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Avoiding Meltdowns and Tantrums While Shopping: Tips for Parents of Kids on the Autism Spectrum

All parents with Aspergers and high functioning autistic (HFA) children have experienced it: the dreaded meltdown in a public place. Your child is screaming at the top of his lungs while an assortment of disapproving eyes are all focused on you. The pressure is on! What can you do? Fear not, you are not alone.

Below are some tips to preventing meltdowns and tantrums while shopping:

1. Anything that reduces uncertainty will help to reduce meltdowns. Give your youngster a visual list of where you are going and the places you will be visiting. Make cards with pictures of the places you are going to, or cut out pictures from a magazine. Let your youngster help you make the list and arrange the order of places where you are going. In this way, he will be able to anticipate where you are going and what will happen next. Take your list along, and every time you have finished one errand, remove the card from the list and ask your youngster to tell you where you are going next. Once all the cards have been removed from the list, you can take him for a treat (if there were no meltdowns).

2. Set expectations. Before leaving the house, set out clear rules so your youngster knows what to expect. Explain you are going for only the items on your list – and nothing else (e.g., say to your youngster “we are not buying a toy today” and ask him to repeat this statement back to you). If your youngster knows what to expect before leaving, there is less chance of him having a meltdown when you say “no.”

3. During meltdown, put your youngster's needs first. It is tempting to worry about “what everyone else is thinking,” but make eye-contact with your youngster and let him know you are "present" to the situation. Stay cool. The last thing your screaming child needs is to be confronted with a screaming mother or father telling him to “stop it” and threatening to take away all of his favorite toys when you get home. Stay calm and talk to your youngster. Verbal aggression is fueled by lack of communication. When parent and child are shouting at each other, this breaks down the communication even more.

4. Avoid a physical struggle when possible. If a meltdown does happen, you may have to physically restrain your youngster to prevent him from harming himself or others, but generally a physical struggle makes things worse. If your child finds comfort in being held, he will see this as a reward for his meltdown, especially in public. As a result, you may see him having more – not fewer – outbursts.


5. Avoid verbal examinations. Although it is a good idea to talk with your youngster when you are shopping, avoid creating the impression that outings are verbal examinations. Sometimes, well-meaning moms and dads present their youngster with a rapid-fire series of questions (e.g., "What color is that balloon?" … "What shape is that?" … "Point to the clown") as they navigate through their shopping trip. Kids on the autism spectrum have speech-processing delays. Because they are already distracted by everything they see during an outing, asking them a series of questions can create additional cognitive demands, and in some cases trigger meltdowns. Allow your youngster's interests to guide occasional questions from you (e.g., if your youngster is staring intently at a poster of a popular kid's book character in a store window, you might ask him the name of the character he sees).

6. Don't make jokes. This is not the time to try and cajole him back to a calm state. If he is shrieking and thrashing around on the floor, put your shopping cart in reverse, tell the check-out lady you will return another time, and physically walk out of the store with your child in tow. Sometimes a different environment is all it takes to calm an Aspergers or HFA youngster down. If he doesn't calm down, leave …quickly.

7. Be realistic. "Special needs" kids can only be “stimulated” for so long. Be considerate and remind yourself how you feel when something over-stimulates you (e.g., the sound of loud screeching brakes). No child is going to sit quietly as you visit seven shoe stores and try on every pair you like. Cut shopping strips down to one hour (two at the most!). Also, consider browsing websites to find the items you want before going in order to cut down on shopping time.

8. Build in opportunities for choices along the way so that your youngster feels he has some control. For example, if you are going to take a break in mid-morning during a shopping spree, you might include a choice of snacks on your youngster's schedule so that he can choose between a fruit smoothie or some chocolate milk. On the visual schedule, the item that comes after the visit to the shoe store can show two images side by side – a fruit smoothie or a container of chocolate milk – from which your youngster can choose.

9. Apologize to bystanders while you attempt to gingerly make your way out the door. You need not gush, simply say, "I'm sorry, we are having a difficult morning."

