Content Warning: Description of Animal Abuse in Historic Experiments
I recently ran across a meme with a troubling message. It said, Never do for a child what he can do for himself. A “dependent” child is a demanding child… Children become irresponsible only when we fail to give them opportunities to take on. I bristled immediately. “Never” do for a child? Absolute statements like this make me uncomfortable. I understand that the point is to be decisive and firm, but then there is no room for children to be imperfect or to have needs. Yes, giving children age-appropriate responsibilities builds competence and self-assurance. However, we should be open to children refusing responsibility in an effort to have their other needs met. Seems a lot of us misunderstand why children might be “irresponsible.” There’s a great fear that we’ll foster learned helplessness if we don’t demand that our kids fulfill their responsibilities. But, is that really true?
In the 1960s, psychologist Martin Seligman conducted a series of experiments to better understand why depression was so defeating. The first experiment involved three groups of restrained dogs. The first group was restrained and released. The second group included dogs who received an electric shock which they could stop by pressing a lever. Dogs in the third group were paired with dogs in the second group and also received an electric shock. However, their levers did not stop the pain. Instead, the paired dog from the second group controlled the only working lever, which meant that the dog in the third group had to suffer the pain with no control over it and, therefore, little hope of ending it.
In the second experiment, the dogs were presented with a similar scenario, except that Seligman introduced an escape option. The dogs in the first two groups, having either not experienced the shocks at all the first time around or having had access to a lever to stop the pain, fairly quickly escaped when the shocks began. However, the dogs in the third group made no effort and were able only to cry out pitifully when they were shocked. That presumed inability to take action is learned helplessness, and it results from hopelessness in the face of failure.
An especially important aspect of these experiments was the finding that “one cause of learned helplessness seems to be learning that reinforcers cannot be controlled” (409). For those who aren’t familiar with the term “reinforcer,” it means a punishment or a reward. So, the inability to control the punishment of these painful shocks directly contributed to the dogs’ acceptance that the pain was inescapable. No amount of punishments or rewards delivered after the learned helplessness had taken hold had any positive effect on the dogs’ behavior.
What you may find interesting is that Seligman did find a cure for the learned helplessness. He discovered that either picking up the dogs and moving them to safety or using a leash to drag them out of harm’s way provided enough motivation for them to take action. He called it “directive therapy” and it was simply an intervention wherein an outside participant showed each dog how to do what the dog didn’t realize was possible. He found that less and less force was required in pulling on the leash as the dogs began to realize that there was hope. The end result of this portion of the experiment was that all the dogs in group three fully recovered and were able to escape completely on their own (410).
…which brings us to helping. Put simply, learned helplessness is giving up because an obstacle is too insurmountable. For children, it may be sitting in the middle of their room unable to clean up, because they don’t know where to start. It may be accepting punishment for not getting dressed quickly enough because they feel that the punishment is inevitable, and they can’t do what’s expected of them to begin with. As noted in the experiment, the cure for learned helplessness is directive therapy, i.e. demonstrating a way to be successful. In other words, helping. When our children become overwhelmed with their messy rooms, we can intervene by helping them come up with a plan and working on the clean-up with them. Over time, they will gain more competence and the process will be less frustrating for them. When our children struggle to dress themselves, the easiest solution is to recognize that we need to take a few steps back and offer to help them dress. It may take a while for them to do things that seem simple to us, but the more we respond to their need for help, the more capable they will become.
There are three overarching lessons I learned from reading up on learned helplessness:
A little failure is good. Letting kids figure things out on their own is crucial for their development.
A lot of failure is bad. Leaving kids to become helpless in the face of challenge does no one any good.
Our responsibility as parents is to help our children learn from failure without losing hope.
Whether a child seeks our help because they don’t know how to do something or because they want to connect with us or because they are weary and need some support or for any other reason, we will always do right by them when we help them, especially when we don’t think they really need the help. In doing so, we invigorate qualities like learning, self-motivation, and confidence… the very things that combat learned helplessness. So, please, help your kids.
If you’re a visual learner, check out this video from therapist Kati Morton! Toward the end of the video, she provides some tools for helping ourselves (and our kids) release these thoughts of helplessness.
This post is a collaboration between Peace I Give and Unmasked. Tee Mone’t runs the page, Unmasked, on Facebook, and Unnmasked on Instagram. Diagnosed as an adult with substantial support needs, she works to help others understand what it means to be autistic. She is here to educate and most importantly, learn.
“My child just got diagnosed with Autism Spectrum Disorder. What do I do?”
If this question is on your mind right now, you’ve come to the right place. We’re here to help. It seems that when caregivers of newly diagnosed Autistic children start looking online for guidance, too often they’re bombarded with recommendations from people who understand autism purely from a professional standpoint. They can miss important posts like this one from Autistic Mama. Misinformation about autism is a quick Google search away, and this article is the antidote. If you want to know what you might really do for your Autistic child in plain language from two #ActuallyAutistic people, we invite you to read on.
Facing a brand new experience can be challenging and your feelings around this new diagnosis are valid. Let us reassure you and tell you that there is nothing to fear and nothing to mourn. Your child is not broken but is the same child you have loved all along. Autistic kids are just like any other child with the same very human need for understanding, support, and love. Parenting an Autistic child is simply parenting a child. All children have a unique composition of strengths, weaknesses, needs, and capacities that caregivers must navigate. The difference when it comes to Autistic kids is that you have the wisdom of an entire community of Autistic adults at your disposal to help you understand where your child is coming from. As you become better acquainted with how to connect with your child and address their specific needs in the healthiest way possible, you and your child will both be empowered.
Now, at the top here, we must include a disclaimer that Autistic people are not a monolith. We don’t all feel the same way or share the same beliefs. As the saying goes, “if you’ve met one Autistic person, you’ve met one Autistic person.” In this piece, however, we will describe how the vast majority of Autistic self-advocates wish to be understood. Neither Peace I Give nor Unmasked criticizes any Autistic person for choosing other forms of self-advocacy that diverge from the majority preferences. However, those decisions lie strictly within the Autistic community. If you are not Autistic, it is not your decision to make.
Autism is a natural neurological variation in humans. Autistic brains are different from allistic brains. Autistic kids are not allistic kids waiting for someone to break them out of a mental prison. They are born as whole and dignified human beings in need of the same care and attention as all children.
When we say “the autistic community”, we mean everyone who is autistic. We mean:
Autistic people who need a lot of support in their day-to-day life, and autistic people who need very little support.
Autistic people who can speak, and autistic people who are nonspeaking.
Autistic people who also have an intellectual disability, and autistic people who don’t.
Autistic people who have other disabilities besides autism, and autistic people who don’t.
Autistic people who were diagnosed by a doctor, and autistic people who figured out they were autistic on their own.
We are all a part of the autistic community, and we have to work together to make sure all of us have our voices heard. Every autistic person belongs in the autistic community. There is no “wrong” way to be autistic. Trying to separate certain groups of autistic people from the autistic community hurts all of us.
