Fostering Emotional Connections with your Child who has Autism – a guest post from Amanda Ronan

Autism and emotional connections

Autism and emotional connections

Welcome to the latest in a series of guest posts from the ORP Library. Today we feature an article by Amanda Ronan entitled “Fostering Emotional Connections with your Child who has Autism“. Ronan is a writer, an editor, an educator and a dreamer. She has her Master’s in Education and was a teacher of elementary and middle-school aged children for nearly ten years. While engaged with her work in the classroom, Ronan rediscovered her first love — writing.

The baby photography package seemed like an over-the-top gift from her in-laws. Briana* didn’t think the family needed pictures of James in different outfits playing with different toys. She’d already posted plenty of those kinds of pictures on Facebook. In the end, though, the baby photographer ended up capturing some stunning shots of James, looking right into the camera while smiling and laughing. Now, when Briana looks at those photos, she is grateful for the gift; the photographer was able to capture a time when James was still engaged in the world around him in typical ways. Not long after that photo shoot, when James was nearly 18 months old, he stopped making eye contact. He stopped giggling when Briana tickled him. He stopped babbling. Suddenly, Briana’s lively, active, and loving baby seemed withdrawn and distant, heartbreakingly indifferent to Briana’s presence.

After a slew of visits to multiple doctors, including appointments to check his eyes and hearing, James was officially diagnosed with Autism Spectrum Disorder (ASD). The news changed Briana’s life forever; the loss she felt when she realized her son would likely never engage with her as he once had — easily, with smiling eyes and playful giggles — was devastating. There were nights Briana pored through that photo album, wondering what she had done wrong, wishing for the past.

As James grew, he continued to be less emotionally connected to the family than Briana’s other children. When they visited the town’s annual fall festival, James would wander off to investigate something that caught his eye, rather than stay close to the family and choose a pumpkin to decorate later. During the holidays, while the family decorated the house, trimmed the tree, and sang carols, James sat on the couch with his headphones on, watching a video on his tablet. For years, it seemed there was nothing Briana could do to encourage James to participate in the family life she and her husband tried to nurture.

Perhaps you currently find yourself in the same position as Briana. Your once happy, cooing, engaged baby is now reserved and distant because of ASD. As a caretaker, you feel as though there’s more you should be doing to help your child engage with your family. Yet so many of your efforts seem ineffective, leaving your child unaffected and disinterested — and your heart broken.

In those moments, it may be difficult to remember that your child is not choosing to be disconnected from you and your family; rather, he or she just doesn’t know how to connect the way you you would like him to. The good news is that many families have had success reestablishing strong emotional connections with their children with ASD. Children with ASD react differently to different environments, stimuli, and therapies, and such connections often happen in unexpected ways and through previously unconsidered activities.

The best way to begin rebuilding your emotional connection to your child is to work with teachers and therapists who have experience working with children with ASD. Professionals can model and teach you different therapeutic strategies and approaches to help foster connections with your child. Here are a few approaches, based upon the DIR/Floortime® model, to consider:

Floortime®. Floortime is a type of developmental therapy that pushes children with Autism Spectrum Disorder to reach their fullest communication potential. Floortime uses playful interactions to mobilize development in areas associated with attention and regulation, two-way communication, and social problem-solving. According to Autism Speaks, “Its premise is that adults can help children expand their circles of communication by meeting them at their developmental level and building on their strengths.” During Floortime, parents engage with their child in activities initiated and enjoyed by the child, rather than vice versa. For example, a child might enjoy blowing bubbles over playing with blocks; during Floortime, a parent would blow bubbles with the child, eventually establishing and nurturing communication through the game, rather than pushing an activity that will become frustrating to both parent and child. Floortime allows parents to better understand their child’s likes and dislikes. Many psychologists, teachers, and therapists are trained in Floortime techniques and can help parents include it in their child’s daily routine.

Pay attention to and understand your child’s specific cues and triggers. All children give nonverbal cues as to how they’re feeling, and your child with ASD is no different. Pay close attention to the sounds, facial expressions, and small gestures your child makes when he is hungry, tired, or content. The more you are able to predict what your child wants or needs, the more responsive you will become, and the greater the trust built between you — as well as the greater the emotional connection. In the same way that understanding cues can build a connection, your misunderstanding of what your child is communicating can easily lead to meltdowns or tantrums. Your child may feel ignored and frustrated when you don’t pick up on the right cues. Likewise, it is also important to pay attention to triggers for your child’s behavioral problems. Common triggers are often environmental, internal, or interactional. Understanding what triggers challenging behavior and meltdowns in your child will make you more responsive and your relationship stronger, especially as you are reacting purposefully and in response to their cues.

