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    One in Five: Episode Six with Anne Currie

    In this episode of One in Five, Anne Currie reflects on her journey after acquiring an incomplete spinal cord injury,...
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    Making Local Change

    In this five-part video series, members of the SCIA Advocacy community share their experiences of making local change.
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    One in Five: Episode Five with Elizabeth Abrahams

    After being diagnosed with motor neurone disease (MND), Elizabeth has found new ways to stay active, maintain her independence and...
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    Understanding NDIS changes

    To help make sense of recent changes to the NDIS, SCIA Advocacy has developed a five-part video series explaining the...
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    One in Five: Episode Four with Stuart Hurst

    After a life-changing motorcycle accident in Nepal, Stuart shares his experience of living with a spinal cord injury and rebuilding...
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    One in Five: Episode Three with Nicki Antonio 

    Accessing healthcare can look very different depending on where you live. For Nicki Anne Antonio, living in Western Australia's Wheatbelt...
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    One in Five: Episode Two with Poonam Shah

    Our latest series ‘One in Five,’ produced in collaboration with Spinal Cord Injuries Australia and NeuroMoves, shines a light on...
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    One in Five: Episode One with Renee Power

    Renee Power is a NeuroMoves client in Joondalup, WA. In this episode of our One in Five series, Renee answers...
    Read More

    A Home Away From Home: Inside SCIA’s Transition House

    SCIA's Transition House in Perth helps people with spinal cord injury try home modifications and daily routines before making decisions...
    Read More

    Anne is smiling and seated next to a green lounge against a teal wall.

    For Anne, movement has always been a big part of life. A keen cyclist and mother of three, she sustained a C6/C7 incomplete spinal cord injury (SCI) while training for a half ironman triathlon. After leaving rehabilitation, Anne was determined to find ways to stay active and discovered the Walk On program, an intensive activity-based therapy program that would later become NeuroMoves.

    In this episode of One in Five, produced in collaboration with Spinal Cord Injuries Australia (SCIA) and NeuroMoves, Anne reflects on her journey, the support of her family and friends, and how movement and exercise has helped her maintain her independence, confidence and quality of life.

    Thank you to Anne for sharing her story so openly.

    Subscribe to our YouTube for more episodes

    For Anne, movement has always been a big part of life. A keen cyclist and mother of three, she sustained a C6-C7 incomplete spinal cord injury (SCI) while training for a Half Ironman triathlon. After leaving rehabilitation, Anne was determined to find ways to stay active and discovered the Walk On program, an intensive activity-based therapy program that would later become NeuroMoves. In this episode of One in Five, produced in collaboration with Spinal Cord Injuries Australia (SCIA) and NeuroMoves, Anne reflects on her journey, the support of her family and friends, and how movement and exercise has helped her maintain her independence, confidence and quality of life. To access a transcript of this episode head to https://scia.org.au/resource-hub/one-in-five-episode-six-with-anne-currie/

    This video is private.


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    YouTube Video UExGUmJkdVFBSEMzUS41MzJCQjBCNDIyRkJDN0VD



    One in Five: Episode Six with Anne Currie


    SpinalCordInjuriesAustralia


    October 15, 2026 4:27 pm


    For Elizabeth, family and staying active have always been a big part of life. Living in Perth with her three children, she was diagnosed with Motor Neurone Disease (MND) after noticing changes to her strength and mobility while playing soccer. Since then, she has adapted many of the activities she loves, finding new ways to stay connected to her family and maintain her independence. In this episode of One in Five, produced in collaboration with Spinal Cord Injuries Australia and NeuroMoves, Elizabeth shares her experience of living with MND, the challenges of adjusting to changing abilities, and how exercise and NeuroMoves have helped her maintain strength, balance and confidence in everyday life. To access a transcript of this episode head to https://scia.org.au/resource-hub/one-in-five-episode-five-with-elizabeth-abrahams/

    For Elizabeth, family and staying active have always been a big part of life. Living in Perth with her three children, she was diagnosed with Motor Neurone Disease (MND) after noticing changes to her strength and mobility while playing soccer. Since then, she has adapted many of the activities she loves, finding new ways to stay connected to her family and maintain her independence.

    In this episode of One in Five, produced in collaboration with Spinal Cord Injuries Australia and NeuroMoves, Elizabeth shares her experience of living with MND, the challenges of adjusting to changing abilities, and how exercise and NeuroMoves have helped her maintain strength, balance and confidence in everyday life.

