Beyond the Surface Therapy

Beyond the Surface Therapy Helping families living with PDA feel seen, understood, and connected. Holding Space Community Hub
https://www.skool.com/holding-space-for-pda-4300/about

Counselling, behaviour support, and real-life strategies for neurodivergent individuals & Families.

As always perfectly written & really describes the complexity of some of our pda families- mine included ❤️Do you recogn...
27/02/2026

As always perfectly written & really describes the complexity of some of our pda families- mine included ❤️

Do you recognise PDA within yourself or your partner?

PDAers often struggle with being perceived.

By that I don’t simply mean being seen. I mean the experience of someone observing, interpreting, forming conclusions, or assuming meaning about what we’re doing, how we’re doing it, or why.
It can feel like someone accessing internal information that we haven’t chosen to share, while perceiving via their own biased lens.
Even when the other person believes they are being helpful, supportive, or insightful, the experience for a PDA nervous system can be exposure and loss of autonomy.

This becomes particularly relevant in co-parenting.

In families raising a PDA child, it is common for one parent to become the “preferred” parent while the other parent has more difficulty in the relationship.
I am frequently asked how to get a co-parent on board. How to make them understand that the child is not doing this on purpose. How to help them see that this is a nervous system response and not manipulation.

There is often an assumption that if the other parent just had the right information, the right explanation, or the right framework, they would change.

But we cannot make another adult understand something they are not ready or able to understand.

Sometimes the other parent is also PDA. There can be an assumption that this should automatically mean deeper empathy or insight in regard to the PDA child. However, adults who are PDA - especially those who do not recognise or accept that in themselves, may already be operating from a chronically activated nervous system.
When they are given information about what they are doing “wrong,” or shown a different way of parenting, or positioned as the one who does not understand, they may experience that as being analysed, corrected, or controlled. In other words, they may experience it as being perceived.

And when PDAers feel perceived in that way, resistance is a very common response.

Equalising often shows up in these dynamics.

Equalising is not a conscious decision to punish someone or make life harder for them. It is not about deliberately sabotaging a partner. Equalising is a nervous system attempt to restore balance when someone feels one-down, criticised, exposed, or stripped of autonomy.

In co-parenting, equalising can take different forms.

If one parent is more responsive, more flexible, more nurturing in accordance with the child's specific needs, and the other parent interprets that as permissive or believes the child is being manipulative, they may feel that their authority or autonomy is being undermined.

A PDA parent in that position may equalise by parenting in a harsher or more rigid way. They may also equalise against the other parent by criticising their parenting, challenging their decisions, or giving them a hard time about the way they handle things.

From the outside, this can look intentional or punitive. Internally, it is often about restoring equilibrium.

Tit-for-tat patterns can also emerge, particularly when both adults are PDA.

Earlier in my own co-parenting relationship, both adult PDAers, there was a lot of tit-for-tat parenting and tit-for-tat arguing.

I assessed everything through the lens of fairness. My brain constantly asked, “Is this fair?” "Am I being fair?"

But what I thought was fairness was not always fairness.

It was balancing scales. "He did this, so I should do this". "I did this, so he should do this". It became a ledger system.

It was not conscious at first. When it became conscious, I had to actively work on being aware of it and changing it. My brain will still default to the question, “Am I being fair?” That reflex is still there.

When you grow up as a PDAer, fairness can become a very abstract concept. Particularly if you grow up in environments where your behaviour is assumed to be volitional, intentional, conscious, and manipulative. You are regularly criticised, punished, dismissed, invalidated, and perceived as bad.

Over time, I internalised the belief that I am inherently wrong.

That creates what I would describe as fairness trauma.

Fairness becomes hypervigilance. Am I being fair? Have I done enough? Have I taken too much? Have I made it even?

I assumed that others perceived me as bad. I assumed that I had always, or was always doing something wrong without even knowing what it was. I learned to expect criticism.

Here’s what stands out to me: PDA children begin by stating “That’s not fair!” about just about everything in life. And this is because they’re children with a very sensitive response to perceived injustice toward themselves and for some, toward others.
My own experience, however, changed across my lifespan to “Am I being fair?” I believe due to being socialised as a female - gender stereotypes, being socialised to be a carer and nurturer (I am also those things naturally), to put myself last and to burn myself out trying to support others.