What is the Autism Spectrum?
A lot of people who first encounter autism assume that the spectrum is a linear progression from “mild” to “severe.” Please understand that functioning labels like “mild,” “severe,” “high functioning,” and “low functioning” can be extremely harmful to Autistic people, including your child. Autism is a spectrum, but that spectrum looks a lot more like an equalizer than it does a line.
Neuroclastic does a great job of explaining the autism spectrum in this post, but in short, the spectrum encompasses a handful of domains including but not limited to social aptitude, intensity of interests, motor control, and so on. Autistic people are measured against allistic people in each domain, which is inherently ableist. It’s like assessing a computer programmer’s untrained singing voice against professional opera singer, Maureen McKay. The computer programmer may have a fine voice, but it certainly won’t be as polished as McKay’s. Each person needs to be embraced for their inherent worth and appreciated for the gifts they bring to this world. Autistic people bring so much good to humanity.
Sadly, in most areas of the world, societies do not operate in a way that is inclusive of Autistic brains, so Autistic people are largely viewed as deficient. In contrast, the neurodiversity paradigm changes the perspective, declaring that a diversity of neurology among humans is normal, necessary, and natural. And, the social model of disability helps to challenge the idea that disabilities must be limiting in and of themselves. The social model demonstrates that, with acceptance, inclusion, and adequate accommodations and technology, nearly every disabled person could have equal access to social spaces. It’s a lofty idea and we can all help to improve the quality of life and access to shared spaces that disabled people deserve.
Disability is not a bad word and, for the majority of us, autism is disabling because society disables us. Functioning labels are part of the way society oppresses us. For example, some of the people who read this article may say to themselves, “the authors of this piece can’t be Autistic” because of the narrow view of autism they have encountered culturally. This is the kind of mindset we want to gently challenge.
Autism as an Identity
Much like other disabled groups that have developed passionate self-advocacy within their ranks, many Autistic people capitalize the “A” in Autistic in recognition that it is part of our identity. It’s who we are. It cannot be separated from us and it cannot be treated or “cured” without destroying us.
If you happen to see someone on social media with an Âû in their name, they likely consider autism to be a critical aspect of their identity. Âû is a reference to the Autistic Union, which has a list of 10 Points describing its ethos. And, Âû is a helpful way for Autistic people to recognize each other quickly in virtual spaces.
Autism as an identity is one of the reasons that Autistic people overwhelmingly reject person-first language (child with autism) in favor of identity-first language (Autistic child). It’s why you’ll notice that Autistic adults often dislike euphemisms like “on the spectrum.” It’s why many of us despise puzzle piece mentality, a position you may be surprised to learn is backed up by science. And, it’s why Autism Speaks is considered a hate group by most within the Autistic community.
Autism is an identity that deserves to be embraced, understood, and accommodated by our greater culture. By the same token, Autistic people have every right to vent about how difficult and painful it is to be Autistic in an oppressive environment.
Many of us engage in a coping technique called masking. If you’ve ever presented yourself differently from the person you really are in order to avoid an argument or get ahead in your career, you probably have an idea of what masking feels like. For Autistic people, it can be a constant requirement in order for us to navigate a world that was not made for us. We pretend to be neurotypical as best we can, so we can avoid uncomfortable situations, “fit in” more readily with others, and go unnoticed. It’s a survival mechanism and it is costly for us. Many Autistic adults must go to great lengths to undo the damage that masking has done to us. So, if an Autistic person lets down their mask around you, consider it a compliment. That means you are trusted to see us as we really are, stims and all.
Check out this post from Tee Mone’t of Unmasked about the raw truth of what masking really is:
Allistic caregivers are crucial to the wellbeing and safety of their Autistic loved ones. A positive, affirming relationship with a caregiver is not only helpful, it may even be life-saving. Caregivers can uphold the dignity of their Autistic loved ones by getting consent before talking about them, limiting the personal information shared about them, not complaining about autism or Autistic people, and taking their needs very seriously. This excellent infographic from the Therapist Neurodiversity Collective provides a snapshot of ways in which to embrace Autistic identity by refusing to pathologize us:
It’s important to note here that there are some Autistic people who are more discreet about their autism, perhaps because they have experienced substantial discrimination or because they view it primarily as a medical diagnosis or because other aspects of their identity are more pronounced. It is up to Autistic people ourselves to decide how we will move through our lives. The best thing our families can do for us is to support us in whatever way we need. Some of us are out and proud about being Autistic. Others are just living life. There’s no shame in any of it.
Generally speaking, it is considered bad form to tell people your child is Autistic without the child’s consent, in the absence of a seriously compelling reason. For instance, you’d likely want to tell medical professionals and your child’s school, so they can better understand your child’s needs. You’d probably not need to tell your family and friends unless they care for your child and require support in providing the best care. You definitely don’t need to tell random strangers or research companies trying to buy your child’s DNA for dubious purposes.
Use great care and discretion with the understanding that disclosing your child’s diagnosis is an extremely intimate and intrusive act. And, finally, consider what information needs to be shared. Do you need to state that your child is Autistic or do you need to let the person know what to expect? For instance, if you’re at a park with friends who don’t know your child’s diagnosis and you know your child tends to elope, you might say, “[Child] sometimes runs off unexpectedly. Would you mind helping me keep watch?”
There is nothing shameful about being Autistic or having an Autistic child. What we’re highlighting here is the importance of respecting the privacy of Autistic people and allowing us the dignity of controlling the way information about our personal identities gets exposed.
Now, if you’re wondering about disclosing to your child their own diagnosis, yes, please! From the moment you know, tell your child. Openly, talk about autism in positive, factual ways as they grow up. Help your child navigate the world by showing them how. Things like social stories (keeping in mind that social stories have a potential to harm) and role playing can be helpful tools to give Autistic kids a concrete view into the hazy, amorphous world of social interaction. Talk with your child and observe their behavior for clues into what you could be doing to better support them. Accept that Autistic is who they are. Not what they have.
Will My Child Ever Fit In?
Depends on who your child interacts with. It’s so important for caregivers of Autistic children to recognize how difficult it is for Autistic kids to make a way for themselves when they’re thwarted at every turn. Autistic children must be given opportunities to connect with other Autistic children as a basic human need. From crucial childhood relationships with both Autistic and allistic children, Autistic kids learn what it means to be a friend. And, guess what, Autistic relationships have been studied! Here’s what we know.
Autistic people ARE empathetic (more on this below).
Autistic people ARE social.
A study on Autistic kids aged 8 to 15 years found that they believed they were good friends to others and also that they enjoyed social interaction.
At least 80% of Autistic children have at least one friend and the majority enjoy their friendships.
Lack of supports is what excludes Autistic kids from social experiences, not autism.
