SoulShift for Carers

SoulShift for Carers SoulShift for Carers offers an exclusive support program to parents and carers of people with a disability - because you deserve to thrive too!

Jade | Nervous System Repair for Special Needs Mums
🧠 Carer burnout is a nervous system injury (not a self care problem)
🧔 Somatic support for autism mums and complex needs parenting
āœ… Start here: Free Toolkit
šŸ’¬ Message ā€œBOOKā€ for session availability Our 1:1 holistic support aims to help you to reclaim your identity, restore and sustain mental, emotional and spiritual wellbeing and rise into empo

wered, purpose-driven living. I know first hand the impact on your whole self that caring for a loved one has and want to support you to live the life you deserve with a sense of peace and purpose. Our goals:
- Improve mental health and emotional resilience
- Build a supportive and understanding community
- Provide trauma-informed holistic healing therapies for carers
- Empowerment & life design guidance
- Support spiritual growth
- Prevent and reduce carer burnout
- Address and reduce the risk of addiction or maladaptive coping strategies
- Support grief and chronic sorrow

I have 12 years of lived experience having a daughter who has a severe disability/rare genetic disorder and years of professional experience supporting families. I also ran a successful business providing support to families and respite for people with a disability. My qualifications include:
- Holistic Wellness Practitioner
- Advanced Transformational Life Coaching Practitioner
- Inner Child Healing Practitioner
- Mental Wellness Coaching Practitioner
- Mindfulness Coaching Practitioner
- Polyvagal Therapy Practitioner
- Certificate in DBT (Dialectical Behaviour Therapy)
- Certificate in Acceptance and Commitment Therapy (ACT)
- Quantum Healing Practitioner
- Crystal Energy Healer
- Certificate IV Alcohol & Other Drugs
- Certificate IV in Training & Assessment
- Certificate III Community Services
- Bachelor of Arts - Youth Studies
- Mental Health First Aid
- First Aid Level 2
- ASSIST (Applied Suicide Intervention Skills Training)
- Currently completing Graduate Diploma in Counselling

23/04/2026

When people ask what it’s really like raising a child with profound autism… šŸ’”

It’s not the cute stereotypes or feel-good clips people usually see online.

It’s sleepless nights.
Self-harm.
Aggression.
Sensory overload.
Constant supervision.
And a level of exhaustion most people will never understand.

Families like ours live this every day.

And we need more than awareness.

We need recognition.
We need support.
And we need funding that actually matches the reality. šŸ’™

23/04/2026

I am so grateful for the support my daughter gets through NDIS (even though it completely burnt me out fighting for it for so many years).. but seriously, a lot of families are going to struggle to maintain out of pocket costs of supports that are beneficial and it’s all a bit scary for some of us.

23/04/2026

Burnout recovery is not about magically finding an extra hour in your day.

Most mums do not have that.

That is exactly why somatic healing can work so well. It is not about adding more to your plate. It is about using tiny nervous system resets inside moments that already exist in your day.

Little by little, when your body starts getting more regular signals of safety, your baseline can begin to shift out of constant fight or flight.

That is when things can start to feel lighter.

Comment BURNOUT and I’ll send you free resources to help you start.

And if you are ready to repair your nervous system more deeply, send me a DM and I’ll let you know the support options I offer.

22/04/2026

What happens when support is taken away?

People talk about ā€œcutting costsā€ like the impact ends on paper.

It doesn’t.

For some families, less support means a parent has to cut back work or stop working altogether just to keep their child safe, regulated, and cared for.

And when income drops but the care load does not, the pressure does not stay small.

That pressure can become missed bills, impossible choices, and real fear about how to keep a roof over your head.

This is the part that is not being talked about enough.

The need does not disappear.

It gets pushed onto families already carrying too much.

Follow me for more support around NDIS funding, evidence, access, and plan reviews.

Comment NDIS if you need help.

Have you ever walked out of an NDIS meeting and thought, they still do not get how hard this really is?That’s the part s...
22/04/2026

Have you ever walked out of an NDIS meeting and thought, they still do not get how hard this really is?

That’s the part so many families are carrying.

Not just the care itself, but the pressure of having to explain, prove, document, and somehow turn your whole life into language the NDIA will actually understand.