That is not PDA itself. That is the trauma that results from being misunderstood and constantly perceived through a deficit lens.

In parenting, this trauma can distort how fairness is interpreted.

Tit-for-tat responses can emerge. Scorekeeping can emerge. Reactions can be about restoring balance or equalising, rather than responding to what is actually needed in the moment.

In my own life now, it is often my ex-husband who will point out that I have done enough and that it is okay. He will sometimes show me more compassion than I show myself. That shift only became possible once I recognised the tit-for-tat pattern and began to separate fairness from scale-balancing tpward myself, internally.

For the preferred parent, watching equalising or harsher parenting can be extremely difficult. You can see what triggers your child. You know what helps and what destabilises them. You want to protect.

However, constantly intervening can intensify the dynamic. It can increase the other parent’s sense of being perceived and escalate equalising or tit-for-tat patterns.

Often, the more stabilising approach is to step back from trying to manage the other adult and instead focus on our own relationship with our child. Allowing the other parent and the child to develop their own relational rhythm, even if it looks different from ours is crucial.

This does not mean ignoring our child’s experience.

We live in a culture that promotes parents presenting a united front at all costs and never speaking in ways that could be interpreted as disloyal. But there is a difference between vilifying a co-parent and validating a child.

If my co-parent raises their voice and my child comes to me and tells me about it, I validate the experience. I might say, “That sounds really disappointing. That must have been hard. It doesn’t feel safe or fair when I am yelled at. How are you feeling about it now?” I offer a hug. I make space for their feelings. I do not need to label the other parent as bad in order to acknowledge that the experience was painful, however if the other parent was being abusive, this is different.

There is a way to validate a child without escalating inter-parent conflict.

Where dynamics move into abuse narratives or genuinely harmful patterns, that requires a different response and a different strategy. That is a separate and important conversation.

For now, the key concepts are these:

- PDAers are sensitive to being perceived in ways that feel intrusive or evaluative.
- Equalising can emerge in co-parenting when one parent feels criticised, undermined, or one-down.
- Tit-for-tat patterns and fairness trauma can distort how adults interpret balance and responsibility.
- Attempting to force insight or control another adult’s nervous system often escalates these responses.

Many will respond by concluding that an adult should know better - that they could somehow magically overcome the very thing that we still struggle to understand and even believe exists in children: Pathological demand avoidance.

We can only work on something we truly know, understand and accept. And for a PDAer, the pressure of someone trying to intervene on this impacts the nervous system to the point where learning is impossible. Being centred, grounded and able to take in new information and perspectives is impossible.

Often, the parent child relationship will find a rhythm once we step back. It will be messy. Sometimes ugly. Different from how we'd do things.

But the increase in trust with our coparent to navigate this pathway helps restore their autonomy and their confidence.

We cannot take responsibility for the other parent’s growth. We cannot fully protect our child from every relational rupture. We can focus on our own regulation, our own relationship with our child, and validating their lived experience without fuelling the dynamic.

That is often the most stabilising work available to us. It might just be the thing that saves us, and our relationship with our child.

KF

𝗥𝗮𝗱𝗶𝗰𝗮𝗹 𝗮𝗰𝗰𝗲𝗽𝘁𝗮𝗻𝗰𝗲 𝘄𝗮𝘀 𝗼𝗻𝗲 𝗼𝗳 𝘁𝗵𝗲 𝗵𝗮𝗿𝗱𝗲𝘀𝘁 𝘀𝗵𝗶𝗳𝘁𝘀 𝗜 𝗵𝗮𝘃𝗲 𝗲𝘃𝗲𝗿 𝗺𝗮𝗱𝗲 𝗮𝘀 𝗮 𝗽𝗮𝗿𝗲𝗻𝘁.🤍Not learning strategies.Not advocating in...
20/02/2026

𝗥𝗮𝗱𝗶𝗰𝗮𝗹 𝗮𝗰𝗰𝗲𝗽𝘁𝗮𝗻𝗰𝗲 𝘄𝗮𝘀 𝗼𝗻𝗲 𝗼𝗳 𝘁𝗵𝗲 𝗵𝗮𝗿𝗱𝗲𝘀𝘁 𝘀𝗵𝗶𝗳𝘁𝘀 𝗜 𝗵𝗮𝘃𝗲 𝗲𝘃𝗲𝗿 𝗺𝗮𝗱𝗲 𝗮𝘀 𝗮 𝗽𝗮𝗿𝗲𝗻𝘁.🤍

Not learning strategies.
Not advocating in systems.
Not sitting through appointments.