Allistic biases against Autistic people disappear when impressions are based on conversation rather than audio-visual cues (meaning, prejudice against Autistic mannerisms keeps allistic people from having wonderful interactions with Autistic people).
Autistic people tend to be more invested in their social partners and prefer to have genuine conversations rather than small talk.
Autistic adults often prefer the company of other Autistic adults (so get your kids into Autistic social experiences early on).
A special note on empathy. The outdated claim that Autistic people lack empathy is a lie. What’s true is that Autistic people struggle with cognitive empathy when it comes to allistic people, meaning, we can miss certain social cues and misunderstand situations. On the other hand, our affective empathy, the ability to bear with others, is in full effect for lots of Autistic people. Sometimes, affective empathy is so intense and unmanageable that it can lead to meltdowns and shutdowns. Many Autistic people feel deep, genuine, visceral emotions. However, while hyperempathy is a well known Autistic trait, different Autistic people experience varying degrees of empathy, just as it is in the neurotypical world. And, our empathy may not look the same as an allistic person’s.
Relating to Autistic people requires effort on the part of allistic people. Dr. Laura S. DeThorne wrote about this in her piece entitled, Revealing the Double Empathy Problem. In it, she pinpoints a most challenging barrier for Autistic people who are trying to relate to allistic people. She says,
Although the misunderstanding may be bidirectional, it disproportionately stigmatizes autistic people when their perspectives are not adequately represented within institutional power structures, like education, research, and medical systems. When autistic perspectives are not heard, it becomes easy for autistic behavior to be misunderstood and pathologized. Note, for example, much of the autism literature focuses on helping autistic individuals understand nonautistic perspectives, rather than the other way around.
As a caregiver, you can work toward understanding your child on their terms and showing them what a healthy and respectful relationship looks like. All Autistic people communicate. Sometimes it just looks a little different from what you might expect.
Is Early Intervention Necessary?
In the United States, children under the age of 3 are eligible for Early Intervention services when they aren’t meeting their expected milestones and/or if they have diagnosed disabilities that require support. When autism is suspected, many caregivers are pressured by medical professionals and peers to get their kids assessed and into some form of “treatment” as early as possible. We have even seen claims that Autistic children will never “improve” if their caregivers wait too long for “treatment.” That’s simply not true. Autistic brains don’t need treatment any more than neurotypical brains for the mere existence of a particular neurotype. If that weren’t enough, a recent meta-analysis found that there is insufficient evidence to recommend early intervention or treatment for children. Pressure to push children into Early Intervention can be wielded as a scare tactic and that helps no one.
Early Intervention is as embroiled in anti-Autistic ableism as any intervention offering “help” to Autistic people from an allistic perspective. The therapies offered generally seek to bring an Autistic child as close to typical expectations as possible, which is ableist. Autistic people do not need to be more allistic in order to move freely through and contribute to the world around us. So, while Early Intervention is not necessary, we do understand that it is a cost effective way to access services like occupational therapy that can help Autistic kids a great deal. Whatever you decide to do, we encourage you to brush off any pressure that comes your way about changing your child.
Autism is simply a natural way of being. That’s not to say Autistic people don’t need any therapy. There are various forms of therapy that can help Autistic people cope with living as strangers in a strange place without having to be subjected to behaviorism. Different people benefit from different things, so having an open mind can help you find exactly what will serve your child the best.
Occupational Therapy: OTs help identify gaps between a person’s needs and their ability to meet those needs. Autistic people often need support when it comes to motor skills (e.g. dressing/undressing and tying shoes), proprioceptive abilities (e.g. tolerating the taste and texture of food, and knowing when it’s time to urinate), and self-regulation. OTs have the knowledge and experience to recognize where there are disconnects and help Autistic kids integrate their senses and practice new life skills.
Speech Therapy: Speech is widely considered the superior form of communication. It’s not. All forms of communication are valid. Some Autistic people prefer speech, some prefer speech some of the time, and some don’t prefer speech at all. There are many reasons for these differences. What Speech Language Pathologists can do is give your child the tools to improve their speech and/or other modes of communication.
Physical Therapy: PTs specialize in human movement. If your child needs support with balance, motion, or spatial awareness, a PT might be able to help. There is some overlap between what OTs and PTs do for Autistic kids, so our general suggestion would be to start with OT and add in PT, if needed.
Dialectical Behavior Therapy: DBT is a cognitive-behavioral therapy that helps people practice regulating their emotions, relate more easily with others, and handle stress, all of which are skills every human person certainly needs. Given the strain of moving through this world as an Autistic person, DBT is often a great fit for addressing lingering traumatic experiences. Side note: Even though DBT and ABA contain the same word, they are NOT the same. DBT is a true behavioral therapy that is beneficial for many. ABA is a behaviorist therapy that is harmful.
And, finally, a note on comorbidities. Autism is a neurology unto itself with its own strengths and weaknesses. Oftentimes, people conflate other diagnoses with autism as though they are one and the same. An autism diagnosis is not dependent on things like IQ, aggressive behavior, hyperactivity, and so on. When present alongside autism, these things may or may not need to be addressed professionally. And, if they do need to be addressed, the supports may be beyond the scope of this particular article. (In other words, we can’t cover every possible therapeutic option, so please seek out support from Autistic adults.)
Will My Child Ever Be Independent?
Are we meant to be? Do you know anyone who is completely off-the-grid and self-sustaining? Seems like it would be a lonely life. We may wonder what the future holds for Autistic kids, but independence need not be a goal. We are, by nature, an interdependent species. We need connection to thrive. So, one of the things Autistic children need to practice is self-advocacy. Empower your child to ask for what they need. Reveal all the avenues available. Some Autistic people do need lots of hands-on assistance into adulthood (which is probably what most people mean when they wonder about independence). That’s totally fine. They are as fully human, fully worthy, and fully deserving of fulfillment as is any person. It’s natural to worry when you’re responsible for the care of a child, but put that nervous energy into helping your child build a network of support.
How Do I Discipline My Autistic Child?
You teach an Autistic child about the world in the same way you’d teach an allistic child, by figuring out how they learn best and presenting information in that way. There is absolutely no need for intrinsic motivation killers like rewards or punishments. Especially not physical punishment. There’s no need to control your Autistic child or force their bodies to do things that are uncomfortable for them (such as demanding eye contact or using hand over hand instruction). When you create an environment where your Autistic child can succeed, your child will have their best opportunity to grow in their relationship with you and to trust you.
As the caregiver of an Autistic child, your child will be best served by your acceptance that most Autistic children have specific needs around sensory processing. Autistic processing of sensory input is different from that of the allistic brain. Responses tend to be more pronounced and overload can be unbearable. Some things to know.