10. Diffuse the problem ahead of time. If you see a meltdown brewing, try to gently diffuse it by stopping, bending down to your youngster, and speaking softly and gently to “nip it in the bud” before it escalates. Explain the expectations that the two of you agreed upon earlier - and that you both promised “no screaming or shouting” - and give him something to look forward to (e.g., trip to the park on the way home, lunch at McDonald’s, etc.).

11. Use distraction. Only a mother or father can recognize and understand the benefit of using the technique called “distraction.” When that bottom lip starts wobbling, you’ll do whatever it takes to prevent a screaming session. To the uneducated eye, it may appear you are spinning around on one foot, singing “Row Row Row Your Boat” while clapping your hands, but in all actuality, over your years of parenting, you have mastered distraction.

12. For younger children, don’t go out before naps. When possible, have your child take a good hour nap before leaving for a shopping trip. If he is tired, he will be quick to explode if he becomes over-stimulated.

13. Don’t go out hungry. A hungry kid is a grouchy kid. Go shopping – especially food shopping – only after a snack or meal.

14. Ignore the minor tantrums. It can be easy to crumble with embarrassment and feel you must reprimand your child as other shoppers look on. By allowing yourself to get angry and raise your voice, you will simply add fuel to the fire. Tantrums are attempts to get your attention so that your youngster can get what he wants. Ignore the milder form of tantrums, and he will tire-out eventually or forget what he was complaining about. (Note: There is a difference between a tantrum and a meltdown. Tantrums are voluntary – meltdowns are not!)

15. Refrain from trying to act like a full-blown, major meltdown isn't happening. Nothing is more maddening to bystanders than witnessing a mother or father attempting – and tragically failing – to ignore her youngster's “totally out-of-control” behavior. It’s a "lose-lose" situation for all concerned to pretend that high-voltage behavior is not taking place.

With the right techniques, you can avoid public meltdowns and tantrums completely, but this takes time, patience, determination – and sometimes, just plain guts!

My Aspergers Child: Preventing Meltdowns and Tantrums

The Holiday Season: Coping Strategies for Aspergers Children

With Thanksgiving and Christmas coming up, I thought we should have a conversation about coping with the holidays – an especially important topic for parents with Aspergers children:

Nov 1, 2010 ... With Thanksgiving and Christmas coming up, I thought we should have a conversation about coping with the holidays – an especially important ...

Dec 18, 2008 ... “Dear Family and Friends:” was written for the purpose of it being sent to relatives and hosts of holiday gatherings who might need a crash ...

Dec 6, 2008 ... This is an article designed to help parents of children who have Aspergers through the holiday seasons. We all have fond memories of our own ...

Nov 25, 2010 ... Holiday therapy can be a temporary bridge to January 2nd. ... Remember that as long as you're using substances to deal with holiday stress ...

Children on the Autism Spectrum and Emotional Dysregulation


Emotional dysregulation is a term used in the mental health community to refer to an emotional response that is poorly modulated and does not fall within the conventionally accepted range of emotive response. Emotional dysregulation may be referred to as labile mood or mood swings.

Possible manifestations of emotional dysregulation include behavioral outbursts (e.g., destroying or throwing objects, aggression towards self or others, anger and rage, etc.). These variations usually occur in seconds to minutes or hours. Emotional dysregulation can lead to behavioral problems and can interfere with a child’s social interactions and relationships at home and school.

Emotional dysregulation is quite common in Aspergers and High-Functioning Autistic (HFA) children. In my practice, the most frequently asked question by parents is: “What do I do when my child loses control of his emotions?” When emotional dysregulation is occurring, the best reaction is to ensure the safety of all concerned. Know that this behavior is not planned, but instead is most often caused by subtle and perplexing triggers. When the behavior happens, everyone in its path feels pain – especially the Aspergers youngster.

When Your Aspergers or HFA Child Experiences Emotional Dysregulation:

1. Acknowledge your youngster’s effect on you. Many HFA kids will calm down if you acknowledge their impact — and get angrier if you don't. You might stop and say something like, "I've stopped the car (or "I am off the phone") and you have my full attention." Then, ask questions like, "What don't I understand?"