Understand your child’s individual differences in sensory processing.  Many children with ASD are sensitive to lights, sounds, tastes, smells, and/or textures. What other children may find soothing or calming may irritate a child with ASD. Finding fun activities to do as a family that elicit positive responses, and take into account sensory sensitivities, can make for improved emotional connections and enjoyment. Some families, for example, have found that swimming calms their children with ASD, and allows them to be better regulated, which enhances quality family time. In fact, sometimes the floating sensation has such a positive impact on the child that he or she will allow for hugs and closeness in the water — a huge boon for a parent longing to connect with their child. Some children with ASD love swinging, so families have installed playground equipment in their backyards. Taking turns pushing the child sparks delight in both parent and child. Likewise, a parent might notice that their child is easily distracted and agitated around loud noises. This family then would try to avoid loud, highly stimulating social trips. A day-long outing at the county fair would then be off limits.

Through therapy, you can learn how to engage with your child. Through observing speech and occupational therapists’ methods of interaction with her son, for example, Briana can start to incorporate more of the things James enjoys in her own interactions with him. Instead of expecting him to join in the family fun, Briana can strive to bring the family into James’s idea of fun. Establishing emotional connections with your child with ASD may at times seem impossible, but with the right perspective, understanding, and tools, you too can experience a positive — even joyful — change.

 

For more information on DIR and Floortime, visit the ICDL website.

*Briana’s story is based on multiple interviews with parents of children with ASD.

Autism and Bullying 2.”MISSION: BULLY-PROOFING MYSELF” – a free example lesson on dealing with bullying!


Autism and Challenging Behavior

Autism and Challenging Behavior

As many of you will have noticed we have been showing our support for anti-bullying campaigns over the last few years.

Do our friends at The ORP Library have asked us to share one4 of their example anti-bullying lessons with you.

 

So check out this free lesson from the workshop guidebook, Those Who Bully and Those Who Are Bullied.

In this lesson, children can:

  • figure out different ways to bully-proof themselves,
  • learn how to create a plan of action for when bullying happens,
  • and parents can use this as a tool to help with communication on bullying.



LESSON 11 – MISSION: BULLY-PROOFING MYSELF

Bullying happens sometimes, but that doesn’t mean you can’t help bully-proof yourself. What does that mean?

Bully-proofing yourself means building your skills, courage, and confidence to handle
bullying if it happens. It also helps you send the message to others that you are not an easy target.

KEYS TO BULLY-PROOFING YOURSELF
• Talk to an adult you trust: Agree on a plan of action if you are bullied or witness someone else being bullied. This way you know that you have support and have an idea of how to handle a situation if you are faced with it.

• Don’t believe a word they say: “Sticks and stones may break my bones, but words will never hurt me” is a popular saying that isn’t necessarily true. Words can and do hurt, but if you know that nothing bullies say about you is true and it’s more about their state of mind, it’s easier to ignore them and not believe what they are saying to you. No matter what they say, you are a valuable and strong person. Don’t believe them.

• Assert yourself: Practice and remember some things you could say in return if someone is bullying you. Example: I know that I’m not stupid. I want you to leave me alone.

• Stay calm: Those who are bullying often pick on people they know will react emotionally. They feel more power and control because they caused that reaction. Instead, just remain calm. Ignore them. Walk away. Don’t give them the satisfaction.

• Basic avoidance: Students who bully often strike when adults are not present. Avoid unsupervised areas like empty hallways, bathrooms away from the main hall, or certain areas of the playground that are out of the line of sight of a teacher or other adult.
• Fake it: Even if you aren’t feeling brave and strong, act like you are. It is important that the person bullying you thinks that you are.
• Build yourself up: Know that you are important, you are cared for, and you matter!
• Use imagery: Imagine situations where you are assertive and the situation ends well.

ACTIVITY
Knowing how to bully-proof yourself is important, but you will still face challenges. Come up with a plan of action to help you navigate your way through those challenges. Post this list somewhere so that you can refer back to it anytime you need to!
1. An adult I can trust to talk to when faced with a bullying challenge:

……………………………………………………………………………………………………………………………………………………………………………………………………………………………………………………………………………………………………….
2. If someone says something to me that I know is not true, I will:

……………………………………………………………………………………………………………………………………………………………………………………………………………………………………………………………………………………………………….
3. Something I can say in return to a mean comment to be assertive and let others know that I am not an easy target is:

……………………………………………………………………………………………………………………………………………………………………………………………………………………………………………………………………………………………………….
4. Ways to remain calm when faced by a bullying challenge are:

……………………………………………………………………………………………………………………………………………………………………………………………………………………………………………………………………………………………………….