Sensory Seeking and Sensory Aversion: For most Autistic people, our experiences with external stimuli can be heightened. Sensory Seeking means craving input to address uncomfortable understimulation of the nervous system. Seeking may look like enjoying being extra loud, using our bodies to crash into the world around us, and generally filling up a space. Sensory Aversion means craving escape to address uncomfortable overstimulation of the nervous system. Aversion may look like extreme discomfort with anything touching our skin, blocking our ears to muffle a cacophony of sounds, and covering our eyes to shield them from bright lights. While many Autistic people tend to experience either seeking or aversion, given the right circumstances, we can all experience them both.
Meltdowns and Shutdowns: To understand meltdowns and shutdowns, think about the most upsetting day you’ve had recently. Maybe your car broke down, causing you to lose your job. Then you tried to take the bus home only to find that you left the gate open and your dog has run away. And so on. Just a rotten day. You can relate to jab after jab sending you over the edge. When the needs of Autistic people are persistently unmet, the descent into overwhelm is like your really bad day. You might go home and cry, call a friend, or try to relax in front of the TV. Autistics can end up so dysregulated that these calming techniques don’t help. The end result is an uncontrollable explosion of emotion and physiological tension (i.e. a meltdown) or a complete reset of capacity (i.e. a shutdown). Both are upsetting for Autistic people. No one wants to feel that way, so it’s helpful for our families to understand what we need in order to avoid getting to that point. Meltdowns and shutdowns are not necessarily a given. They can often be prevented by addressing our needs.
If you are interested in a gentle discipline approach to guiding both Autistic and allistic children, these articles may help you as you figure out exactly what your child needs most in order to feel safe, secure, and supported.
While this post is about how to proceed with a new diagnosis, we have included this response to those who may ask about how to obtain a diagnosis. Generally speaking, in the United States, autism assessments for children are conducted by developmental pediatricians and pediatric psychologists. Your child’s standard evaluation may involve questionnaires and interviews for the caregivers, observation of the child, and administration of the Autism Diagnostic Observation Schedule (ADOS) and/or the Autism Diagnostic Interview-Revised (ADI-R), along with a review of observations from the child’s teachers and other professionals, if applicable. Be aware that masking (as described in the Autism as an Identity section) can interfere with a medical professional’s ability to diagnose your child. The very thing that helps keep us safe in other circumstances can end up making it more difficult to get the accommodations we need. Please let your child know they don’t have to hide who they are with the doctor.
If you are in the United States, be aware that your insurance company may require a referral from your child’s pediatrician or family doctor. If you cannot afford a standard evaluation or are uninsured, organizations like Easterseals may be able to provide you with discounted services. Be aware, however, that these organizations are not typically autism-forward and may recommend ABA therapy.
In order to be diagnosed, your child must meet the criteria set out in the Diagnostic and Statistical Manual of Mental Disorders (current edition, DSM-5), which includes an unfortunate “severity” scale of 1, 2, and 3, each corresponding to an increasing need for supports and services. These numbers represent how burdensome the doctor expects your child to be and that is a problem. The severity scale also does not account for changes in capacities as your child grows up and it is heavily influenced by your child’s ability to speak. However, speech is not required for communication. Do not be overly concerned if your child doesn’t speak. Take note of the number your child is assigned, but don’t allow it to dictate your acceptance of your child’s capabilities.
Many caregivers question if pursuing a diagnosis is worthwhile. The Autistic community is somewhat split on this. A medical diagnosis can open many doors for your child to receive accommodations and modifications. It can also, sadly, present unwanted barriers, such as being barred from certain jobs, military service, and even being disallowed from emigrating from one’s home country. Despite the potential challenges, childhood diagnosis tends to be easier to obtain. It is incredibly difficult to obtain a diagnosis as an adult, which is why the Autistic community embraces self-diagnosis. We encourage you to read this beautiful post from Autistic Mama about the reasons why early diagnosis can be life-changing. If you want to wait or not pursue a formal diagnosis at all, your child may still be eligible for supports in school. In the United States, schools can conduct their own internal assessments to provide your child with appropriate accommodations and modifications while in school, even absent a formal, medical diagnosis.
On IEPs and 504 Plans
We promised plain language at the beginning of this post and we’re about to take a dip in the blistering world of federal law, so please bear with us as we keep this as simple as possible. We strongly recommend checking out Wrightslaw and the Wrightslaw books if you want to get the most accurate information about accommodations and modifications.
In brief, the federal Individuals with Disabilities Education Act (IDEA) guarantees the right of your child to a Free and Appropriate Public Education (FAPE) in the Least Restrictive Environment (LRE). Part of giving your child a FAPE involves establishing a customized blueprint for their educational track via an Individual Education Program (IEP) or a 504 Plan.
IEPs are comprehensive action plans that detail precisely which combination of services will provide the ideal learning environment for your child in a special education program. The custodial caregiver (e.g. parent, grandparent, etc) is part of the IEP team and advocates on behalf of the child. The assessment process to be deemed eligible for an IEP can be lengthy and tedious. If your child already has a medical diagnosis, this is one of the times when it comes in very handy. IEPs are nearly limitless. If your child needs a solution, this is where you put it. The IEP is also where the IEP team declares the LRE for an individual student be it a specialized separate class or some form of integration into general education.
504 Plans are guaranteed under the Rehabilitation Act of 1973. Unlike IEPs, 504 Plans do not entitle children to the extensive services of special education. You can think of them as a less stringent counterpart to IEPs that are especially useful for general education students who have specific areas where they need support, such as dyslexia. Students can technically have both an IEP and a 504, but having both is not necessary. It’s important to note that IEPs can and usually do include everything that would be written into a 504 Plan, but the reverse is not true.
In order to obtain supports for your child through an IEP or a 504 Plan, the first step is to contact the school (typically a school/guidance counselor or an assessment coordinator) to request an evaluation. You’ll want to be prepared with as much information as you have about what your child needs. Check out this write-up for a detailed overview of the process.
ABA: Applied Behavior Analysis is billed as a “treatment” for autism, but it has widely been met with scorn due to its proclivity for causing post-traumatic stress disorder in Autistic children. It’s no wonder as the “father” of ABA had this to say about Autistic people, “You see, you start pretty much from scratch when you work with an autistic child. You have the person in the physical sense – they have hair, a nose and a mouth – but they are not people in the psychological sense.” For more information on why ABA isn’t welcomed by Autistic people, check out ABA Treats a Problem Your Child Doesn’t Have.
Asperger’s: In the United States, Asperger’s has fallen into medical disuse as a diagnosis as the DSM-5 rightly condensed autism into a single diagnosis. Many Autistic people who were originally diagnosed with Asperger’s continue to use this term. However, allistic people should be aware that Hans Asperger was a Nazi eugenicist who was responsible for the murder of hundreds of disabled children (warning: linked article contains functioning labels). Some people have pointed out that he may not have been a Nazi sympathizer, but rather a person who fell in line in order to save his own life. Even if that is the case, he still sent hundreds of children to their deaths and does not deserve the honor of being associated with Autistic people. Please use “Autistic” instead as a caregiver.