2. Avoid physical power struggles. Using your size and strength only exacerbates the problem. Imagine your youngster is feeling furious and picks up a stick. If you grab it before he has time to give it up voluntarily, he might try to hit you with it. Instead, you can avert danger and acknowledge your youngster’s power by saying, "Please put that down. You could hurt someone you love." (Obviously you would never allow someone to hurt or be hurt.)

3. Don't extend your child’s dysregulated state with too much discussion. If your youngster is feeling out of control or in a rage, a lot of talking may not help – in fact, it could prolong the problem.

4. It's natural for HFA children to sometimes have big feelings. You haven't done something wrong if your youngster has an occasional blow-up or melt-down. Moms and dads should only worry if the youngster is chronically, constantly out of control.

5. Keep breathing and stay relaxed. It's hard not to tense up when your youngster is getting out of control, but if you stay relaxed, he's more likely to follow. Sometimes we start holding our breath when things get tense. Instead, inhale, exhale and then talk through your own feelings in a clear and (if necessary) firm way.


6. Keep your own strong feelings separate from your child’s behavior. While it's often important to show your youngster what you feel, entering into his dysregulated state with your own anger will only escalate the situation. Take a breath, speak calmly, even leave the room and give yourself a time out if you need to.

7. Let the emotional dysregulation run its course as long as no one is being hurt. This is really crucial. A youngster who is filled with raw feelings may not know how to manage them. But he may feel reassured by your calmer presence. Then, you get back to the business of communicating.

8. Let your youngster express negative feelings without judging him. Imagine if every time you were upset, some bigger, taller, frowning person looked down at you and said, "Don't feel that way," or "Don't tell me that." Would you feel like calming down - or acting out?

9. Reflect your youngster’s feelings. You might say, "I can see how frustrated you are. Can you tell me what made you feel that way?" ("What" is always more important than "Why" — it asks for specifics.)

10. Seek professional help if you see a repeated, chronic pattern that you can't figure out. If your child’s destructive behavior escalates and becomes increasingly difficult to deal with, and if nothing works over a period of weeks or months, there may be an underlying issue that needs professional help. You can find a referral through a doctor, guidance counselor at your youngster’s school, a friend, neighbor, community center or place of worship.

11. Set limits that your youngster will find comforting. A limit is not a punishment. Limits may help your youngster learn how to calm himself down. Aspergers and HFA children find the “setting of limits” comforting and soothing. They need to know that you (the parent) are in control.

12. Slow down the process by saying, "I need a moment to think about this." If your youngster is starting to lose control, you can slow things down by giving feedback. You might say, "I can see you're upset. Let's talk."

13. Try not to take your youngster’s strong feelings personally. Many moms and dads feel frustrated or personally attacked if their youngster explodes at them. Don't take his strong feelings personally. “I hate you” is not actually a personal statement. What your youngster really may be saying is “I hate being out of control.”

14. Try to avoid threats in the heat of the moment. The moment you make irrational threats with punishments that do not suit the occasion, you are not talking about the topic anymore. In the heat of the moment, if you say, “If you throw that toy – I’ll ground you,” then the youngster may start to fight the grounding, and the original issue is lost.

15. Try to comfort your youngster physically. Each kid on the autism spectrum reacts to emotional dysregulation differently. Some will want to be held, others want to be left alone. If it seems right, you might try holding your youngster, if he will let you. If your child struggles ferociously, let go as long as no one will get hurt.


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

What causes Aspergers and HFA?

Scientists don't know the exact causes of Aspergers or High-Functioning Autism (HFA), but research suggests that both genes and environment play important roles. In identical twins who share the exact same genetic code, if one has Aspergers, the other twin also has Aspergers in nearly 9 out of 10 cases. If one sibling has Aspergers, the other siblings have 35 times the normal risk of also developing the disorder. Researchers are starting to identify particular genes that may increase the risk for Aspergers. Still, scientists have only had some success in finding exactly which genes are involved.

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

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

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


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

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

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

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

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

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

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

Following extensive hearings, a special court of Federal judges ruled against several test cases that tried to prove that vaccines containing thimerosal, either by themselves or combined with the MMR vaccine, caused autism.

