Meltdowns In Kids With AuDHD Are Never A ‘Choice’ – Trying This With Your Child Might Help

Every parent knows how difficult it can be when their child is struggling to regulate themselves.

But for parents of children with AuDHD – those who are both autistic and have ADHD (attention deficit hyperactivity disorder) – it can be especially tough to navigate emotional outbursts that seem to come out of nowhere.

In my experience, understanding the difference between a meltdown and a tantrum is crucial in knowing how to respond – and how to help.

What’s the difference?

A tantrum is a way of expressing frustration or attempting to get something. It is typically goal-oriented and usually the child has some control over it – for example, if they get what they want, they are usually able to calm down.

A meltdown is not a choice. It’s a neurological response to overwhelm – whether that’s too much sensory input, emotional stress, or cognitive demand.

Meltdowns are associated with the range of intense emotional regulation challenges that can accompany AuDHD. Importantly, meltdowns stem from a loss of control, not a desire to gain it.

An emotional safety plan can help

An emotional safety plan is a proactive, collaborative tool that helps children identify their emotions, recognise their triggers, and explore personalised strategies for managing distress.

It can be as simple as a colourful chart or journal page created together with your child, divided into spaces to note what each emotional state looks and feels like, what might have caused it, and what helped in those moments.

Involving your child in building their plan is key: it not only gives them a sense of ownership, but also helps them reflect on their own needs, feel heard, and develop vital self-awareness skills over time.

This can provide children with the tools to “name it to tame it”, putting words to feelings, to help reduce distress. This can be empowering, in addition to providing a sense of validation and control.

Key emotional states you can map together

Here are some common emotional states your child may experience, and ways you can support them through each one:

Hyper-arousal (meltdowns)

A meltdown is an intense, involuntary reaction to being overwhelmed, often as a result of stress and exhaustion. It may present physically, such as kicking or self-harming; verbally, such as screaming or shouting; and/or emotionally, such as through crying.

Meltdowns are highly individual and situational, with many potential causes, such as sensory overload, changes in routine, loud environments, and an inability to communicate effectively.

Co-regulation is a highly effective strategy to manage a child’s meltdown – stay calm and regulate yourself, while validating their experiences.

Reducing demands and sensory input, such as turning off lights or providing noise-cancelling headphones, can also be very helpful.

Establishing a safe physical space and toolkit for when a meltdown occurs, tailored to an individual’s needs, can provide an important foundation of safety.

Identifying potential triggers can flag opportunities to plan effectively, such as by using visual aids to plan transitions or changes.

Dysregulation (overwhelm)

Dysregulation is linked with overwhelm, such as from sensory input, emotional demands, or social expectations. Masking (suppressing natural responses to ‘fit in’) takes a toll on the nervous system, often resulting in emotional outbursts when this becomes unsustainable.

For example, a common scenario is when an AuDHD child arrives home from school and ‘releases’ overwhelm in a ‘safe’ environment, having masked all day. This can be referred to as the ‘shaken Coke bottle’ effect, where dysregulation builds up pressure internally, until this becomes external.

Overwhelm could appear as ‘naughty’ or ‘rude’ behaviour, which may be more accurately described as decompressing and adjusting.

Identifying these experiences with your child can help signpost potential strategies for support. For example, providing predictable decompression time before any conversations or demands after arriving home from school, or predictable rituals, can provide space for healthy decompression.

‘Normal’/balanced

Many AuDHD children grow up feeling like they need to adapt to what others expect – smiling when distressed, hiding self-soothing activities, or mimicking social behaviours, for example. This can make it difficult for them to understand what they actually need, or what it feels like to be authentically themselves.

Helping them to identify their own version of ‘normal’ (by identifying situations where they feel safe to unmask) and their sensory preferences can empower them to know their own baseline. This enables them to better recognise dysregulation, including when and how to seek support.

Reframing masking in this way can help AuDHD children (and adults) understand the difference between harmful suppression and strategic adaptation in masking, moving towards conscious choices, as opposed to involuntary reactions.