Autism is a Superpower: The belief that Autistic people have superhuman powers is a form of inspiration porn that dehumanizes and others us. We are as human as any other person. Our autism is often disabling, because it has not yet been normalized by the broader culture in which we live. Because of our different neurology, there are some areas where we might excel. It’s ok to celebrate accomplishments by virtue of our efforts. It’s not ok to celebrate accomplishments because we are Autistic.
Autism Parent: Curiously, many allistic parents of Autistic children proclaim themselves as “Autism Parents” but are often unwilling to adopt the identity-first language most of us prefer (i.e. Autistic person). “Autism Parent,” and the use of autism as a lead into any conversation about their kids, gives the impression that the caregiver is donning their child’s identity as a sort of uniform to showcase their experience caring for an Autistic person. And, worse, “Autism Parents” often say things like “Autism won today” to indicate they’ve had a bad day. Imagine saying such a thing about any other identity. Please use “Parent of an Autistic Child” instead.
Functioning Labels: “Mild,” “Severe,” “High Functioning,” “Low Functioning,” “end of the spectrum” and so on. These are functioning labels that are meant to communicate to allistic people just how much Autistic people diverge from neurotypicality. Even the levels assigned by diagnosing doctor’s that are meant to indicate anticipated support needs end up communicating how burdensome we are expected to be for our caregivers. Yet, Autistic people’s capacities can slide all over the place, even hour to hour. Functioning Labels provide no useful information. When talking about Autistic people, avoid discussing deficits. Instead, help us advocate to meet our needs. For example, rather than saying “my child is non-verbal,” try “my child uses augmentative and alternative communication (AAC).”
Person with Autism: Survey after survey demonstrates that Autistic people, on the whole, prefer identity-first language. Autism isn’t a feature. It is the very lens through which our brains process the world. Every Autistic person has an Autistic mind. We cannot be allistic. We cannot “age out” of autism and we cannot be “cured.” It is who we are, therefore, it is always appropriate to use identity-first language (Autistic person) unless you’re speaking about an individual who has specifically indicated that they prefer person-first language.
Puzzle Piece: Since the puzzle piece is ubiquitous, you might not realize that Autistic people generally do not identify with it. The puzzle piece was created by an allistic member of the National Autistic Society and it originally featured a crying child as a symbol portraying autism in contrast to the way “normal” people are supposed to be. It says Autistic people are a baffling mystery. That our minds aren’t complete. And, it garners such ableist phrases as “Until All the Pieces Fit.” Parents of Autistic kids – the group most likely to use it – go to great lengths to explain why they don’t see the puzzle piece as a negative thing. However, a 2018 study confirmed once and for all that the puzzle piece is harmful to the Autistic community. The Autistic community has embraced the gold infinity loop as a more appropriate representation of who we are. (The rainbow infinity loop is a positive symbol for neurodiversity.)
Sesame Street: In April of 2017, Sesame Street debuted Julia, an Autistic girl who would introduce children worldwide to autism. Many Autistic adults were overjoyed, especially given the fact that Sesame Street had spent years developing Julia with the Autistic Self-Advocacy Network (ASAN). We knew she would be a genuine reflection of Autistic people. Sadly, in 2019, the partnership between Sesame Street and ASAN ended. In a devastating betrayal, Sesame Street elected to partner with Autism Speaks instead and promote their stigmatizing resources for parents of newly-diagnosed Autistic children.
Symptoms: Autistic people have traits, not symptoms. The way we think and behave is not the result of an illness. It is a manifestation of our neurology and our individual personalities. Use of the word symptom is an example of the pathologizing of autism. Because we are different, there is a tendency from a medical perspective to pinpoint and correct those differences and that tendency makes its way into the literature around autism.
Violence: An unfortunate stereotype exists that Autistic people are prone to violence. In reality, violence is not part of the criteria for a diagnosis. It is not indicative of autism. So, why do caregivers of Autistic kids talk about violence so much? It’s a misunderstanding of what the “violence” actually is. All of us, Autistic and allistic alike, understand what it’s like to be worn down by life and pushed to the limit. This stress is the root of much discomfort, frustration, and even anger. It’s something that Autistic people experience significantly more often than allistic people, because we are moving through a world that does not operate with our needs in mind. Some Autistic people, particularly children, become so overwhelmed that they lash out. It is a form of communication that tells everyone around them that they need help. Not censure. Autistic people are not inherently violent.
How Do I Best Love My Autistic Child?
This one isn’t just about feeling a tender, nurturing draw toward an Autistic child. We know you love your child deeply or you wouldn’t be here. This one is about loving an Autistic child for who they are. Not for who they might be if they weren’t Autistic. It’s about recognizing your child’s stimming and supporting them by providing stim toys and room to stim without judgment. It’s about engaging with, rather than pathologizing the great interest your child takes in the things they love the most. It’s about viewing Autistic people as creative communicators rather than awkward and socially inept. It’s about going directly to Autistic adults, and professionals who listen to Autistic adults, to ask questions about how to support your Autistic child. And, it’s about folding your Autistic child into your family life in the most natural ways. Full acceptance. Unconditional love. Exactly what every caregiver should do for every child. It’s nothing remarkable and it’s the most remarkable thing of all.
We’ll leave you with this video that sums up how we want parents of Autistic children to choose to view their kids in hopes that the more our world understands autism, the higher quality of life all Autistic people can enjoy.
Looking for More?
Our friend, Autistic Mama, is working on another resource she’s calling Autism Diagnosis Journal: A Parent’s 30 Day Guide to Confidently Process Their Child’s New Autism Diagnosis. Autistic Mama, Kaylene George, is an Autistic mother of 6 neurodiverse kiddos, including one Autistic child. Her life’s work is helping parents of Autistic children become better parents, advocates, and autism allies. Her efforts serve to make our society more accepting and inclusive to Autistics. Her newest project promises to be comprehensive and thoughtful, and we encourage you to keep watch for when it drops.
*Please comment below or message Peace I Give with any questions you may have. We consider this to be a living guide to be updated as new pressing questions arise.We are open to criticism as well. Thank you for reading!
My family has been going through it the past couple weeks. It’s just more of the same 2020 nonsense that everyone is experiencing, but that doesn’t make it any easier. I’ve been thinking about a post on executive functioning, as I can imagine we’re all working a little harder on this skill of late, but also because I recently ran across something that might help our kids be a little more effectual with a lot less work and frustration.
Executive function is the term for the overall management of the brain. It is what allows us to prioritize tasks and get things done and it involves three overarching areas: working memory, cognitive flexibility, and inhibitory control (including self-control). The eight executive functions are self-control, self-monitoring, emotional control, flexibility, task initiation, organization, working memory, and planning & time management.
