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At Two Way Street, we’re passionate about creating a world where everyone can communicate with confidence.
Imagine navigating daily life when the world around you isn’t built with your communication in mind. That’s the daily experience for more than 1.2 million Australians living with communication disability.
We believe inclusive communication is more than just a tick box. It is the key to dignity, independence and connection. We are proud to support organisations taking steps – big and small – toward creating environments where everyone can feel included and confident communicating. And when large organisations like Uniting Communities and SA Water prioritise accessible communication, we see just how powerful this can be.
In the latest Unite Magazine (Autumn 2025, pages 10-12), Uniting Communities shared their story in ‘The Power of Being Heard’, a feature article that brings inclusive communication to life through powerful stories and heartfelt short film ‘It Takes Two’.
The film captures real experiences from aged care residents, volunteers, and staff living with hearing loss, dementia, vision impairment, and culturally and linguistically diverse backgrounds. The message is clear: small communication barriers can have a big impact—but so can thoughtful, inclusive strategies.
“When people feel heard, they feel valued – and that’s where real change begins.” Unite Magazine, Autumn 2025
Two Way Street has proudly partnered with Uniting Communities to guide several of their sites through the Communication Access Accreditation process. This means staff are trained in inclusive communication strategies, environments are adapted to meet different needs, and resources are in place to support everyone to understand and be understood.
When a site earns the Communication Access Symbol, it signals a genuine commitment to breaking down communication barriers—not just for customers or residents, but for every single interaction.
👉 Read the article (pages 10–12)
📽️ Watch the video
Inclusive communication isn’t limited to specific settings, it’s needed everywhere that people connect. SA Water’s efforts show how thoughtful universal design and inclusive service delivery make an impact.
Through their ‘Wider World’ program, SA Water identified key barriers faced by customers with disability, older Australians, and people experiencing digital or language exclusion. Their response included customised communication boards developed by Two Way Street to support customers during essential works, as well as easy read materials and accessible visitor guides.
📽️ See the communication boards in action
Adding a communication board to a customer service point, creating an easy-to-read resource, or training staff on how to support people with different communication needs are all small steps that can make a big difference. They show customers, clients, and the wider community that you’re actively creating a space where everyone is welcomed, can understand and be understood.
Inclusive communication isn’t about flashy tech or complex systems. Often, it’s about slowing down, using plain English, offering visual support, and genuinely listening. And when these strategies are embedded across an organisation, everyone benefits.
Whether you’re a council, service provider, community group or customer-facing business, you have the power to make communication accessible for everyone. And at Two Way Street, we make that journey achievable.
We can work with you to:
When you take steps toward communication access, you’re telling your community: “You’re welcome here. We’ll meet you where you are.”
And that’s where real inclusion begins.
It takes intention.
It takes care.
It Takes Two.
We’re incredibly grateful to Uniting Communities and SA Water for sharing the inspiring work they are doing, and reinforcing the importance of breaking down communication barriers across all settings. This work is a great example of how thoughtful design and genuine commitment can remove barriers and create environments where everyone can participate.
If you’re ready to take steps toward inclusive communication, we’d love to help. You don’t have to do it all at once – but you can start today.
Let’s talk about what’s possible for your organisation. Connect with us:
🌏 – https://twowaystreet.com.au/contact/
📞 – 0434 266 237
✉️ – [email protected]
Find out more about what Communication Access means, why it is important and how you can become certified here: Communication Access
Building an inclusive learning environment is a commitment to recognising and addressing the diverse needs of every child. It also means creating an environment where all children feel welcome, valued and that they belong, without having to ask!
Being intentional in the set up of your learning environment will drive successful outcomes in engagement and positive behaviour. Children who experience an inclusive learning environment develop not only academically, but also socially and emotionally.
Just as inclusive architecture focuses on creating environments that are usable by all people – in education, resources and adjustments that may be a priority for some, can be used by all to enable opportunity.
When you minimise the barriers to learning and create an inclusive environment, ALL students are set up for success. This approach is particularly important in the early childhood setting, when needs may not yet have been identified and children are at different stages of development, with varying abilities.
There’s another buzzword you may have heard in education – Universal Design for Learning (UDL).
UDL guides the creation of learning outcomes, resources and assessments that work for everyone. While some children will need more individualised adjustments and tools to participate in an environment, UDL closes the gap that needs to be filled by an individual.
