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Muscular dystrophy goes beyond a medical diagnosis — it’s a journey that alters daily living, impacting movement, autonomy and emotional health. But let’s be honest: nobody needs to go through this alone. Join the Support Network family today, where we don’t just provide seamless care, but we become your family, standing next to you with unfailing support every step of the way, so you or your loved one can receive the best, most personal, compassionate and expert care in Australia.
Muscular dystrophy impacts each individual in unique ways, and that is why the care we provide isn’t just about meeting the basic needs of a living being — it is about building a life that feels fulfilling, dignified and supported in every possible way.
From early-stage muscle weakness to advanced mobility challenges, we tailor our care to your changing needs. Whether you need light help with daily activities or full-time care with clinical supervision, we exist to support the transition of what is to what’s possible.’
Our care plans are based on you—not on standard templates. It means knowing your routine, your likes, your struggles and your goals. Be it ensuring independent mobility, minimizing discomfort or simply serving as a trusted companion, we create every care plan as if we were caring for our family.
The small things? They’re not small. The ability to get in and out of bed without difficulty, to take a shower without struggle, to eat a meal without battle — those moments are dignity, and we guard them with our lives.
Here are some of the things we help walk you through:
The goal of our approach isn’t just to do things for you — it’s to help you maintain as functional of a lifestyle as possible. We are there to help when needed, but we are also there to empower when possible.
Some people perform better in the privacy of their own home, while others thrive on engagement within the community. We provide both options because no two people whose lives include muscular dystrophy are alike.
If you would rather receive care at home, we also offer the convenience of professional medical and personal care right in your own home so you can stay where you feel most comfortable.
For those who have it all but still need engagement based on the community, we help them reach out social activities, therapy programs and disability-friendly events as no life should be limited to four walls.
We’ll be there wherever you feel most comfortable—supporting you in whatever way feels right for you.
Medication is not just a prescription, it’s a lifeline. With the right dosage, timing, and adjustments, muscle function and symptom management can be optimized.
My trained carers ensure that medication schedules are followed strictly, but we work with health care providers to monitor responses, manage side effects and make any adjustments as conditions change. We also help with pain management strategies and light physical therapy exercises, and overall symptom-control, so that each day is as bearable and comfortable as possible.
Eating is not only about consumption, it’s about feeding the body for strength, energy and long-term health. Meal plans focusing on muscle health These plans are built around the need for proteins, vitamins and minerals that are crucial for individuals dealing with muscular dystrophy, as our carers closely recommend.
Whether it is helping with eating or creating highly nutritious meals that are easy to swallow, we take care of nutrition, never making it a struggle but something that provides nourishment and energy.
Muscular dystrophy is not merely a condition of the body, but one of the heart; it is not only a challenge of the legs but one of the spirit, not just a limitation of the limbs but of connection. Time and again, individuals and families with this condition feel isolated, overwhelmed, or just needing someone that really gets it.
More than care, we are with you along the way, so you or your loved one has the emotional and social support to live, thrive and be connected. Whether it means companionship, social inclusion, or mental health support, our team is ready and able to provide unparalleled care, connection, and encouragement.
Need to speak to someone who gets it? Only then can we can create a support system that actually helps.
(pink) Care laren’t simply about assisting with activities of daily living — it’s about being present in the process of living in a manner that makes life meaningful.
Our caregivers at Support Network are not just professionals; they are also trusted companions who truly care. We cultivate a pillowing, scandal-less environment in which people feel:
We also know families need support as well. Seeing a loved one struggling with muscular dystrophy can be emotionally taxing. That’s why we’re here—not just for the individual but for all the family members who want help but don’t know where to turn for reassurance, guidance or a shoulder to cry on.
Want to talk to someone who actually knows what you’re facing? Contact Call Support Network on 1300 671 931 now.
Muscular dystrophy should never mean missing out on life. Unfortunately, so many of us are challenged by limited mobility, lack of access to disability-friendly events, or just plain feeling disconnected from the rest of society.
At Support Network, we fill in that gap to ensure that our clients stay active, engaged, and socially connected.
We offer more than care—we offer a way back to the life you love.
Find out how we can help. Pick up the phone now at 1300 671 931 and let’s get started.
Receiving a diagnosis of muscular dystrophy is a storm of feelings — confusion, frustration, sadness and sometimes fear. But no one should have to sort through those feelings in a void.
We help individuals and families access counselling and mental health support to equip them with the emotional tools to cope, adapt and thrive – Support Network
Physical health is not the only thing that matters. We ensure that no one goes through this journey alone.
Need someone to talk to? If you need to talk, support is only a phone call away — 1300 671 931.
Muscular dystrophy is not just a diagnosis; it is a life-long journey requiring specialised care, adaptive support and financial assistance to achieve the best possible services. But the stark reality is that understanding how government funding, NDIS and disability support programs work in Australia can be daunting. Forms, applications, assessments — it’s a system that so often seems designed to be complex.
That’s where Support Network comes in. We not only show you the options you have to fund your treatment, we guide you all the way through to getting everything you’re entitled to. Because this is more than just paper work — it’s about making sure that you, or someone you love, receives the care, support and quality of life you deserve.
Click here to ask us a question about NDIS or My Aged Care. We’ve got you covered. Just call us on 1300 671 931 and we’ll help you every step of the way.
