be alone.
•    Anonymous said… Terrifyingly,on many occasions, somehow we survived into adulthood, able to drive, catch flights and use public transport although even that is less straightforward than one would like.
•    Anonymous said… That is why he is never unattended. Ever.
•    Anonymous said… that's why we have the Gizmo watch phone now. It allows us to track her. She can call only 4 numbers on the phone. It's been very handy. She feels independent and the wandering off has stopped. Also the best part: when I call: it auto picks up and I can talk and she has to listen.
•    Anonymous said… Twice, law enforcement searched.
•    Anonymous said… When he was little ... All the time
•    Anonymous said… When my son was around 8 he bolted through a pasture full of horses & cows. I was afraid he was gonna get trampled!
•    Anonymous said… every time it was because of anxiety. My son did this a lot when he was younger. He's now 16 and we don't have the issue. We've also worked hard to prepare him for change and limit his anxiety.
•    Anonymous said… Yes and he got sooo grounded. He took off a few times last year he hasnt done it since.
•    Anonymous said… until around 4. Had to have a whole shop shut down once as he managed to unclip himself from the stroller and was found hiding amongst the clothes rails...I died a million times in those minutes.
•    Anonymous said… Yes with fire! Would never learn it was hot
•    Anonymous said… He was a runner when he was 4-5 years old.
•    Anonymous said… No sense of danger. Fear is not an emotion he possesses.
•    Anonymous said… When I was younger because I did not want to be at school. Not anymore.

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Teaching Your ASD Child "How To Be A Good Friend"

Many children on the autism spectrum tend to have an Avoidant/Anxious attachment style in which they typically repress the desire to seek comfort from their parents or other caretakers when scared, distraught, or in pain. Instead, they rely heavily on self-soothing behaviors as a way to deal with such uncomfortable emotions. For example:
  • rocking
  • pacing
  • twirling hair
  • sucking thumbs and various objects
  • hitting or head banging
  • pulling hair, eyebrows or lashes
  • picking skin or nose
  • grinding teeth
  • cracking knuckles
  • biting nails, lips, cheeks, pencils, etc.

Even at a very young age, many Avoidant/Anxious kids tend to be independent “little adults,” relying very little on others for help. Unfortunately, their tendency to be self-sufficient and unsociable can leave parents feeling a bit rejected. Furthermore, the fact that they rarely demonstrate a desire for warmth, love, closeness or affection tends to discourage support from parents – and even siblings. Many moms and dads have reported that their High-Functioning Autistic (HFA) child is often aloof and doesn’t like to be touched or hugged.

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

As these children enter school, many appear to be more aggressive, hostile and emotionally isolated than their “typical” peers. On the playground, they may be the students who bully their classmates. As teenagers, they tend to be disliked by both peers and educators. Also, they are less emotionally involved with their parents and siblings.

Perhaps the saddest aspect of this attachment style is that these children have great difficulty in finding and keeping friends. This is often due to the fact that they lack an understanding of basic social skills, don’t know what to say or do around their peers, withdraw from others and choose to spend time alone rather than run the risk of trying to “connect,” and decide that staying to oneself is the less painful option. Many parents report that their HFA child prefers to play alone. In addition, these children often annoy their peers by butting-in during games, interrupting conversations, rambling on about their special interest or favorite topic, cut in line, make rude comments (with no intention of being rude), and so on.

Some children with an Avoidant/Anxious attachment style are significantly “asocial” (i.e., they lack the motivation to engage in social interaction, have a preference for solitary activities, have limited social expressiveness, have low sensitivity to social cues, emotions, and pragmatic use of language). Asocial tendencies become acutely noticeable in these kids from a young age due to deficits in crucial social development skills (e.g., social and emotional reciprocity, eye-to-eye gaze, gestures, normal facial expressions and body posture, sharing enjoyment and interests with others, etc.). Some of these young people really want to be social, but fail to socialize successfully, which can lead to later withdrawal and asocial behavior – particularly in the teenage years.

Friendship skills come fairly easily to “typical” kids. But, unfortunately for children on the autism spectrum, these skills must be taught. If you have a child on the autism spectrum, then you have a child who is socially and emotionally immature. Thus, parents must coach their child in social and friendship skills. In order to find and keep friends, your child must cultivate the skills to BE a “good” friend. Then – and only then – will he or she attract peers and turn the relationship into a friendship.


Here are a few tips for how parents can coach their autistic child on how to be a good friend:

1. Be a good role model. Try to find a lot of opportunities for your child to observe you being nice to someone (e.g., having a casual conversation with a stranger in the line at the grocery).

2. Give your youngster the words and behaviors to enter into - and exit - others’ play group (e.g., “If you want to join in the game that they are playing, then ask ‘can I play too’.”). Also, give him the words and behaviors to include other peers in his play group (e.g., “Would you like to play with us?”).

3. Help your child to be a “behavior observer.” Teach him to pay attention to the actions of other kids as they relate to one another (e.g., at the park, playing a board game, etc.). Then discuss with him what was observed and what things demonstrated good friendship skills (e.g., “Did you notice that Michael is being good about waiting for his turn?”), as well as the things that did NOT demonstrate these skills (e.g., “Did you see Sarah jerk that toy away from Carlie? That’s not being a very good friend.”).