Dysregulation (numbness)

Not all dysregulation looks explosive – sometimes, it can manifest as becoming numb, distant, or zoned out, failing to follow instructions. This stress response may be a form of dissociation, where the brain temporarily disconnects to protect itself from overwhelm or perceived danger.

Such behaviours may be misunderstood as ‘rudeness’, ‘laziness’ or ‘not paying attention’, when the individual is in fact likely freezing up mentally and physically.

Triggers could include high pressure environments (such as classrooms), feeling criticised or misunderstood, or sensory overload, which builds up slowly.

Helping children to identify that these experiences aren’t ‘normal’ – or their fault – can be empowering. This can not only enable children to identify early warning signals, but also helpful activities to move through such states.

For example, creating mindfulness routines, such as counting breaths or colours, can help to centre their focus, in addition to identifying tools such as fidget toys to offer grounding through sensory input.

As a parent, providing non-intrusive presence, or grounding activities such as a firm hug (if your child is comfortable with this) can be highly effective. Ultimately, compassion can help them move into a state of safety.

Hypo-arousal (or shutdown)

Hypo-arousal is an intense state of nervous system under-action, often referred to as a shutdown. This is an internalised response, where the body and brain effectively go into ‘power-saving mode’ to survive overwhelm, effectively switching off.

Although highly individual, signs of shutdown can include selective mutism, where they become unable to speak. Children might become non-responsive, and extremely fatigued, withdrawing from interaction or situations and becoming detached from their surroundings.

Triggers for this involuntary response could include being told off, a lack of sleep, or an inability to communicate their needs. Certain sensory stimuli – such as smells, lights, noises, textures or movements – could also result in a shutdown.

In all situations, it’s crucial to prioritise the safety and wellbeing of the child, such as gently guiding them to a less stimulating, safe environment, and respecting their personal space. Avoiding pressure, such as to talk or communicate, is important, and pre-identifying alternative communication methods such as hand signals can be highly effective.

Practicing grounding and self-soothing techniques in a safe environment, such as deep breathing, or identifying calming activities such as colouring or journaling, can also help to form the basis of an emotional safety plan.

These plans can help empower children

Every child’s experience will be very different, but they likely already have a lifetime of experiences to draw upon and identify their own unique triggers and strategies that have helped them.

Having a step-by-step list of things to do in situations that trigger emotional dysregulation can be a highly empowering touchpoint, especially within states of overwhelm.

Just like you wouldn’t be able to stop crying just because someone told you to, neither can children – especially when they’re AuDHD. However, these plans can bridge the gap, providing a window into their invisible experiences, enhancing awareness and empathy.

Ultimately, kindness and understanding are key to supporting AuDHD children. Avoiding judgement, demonstrating reassurance and providing well-informed, tailored support is key to creating environments where AuDHD children can thrive – not just survive.

The experiences I’ve mentioned above are not ‘bad’ – they are simply part of a normal reaction to a world that isn’t designed for their unique neurological makeup, but all AuDHD children deserve to feel happy, safe, and empowered as they are.

Leanne Maskell is the founder and director of ADHD coaching company ADHD Works, and the author of AuDHD: Blooming Differently – a new book offering practical help and advice for AuDHD individuals and those who support them.

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People Love To Ask Invasive Questions About My Son’s Autism. These Are The Only Ones I’ll Answer

My son, who starts second grade soon, is autistic and largely nonverbal.

We don’t live in a world that’s made for neurodiverse folks. And while there’s so much out there that tries to push kids like mine to conform into neurotypical spaces, it’s really on us to bend the world for them.

That’s why I talk to our neighbours, the folks running nearby stores, members of our community, about his autism. As a result, he has a favourite corner deli, where the owners know him. A thrift store where, when we walk in, an employee turns the music down, smiling at me from across the aisles. A bookshop where the booksellers don’t mind him sitting at the little kid’s table for half an hour, even when he unpacks a bag of Lego.