What many families don’t even know, is that if you or your loved one has muscular dystrophy, you can receive NDIS (National Disability Insurance Scheme) funding. The NDIS is not simply a financial program, rather a lifeline that allows funding for necessary services, so people with muscular dystrophy can live as independently and comfortably as possible.
Through NDIS, you might be entitled to:
We work hand-in-hand with the NDIS at Support Network to develop a care plan that is tailored to your individual needs. We do not just offer services, we advocate for you to make certain that your funding accurately correlates with your care needs.
Still unsure if you qualify? Give us a ring on 1300 671 931, and let’s get it sorted out together.
Applying for NDIS can be a scary thing. The forms, the evaluations, the back-and-forth — it can leave anyone feeling bewildered. But here is the good news: you don’t have to do it alone.
Here is where Support Network take the stress out of the whole NDIS application process. We handle everything from preliminary eligibility checks to obtaining the appropriate funding facility. Here’s how we help:
NDIS can seem like a lot of juggling but we keep it simple. Need help getting started? It's time to talk—speak to us on 1300 671 931 today.
People over the age of 65 with muscular dystrophy can no longer access the NDIS. Rather, My Aged Care takes over as the main funding source for additional support. But this is where so many families feel stuck – how to go from NDIS to My Aged Care? How about if the level of care increases?
At Support Network, our expertise lies in bridging families through this transition to ensure there are no gaps in services or funding.
Changing systems from NDIS to My Aged Care can be stressful and complicated—and we cover it all. From the coordination of assessments through to ensuring the ongoing funding of care, we will ensure you, your loved one, will receive the highest standards of care, uninterrupted.
Feeling lost? We’re here to help — call the Support Network on 1300 671 931 and we’ll sort it all out for you.
As muscular dystrophy advances into the later stages, the needs become more nuanced, fragile, and deeply emotional. And it’s no longer just a matter of physical care—it’s the compassion, companionship and understanding that, when coupled with physical needs, takes on a quality that goes beyond traditional support.
Support Network is not just a caregiver; we are here for you as support, your partners in this process. From short-term relief for you as a family caregiver, to long ongoing advanced care, or perhaps endoflife support for a loved one — we will not only support you on your journey, but walk alongside you through each aspect of it.
And this isn’t just about your support team. It’s having people who really know what you’re feeling — who listen, who feel, who care like family.
If you need someone to share the burden of this journey, we are here. Call Support Network on 1300 671 931 – we’re there to listen.
There are times in life when care moves from buying time to delivering comfort, peace and dignity.
For families working through this stage of muscular dystrophy, the emotions can be a lot to manage — grief, exhaustion, uncertainty and an inseparable love that renders each moment that much more precious. You don’t just need care for your loved one; you need people who will stand alongside you, who will grieve with you, who will make sure no one walks through this alone.
At Support Network, palliative care is about dignity, comfort and a space where love outweighs fear.
This stage of care isn’t just about the individual: It’s about the entire family. If you require a team that really gets it, we're here—1300 671 931.
Breathing is a function most of us take for granted — until it becomes a struggle.
For patients with severe muscular dystrophy, respiratory issues can be terrifying and tiring. But no one should have to fight for air.
Support Network offers advanced respiratory care focused on relieving discomfort, preventing complications, and making breathing as easy as possible.
Above all, we offer peace of mind. When it’s hard to breathe, we’re here to make things a little easier — not just for the individual but for the whole family too.
Looking for specialist respiratory support? Anyway, call 1300 671 931 — let’s have answers for you.
Having muscular dystrophy does not mean you should have to lose the ability to live life.
And with the proper technology use, adaptive equipment and modifications, we keep individuals functioning independently, comfortably and in control, regardless of where they are in their journey.
At Support Network, we can help:
We don’t just offer the equipment, we teach families how to access the technology that makes life easier. We can help you with expert advice on the best adaptive solutions on 1300 671 931.
Caring for someone with muscular dystrophy isn’t merely a matter of getting through tasks and routines — it’s about understanding, connection and trust. At Support Network, we are not just service providers; we are your support team, based on caregivers for caregivers, to ensure your or your loved one is supported by people that understand.
We are not only carers— we are advocates, companions, and a constant reassurance.
Heart matters just as much as experience, however. Our care was medically trained, extremely skilled, listen to you, support you, and stand with you throughout the process. Muscular dystrophy has a unique set of challenges, and we customize our care model to meet your unique needs, because each journey is different.
It’s hard to navigate the system — but you’re not alone. We ease the complexities as NDIS-registered providers and ensure you maximize the support and funding you deserve.
We hail from all walks of life, and our legacy spreads across Australia, a testament to our trusted experience and dedication to treating everyone as we would our kin. From daily help to advanced medical care and emotional support, we ensure that no need is left unmet.
Muscular dystrophy and other neuromuscular conditions can bring many questions—whether it’s understanding genetic testing, managing care, or finding the right health care professional to support daily needs. At Support Network, we provide a wide range of services, from in-home support to expert guidance on genetic conditions like limb-girdle muscular dystrophy, one of the most common forms of muscular dystrophy.
Our team includes occupational therapists, social workers, and skilled caregivers who work closely with individuals facing skeletal muscle deterioration due to various neuromuscular diseases. Whether you're navigating muscle biopsies, mobility challenges, or seeking advanced care solutions, we’re here to walk this path with you.
Need support, advice, or just someone who truly understands? Call us at 1300 671 931, and let’s talk about how we can help.
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