    To access a transcript of this episode head to https://scia.org.au/resource-hub/one-in-five-episode-five-with-elizabeth-abrahams/


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    YouTube Video UExGUmJkdVFBSEMzUS4xMkVGQjNCMUM1N0RFNEUx



    One in Five: Episode Five with Elizabeth Abrahams


    SpinalCordInjuriesAustralia


    September 28, 2026 11:53 am


    For Stuart, independence is one of the most important things in life. Following a motorcycle accident while travelling in Nepal, which resulted in a spinal cord injury and traumatic brain injury, he has found new ways to continue doing the things he enjoys, including travelling, spending time with family and staying active in his community. In this episode of One in Five, produced in collaboration with Spinal Cord Injuries Australia and NeuroMoves, Stuart shares his experience of living with disability, the role patience and positivity have played in his journey, and how NeuroMoves has become an important part of his routine. Thank you to Stuart for sharing his story with such openness and generosity. To access a transcript of this episode head to https://scia.org.au/resource-hub/one-in-five-episode-four-with-stuart-hurst/

    For Stuart, independence is one of the most important things in life. Following a motorcycle accident while travelling in Nepal, which resulted in a spinal cord injury and traumatic brain injury, he has found new ways to continue doing the things he enjoys, including travelling, spending time with family and staying active in his community.

    In this episode of One in Five, produced in collaboration with Spinal Cord Injuries Australia and NeuroMoves, Stuart shares his experience of living with disability, the role patience and positivity have played in his journey, and how NeuroMoves has become an important part of his routine.

    Thank you to Stuart for sharing his story with such openness and generosity.

    To access a transcript of this episode head to https://scia.org.au/resource-hub/one-in-five-episode-four-with-stuart-hurst/


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    YouTube Video UExGUmJkdVFBSEMzUS4wOTA3OTZBNzVEMTUzOTMy



    One in Five: Episode Four with Stuart Hurst


    SpinalCordInjuriesAustralia


    September 15, 2026 8:17 am


    Accessing healthcare can look very different depending on where you live. For Nicki Anne Antonio, living in Western Australia's Wheatbelt region has meant navigating additional barriers while adapting to life after a diagnosis of transverse myelitis. In this episode of One in Five, our series produced in collaboration with Spinal Cord Injuries Australia and NeuroMoves, Nicki shares her experience of acquiring her disability later in life and the journey of accessing support in a regional area. She also reflects on how her experience working with the NeuroMoves Fremantle team has transformed her relationship with movement and supported her independence. Thank you to Nicki for sharing her story with such openness and kindness. To access a transcript of this episode head to https://scia.org.au/resource-hub/one-in-five-episode-three-with-nicki-antonio/

    This video is private.


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    YouTube Video UExGUmJkdVFBSEMzUS41MjE1MkI0OTQ2QzJGNzNG



    One in Five: Episode Three with Nicki Anne Antonio


    SpinalCordInjuriesAustralia


    September 4, 2026 9:15 am


    In this episode of our series 'One in Five', we meet Poonam Shah, who trains at NeuroMoves Joondalup in WA. Poonam shares her experience of living with Neurosarcoidosis, reflecting on her path to diagnosis and the important role movement and the outdoors has played in her life. She is joined by her mother, Chandrika, who offers a parent's perspective on supporting a loved one through this experience. We would like to thank Poonam and Chandrika for sharing their stories so openly and generously. To access a transcript of this episode head to https://scia.org.au/resource-hub/one-in-five-episode-two-with-poonam-shah/

    This video is private.


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    YouTube Video UExGUmJkdVFBSEMzUS4wMTcyMDhGQUE4NTIzM0Y5



    One in Five: Episode Two with Poonam Shah


    SpinalCordInjuriesAustralia


    August 24, 2026 1:01 pm


    In Australia, one in five people live with a disability and behind this statistic are millions of individual stories, experiences and perspectives. Our new series ‘One in Five’ is dedicated to bringing those stories to life. Produced in collaboration with Spinal Cord Injuries Australia and NeuroMoves, each episode offers a candid and reflective look into an individual’s experience of disability, how it has shaped their lives, their routine and the people around them. Our first guest is Renee Power, who trains at NeuroMoves Joondalup in Perth's northern suburbs. In this episode, Renee speaks openly about her encephalitis diagnosis, what came after, and how she found her way to NeuroMoves. Thank you, Renee, for sharing your story so honestly. To access a transcript of this episode head to, https://scia.org.au/resource-hub/one-in-five-episode-one-with-renee-power/

    In Australia, one in five people live with a disability and behind this statistic are millions of individual stories, experiences and perspectives. Our new series ‘One in Five’ is dedicated to bringing those stories to life.