For example, height adjustable desks in a classroom mean that a child who uses a wheelchair some or all of the time, can still sit at the same desks and in the same space as all of the other children. In addition, taller children and smaller children can also set the desk to the height that best suits them rather than needing a cushion or having to sit at a different desk. These children ‘just fit’ in their classroom and there is no requirement to apply for extra funding, have special meetings to organise an appropriate desk, nor to encounter challenges when the class moves to a different room where the ‘special desk’ is not available. There may also be some days where all children would benefit from alternating between standing and sitting.
Communication is no different. Though the majority of children in our childcare and school settings communicate with spoken words, many need or prefer other methods such as sign, symbols, typing, body language and more. Many children benefit from alternate methods some of the time, or to enhance their expression or understanding through visual channels.
Just as PowerPoint, photos, maps and pictures add visual meaning and interest to our conversations and learning, visual displays can do the same for our children by expanding on the spoken word. All children can benefit from the inclusion of symbolic communication displays to enhance understanding, idea generation and expressive communication. With varied methods of communication available, those who need or prefer to use them will ‘just fit’ into their learning environment too. The communication displays also have a beneficial impact on those who may not speak English as a first language, may be shy, or as yet have not been identified as someone who may benefit from a personalised communication system.
Remember that preferences are part of the equality equation and are an important component in creating your inclusive learning environment. Taking preferences into account is crucial because it acknowledges that children have different ways of processing information and engaging with their surroundings. And those preferences may change based on the activity or environment.
Considering preferences promotes a sense of autonomy and agency among children. When children have choices in how they learn and demonstrate their understanding, they are more likely to be actively engaged and invested in their learning process. It’s empowering to feel valued and supported when exploring your own unique interests and strengths!
As we aim to create an inclusive world that includes communication accessibility opportunities, we need to ensure that symbolic communication starts in the early years as a component of UDL (also referred to as Tier 1 support). We can not know which children may need or prefer to use symbols for communication later in life, nor those who benefit from the symbols to enhance their comprehension of speech. Rather than waiting to find out, let’s give opportunities early.
It’s better to be glad we did, than to regret we didn’t
Integrating symbolic communication into existing curricula can be done with a few simple adjustments. By incorporating visual aids alongside other forms of communication, all children will feel empowered to express themselves effectively. And as we mentioned earlier, embracing inclusive communication practices early, not only benefits people with specific needs, but fosters empathy and understanding among all children preparing them for a diverse and interconnected world.
At Two Way Street, we’ve started our quest to ensure that people see symbolic communication as ‘just part of it’ rather than it being different or special.
Our first Communication For All Pack is available now, for the Early Childhood setting. We’ve done all the work, so you can create a truly communication inclusive environment. The pack includes symbolic communication displays for common activities in kindy or childcare settings, along with posters that value, respect and represent symbolic communication, plus downloadable templates to help you implement inclusive communication practices.
Take a closer look at the Communication For All Pack – Early Childhood. And get in touch with the team at Two Way Street for more information.
Most of us spend well over a decade of our younger lives at school. The transition from school to work, school to university – or to whatever life after school looks like – can be a tough one! And it becomes even more complex when you have a communication disability.
In this insight article, we share some strategies and ideas for you to help prepare your person to begin their new life after school, and be ready for whatever the future brings.
You don’t need to prepare anything for this, just talk as you normally would. If possible, use your person’s communication system to model the messages. Here are some ideas:
Create a story using Microsoft Word or the Pictello App outlining what will happen. Use photos and symbols. It’s ok if you don’t have all of the answers when you first introduce the story, you can add to it as you go along. Try to include photos of the school, your person and the key people in their lives. If you know where your person is transitioning to, whether it be further education, work or something else, start introducing this.
When you know where your person will be transitioning to after they finish school, organise some on-site visits as early as possible. It is important that the new setting, whether it is another educational facility, a workplace or somewhere else, becomes a familiar place for your person, to reduce anxiety they may experience about leaving school. Take photos if you can. Ask your person their thoughts about the visits each time they go. Try to gradually work up your days at the new location, so your person has an opportunity to get used to their new routine after school has finished.
A visual calendar is a great way to support the lead up to finishing school and the start of their life after school. This may help you to talk about changes in their routine with symbols. A visual schedule may also help your person with new morning or afternoon routines once school has finished.