5. Ways to avoid being in a bullying situation are:

………………………………………………………………………………………………………………………………………………………………………………………………………………………………………………………………………………………………………
6. When I’m feeling weak and afraid inside but want to appear to be brave and strong on the outside, I will:

……………………………………………………………………………………………………………………………………………………………………………………………………………………………………………………………………………………………………….
7. One thing I will tell myself everyday to remind me that I am valuable and important is:

……………………………………………………………………………………………………………………………………………………………………………………………………………………………………………………………………………………………………….

Personal, Solitary, Parenting Pain: The Emotional Turmoil Surrounding Extremely Aggressive and Behavior in Your Child with ASD – a guest by Amanda Ronan shared by Round Table Companies

Advice for autism parents

Advice for autism parents

Our friends at Round Table Companies have shared with guest blog post , by Amanda Ronan, with us.

Ronan share tips and ideas for helping parents with a child on the spectrum who live through extreme meltdowns and aggressive behaviour. You can read the original article here Personal, Solitary, Parenting Pain: The Emotional Turmoil Surrounding Extremely Aggressive and Behavior in Your Child with ASD.

Ronan writes “Please . . . please don’t wake up, Nora pleaded silently. A dog barking somewhere in the neighborhood had startled her fully awake, though she hadn’t really been sleeping; she’d been in the half-sleep state she’d been surviving on for as long as she could remember.

Yesterday had been the hardest day yet, and that was saying a lot, given what her family had been through over the past 15 years of living with her son who had an autism spectrum disorder (ASD), and extreme behavioral problems. They had been heading into lunchtime after a morning during which Ander had enjoyed all of his normal routines—the same breakfast he’d eaten every day for years, a quick shower, and a few hours of homeschool instruction. Now he was engrossed in his normal weekday TV show as she prepared to make his normal lunch. Routines were important, even crucial, to Ander—and to the peace of the household—so Nora had arranged her life in order to maintain them. Spontaneity, and doing things in the spur of the moment, were four-letter words in their home.

Ander would only eat nachos. There had to be only a small pile of chips, whole triangles with rounded corners, not pointy. The cheese had to be a Mexican blend with both white and yellow-orange shreds visible. The salsa had to be red and mild, pureed with no chunks. This was part of the obsessive-compulsive disorder that the new psychiatrist said her son had, along with ASD and attention-deficit hyperactivity disorder. But as Nora looked in the refrigerator, she cursed under her breath. They’d run out of cheese the day before and she hadn’t had time to visit the store.

“Hey buddy?” she called out. “How about I make us some pizza for lunch today? I know you love pizza and it’s pepperoni – your favorite!” She peeked around the corner into the living room.

Though Ander had headphones on, she could hear the sound. His expression was one of concentration, as though he’d found a moment of peace from his constant struggle to self-regulate, communicate, and actively participate in the world. She waved a hand at him. He didn’t respond.

She knew better than to remove the headphones for him. She’d tried that a few years ago, right after he hit puberty. That was the first time he’d hit her hard, a succession of several slaps to her head until she dropped the headphones and backed away. It was shocking and gut-wrenching. Before that he would lightly hit her—more in a way to get her to leave him alone.

Aggression itself wasn’t new; it had started a few years before kindergarten when he bit both his sister and the family dog, just days apart. Both had howled and become nervous around him after that, having lost trust for a period of time. Nora lost something, too at that time—the hope he’d be ready for school. Despite all the interventions, medical appointments, and therapies, she realized as she tended to her daughter’s wound that Ander might not successfully go off to kindergarten, play with the other kids, and maybe become a teacher’s pet. The journey ahead could be long and difficult; she could no longer deny it.

Not long after the biting, his meltdowns, which once had resembled a whining child’s tantrums, took another unexpected and dangerous turn when he started to throw things in the house and punch the walls. The sound of his knuckles against drywall made her stomach turn. She learned to go into the kitchen for some bandages and ice to apply to his hand when he had calmed down.

Then came the day of the windows. She would never forget the first time she heard the sound of glass shattering. Ander had put his head through the window; incredibly, though, he was unscathed. He turned around to face her, then curled up on the floor and rocked himself until he fell asleep. It took two more broken windows for them to hire contractors to install shatterproof glass windows.