As a father, I will pry the world apart with my bare hands if I have to, if it means he can find a way through. But outside of these specific situations, I’ve never liked talking about my son’s autism with other people.

Growing up as a marginalised person, particularly as an adopted person of colour who didn’t really fit into any one space, a lot of irritating questions regularly came my way. “Where are you from, from?” perhaps being the favourite.

And while I had plenty of canned responses, none were ever satisfying, and I was always tired. No one likes to continuously explain their existence.

It wasn’t until I was an adult that I learned the concept of “it’s not your job to educate everyone”. It quickly became a core part of how I walk through the world. I was frustrated. I didn’t want to keep justifying myself to people who didn’t understand.

They could just go Google. It’s not that hard to learn about adoption, or what being a transracial adoptee means. Why waste my time, why make me cut myself open for you?

When our son was first diagnosed, there were a lot of questions from family and friends. Most of them were genuinely well-meaning, but as he grew older, some of them started to feel more and more ignorant and intrusive. I got angry. I snapped on phone calls, out at dinner. And that shield went up once again.

It wasn’t my job to educate everyone.

But in the last two years, something has changed. My child started going to school, then started wanting to go to the park, to playgrounds. He was trying to be social, even without the words. And in that world that tries to make neurodiverse folks bend and change, he deserved every opportunity, every run on a slide, every jump in a splash pad. A classroom, a summer camp. A childhood.

Then the questions started to happen again.

But they weren’t coming from the adults. The other parents mostly looked at us silently, from the corner of their eyes, as I showed up with my kiddo in a wagon while the rest of their children walked; or when he jumped around as their kids sat still; or when he got wildly upset over someone touching his backpack and had to unpack the entire thing so he could make sure everything was just the way he needed it to be.

The side eyes and furrowed brows are seared in my brain. Even if they don’t recognise me at the local grocery store, I sure remember them. I’m a father first and a Scorpio second.

So no, the questions didn’t come from those adults. They came from their kids.

“Hi, are you his Dad?”

“Why do you take him everywhere in that wagon?”

“What’s wrong with him?”

“Why doesn’t he talk?”

“He won’t play with me, why not?”

“Why does he keep spinning around like that?

“How can I help?”

At 6 or 7 years old, they were full of questions, but they were also full of empathy. Between drop off and pick up at school, at neighbourhood block parties, and at this year’s summer camp, little kids frequently asked these gentle questions, sometimes while a nearby parent tried to shoo them away or tell them what they were asking was inappropriate.

Maybe Past Me would have felt the same. The part of me that insisted “it’s not my job to educate everyone”. But I think that changes when the person you’re trying to educate people about can’t do it for themselves. When you have a chance to alter the world for your child, even a little bit.

So, I started to answer the questions. Just a quick sentence here or there.

“Oh, well he’s autistic. He experiences the world in another way.”

“Sometimes he gets overstimulated, and moving around helps. It’s called stimming.”

“It’s called being nonverbal. Words are hard, but he does communicate.”

“He experiences sensory things differently. So touching is sometimes very uncomfortable.”

And so on. My responses were always met with a thoughtful look, a smile. An “I want to try that!” and a kid spinning around themselves, arms stretched out in the morning sun.

I’m hopeful, staring down second grade. He’s got great teachers and a great community. And there are kids with empathy everywhere, even if some of the adults have lost it over the years.

Where I once thought it wasn’t my job to educate everyone, now I wish that more people would ask these questions in the gentle, well-meaning way kids do. That instead of the stares and the whispers, they would be curious and brave, like children who only want to understand.

Do you have a compelling personal story you’d like to see published on HuffPost? Find out what we’re looking for here and send us a pitch at pitch@huffpost.com.

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RSD May Be ‘Common’ With ADHD – Here Are Its Symptoms

Rejection-sensitive dysphoria, or RSD, is not an officially recognised diagnosis, the Cleveland Clinic says. But it is sometimes used in connection with formal diagnoses, like ADHD.

“This condition is linked to ADHD and experts suspect it happens due to differences in brain structure,” the Cleveland Clinic adds.