More 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

==> 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

==> Highly Effective Research-Based Parenting Strategies for Children with Asperger's and High-Functioning Autism

How To Parent An Aspergers Child: From Childhood To Adulthood

What works for your Aspergers (high functioning autistic) child at the age of 3 may not work for him/her at the age of 13. Here are some important tips for parenting children on the spectrum  across the lifespan:

Childhood—

After your youngster is diagnosed with Aspergers, you may feel unprepared or unable to provide him/her with the necessary care and education. Know that there are many treatment options, social services and programs, and other resources that can help.

Some tips that can help you and your Aspergers youngster are:

• Contact your local health department or autism advocacy groups to learn about the special programs available in your state and local community.

• Keep a record of conversations, meetings with health care providers and educators, and other sources of information. This will help you remember the different treatment options and decide which would help your youngster most.

• Keep a record of the doctors' reports and your youngster's evaluation. This information may help your youngster qualify for special programs.

• Talk with your youngster's doctor, school system, or autism support groups to find an autism expert in your area who can help you develop an intervention plan and find other local resources.


Adolescence—

The adolescent years can be a time of stress and confusion for any growing youngster, including adolescents with an autism spectrum disorder. During adolescence, teens become more aware of other people and their relationships with them. While most adolescents are concerned with acne, popularity, grades, and dates, adolescents with Aspergers may become painfully aware that they are different from their peers. For some, this awareness may encourage them to learn new behaviors and try to improve their social skills. For others, hurt feelings and problems connecting with others may lead to depression, anxiety, or other mental disorders.

One way that some Aspergers adolescents express the tension and confusion that can occur during adolescence is through increased aggressive behavior. Teens with Aspergers will also need support to help them understand the physical changes and sexual maturation they experience during adolescence.

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

Transition to Adulthood—

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

Long before your youngster finishes school, you should search for the best programs and facilities for young adults with Aspergers. If you know other moms and dads of Aspergers adults, ask them about the services available in your community. Local support and advocacy groups may be able to help you find programs and services that your youngster is eligible to receive as a grown-up.

Another important part of this transition is teaching young people with Aspergers to self-advocate (i.e., take on more responsibility for their education, employment, health care, living arrangements, etc.). Grown-ups with Aspergers must self-advocate for their rights under the Americans with Disabilities Act at work, in higher education, in the community, and elsewhere.

There are many options for grown-ups living with Aspergers. Helping your adult child choose the right one will largely depend on what is available in your state and local community, as well as your youngster's skills and symptoms.

Below are some examples of living arrangements you may want to consider:

Independent living. Most grown-ups with Aspergers are able to live on their own. Others can live in their own home or apartment if they get help dealing with major issues (e.g., managing personal finances, obtaining necessary health care, interacting with government or social service agencies, etc.). Family members, professional agencies, or other types of providers can offer this assistance.

Living at home. Government funds are available for families who choose to have their adult child with Aspergers live at home. These programs include Supplemental Security Income, Social Security Disability Insurance, and Medicaid waivers. Information about these programs and others is available from the Social Security Administration (SSA). Make an appointment with your local SSA office to find out which programs would be right for your adult youngster.

Long-term care facilities. This alternative is available for those with Aspergers who need intensive, constant supervision.

Other home alternatives. Some families open their homes to provide long-term care to grown-ups with disabilities who are not related to them. If the home teaches self-care and housekeeping skills and arranges leisure activities, it is called a "skill-development" home.

Supervised group living. People with disabilities often live in group homes or apartments staffed by professionals who help with basic needs. These needs often include meal preparation, housekeeping, and personal care. People who are more independent may be able to live in a home or apartment where staff only visits a few times a week. Such residents generally prepare their own meals, go to work, and conduct other daily activities on their own.

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

==> 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

==> Highly Effective Research-Based Parenting Strategies for Children with Asperger's and High-Functioning Autism

2024 Statistics of Autism in Chinese Children

Autism Spectrum Disorder (ASD) has emerged as a significant public health concern worldwide, and China is no exception. As of 2024, new rese...