Nora knew that the increased agitation, self-injurious behavior, and aggression stemmed from Ander’s difficulties with communication, social interaction, and self-regulation and that he never truly meant to cause harm and hurt himself or others. But there were times when, for his own safety and the safety of their daughter, Nora and her husband Peter had had to use the physical intervention techniques they’d learned from Crisis Prevention Institute (CPI): carefully wrap their arms around him, remove him from the circumstances, and attempt to defuse the situation. Physical restraint was always a last resort; no parent, Nora was sure, ever wanted to restrain his or her child. As he got bigger, though, she worried about what would happen if this “last resort” was no longer an option due to his size.

She found this out the day there was no cheese in the refrigerator.

When Ander saw that lunch was not what he’d expected, there was a sudden shift in his demeanor and affect. His eyes narrowed, his head shook from side to side, and his feet stomped the ground. A flush also began to creep up his neck.

“It’s okay, buddy,” she said. “The pizza is just for today. We’ll have nachos again tomorrow, just like we always do, ok?”

Ander opened his mouth and screamed at her, flapping his arms so that one palm smacked the glass breakfast table making it jump a bit. Nora jumped herself, backing up slightly. She couldn’t help it: she was actually feeling afraid of her own son. He had hit the table so hard…It wasn’t supposed to be this way…she thought to herself.

And then, in a sudden burst of movement, Ander jumped up, ran towards her, and tackled her. Nora fell backward, her elbow cracked against the tile floor, and the impact knocked the air from her chest. She was gulping like a hooked fish when Ander landed his first punch on her cheekbone. The next one caught her neck and the third her right ear, and her head reverberated with shrill ringing. Finally, with a gasp, she filled her lungs, but she couldn’t push free. Ander was stronger. So she cried helplessly as her baby boy howled and beat her. The once chubby hands that used to grasp at toy cars had become powerful fists that continued striking her until, mercifully, her husband opened the front door. Then it stopped as quickly as it had begun; Peter was still strong enough to pull Ander away from Nora—for now.

After the barking dog woke her, Nora wondered through her familiar exhaustion whether she really knew her own child, knew how to care for him, what he needed, or even knew how to be a good parent. She closed her eyes and willed the barking to stop. When it finally did, she exhaled, not even realizing she’d been holding her breath.

Nora strained to listen for any slight noises, any movements that might indicate that Ander’s sleep had been disturbed. Not hearing anything, she let her neck muscles relax and her head sink back into the foam pillow. The bedside clock saturated the otherwise dark room with the same deep red hue as the bruises on her body. In two hours, a new day would start. And she had no idea what it might bring.

As a parent of a child with ASD and extremely aggressive behavior, perhaps you can envision yourself in this story, which reflects actual parent interviews and other informed sources. Maybe you, like Nora, are feeling alone, lost, hopeless, and more disconnected than ever before.

If you are living constantly on the edge of your seat, “walking on eggshells”, trying to avoid another meltdown or manage the aggression, the self-injurious behavior, and the violent outbursts, you aren’t alone. With the U.S. Centers for Disease Control and Prevention reporting that one out of every 68 children is being identified with ASD—a huge increase from 2000 to 2010 alone—the emotional and physical turmoil associated with ASD and extremely aggressive behavior is becoming is becoming a more common scenario.

When you begin to fear your own child, it’s time to ask for help. Here’s what some parents and experts recommend:

* Build your team. Seek the assistance of a therapist with expertise in autism spectrum disorder and behavioral approaches. This person can help you assess your environment, identify triggers for behavioral problems, help with structure and routine, and provide strategies at home to prevent meltdowns and aggressive behavior. Speech therapists, occupational therapists, special education teachers, and autism in-home providers can also provide you with strategies to teach communication, social, and self-regulation skills. Respite providers and support groups can also offer provide a great deal of support for you and your family.

* If what you’re doing isn’t working, then try something different. Maybe it’s time to consider medication. Psychotropic medication does not “cure” ASD but it is often helpful for extreme emotion and behavior problems. While many parents feel fear or hesitation about using medication with their child, the right form of psychopharmacological intervention may be helpful for symptom relief and also allows therapeutic approaches to be more successful, ultimately, so that medication is not necessary in the future. Also, if your child’s therapist is not providing you with ideas and strategies to try at home to minimize the behavioral outbursts – and it seems like they are just doing a lot of “talk therapy” with your child – then it might be time to seek a second opinion. Most insurance companies will cover this type of service. If your child is in special education, and you believe that there is not a “good fit” between his needs and the services provided through the IEP – remember: you have the right as a parent to meet with the IEP team to discuss your concerns and potential changes to the plan.