There are many brain differences that impact executive functioning including things like autism, ADHD, depression, and trauma to the brain. And, if you’ve spent time around kids, you’ll recognize that their executive functioning is still under construction. In fact, executive function develops all the way into adulthood. Kids who are struggling with it might not be able to pay attention, hold onto a series of instructions, transition from one task to the next, or plan out action steps. As a child, I had many, many hours of therapy to help me improve my executive functioning skills, so I was intrigued when I recently ran across a strategy that promises improvements in executive function.
Kristen Jacobsen (MS CCC-SLP) and Sarah Ward (MS CCC-SLP) are two speech language pathologists who have been studying executive function for the past 20+ years and now co-direct Cognitive Connections, a specialty practice in Massachusetts. Together, they created the 360 Thinking™ Executive Function Program that includes a strategy developed by Sarah Ward called Get Ready, Do, Done. This strategy coaches children to identify what needs to be done at a future time, imagine what “done” looks like, work backward to plan out the steps to get there, and then collect needed materials to accomplish the task. It is a way to lay out each step for those whose brains don’t automatically do the planning for them. The model plans backward before taking steps forward.
What will it look like when I am done?
What steps do I need to take to be done? How long will each step take?
What do I need to get ready?
What materials do I need to do the steps?
Time to do the task. Create a timeline and time markers.
Know when to stop and close out the task.
When I was little, I used to get frustrated to the point of shutting down when I was told to clean my room. In childist terms, I might have been called lazy or stubborn, but the problem I had was that I simply didn’t know what to do! I needed someone to show me my room clean and straight several times, so I’d have the picture in my mind. I needed to be walked around the room and shown where each item was supposed to go. I needed a step-by-step plan, like:
Get cleaning supplies.
Clear off and make the bed to use as a staging area if needed.
Pick up and put away items from the floor as follows: trash, dishes, clothes, toys, books, and everything else.
Organize wardrobe and trunk.
Wipe dust and grime from surfaces.
That never happened for me. I stumbled through housework until well into adulthood when I came across the organizing and cleaning industries and learned how to properly do housework. Even with small children now, I’m able to keep my house nice and clean. I even put laundry away after it’s dried, which is something I never did as a young adult. Check out this quick video that uses cleaning a room to explain executive functioning:
If you’d like to give Get Ready, Do, Done a try, check out these free resources:
Almost all children will go through periods where they lash out in some way and spitting, hitting, biting, and kicking seem to be the most common behaviors. What should you do when your child lets loose? It’s critical to understand what underlies the behavior. We could fancy ourselves investigators for this purpose. What precipitated the event? Here’s a list of replies your child might give you if they could.
I just felt like it.
I need your attention.
I need freedom. Give me space.
It’s too noisy in here.
My sibling took my toy.
Stop touching me!
You’re not listening to me.
This is fun!
Let me do it my way.
I saw my sibling doing this and I wanted to try.
I was curious what would happen.
My body doesn’t feel good.
Both my 2 year old and my 4 year old spit, hit, bite, and kick at one time or another, so I completely understand the frustration and that gut feeling of wanting to react in an unkind way. But stop! Stop for a minute and think about what’s happening. Let’s categorize the “whys” for greater understanding.
I need your attention. You’re not listening to me.
Sadly, we’ve been conditioned to see children as annoyances who drain our time and our energy. We don’t want to “give in” when our kids express their need for our attention in undesirable ways. However, empathetic communication actually increases well-being. It’s not simply a way to meet our children’s needs. It also improves our relationship. If your child needs your attention, try a little active listening.
Some of the pitfalls I face when it comes to listening to my kids include thinking of something else while my child is communicating, trying to figure out what I’m going to say next, and attempting to manipulate the direction of the conversation. If you’re anything like me, one or more of those statements might resonate.
Professional communicator and educator, Julian Treasure, recommends a four-step approach to listen with investment:
Receive: Absorb what the child is telling you
Appreciate: Pause and think
Summarize: Paraphrase what you’ve understood
Ask: Learn more
If you know your child needs your attention, give it freely. Silence those harmful voices telling you not to spoil your child. You cannot spoil a child with love and affection. Quite the contrary, kids who are perceived as spoiled tend to be those children who have a) not had their boundaries respected so they react with belligerence or b) not been given enough attention and therefore do not trust that their needs will be met.
I need freedom. Give me space. My sibling took my toy. Stop touching me! Let me do it my way.
In our childist culture, it’s easy to get caught up in “what’s mine is mine and what’s yours is mine” thinking when it comes to children. We’ve got to work toward flipping that perspective around and radically respecting our children’s autonomy.
Years ago, sexuality educator, Deanne Carson, made headlines when she advocated for asking infants if it was ok to give them a diaper change. She acknowledged that they wouldn’t be able to consent, but said that asking for consent and pausing to acknowledge them lets children know that their response matters.
I fully admit that I scoffed at her comments at the time, even though I was already three years into my Peaceful Parenting journey, as I was sorely lacking an understanding of childism.
Yes, you can let your baby know you’re about to change their diaper. Consent does start from birth and it never ends. We must prioritize navigating our children’s demands for bodily autonomy and their health-related needs. It’s not easy or simple, but it’s our responsibility.
If you know your child is enforcing a boundary, respect it. Bottom line. For guidance on helping siblings through the tough task of sharing/turn-taking, check out this article.
I’m tired. I’m hungry. It’s too noisy in here. I’m anxious. My body doesn’t feel good. I’m frustrated.
Discomfort shows up physically and mentally. Both are completely real and valid. In our culture, we tend to tell children how they’re feeling. We dismiss skinned knees with “You’re ok” and toileting urgency with “You just went!” Children are too often forced into the constraints of our schedules and whims, and it’s not ok. Kids deserve for their needs to be met. Where the dominant culture tells us that our children are manipulatinrg us, it is incumbent upon us as Peaceful Parents to reject that perspective wholesale. If our children need to use the bathroom, they will. If they feel sick, we listen. If they are anxious, we soothe.
And, a note to those who fear all this responsiveness will lead to spoiling children. It won’t, but as we get into more complex needs, our responses may need to evolve. All children need accomodations, some more than others. Autistic Mama wrote a fantastic piece called Are You Accommodating or Coddling Your Autistic Child and really it applies to all children. In it, she explains:
The line between accommodating and coddling boils down to one specific question.
What is the Goal? You have to ask yourself, what is the goal here?
Let me give you an example…
Let’s say your child has a history assignment and is supposed to write two paragraphs on the civil war.
What is the goal of this assignment?
To prove knowledge of history.
Now any tool or strategy that doesn’t take away from that goal is an accommodation, not coddling.
So typing instead of writing? Accommodation.
Verbally sharing knowledge of the civil war? Accommodation.
Writing a list of civil war facts instead of using paragraphs? Accommodation.
Because the goal of the assignment is a knowledge of history, not the way it’s shared.
We can empower our children to solve their own problems by showing them how to be problem-solvers from a young age. We can teach our children to ask for what they need and demonstrate that their needs matter by obliging their requests. As they get older, we can empower them to seek reasonable accommodations in a variety of environments by considering what needs they must have met in order to succeed and to advocate for themselves.