ADHD resource ADDITUDE calls RSD a “common ADHD trait”, though experts are in disagreement about whether it’s a trait or side effect. Nonetheless, a 2024 paper suggested a strong relationship between the two.

So, what exactly is RSD?

RSD is an extreme sensitivity to feelings of rejection. The term’s last word, “dysphoria”, comes from an Ancient Greek word meaning “uncomfortable” or “hard to bear”.

Cleveland Clinic says: “While rejection is something people usually don’t like, the negative feelings that come with RSD are stronger and can be harder to manage or both.

“People with RSD are also more likely to interpret vague interactions as rejection and may find it difficult to control their reactions.”

For those with RSD, something which might be a throwaway comment for one person can come across as a hostile, hurtful insult.

It may be linked to issues with emotional regulation, which neurodivergent people and those with personality disorders might struggle with more.

What are the signs of RSD?

People-pleasing, overreacting to perceived rejection, and struggling to interpret vague or neutral interactions as anything other than bad are common signs, the Cleveland Clinic says.

Feeling easily embarrassed or self-conscious, having low self-esteem, avoiding projects or tasks that include a risk of failure, and being preoccupied with perfection can also be symptoms.

It may be passed down genetically.

NHS Devon Partnership Trust writes that while “people with ADHD might identify with the definition of RSD… it won’t be given as a diagnosis in the UK”.

But while you are unlikely to receive a formal RSD diagnosis, you should speak to a doctor if you’re experiencing persistent difficulties with: attention, mood, focus, sensory processing, social interactions, or learning that disrupt your day-to-day life.

According to private medical centre, the Dr Jenni Clinic, talking therapies and emotional regulation techniques might help manage RSD. Some ADHD medications can also support emotional regulation, “reducing the intensity of RSD symptoms”.

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There Are 8 Key Autism Terms – It’s Time You Learned Them

Recent studies reveal that about 700,000 people in the UK are autistic, which works out as around one in every 100 people in the population. Research also indicates that the numbers could be twice as high, as there are so many people still undiagnosed.

With this in mind, Dr Selina Warlow, a clinical psychologist and owner of The Nook Neurodevelopmental Clinic, has shared a glossary of terms that give insights into some of the traits of autism, providing support when it comes to recognising symptoms.

She says: “Conversation around neurodiversity is becoming normalised, and that’s so positive to see.

“But the figures show a need for more awareness to help people identify whether they [are autistic], so they can start their assessment journey. Receiving a diagnosis can open access to expert resources that support autistic people to thrive in society.”

From masking to autistic burnout – a psychologist explains 8 traits of autism

Stimming (Self-Stimulatory Behaviour)

Stimming is a term that refers to repetitive movements or sounds often associated with autism to manage sensory overload. This includes rocking, tapping, hand-flapping and spinning”, explains Dr Warlow.

While these aren’t exclusive to autistic people, autistic people are more likely to use them as tools of self-regulation.

Masking is behaviour autistic people may use to hide their true characteristics to match those of neurotypical individuals”, says Dr Warlow.

“This could involve copying facial expressions, planning conversations in advance, or holding in ‘stimming’, for example swapping hand clapping, with playing with a pen.”

Autistic burnout

“Autistic burnout – being extremely tired both mentally and physically – can be associated with the act of ‘masking’ (concealing autistic behaviours) for a long period of time, or sensory or social overload.”

Dr Warlow shares that some of theymptoms of autistic burnout include withdrawal from social life, reduced performance, and increased sensitivity to certain stimuli.

Literal thinking

For some autistic people, language is always very literal, which can result in confusion with figures of speech, irony or indirect requests.

“For instance”, Dr Warlow adds, “being told to ‘pull your socks up’ might be understood literally, not as a motivational phrase, so using exact words may be more helpful during conversations.”

Assessment

Prior to diagnosis, a person showing signs of being autistic may choose to be assessed. This process can either happen through the NHS by visiting your GP or you can seek a private assessment.

