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Let's talk about what matters to you.
Whether you're navigating a new diagnosis, planning your loved one's care after hospital, or looking for support that sees the whole person — we're here to help.
What happens after you reach out
1. We listen first
A calm conversation where you share what's happening and what matters most to you.
2. We help you understand what else might be important right now
We'll highlight patterns, changes, or transitions to pay attention to — without overwhelming you.
3. We outline what support could look like
We'll explain how our Compass, Adapt, and Modules approach could help — and what the next steps might be.
You might reach out if...
You or a family member is navigating a diagnosis
You or a family member has an acquired brain injury or neurological condition. You're looking for a care provider who understands the complexity, sees the whole person, and looks ahead.
Planning care after a hospital stay
You're planning care after hospital, or your care needs have changed. You need a care provider who's prepared, attentive, and ready to adjust support thoughtfully.
Exploring NDIS, SDA or SIL options
You're considering Specialist Disability Accommodation or Supported Independent Living and you're looking for care that understands how the home environment affects wellbeing, comfort, and independence.
How we can support you
Personal care
Support for everyday living.
Community support
Staying connected beyond home.
Health & nursing care
Care that supports health needs.
24/7 In-home support
Round-the-clock responsive support.
Onsite shared support
Supported independent living support.
Hospital transition
Preparation for coming home.
You don't have to figure this out alone
Get our free 5-day email guide for people and their families navigating finding personal care and support following a brain injury, stroke or neurological diagnosis.
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The questions that reveal what care will really look like
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How to watch for changing needs (and what to do)
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What makes care reliable — and how to recognise it
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I'm Jonathan, the founder of La Vita Care.
After supporting my mum through Motor Neurone Disease and realising how much families need care that truly sees the whole person – we have built La Vita Care to deliver that. Over the years, we've supported hundreds of people and their families through personal care and support.
The insights in this guide come from that collective experience — what we've learnt works, what people and their families wish they'd known earlier, and how to think about care in ways that make a real difference.
I hope it helps.
Jonathan