4. Help your child to recognize what traits HE wants in his friends (e.g., someone who shares, plays fair, doesn’t push or hit, doesn’t call people bad names, etc.).

5. Help your youngster to develop the ability to observe the impact of his behavior on others (e.g., “I noticed that when you called your friend ‘stupid’, she looked like her feelings were hurt.).

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

6. Let your child witness you spending time with YOUR friends.

7. Notice and acknowledge successes. In order to help your youngster see when he is using good friendship skills, comment specifically on what he does in his friendships that shows he cares (e.g., “When Kayla fell down and hurt her leg, you offered to help her up and took her to a chair so she could to sit down. That’s you being a good friend!”).

8. Watch movies and read books about friendship.

9. Role play how to be a good friend.

10. Lastly, post the following (with pictures if possible) in a very prominent place (e.g. refrigerator door):

I am a good friend because...

•    I am reliable
•    I do kind things for my friends
•    I use kind language with my friends
•    I like to have fun with my friends
•    I help out when my friends are sad or have a problem
•    I like spending time with my friends
•    I remember my friends’ birthdays
•    I like to share with my friends

In a worst case scenario, the HFA child wants so desperately to “fit-in” with his peer group, but fails miserably – time and time again – due to the lack of skills in this area. As a result, he “gives up” and even has a pervasive sense of anxiety about ever trying again. He simply avoids “connecting” to friends as a way to cope with feelings of rejection.

If your best efforts to help your child “be a good friend” fall short, a mental health professional can design a treatment plan that is appropriate for the child who exhibits an Avoidant/Anxious attachment style. Treatments vary, but they will likely include cognitive-behavioral therapy (CBT). If a co-existing condition (e.g., depression, anxiety, etc.) is also diagnosed, appropriate medications can be used.

Share with your child:


 
Resources for parents of children and teens on the autism spectrum:
 

==> Videos for Parents of Children and Teens with ASD
 
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Unraveling The Mystery Behind Asperger's and High-Functioning Autism


Does your AS or HFA child's behavior confuse and frustrate you? Have you often wondered how his mind works? Are you frequently stressed-out due to your child's meltdowns and tantrums? Do you feel that you have wasted a lot of time and energy trying to get him to change?

Then listen to this: Unraveling The Mystery Behind Asperger's and High-Functioning Autism.

Parenting High-Functioning Autistic Children


Announcing our new Facebook support group:

==>  Parenting High-Functioning Autistic Children <==

This is a support group and educational resource for parents raising children on the "high functioning" end of the autism spectrum (i.e., HFA, Asperger's).

Join Today!

Helping Non-Autistic Children Cope with Their Asperger’s or HFA Sibling

"What suggestions have you tried regarding helping the siblings of your autistic child to have more compassion. When they try to play with our autistic child, it always ends badly as he has to make up and enforce a set of rules for whatever game they are playing at the time - so we are in the position of having to keep them apart."

As a mother or father, you want to give all your kids equal attention. But when parenting a youngster with Asperger’s (AS) or High Functioning Autism (HFA), that can be difficult. Your “special needs” youngster has more challenges and obstacles – and may take more of your time. As a result, your other children may begin to feel left out.

In addition to feeling left out, siblings of an AS or HFA youngster may experience the following:
  • trying to make up for the deficits of their sibling
  • frustration over not being able to engage – or relate to – their sibling
  • embarrassment around friends
  • concern regarding their parents’ anxiety
  • concern over their role in future caretaking
  • being the target of aggressive behaviors



Due to the nature of AS and HFA, it may be tough for your non-autistic children to form a satisfying relationship with the sibling who has the condition. For instance, their attempts to play with their sibling may be rejected, may turn into a fight due to his or her lack of play skills, or may end suddenly due to his or her meltdowns and tantrums.

The parent needs to understand what the non-autistic kids may be thinking and feeling. These kids love their AS or HFA sibling. They want to understand why there are some things that he or she can’t do, and how they can help. By honestly answering their questions in an age-appropriate way, the parent can clear up any confusion, help ease worries, and give the other children a chance to help out.

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

How to help your non-autistic children cope with their AS or HFA sibling:


1. Preschoolers are self-centered by nature. Your non-autistic preschooler may feel that everything is about him and what he wants — from the toy he wants to play with to the game he asks for at the mall. As a result, helping him understand why his AS or HFA sibling needs more of your time and attention can be difficult. When possible, try to spend one-on-one time with your non-autistic youngster. Even a few minutes spent watching a cartoon or allowing him to help you cook a meal can provide the quality parent-child time that he needs.

2. When your children ask about their AS or HFA sibling's disorder, explain it using simple, honest descriptions they can understand. For example, if they ask why their brother only eats chicken nuggets and fruit, you can say something such as, "He has trouble eating certain foods because he has Asperger Syndrome." If they ask, "What is that?" …state in simple terms that it's a disorder that makes certain foods taste bad.