Leaving school is a big change, so it is important to give your person access to the vocabulary they need to talk about it. If your person uses a communication app as part of their overall communication, you can program additional vocabulary to support the transition from school. Include the name of the place they are transitioning to once they leave school and the key people that will be in their lives. You could also create a chat page about the transition from school and questions that your person may ask. Be careful not to erase their school vocabulary. Most young adults still want to talk about school after they have left.
If your person is transitioning to a new place such as a workplace or day options program, it is important that their new team understand how they communicate. You, your person and/or your speech pathologist can create a communication video talking about:
These videos are an accessible and engaging way for others to get to know your person.
Once your person leaves school for the final time, find ways to stay connected and enable them to have conversations about their school experiences.
Learning doesn’t stop with school! Your person will have the opportunity to consolidate skills they have learned at school and pick up new skills on their post-school journey. Using these strategies, your person will be better prepared for life after school and empowered to embrace whatever the future holds. This is a new chapter full of possibilities and with your support and the right tools, your person will continue to thrive and grow in their own unique way.
Is your person already a client with Two Way Street? Talk to your Speech Pathologist about creating resources to support the transition from school.
Written by: Erin Morley, Speech Pathologist
On October 14th, the people of Australia will vote in a referendum. The question on the ballot paper is: “A Proposed Law: to alter the Constitution to recognise the First Peoples of Australia by establishing an Aboriginal and Torres Strait Islander Voice. Do you approve this proposed alteration?”
Voters will be asked to vote ‘yes’ or ‘no’ to this question.
At Two Way Street, we think it’s important that everyone has a voice. If you are over 18, then you are entitled to vote in the election. If you are under 18, then it’s still a very important topic of conversation. Not just for the outcome of this vote, but to consider and understand significant events occurring in our country and the world. This will help you to relate to information you might hear in the news or on social media, as well as to be part of conversations both in person and online about current events.
Voting is both a right and a privilege in Australia, as well as being compulsory for those over 18 (remember to enrol to vote if you haven’t already!). For those under 18, events like this referendum give us opportunities to talk about voting, laws and topics that help to build our understanding and capacity to make decisions, and to vote as an informed citizen after we turn 18.
The Australian government and others have created some accessible resources relating to this referendum. We’ve included links to these below.
We also think it’s important to provide opportunities for people to talk about the referendum, their reasons for voting ‘yes’ or ‘no’ and to ask questions before they make a decision. Good decisions include more than just being told information. Most people have conversations with friends, family, colleagues and even those who disagree with us in order to make decisions and prepare to vote.
To get the conversation started for people who use communication symbols to augment their communication, we have created a ‘Talking about The Voice’ aided language display (ALD). Of course there may be many more words required for a robust discussion on this referendum. This ALD is just to get the conversation started.
The first page has vocabulary to talk about the Voice and express opinions. The second page (reverse side) includes some common questions as well as space to add the individual’s own questions that they might like to ask people. We’ve also included some spaces to add personal opinions or preferences to share with others once you’ve had a chance to think about it. If you are a parent or support worker, be sure to only add messages that have been created by the person or at a minimum, agreed upon by them.
After these discussions, you might also like to add messages to the person’s own AAC system for use in all situations, or consider sharing information on social media, or by joining their selected campaign. It is crucial that you gain consent for any action you take on their behalf and that you keep your preferences separate from theirs when sharing their message.
Enjoy the conversations and we look forward to a referendum where everyone has a voice about the Voice!
The Voice website, includes:
Visit the Australian Electoral Commission for more accessible resources and information on enrolment and voting.
Civics Australia also provides information about the referendum in an engaging way.
I was born with Cerebral Palsy and grew up using my natural speech with what I like to call a ‘Cerebral Palsy accent’ (some of you may call this a communication disability). It was an era when talking freely about emotions just didn’t occur. Limited options for speech generating devices made it difficult for me to communicate effectively, and when I did try to express my feelings, the outcomes were often disastrous for me and those around me.
My parents did their best to create a happy and nurturing home environment. Dinner time was a fabulous time of sharing laughter and conversations, but it would have been immensely valuable if my parents had access to a program like Talking About The Important Stuff to support my emotional development, just as they could with my brother. This would have provided strategies not only to talk about emotions, but to provide children with complex communication needs (CCN) with avenues to express thoughts and feelings, just like any other child. We now recognise the significance of supporting parents and caregivers in this journey as well.