* If it’s an emergency at home – then act like it – call the police or a crisis response team. Contact the Department of Human Services (DHS) in your county or jurisdiction and inquire about emergency crisis services. This is a good proactive step. The police should always be contacted if necessary but remember their primary responsibility is to ensure safety – and they are not usually very familiar or trained in how to effectively work with children with special needs. Always take necessary action to keep yourself and your family safe.

* If you’ve truly exhausted your emotional resources–then consider out-of-home care. Community-based homes and therapeutic residential treatment programs are available through county and school district funding and provide access to therapeutic care that is consistent with the individual needs of your child. They can be short-term or more long term options. Contact your local DHS or do a websearch on programs in your area – and then start making phone calls to learn more.

Parents: Remember, you don’t have to feel afraid and isolated in your own home. If you are in a very difficult situation with your child with ASD and extreme aggression, remember that you have not failed. You’ve done your best with what you’ve been given – and it’s time for more help. You are a loving, concerned parent who is trying to manage a situation that has become unmanageable. Having an awareness that you need help – and it’s okay – is one of the first steps necessary in doing what’s best for you, your family, and your child.”

Amanda Ronan is a writer, an editor, an educator and a dreamer. She has her Master’s in Education and was a teacher of elementary and middle-school aged children for nearly ten years. While engaged with her work in the classroom, Amanda rediscovered her first love — writing.

Autism and Parenting – how does parenting influence the emotional development of children with autism? Please help students at West Virginia University with some important research.


West Virginia University

West Virginia University

As many of you know I come from a survey research background. So am aware of both value and the pitfalls of research. That being said more needs to be done in and around the world of autism. Indeed I consider surveys to be a great way of giving people in the ASD community a voice.

I few days ago I was contacted by some students studying the impact of parenting on the emotional development of children with ASD.

The study is being conducted by This study is being conducted by Hilary Bougher and Amy Root in the Department of Learning Sciences & Human Development at West Virginia University.

Bougher and Root write:-

“ATTENTION PARENTS OF CHILDREN WITH AUTISM SPECTRUM DISORDER BETWEEN THE AGES OF 3 AND 11: I am currently conducting a study examining how parents of children with autism promote their children’s emotional development. We are interested in examining the unique experiences and ways in which parents of children with autism respond to their children’s emotions and teach them to regulate their emotions. If you are a parent or guardian of a child aged 3 – 11 years with autism spectrum disorder, you may be eligible to participate in a West Virginia University IRB-approved study on parenting. We are interested in learning about the parent-child interactions of parents of children with autism between the ages of 3 and 11. If you are eligible to participate, you may opt into a drawing to receive a $100.00 gift card for completing a 45-minute survey. Surveys can be completed online. Please note, your answers will be completely anonymous and no identifying information will be linked to your answers. IRB Approval is on file for this study. ”

You can take part in the study by following the link here.


Looking for parents of children with autism! Please help a student at The Irish Centre for Autism and Neurodevelopmental Research with a survey.


Over the last

Irish Centre for Autism and Neurodevelopmental Research

Irish Centre for Autism and Neurodevelopmental Research

year we have help promote a number of research projects run by the Irish Centre for Autism and Neurodevelopmental Research (ICAN) . Which is part of National University of Ireland.

A few days ago one of their PhD students, Arlene Mannion, contacted us to ask for some assistance from our readers with a survey she is running on sleep problems or gastrointestinal symptoms in children with autistic spectrum disorder (ASD).

It would be great if you could help her with the research as we think it may prove very useful to all the ASD community going forward.

Mannion writes “Does your child with autism spectrum disorder (ASD) experience sleep problems or gastrointestinal symptoms?

Some children with autism have both sleep problems and gastrointestinal symptoms, while other children have one of these issues or none at all. The Irish Centre for Autism and Neurodevelopmental Research (ICAN) in National University of Ireland, Galway is interested in hearing about your experiences with your child or adolescent aged 3 to 17 years with autism. We are interested in understanding how sleep problems and gastrointestinal symptoms affect both child and parent. Even if your child doesn’t have sleep or gastrointestinal problems, we can still learn a lot from your information on why some children have these issues and others do not. If you wish to participate, please use the link below.

https://docs.google.com/forms/d/1rdm3IrSWzZcrG14jezW1FjrjoF5T62zUH4cX26ecs2k/viewform?c=0&w=1

If you need any more information on the survey you can contact Ms Mannion at a.mannion3@nuigalway.ie.

Thanks very much in advance!