Acceptance.

True acceptance.

The kind that asks you to stop fighting reality in your own mind.

When you’re parenting a child with a PDA nervous system, radical acceptance can feel like grief.

Grief for the parenting scripts you were handed.
Grief for the idea that consistency and consequences would “fix it.”
Grief for the belief that if you just found the right approach, everything would settle.

Because at some point, you realise…

Your child is not being difficult.
Their nervous system is experiencing everyday demands as threat.

And no amount of sticker charts, firmer tone, or better routines will change the way their body interprets safety.

That realisation is confronting.

It asks you to let go of comparison.
It asks you to tolerate misunderstanding from others.
It asks you to soften your own urgency to make things look “normal.”

It can feel like giving up.

But it isn’t.

Radical acceptance isn’t resignation.
It’s not permissiveness.
It’s not dropping your boundaries..

It is choosing to respond to the nervous system in front of you instead of the rulebook in your head.

And when that shift happens — truly happens — something changes.

Power struggles reduce.
Shame reduces.
Your child feels less opposition.
You feel less internal war.

There is more creativity.
More collaboration.
More connection.

But getting there is emotional work.

It often requires unlearning, grieving, and re-building your understanding of what support actually looks like.

I’ve done that work. I continue to do that work.

And because of that, when I support families navigating PDA, it comes from a place of lived understanding as well as professional knowledge.

If you’re in the stage where nothing seems to work…
If you’re exhausted from trying harder…
If you’re quietly questioning everything you thought you knew about parenting…

You’re not failing.

You may be standing at the doorway of acceptance.

And you don’t have to walk through that alone.
www.beyondthesurface.au

17/02/2026

Morning Everyone,

I have received quiet a few enquiries from my website over the last couple of weeks- If you have sent one & wondering why i haven't replied... I have, but I've recently found out off a client that my emails are going to their spam.

Please check your folders or search my email hello@beyondthesurface.au.

I still have a couple of spaces left for individualised support.

Thank you,
Sarah x

There’s still so much misunderstanding around PDA.So I’ve put together a concise, professional one-page guide you can sh...
11/02/2026

There’s still so much misunderstanding around PDA.

So I’ve put together a concise, professional one-page guide you can share with:

• School staff
• Family members
• Colleagues
• Multi-agency teams

It explains PDA clearly — without overcomplicating it.

If you’d like a copy, comment "GUIDE" and I’ll message you the link.

Looking for in depth support? I currently have capacity for individualised wrap around PDA family Support
OR
Come & join our wonderful community hub where we hold space for PDA- build your resources & connections⬇️⬇️
https://www.skool.com/holding-space-for-pda-4300/about

This is wonderful, for any of our families that are also navigating ARFID ontop of our pda 🩵
10/02/2026

This is wonderful, for any of our families that are also navigating ARFID ontop of our pda 🩵

Hello everyone 👋Incase anyone has reached out to me over the last week & you haven't heard back- I promise I'm not ignor...
04/02/2026

Hello everyone 👋

Incase anyone has reached out to me over the last week & you haven't heard back- I promise I'm not ignoring you.

My beautiful pdaer in a moment of equalising with me, felt breaking my work computer would do the trick, so it's in getting repaired.
(Yep I'm not excluded from it all)

Hopefully I'll have it back in time foe next week.

Thank you for your patience 🦋

🦋🦋🦋
02/02/2026

🦋🦋🦋

31/01/2026

TRIGGER WARNING 🚩

with the tragic & absolutely heartbreaking news of the deaths of a full family in our disability community over in Perth, I want to let all of you know that please you are not alone.

I know how hard it is to keep pushing through, I know most of us have at some staged wished for a way out. I know we financially can't afford the required supports we need & that the governments dont get it but I am only a phone call away.