I would be remiss not to mention one thing here of great importance to the Autistic community. AUTISTIC PEOPLE ARE NOT INHERENTLY VIOLENT. Violence is not a criteria for diagnosis. So many people ponder why it seems like Autistic children tend toward aggression. Well, imagine having to endure all the little things you dislike (flavors, sounds, textures, etc.) all the time and then being treated as though you’re a burden for asking for it to stop. You might be driven to aggression as well. It’s hard being Autistic in a world that isn’t made for you. Meet the needs of Autistic kids and you’ll see a drastic decline in any aggression.
If you know your child is uncomfortable, try to help relieve that discomfort. Some children are unable to clear saliva and may spit or drool as a result. This is common with children who need lip or tongue tie revisions. If your child is anxious, try these measures. Whatever is going wrong, seek out a solution to support your child rather than punishing them.
This is fun! I saw my sibling doing this and I wanted to try. I was curious what would happen. I just felt like it.
Our children’s top job is to learn through play. We must leave some room for childlikeness, even when it comes to things that are as upsetting as aggression. As strange as it might seem to us, children do many things because they’re testing out how their bodies move and what effect they can have on their environment.
If you know your child is playing, try directing their play into a form that is more conducive to your family’s lifestyle. Getting down on the ground to wriggle around kicking can be fun. Just make sure the goal truly is play or your actions could come across as mocking.
Tips for Interrupting Aggression
Respond Gently. First and foremost, try not to meet force with force. Understand that children start out several steps ahead of us in terms of emoting because of their stage of brain development. The calmer we are, the better we can respond. And, if you need to physically stop your child from harming you, use the least force you possibly can.
State Your Boundary. Let your child know your expectation in clear, unambiguous terms. Try “I know you want to hit me because you’re angry. I can’t let you” or “I won’t let you hurt me.”
Engage the Three Rs. When you need to engage with a dysregulated child, remember to Regulate, Relate, and Reason. For many children, just acknowledging and empathizing alone will resolve the aggression, so that you can work toward meeting the need.
Give Your Child an Alternative. Understand that there are two types of aggression: the type you can mediate, like hitting and the type you can’t, like spitting. You can stop a child from hitting, biting, and throwing. You can’t stop a child from spitting, peeing, or pooping. In all cases, it’s crucial to address the underlying need, but you may also be able to introduce an alternative such as giving a child a chewie to chomp in place of spitting or even a towel to spit into. Whatever alternative you choose must be desirable to your child and easy to access when the need calls.
Resolve the Underlying Need. I cannot stress enough how important this one is. You’ve got to figure out what’s going wrong for your child and help them fix the problem. For example, when a child is pushing his sister down over and over again, take notice of why it’s happening. Is the sibling standing too close? Bothering the child while he’s playing? Once you figure out the need, the solution is often simple enough. Help the kids regulate and then invite the other child to help you in the other room.
Give Children the Words.Kids do not instinctively know how to ask for what they need. I hear a lot of parents telling children to “Use your words.” Let me tell you how very unhelpful that is! Parents, please use YOUR words. Give your child the language they should use to have their needs met, even if you have to do it over and over and even if you have to ask questions to get there. The more you model how to use language under stress, the more capable your children will be in following suit.
Avoid Confusing Messaging. While you’re giving your child the words, remember that children think in very concrete terms. There’s a series of books by Elizabeth Verdick called the Best Behavior Series and it includes such titles as Teeth Are Not for Biting, Feet Are Not For Kicking, and Voices are Not For Yelling. Read those titles again… carefully. How do we chew our food without biting? How do we swim without kicking? And how to we call out for help without yelling? It’s not logical, so it’s not going to make a lot of sense to a child. Kids might learn in spite of these messages, but it’s best to avoid them if possible.
Consider an Assessment. If your child’s aggression doesn’t seem to be manageable using any of the tips above, consider that something deeper may be going on and that you might not have all the information you need to meet their needs. Put aside concerns about stigma and work with a professional to help you and your child understand what’s happening.
As parents, we will harm our children in some way. It’s the nature of genuine relationships to expand and contract in closeness, to struggle in balancing boundaries, and to waver between selfishness and selflessness. Committing to do the least harm requires that we spend much time considering the impacts of our actions, which is what makes peaceful parenting so challenging for many of us. Reacting is easy. Thoughtfully responding to our children gets exhausting fast, even for those of us who have been doing it for a long while.
This past week, a reply to one of my Facebook posts got me thinking about my own inclination toward defensiveness around my parenting choices. I had posted a meme that compared two ways to speak gently with a child who doesn’t want to take a nap. A reader remarked that a third potential solution was to allow children to choose for themselves when they want to sleep. Gasp! I was poised to explain why their solution couldn’t work for me rather than admitting their suggestion was the gentler, more respectful approach. My childist reaction was to defend my situation whereas the anti-childist response was to simply sit with the suggestion, however uncomfortable it was.
You see, I’ve battled lifelong insomnia. Aside from medication, nothing helps. It is just one of the many symptoms of autism that I experience. Anything that makes it more difficult for me to sleep, including my children, becomes an object of great consternation for me. And, the reality is that different kids have different internal clocks, so my best solution has been to get the whole family on a united sleep schedule. Unfortunately, imposing a a schedule onto my kids is not the ideal option for me as a peaceful parent. My preference will always be to give my children autonomy over their lives.
And, that’s what this reader was offering… an opportunity to make a better choice. I often hear people say things like, “every child is different,” implying that parents should have free license to use whatever approaches we deem necessary. I disagree. While every child is different, children have a right to be free from coercion, punishment, and violence. It is never okay to yell at or hit a child. And it’s not okay to pressure children to bend to the will of an adult. I can’t excuse the childism that influences the way I interact with my kids and neither should you. Our goal must be to reject childism and to choose to be anti-childist.
Ultimately, my anti-childist decision was to like react this reader’s nap alternative and withhold my defensive reaction. Other readers needed to know the clearly anti-childist solution and I needed the reminder. It’s not really about naptime at all. It’s about investigating and diminishing the adult-centric way we address the challenges our children experience.
When we are deciding how we will approach these challenges, there are some questions we need to ask ourselves and wrestle with:
What does my child need?
What do I need?
How can I address both our needs while respecting my child’s autonomy?
Are there alternatives I haven’t tried because they’re inconvenient?
How is childism affecting the decision I’m about to make?
How might this decision harm my child?
How might this decision harm our relationship?
As we seek to do the least harm, we will be challenged by people who have better solutions than the ones we’ve been using. Instead of explaining why we can’t choose the anti-childist option, let’s look for ways to incorporate those better solutions into our approaches. In doing so, our anti-childist orientation will grow and mature with the help of our partners, our children, and our peaceful parenting community.
