The Dizziness of Doing Too Much: The System Weary Parent

“I wish I could wake up one day and not be dizzy.”

Those were the words I said to my mum as a young girl. She remembers them not because they were dramatic - as a child they were matter-of-fact, but because of what came after them: silence. This was not the silence of indifference, but of a parent who loved me and had no power to fix this problem. She walked beside me, often literally, and I know now that her presence was everything. But the one thing she wanted to do, she could not: she couldn’t take the dizziness away.

I was deaf from babyhood and diagnosed with a rare condition at eleven after years of uncertainty. By then, I had already spent many days spinning, off school, unable to participate in the ordinary rhythms of childhood. What followed was surgery, treatment of last resort, and the long road of learning to walk again. I had a body permanently altered with balance issues and a disability that would not leave.

I don’t share this to frame my childhood as a tragedy, it wasn't, but because it is the ground from which I now work as both a psychological therapist and a physiotherapist. When I sit with parents navigating the complex world of Special Educational Needs (SEN) or disability, I carry that memory of my mother: present, steady, and quietly unable to do the one thing she most wanted to do.

THE WEIGHT THAT DOES NOT SHOW UP IN THE REPORT

In my practice and my own home, where I parent two children with SEN, I see the 'picture on paper' rarely captures the lived reality. Navigating 'the system' has a particular, exhausting texture. There are the EHCP (Education, Health and Care Plan) processes, the school reviews, and the letters that demand responses on timescales that assume you have no other life.

When I work with families, I hear a version of the same exhaustion: it isn't just from doing, but from the relentlessness of having to know. Having to be a researcher, a record-keeper, and a translator between what the system asks and what your child needs. I highlighted in my last post that a significant recent report raised the concept of Systems Generated Trauma - the way disabled children and their families are traumatised not by their condition, but by dysfunctional public services when they reach out for support.

WHEN EVERYONE HAS A 'TOOL' AND YOU JUST WANT TO BE 'MUM' (OR 'DAD')

There are a lot of tools and strategies in the professional world. I use them; I teach them. But I also want to say plainly: the role of parent is not a lesser role because it does not come with a certificate. The ordinary relationship, sitting together, eating, being bored in the same room or attempting anything or these things, has its own therapeutic function. When professionals suggest strategies, there is often an implicit message: if you do this consistently enough, things will change. That may be true, but it is also a staggering amount of pressure on people who are already at capacity. Not every moment needs to be an intervention. Sometimes you just want to be, and that is absolutely okay.

MAPPING THE CHAOS: CIRCLE OF CONTROL

1. The Outer Ring: No Control

In the context of disability or SEN, this ring is often very full. Naming this honestly is not defeat; it can help understand where you put your energy and your emotions. Examples include:

  • The System: How quickly services respond or the length of waiting lists.

  • The Environment: How other children respond to 'difference' at school.

  • The Timeline: The organic pace of your child’s development.

2. The Middle Ring: Influence

These are things you can shift, even if you cannot determine the final outcome. Examples include:

  • Advocacy: How you frame and evidence an EHCP request.

  • Relationships: The quality of communication and the rapport built with school staff.

  • Preparation: Organising for appointments so limited time is used well.

3. The Centre: Direct Control

This is the most important area, and often the first to be neglected. This includes:

  • The Home Rhythm: Creating predictability and a 'safe harbour' environment.

  • The Repair: How you reconnect with your child after a difficult, dysregulated moment.

  • Your Regulation: Whether you are getting any rest, support, or time that is purely yours. This is probably the most forgotten in the generous parenting I see.

PRESENCE IS NOT PASSIVE

I want to be careful here: the Circle of Control is not a saying that you have passive input across the board. My mother was not passive when she walked beside me. She attended every appointment and persisted when doctors did not know what was going on. She did all of this without being able to change the fundamental fact of my condition. She has been with me and my confusion, exploring what is going on for me through adulthood.

There is a difference between expending energy where it cannot move anything and choosing where to direct effort wisely. When I was spinning as a child, the thing that mattered most was not that my mother could stop it. It was that she was there. The steadiness of her presence was its own kind of stabilisation for my nervous system.

That does not require a strategy; it requires showing up. What I wish most for my Mum was that she looked after herself. I never blamed her for how I was, and I would not want her blaming herself.

A PERMISSION STRUCTURE

Nothing here is intended to suggest you are doing it wrong. If you are parenting a child with complex needs, you are likely doing more than is ever acknowledged.

What I hope this framework offers is permission. Permission to stop spending energy in places where it cannot land.

  • Permission to tend to your own wellbeing and the relationship.

  • Permission to just be a parent for an afternoon, without it being a 'therapeutic activity.'

The dizziness did not go away, and my mother could not make it. But because she walked beside me, I learned to navigate a body I hadn't chosen. That navigation required both of us, and it started with her just being there.

Let us know what you think in the comments!

YOU MIGHT ALSO LIKE

A picture of Verity Green head and shoulders - brown bob, smiling, black top

V.G.

About Verity Green

Based in Catterick Garrison, Richmond, Bedale, North Yorkshire and Online. Therapy and training with trauma, long term conditions and disability, adoption, care leavers, managing high conflict environments in the home, recovering from high control, and managing change from intense environments (such as sport, Armed Forces Community).

Updates in your Inbox!
A picture of a newsletter generated from the system

Free Signup

You can Unsubscribe

Information is NOT sold

Approximately once a month