Dr Warlow says that a diagnosis can be both “an emotional, but also empowering time”, while you learn about autism and adjust your lives to cater for its strengths and needs.

Hyperfocus

Hyperfocus is where an autistic person is able to focus intensely on an activity, and can become absorbed in it to the point of forgetting about the time. This is useful in work or hobbies but can result in neglect of other aspects of life such as food or rest.

Dr Warlow advises: “If it is possible to identify hyperfocus patterns, alarms can be used to help keep tasks moving.”

Special interests

Autistic people can have a particular interest which they find fascinating and dedicate lots of time to learning about. Special interests usually begin presenting in childhood but can also form as an adult. Special interests could include anything from dinosaurs or superheroes to hobbies like gardening.

Dr Warlow adds: “Chris Packham is an example of a person with autism who turned his childhood special interest in animals into a successful career, becoming one of the UK’s best-loved natural world TV presenters.”

Dr Warlow reveals that the term AuDHD – a combination of Autism Spectrum Disorder (ASD) and Attention Deficit Hyperactivity Disorder (ADHD) – is gaining traction in the neurodiverse community, with over 12,000 monthly Google searches, 375,000 posts on TikTok and 172,000 hashtags on Instagram.

“Many autistic people also have ADHD, which can bring certain benefits and difficulties at the same time. While autism is characterised by a desire for sameness and a focus on details, ADHD is defined by impulsivity and difficulty focusing.”

If you think you may be autistic, speak to your GP for a referral.

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People With Suspected ADHD Are Facing A Crisis In The UK

While the UK ADHD population is still grappling with ongoing medication shortages, new research from Mamedica has found that not only are the 2.6 million people diagnosed being left behind but a further 4.5 million Brits believe that they have undiagnosed ADHD.

Undiagnosed ADHD can come with a myriad of complications which leads to a reduction in quality of life for neurodivergent people. According to ADDitude Magazine, undiagnosed ADHD can lead to impulsivity, emotional instability ,and feelings of anger and worthlessness.

How long are NHS waiting lists for ADHD diagnosis?

Of course, throughout the UK, waiting list times differ but a report by ITV released in October found that in some areas of the UK, adults could be waiting up to 10 years for a diagnosis.

Speaking to ITV, a Department of Health and Social Care spokesperson said: “We know how vital it is to have timely diagnoses for ADHD, and we are committed to reducing diagnosis delays and improving access to support.”

Additionally, Sheffield magazine Now Then has reported that in the 12 months between June 2022 and June 2023, only 21 adults received an assessment from The Sheffield Adult Autism and Neurodevelopmental Service (SAANS), which resulted in nine diagnoses.

Now Then stated that with 5,481 service users on the waiting list at the end of the same period, with current assessment rates, it would take 261 years to get through the current waiting list.

How this crisis is affecting women

According to the ADHD Foundation, 50-75% of the women in the UK with ADHD are undiagnosed, and as a result may be experiencing poor health and socio-economic outcomes.

While awareness of ADHD in women and girls has improved in recent years, ADDitude Magazine warns that there is still a lot of information gaps with professionals such as teachers and gynaecologists.

They said: “We now know that fluctuating female hormones worsen ADHD symptoms, yet this important issue is largely neglected. Gynaecologists are not educated about ADHD; psychiatrists don’t study the effects of female hormones on the condition; and many females feel minimised and mistreated.”

How is the ADHD diagnosis crisis being tackled?

The shortage in medication has led to doctors in England being told to not prescribe new patients with ADHD medication but this is expected to be resolved by December. From there, it is up to individual health boards to tackle backlogs.

However, back in May of this year, MPs on the All Party Parliamentary Group (APPG) for Attention Deficit Hyperactivity Disorder (ADHD) called on the government to prioritise tackling NHS waiting lists to assess people who could have the disorder.

Tory MP James Sunderland, a vice chair on the APPG, said to PoliticsHome that he wants the government to “throw the kitchen sink” at tackling NHS backlogs relating to ADHD, particularly for school-aged children.

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