If you have seen the news & completely distressed by it or are really not coping

The below is also available

Lifeline 13 11 14

Heads pace 1800 650 890

Beyond blue 1300 224 636

Its not enough for our families or individuals living with PDA, to access therapies but don't walk alongside you on your...
31/01/2026

Its not enough for our families or individuals living with PDA, to access therapies but don't walk alongside you on your journey while everyone is enjoying their day to day lives and your family is struggling to survive.

for a lot of us its the help behind the closed doors we need, the support once we have left a therapy session.

I remember early on our journey, i begged and begged professionals to "Please, come & be a fly on our wall- you don't understand how bad it is"

Or as an individual how much you feel & experience life with PDA.

I see you all, no matter where you currently are.
The exhaustion, the burnout, the violent outbursts, the damage to your homes, the unlivable bedrooms, the guilt of not being able to keep up with hygiene, the expectations from society & family to have your kids in mainstream schooling, the weight you carry as a "safe" person, as a child the heaviness you feel from everyone's energy around you, the disappointment you aren't succeeding in what is wanted from you.

My support is offered with first hand experience layered with professional expertise, its delivered alongside you authentically & around your whole family to support PDA everyday.

www.beyondthesurface.au

You have done the therapies, the parenting programs, the constant advocating, consequences, rewards and tried to adapt y...
28/01/2026

You have done the therapies, the parenting programs, the constant advocating, consequences, rewards and tried to adapt your approach but its still not working.

You are still struggling to see the light living with PDA & neurodivergence.

What if i told you there was another way?

My Wrap around family support is just this and i have 2 places available for support.

𝐀 𝐋𝐢𝐭𝐭𝐥𝐞 𝐑𝐞𝐢𝐧𝐭𝐫𝐨𝐝𝐮𝐜𝐭𝐢𝐨𝐧 𝐅𝐨𝐫 𝐎𝐮𝐫 𝐍𝐞𝐰 𝐅𝐚𝐜𝐞𝐬 𝐇𝐞𝐫𝐞🤍I’m Sarah.I’m AuDHD, a PDAer, and I’m raising four neurodivergent childre...
27/01/2026

𝐀 𝐋𝐢𝐭𝐭𝐥𝐞 𝐑𝐞𝐢𝐧𝐭𝐫𝐨𝐝𝐮𝐜𝐭𝐢𝐨𝐧 𝐅𝐨𝐫 𝐎𝐮𝐫 𝐍𝐞𝐰 𝐅𝐚𝐜𝐞𝐬 𝐇𝐞𝐫𝐞🤍

I’m Sarah.
I’m AuDHD, a PDAer, and I’m raising four neurodivergent children — two with PDA.

I’m also a registered counsellor.
My lived experience shapes how I work, and PDA is an area I care deeply about — but my support is open to anyone needing counselling, space, or family support.

I work in a low-demand, neurodivergent-affirming way, focusing on nervous system safety, connection, and realistic support across a persons lifespan — from young children learning to manage big emotions, to teens and adults navigating life, relationships, and overwhelm.

This space & time with me is about safety, understanding, and support that meets you where you are.

You don’t have to fit a label to be here.

Thank you whole body nutrition ❤️
27/01/2026

Thank you whole body nutrition ❤️

With school going back I thought this post might be helpful for parents and carers to understand why a child may not be eating at school.

Below are some common reasons why this might happen..

💥Sensory overwhelm - Maybe there is something smelly in the air, their clothing feels itchy, it's loud, it's hot. Everyone has different sensory triggers. People with misophonia have a negative emotional reaction to different sounds e.g. chewing. This can result in anxiety, agitation and annoyance. Fight or flight mode becomes activated.

💥Safe foods are not accessible - Food might need to be at a certain temperature or have a certain texture which just can't be achieved at school.

💥Sympathetic nervous system dominance & stress - perhaps they are overwhelmed and in fight or flight mode so their body doesn't feel hungry, they have no appetite or they might even feel nauseous.

💥Interoception - perhaps they struggle with feeling hunger cues.

💥Eating with others does not always feel safe - it’s true, some kids find it difficult eating in front of other people and this could be for many different reasons.

💥Perhaps there is not enough time given to eat - especially if they are slow eaters. Also sometimes going outside to play is just more appealing.

💜🧡

Disclaimer: The information shared on this account is for educational purposes only and is not a substitute for professional medical advice, diagnosis, or treatment

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Wangaratta, VIC
3677

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