As a child with communication difficulties, my Dad tended to over-protect me, wrapping me in cotton wool as the saying goes! However, I have come to appreciate the wisdom in quotes from people with lived experience of CCN in Talking About The Important Stuff. Quotes like “throw them out of their wheelchair (gently) and let them eat dirt” and “the kid with disability should not be the centre of love all the time”. These quotes serve as powerful reminders that children with CCN deserve to experience everyday life and be exposed to the realities of the world, just like any other child. Over-protection hinders our growth and independence, whereas providing us with opportunities to learn, explore, and be understood promotes our emotional development and self-empowerment.
While it is crucial to start conversations about “the important stuff” during childhood, I am a strong advocate for providing tools and strategies that continue to support individuals with CCN throughout adulthood. Conversations around independence, personal safety, and self-empowerment are long overdue for anyone with a disability, and they hold even greater significance for people with CCN.
Speech Pathologists can work with children and adults with CCN to support them to build on their natural speech. They can also support by introducing Augmentative and Alternative Communication (AAC) as a way to supplement this speech or to give them another way of communicating. AAC systems can take many forms e.g., sign, aided language displays (ALDs), comprehensive communication books (PODD), speech generating devices and many more.
Thinking back to when I was young and having speech therapy, I remember having to listen to the words on a flash card, repeat the words and then sound out each word as I said them. I’m pleased to say, especially during Speech Pathology Week 2023, that nowadays speech therapy looks different. Speechies are much more involved in advocating what works best for their clients and ensuring that all ways that a person communicates are valued. This is important, especially when considering the future “voice” for their individual client. #SPWeek
Through my journey with communication disabilities, I have come to realise the immense power of words in shaping our understanding of one another. By embracing the voices of children with CCN and providing them with the means to express themselves, alongside continued support throughout adulthood, we create opportunities for meaningful connections and a life that flourishes with possibilities.
When you’re little, emotions are big! Think back to when you were young. Did you throw an occasional tantrum? Did you have a bad day and go over it again and again in your head? Until you eventually talked about it with someone you trust and finally felt that huge sense of relief from a problem shared… Probably.
We’ve all had a tough few years and kids have watched their world evolve in ways we could never imagine a short time ago. One of the main messages conveyed when the world was in the turmoil of a pandemic was to ‘stay connected’. We stay connected with one another through sharing stories, ideas, thoughts and even our sense of humour. And we use language to manage our emotions – to tell people how we’re feeling, to validate ourselves, to get help and to regulate ourselves.
So just imagine, you have a million thoughts in your head – some are worries about the future, some are funny stories about your day, some are wondering about what’s happening with your body… but, you need an augmentative communication system like a PODD or communication device, and maybe also a communication partner to share your thoughts clearly. You may not get the same opportunities to talk things through like your siblings or peers.
Emotional development is extremely intertwined with language development. During early years of communication, parents describe their own emotions and the emotions of their child. This ‘emotion talk’ is how we navigate our feelings and start to create our belief systems that stay with us through life. So it’s time to start talking about the important stuff with children with a communication disability, as early as possible, so they too can build a strong foundation for emotional well-being.
Just being aware that emotional development and language development go hand-in-hand is important. Think about all the things that happen in a day that can affect a child emotionally. Create a supportive environment, where you notice when your child may have had strong feelings about something. Celebrate and acknowledge those feelings when you notice them, and do that often! There may not be a response from the child yet, but it’s a great way to ensure they feel heard and can navigate those feelings. And keep talking about stuff in age appropriate ways!
Make vocabulary available. Further to that, model emotional conversations. These conversations may be about something that happened that day or what’s happening in a story you’re reading. You can also scaffold and co-construct messages, to figure out what is happening for your child and help them learn what it means to feel a certain way, how to share their feelings with others and how to indicate why they’re feeling that way.
It is crucial to encourage independent exploration and problem solving from an early age, no matter how a child communicates. Ask children to direct you when appropriate, respect preferences and begin to negotiate. Perhaps you could include your child in interviews with support workers. Any time you find yourself advocating for your child, add those messages to their communication system and show them how to advocate for themselves. Let them hear from people with lived experiences of communication difficulties. Always respect and enable privacy and authorship for anyone using AAC. Do they have the opportunity to talk privately? Can they tell you ‘don’t say that’ or ‘don’t tell anyone’? Can they clarify a message, or say ‘that’s not what I meant’?