And when you are already exhausted, that is a lot.

This is why I care so much about helping families prepare properly for NDIS access, plan reviews, reassessments, and change of circumstances.

Because the right evidence, the right wording, and the right strategy can make such a big difference.

Follow me for practical support with NDIS funding, evidence and plan reviews.

Comment NDIS if you need help.

Note: Use me as a last resort - you should be able to get support from your Local Area Coordinator, Support Coordinator if you have one, or local NDIS Disability Advocacy Services 🧐

22/04/2026

If you have a child on the NDIS who is aged 9 or older, this is the part of today’s announcement I really want families paying attention to.

A lot of the concern is around functional capacity and how much a child’s disability impacts day to day life, not just diagnosis.

And that matters because so many children can mask in appointments.

So many can look ā€œfineā€ on paper.

So many can hold it together for a short assessment, while families are managing aggression, school refusal, emotional outbursts, poor sleep, elopement, feeding issues, toileting issues, lack of safety awareness, and constant supervision behind closed doors.

This is why NDIS funding, NDIS access, and NDIS plan reviews need to be based on the real day to day impact.

Not just what a child looks like in a short appointment.

Not just a diagnosis on paper.

If you are a parent of a disabled child, autistic child, ADHD child, or child with high support needs, please do not minimise what life actually looks like.

Document the supervision needs.

Document the safety risks.

Document the impact on school, community access, family life, and your capacity as a parent.

That real functional impact is what matters.

Follow me for more support with NDIS funding, NDIS access, evidence, and plan reviews.

Comment NDIS if you need support around accessing NDIS funding or preparing for a plan review.

21/04/2026

How many times have you been told it’s just parental responsibility when you know your child’s needs go far beyond that?

This is one of the biggest reasons families miss out on the support they should be fighting for through the NDIS.

Because it’s not enough to know your child needs more.

You have to show, in the right language, exactly how their care needs go above what would usually be expected of a parent.

That’s where so many families get stuck.

If you need help understanding what evidence matters, how to explain functional impact, or how to strengthen your case, comment NDIS and I’ll send you the link to my support options.

Follow me for NDIS funding help and carer burnout recovery and prevention support

21/04/2026

Have you been told that your child can’t access respite through NDIS funding because they are under 18? If that was the case I wouldn’t have been able to run a disability respite business for a few years ONLY working with children.

Always check your facts.

Comment NDIS if you need support

If you’re a special needs mum or autism mum holding everything together on broken sleep, constant hypervigilance and a n...
21/04/2026

If you’re a special needs mum or autism mum holding everything together on broken sleep, constant hypervigilance and a nervous system that never really gets to exhale, this is for you. šŸ’›

These coping thoughts are not about forcing positivity or pretending things are okay when they are not.

They are gentle reminders to come back to when your body is in overload, your mind is racing, and everything feels too loud, too heavy or just too much.

Save this carousel for the moments when you are running on empty.

And if one sentence really hit, drop it in the comments. Sometimes seeing the words written out helps them land when you need them most.

Follow me for support with carer burnout, nervous system overwhelm and the reality of special needs motherhood.

Comment FREE and I’ll send you my free burnout resources.

20/04/2026

For so many special needs mums, the question is not just:

ā€œHow do I help my child more?ā€

It is also:

ā€œHow do I keep going like this?ā€

Because when your body has been living in survival mode for too long, everything gets harder.

Your patience.
Your capacity.
Your ability to stay soft.
Your ability to co-regulate.
Your ability to rest and actually feel rested.

That is why your own healing matters so much.

Not because it is selfish.
Not because it is about putting yourself before your child.

Because your nervous system is part of the environment your child lives in every single day.

And when you start to feel safer, softer, less braced, and less overwhelmed, that changes things.

It changes how you respond.
It changes how much pressure your body is carrying.
It changes the energy in your home.
It changes how much of yourself is actually available for connection.

That is exactly why I created these grief healing sessions.

Because so many special needs mums are not just burnt out.

They are carrying grief, pressure, heartbreak, and emotional weight their body never got to process.

And when that starts to move, everything can begin to soften.

These live grief healing sessions are this week only and spots are very limited.

Comment GRIEF and I’ll send you the details šŸ’›

Address

Melbourne, VIC

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