3. Younger children tend to have a wild imagination. So, the monster in the closet is very real, and the tea at the tea party is very hot. When children have a sibling with AS or HFA, their imagination might lead them to worry that their sibling’s disorder is contagious, like the flu. Reassure them that they can’t "catch" a disorder like Asperger’s, and that nothing they did caused their sibling to have this disorder – it is nobody’s "fault."

4. Don't let your children make you think that everything always has to be "fair" and "equal" — sometimes one kid needs more than the other, whether or not he/she has a disorder.

5. As your children start to better understand the "why" of their sibling’s diagnosis, you will probably get more complicated questions from them. For instance, for questions about their sibling’s meltdowns, your response may be: "He has trouble putting his feelings into words, so he throws things to express his feelings." Then, the next question may be, "Will he ever be able to tell us how he feels?" …to which you can answer honestly: "Yes he will, but we have to help him calm down and show him how to use words instead of acting-out. That's why he goes to his therapist.”




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

6. Don't spend any time trying to figure out which youngster is to blame for a dispute. It takes two to argue — everyone involved is partly responsible. That includes your AS or HFA child.

7. If arguments between your AS or HFA child and his/her siblings are frequent, consider holding weekly family meetings in which you repeat the rules about fighting – and review past successes in reducing conflicts.

8. At some point, your children may try to explain their AS or HFA sibling's disorder to their peers. Some of their friends may ask rude questions, make inappropriate comments, or even engage in teasing and bullying. This, of course, can leave your AS or HFA youngster feeling ashamed, hurt, or angry. Parents can help their children cope with this situation by rehearsing some conversations. For example, “If one of your friends says ‘what's wrong with your brother?’ … you can say ‘he has autism’. If your friend says ‘what’s that?’ …then you can say ‘it’s something that makes my brother act differently than we do’.”

9. Consider establishing a program where all your children earn points toward a fun family-oriented activity when they work together to curtail arguing and fighting.

10. Sibling rivalry occurs in all families, but in those cases where one child has “special needs” – and therefore gets “special attention” – the incidents of sibling rivalry can be more frequent and more intense. Jealousy is common, and claims that “you love him more than me” abound. After all, they may see their AS or HFA sibling occasionally being allowed to stay up later, being excused from doing chores, getting extra help with homework, not being made to eat his vegetables, and so on. Comparisons are typical, but parents can explain to their non-autistic children that while it seems unfair, their AS or HFA sibling has to have this extra help due to his disorder. As an analogy, one parent stated, “If your brother was crippled and had to have a wheel chair to get around, would you complain that he has a wheel chair and you don’t?”

11. If your kids frequently quarrel over the same things (e.g., video games, the TV remote, etc.), post a schedule showing which youngster "owns" that item at what times during the day or week. If this doesn’t work and they keep arguing about it, take the item away altogether.

12. As your children become adolescents, you may find that you rely more on them to keep an eye on their AS or HFA sibling or to help around the house. As a result, they may feel increased pressure to care for their sibling, and may even become resentful. So, try not to ask too much of your non-autistic children. Make some responsibilities (e.g., helping with homework, babysitting, etc.) a choice. This will help them feel that they have control over how much assistance they provide. For instance, you might say, "It would be great if you could help your brother with his Math homework, but if you have other plans, that's fine."

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

13. Make sure children have their own time and space to do their own thing (e.g., to enjoy activities without having to share, to play with friends without a sibling tagging along, to play with toys by themselves, etc.).

14. Remember, as children deal with sibling-conflict, they also learn important skills that will serve them well later in life (e.g., how to compromise and negotiate, how to control aggressive impulses, how to value another person's perspective, etc.). So in essence, some sibling conflict is actually a good thing.

15. In some families, the sibling rivalry between the non-autistic child and his or her “special needs” sibling is so severe that it disrupts daily functioning, or drastically affects one or both of them psychologically and emotionally. In this case, parents should seek the assistance of a mental health professional. Get outside help if the conflict is related to other significant concerns (e.g., anxiety, depression, etc.), is so severe that it's causing marital problems, is damaging to the psychological well-being or self-esteem of any family member, or creates a real danger of physical harm to any family member.

On a positive note, siblings of a youngster with AS or HFA often admit that there were many positive things that resulted from growing up with a “special needs” brother or sister. For example, they developed confidence when facing difficult challenges, learned how to handle difficult situations, and learned patience, tolerance and compassion. Research reveals that non-autistic children viewed their relationship with their AS or HFA sibling as positive when they experienced positive responses from parents and friends toward their sibling, had a good understanding of their sibling’s disorder, and had well-developed coping skills.

Moms and dads should support their non-autistic children to find ways in which they can relate to – and share an interest with – the AS or HFA youngster. By utilizing the suggestions listed above, all siblings can bond with one another and show affection by laughing and playing together.

Helping Autistic Children Navigate the Holidays: Strategies for a Joyful Season

The holiday season is often seen as a time of joy, celebration, and togetherness. However, for families with autistic children, this time of...