By adopting these simple strategies, you can help your little one manage big emotions and navigate their world with confidence and resilience.
To learn more about positive emotional development in children with communication difficulties, take the FREE Two Way Street online course ‘Talking About The Important Stuff’. The course gives parents and key communication partners the skills and knowledge they need to enable meaningful conversations with their kids.
If you’re a white, middle-class male or female living without disability, you won’t need to look far to find someone you can relate to in the media. People just like you are on TV, in movies and can be seen on the pages of catalogues and magazines.
Yet, if you’re living with a communication difficulty, or any type of disability for that matter, you’d be hard pressed to find relatable characters on your favourite media outlet. And when you consider that 4.4 million people in Australia live with disability, there’s a huge gap. That’s 18% of our population, or 1 in 6 people, unrepresented. It’s definitely time for a change.
Media is a powerful creator of perceptions. And it can also be used to create the cultural change that people living with disability would love to see.
Our very own Communication Access Consultant, Margie Charlesworth, lives with Cerebral Palsy and has a communication difficulty. She uses her natural speech to communicate and also uses AAC when creating videos or presenting at conferences and to businesses looking to increase their communication accessibility. She is one of the smartest, funniest, most driven people you will ever meet and a great work mate to everyone at Two Way Street. And yet, Margie faces all kinds of perceptions around her ability to communicate. People STILL finish her sentences for her ‘to help’. And she goes from being respected for her knowledge and experience one minute, to being infantised and called a ‘good girl’ the next.
In one of her ‘Street Talk’ moments, Margie explained how it feels to have people finish her sentences. “Finishing my sentences implies many things. It implies that the person who I am communicating with can read my mind, or that I can’t communicate my own messages. It also implies that I have difficulty expressing myself or trouble figuring out how to say it myself. And finally, it implies that people would rather not listen to my voice…”
Imagine if Margie’s experiences were depicted somewhat realistically in the media! Those assumptions of Margie not being able to get her message across, or not being mature due to her communication difficulty wouldn’t exist. A person’s disability is an important part of their identity and is something we would love to see normalised in media representation.
We’ve seen Target Australia using a model in a wheelchair to advertise kids clothing. Was that the first time a child in a wheelchair rolling through Target saw someone like them on an in-store advertisement? Potentially, yes!
We’ve just seen Disney release a remake of The Little Mermaid featuring a non-caucasion Ariel played by African American actress and singer, Halle Bailey. Reactions from little girls seeing their all-time favourite mermaid as someone they can relate to, again maybe for the first time, made the internet explode.
Our team was just as excited to see Val Kilmer using AAC in the Top Gun 2022 sequel, Maverick. In the movie, Iceman’s battle with throat cancer rendered him unable to speak without causing pain (emanating a little of what was going on for Val Kilmer in real life). He is seen typing sentences and pointing to his screen to get his message across.
It’s this type of representation that needs to be included in mainstream media more. The every-day lives of people, all people, as valued members of society. This is why inclusion is important and representation matters.
Representation can also be achieved through communication modes. We have all become very familiar with the sign language interpreters during community announcements and emergency services briefings. Imagine if other modes of communication were as prevalent. Imagine if people who use modes other than mouth speech to communicate, could see their mode of communication used in advertising, signage and information media.
We work with a range of agencies to create signage that is not only useful for people who need the symbols to communicate, but also represent this mode of communication within the community. Our playground communication boards are a great example. We’ve also been busy creating beautiful products, like our AAC cushion covers, to ensure that symbolic communication is seen and valued around the home. And we have more to come, so if you haven’t already, join us over on Facebook and LinkedIn to stay up to date.
We’re strong believers in that world where communication brings autonomy, belonging, connection and opportunity for everyone. But we still have a long way to go…
If you are a business or organisation and would like some representation at your site, online or within your advertising, give us a call on 0434 266 237.
Do you have a communication difficulty? Are you comfortable using AAC? If you answered yes to both of those questions, then we’d love you to join us on our mission. Get in touch with Two Way Street to find out more about employment opportunities. Email [email protected] and tell us a little about yourself.
Presented by Margie Charlesworth and Janelle Sampson at the AGOSCI National Conference in Hobart on September 4-6, 2022.