Ever have moments when you feel like you’re in sync with your kids and things are amazing? If so, did you know you can have even more of those moments? Kids do well when they can, and you can help them out by understanding better where they’re coming from.
Marriage and Family Therapist, Galyn Burke, put together a fantastic resource on the way children’s brains develop. She explains that the three major parts of the brain (hindbrain, midbrain, and forebrain) develop on different timelines. They have to. Our brains are complex with high energy demands. It takes a while to get everything in order.
The reptilian hindbrain looks like someone dropped a crocodile brain into our heads. This part of the brain serves the most basic purposes including regulating autonomic functions like breathing and instictive behaviors like threat patrol.
The limbic midbrain is our emotion center. It’s what allows us to be empathetic, social creatures. This is the part of the brain where children process their world.
The neocortex forebrain is where our rational mind lives. This part doesn’t fully develop until the mid-20s in humans. We like to think of this area as the logic center, but without the midbrain, our logic is incomplete.
Childhood is an incredibly crucial time in the life of a human being when we learn how to be human. We figure out what emotions are and how to work with them. We learn how to love each other and respect boundaries. And, we learn our personal signs of dysregulation and how to cope. If children are not treated gently and responsively, any of these skills can be hindered.
So, you know that brain development isn’t as simple as 1, 2, 3, but did you know that even babies can think logically before they can talk? Turns out, our ability to reason doesn’t depend on language or understanding. A study that came out a few years back found that preverbal infants notice when something is wrong and try to work out a solution. The scientists figured out that “at the moment of a potential deduction, infants’ pupils dilated, and their eyes moved toward the ambiguous object when inferences could be computed, in contrast to transparent scenes not requiring inferences to identify the object. These oculomotor markers resembled those of adults inspecting similar scenes, suggesting that intuitive and stable logical structures involved in the interpretation of dynamic scenes may be part of the fabric of the human mind.” And our ability to reason explodes from that point.
Alison Gopnik, Professor of Psychology and Affiliate Professor of Philosopy at the University of California at Berkeley and author of The Gardener and the Carpenter, has been studying children for a long time. What she has found is that children have a greater capacity for innovation and creativity than college students all while applying clear logic. She explains that 3-year-olds will offer a stream of consciousness when asked to give us their thoughts, but if you use their own language to ask them concrete questions, the responses will be sensible and surprising.
Check out this piece explaining some of her experiments. You might just find something useful (Hint: Don’t miss the part where the researcher notes that having children explain something themselves increases their understanding of it.)
Now that you know just how brilliant your child is and you know why they can appear to be illogical, you might be surprised to learn that a very simple solution can flip a switch for your child. When a child’s limbic system is on overload, top to bottom exercises can be useful. These are exercises that require movement across both the top and bottom parts of the body. Things like standing stretches and light weight lifting can help your child’s brain regulate itself.
One final thought that comes to mind is Dialectical Behavior Therapy (DBT) with its focus on integration. In DBT, there exists a concept of the Wise Mind, which is “the balanced part of us that comprises our inner knowledge and intuition, where our emotional thinking mind (thoughts driven by distressing feelings) and rational thinking mind come together, the part of us that just ‘knows’ that true reality.”
Many adults need therapeutic intervention to learn to live into their Wise Mind. Children, whose brains are still forming, need direction and practice to find this place. When you recognize that your children are logical, but not logical in the exact same way that you are, it can become easier to learn to speak their language and to offer responses that help them integrate all the parts of their brains. I firmly believe that children are perfectly reasonable and I hope that, now, you do too.
So, you’re on-board with Peaceful Parenting. You try to co-regulate with your kids, empathize, and collaborate with them toward solutions that are mutually beneficial. You’ve been cognizant of your attitude and you’ve been working toward remaining calm most of the time. But, then something happens and you snap. You yell or you spank or you threaten or otherwise forcibly control your child, even though this isn’t who you want to be.
I hope you’re not looking at me thinking that I’ve got it together. That I must never yell or act out in a non-peaceful way. Nope. I’m working toward being a Peaceful Parent just like you are and stumbling all over myself along the way. Here are some of the things I’ve committed to that have helped me push forward.
Punishment Rejection Action Steps
1. Start With a Choice. You have to decide before you ever get angry what your limits are. Yelling is my vice. It’s deeply ingrained from my childhood and it is the language of my hot temper. But, yelling is a punitive act. We use our adult voices to suppress and control our children, leaving them with unseen scars. It may not be as clearly punitive as time out or spanking, but it is undesirable as a tool in our Peaceful Parenting kit. What’s your go to? What punishment do you turn to when you feel you can’t bear anymore? Make a commitment right now to stop. Draw the line in your mind and say, “I will not fall back on this action.” Even if you do it again, reinforce your belief that your actions are unacceptable and then try again the next time.
2. Engage in Prevention. As you may know if you’ve been following my posts, I am a big advocate of the Three Rs: Regulate, Relate, Reason. When my children begin to dysregulate, I intervene then. I try not to wait for the situation to escalate. Most of the time, prevention also helps me avoid dysregulating myself. It gives me a chance to get a grip on my emotions and fully invest in the moment when my kids need me most.
3. Have a Game Plan. Decide, in advance, what it is you’re going to do when you’ve gotten to a point where you’re about to blow your top. The Learning Parent SG put together a fantastic series on what she does as she nears her breaking point. She calls her approach, “Reactive Distancing.”
During a calm moment, take some time to put your game plan together. Decide what it is you can commit to doing when your thinking mind begins to struggle.
4. Think Like a Child. Ever notice how small children go from huge emotions to giggling in no time flat? They aren’t weighed down by the self-judgment and mental turmoil that adults experience. A dear friend of mine told me she takes a cue from Daniel Tiger. When she starts to feel dysregulated, she says, “If you feel so mad that you have to roar take a deep breath and count to 4.” As she counts, her jaw and fists start to relax, and she finds she’s more able to breathe. Then, she makes an effort to speak to her children in a neutral way in an effort to de-escalate the situation. Sometimes neutral is the best she can do and sometimes she’s able to nurture. Either way, she and her children both benefit from her efforts. She shared that she’s learned how valuable things like hugs, cuddles, and tickles can be as she works toward co-regulating with her kids. Play is always called for when tensions are high.
6. Never Stop Trying. Every time you choose to be gentle with your children, you are reinforcing to your own psyche that what you’re doing is good and it’s achievable. Even when you mess up, and oh will you mess up, brush yourself off and make a better choice at the next opportunity. Parenting is about relationship. When we push our kids away with our attitudes, we have to focus on reconciling and confirming to them that the issue is us not them. In the backs of our minds, we have to give ourselves grace enough to say, “I will do better next time” and really mean it.
I yell less than I did a year ago and still less than I did a year before that. Things are improving over time and, before too long, I will consistently react neutrally when members of my family touch a raw nerve. That’s my commitment to them and to myself. What are you willing to commit to today?