Abstract:
The ‘Talking About Important Stuff’ project aims to help children with complex communication needs (CCN) and their parents talk about important topics such as health, hopes, worries, fears and the harder subjects such as death and loss.
The program will target early development of skills such as emotional development, well-being, and self-advocacy with a particular focus (as a pilot program) on young children and their parents. At completion of the project, a free online training program will be available that includes video lessons, real stories, examples and practice activities so that parents can share and teach their children how to talk about stuff. The training program will support opportunities for children and their parents to learn and practice vocabulary, skills, and habits. We also hope to build on their attitudes and insights into the uniqueness and autonomy of their children.
It is important to acknowledge that this project is not about doing or expecting anything extra than the natural conversations that occur for parents and their children who do not have CCN. We simply aim to ensure that children with CCN do not miss out on this valuable learning and connection with their parents and/or people.
This presentation will share the progress of the project to date including a literature review and input from the project advisory committee and content contributors, many of whom have CCN, or are parents of children with CCN. This information will make up the key messages to be presented in the online program.
Presented by Janelle Sampson at the AGOSCI National Conference in Hobart on September 4-6, 2022.
Abstract:
As providers in the disability space and in particular, augmentative and alternative communication (AAC), we know there is no magic bullet. We also know that 1:1 therapy is only part of the answer, and often the more meaningful outcomes are achieved outside of therapy sessions where motivation and engagement is much higher. The NDIS however has structured services so that the 1:1 becomes the standard and most sought after service for therapeutic intervention. In many places, we are frequently finding that demand outweighs supply for individualised therapy, particularly when it comes to those with knowledge and experience in AAC. We are left with long wait lists for individualised services and difficulty finding funding or justifying the costs for innovative programs that may not easily fit within the square (or price guide).
At Two Way Street (TWS), we have been negotiating the NDIS (formerly Better Start and HCWA) as funding for private services for 10 years. During this time, we’ve always had our eyes on the prize that is the bigger picture beyond 1:1 services. It has taken time, patience, dedication, hard work and financial risk on many occasions to expand our services beyond just individual therapy sessions and we are still only part of the way there.
In this presentation, the TWS team will share the milestones and challenges we’ve encountered on our way toward our BHAG (Big Hairy Audacious Goal) for the business that includes individual services alongside capacity building and community development, while maintaining a niche focus on people with CCN at the heart.
Recent changes to the National Disability Insurance Scheme (NDIS) are aiming to make things easier for participants. With these changes, come differences to the systems we’re all accustomed to. It’s important to be aware of how these changes may affect you and what you can do to be prepared.
As we move towards longer plan duration and fewer meetings with the NDIA, you will notice new terminology and processes regarding your plan.
What was previously known as a ‘plan review’ will now be called a ‘plan reassessment’. Your review date will remain as-is. To ensure participants aren’t left without services, all plans that reach their reassessment date without a reassessment being completed will be automatically extended by 12 months.
You will continue to receive Participant Check-In calls from the NDIA to discuss your wellbeing, your goals and the support you need. These calls will determine whether you need:
While likely to be towards the end of your plan duration, we’ve heard that the Participant Check-In call can happen at any time, and possibly with very little notice. This highlights the need to be prepared, with your goals and budget in mind.
You can now request a ‘plan variation’ at any time. This means, in some circumstances, you can make changes to your plan without needing to replace the entire current plan. The aim here is to speed up the process for accessing new supports.
You can read the full information shared by the NDIS on 30 June 2022. This is how the NDIS has outlined the process for changing your plan.
Here are some of our recommendations to ensure you’re prepared and won’t need to wait for access to new supports:
The work we do helps people meet their daily communication needs, and therefore, funding for most Two Way Street services comes from ‘Capacity Building Supports’ and funding for communication resources may come from the ‘Core Supports’ part of your plan. We recommend discussing which Support Budget to use to claim for services with your Support Coordinator, Plan Manager or directly with the NDIS.
Key points to remember:
It can be frustrating when things change and just knowing where to look for the right information can be half the battle. We hope this article has helped with your next steps to ensure successful changes to your plan at your next variation or reassessment.
We’re here to be your teacher, your ally and your cheer squad – even for the maze that is the NDIS. Please reach out if you need any further information on accessing the resources and services you need from us.
We share and we listen. It’s a Two Way Street.