    Produced in collaboration with Spinal Cord Injuries Australia and NeuroMoves, each episode offers a candid and reflective look into an individual’s experience of disability, how it has shaped their lives, their routine and the people around them.

    Our first guest is Renee Power, who trains at NeuroMoves Joondalup in Perth's northern suburbs. In this episode, Renee speaks openly about her encephalitis diagnosis, what came after, and how she found her way to NeuroMoves. Thank you, Renee, for sharing your story so honestly.

    To access a transcript of this episode head to,


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    YouTube Video UExGUmJkdVFBSEMzUS41NkI0NEY2RDEwNTU3Q0M2



    One in Five: Episode One with Renee Power


    SpinalCordInjuriesAustralia


    July 21, 2026 9:30 am




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    Transcript

    I think I’m lucky that I’m in a reasonably healthy condition right now…so I think that’s what I’m looking forward to. I mean, every other part of my life is being made possible by what I do here and I will not stop doing this until I can’t ever get out of bed,

    Hello, my name is Anne Currie and I currently attend the NeuroMoves in Freo (Fremantle) and I work for SCIA in the Peer and Family Support.

    Twenty years ago, I was training for the half ironman triathlon down in Busselton and I had an accident on my bike on the roads as I was training and I suffered a C6/C7 incomplete spinal cord injury…so the C6 and C7 vertebrae in the neck. So I’ve been affected from the chest down.

    I think I wasn’t really fully aware of what had actually occurred and what the outcome was going to be long term. So much was kind of happening in the initial few first days and weeks of that accident that a lot of things were going through my mind. I was a mother of three young children at home with a very busy husband, so I think part of it was also I can’t do any of those tasks anymore and I need to rely on other people to help me with that. I was still going to be in hospital for at least six months for rehabilitation, so that was a long way down the track. But I guess it was hard to initially, especially with all the personal things that go on with that regarding personal care that I could no longer do myself. So that was a little bit hard to get my head around. I think there is a lot more support now in the hospital system for that kind of emotional and I guess physical dependence as well.

    Before I was one of those Mums just took everybody around wherever they wanted to go, do all their sports, wherever they wanted to do, sleepovers at people’s houses. I was a taxi driver, cooking, cleaning, I did it all. So I think I realised I was going to need help with that, which I did get. I was lucky I could get full-time carers, so I had people coming during the week. From 8am in the morning till 5pm in the afternoon. So they took over helping me, getting kids ready for school. And the good thing was I think they were all young teenagers. They learnt very early on how to look after themselves, which was really lovely. They were amazing. I was so lucky that… I’ve got two daughters and a son and my 2 oldest daughters basically took upon themselves to say, how can we help mum do what she needs to get done? They were just amazed. My kids were just onto it. I was so lucky that they don’t really see it as an issue anymore.

    We are fully onto if we’re going to go anywhere, we’ve got it all sorted as far as accessibility. One of my daughters is really into finding different ways of being able to help me in many ways with equipment and so forth. They’re just really, I mean they’re all grown up now and adults, but they were just amazing.

    I was lucky in the fact that I had that experience of wanting to be physically active when I had my accident because I thought I don’t want this to stop. I want to find out many ways of being able to do physical activity after, how to swim, possibly how to ride a bike, do all that kind of stuff. So I came, I think coming from that background was really good for me as well. I was really lucky that when I was, because I was into cycling a lot, that my group of friends that I was with at the time when I was cycling continued to be my group of friends from all these years. They never stopped. You often hear the stories of you find out who your friends really are when something dramatic like this happens to you, but they stuck by me, which was really great. So that continued on for me.

    Nothing else much really changed, I think. I still, I mean, we like to go to the movies a lot, so I never stopped going to the theatres. We still continued to travel when we needed to, going overseas and things.

    So when I left Shenton Park after the six months and I said, are there any physical therapy programs out in the community? The answer was basically no back then, and to just go and have a good life. And I said, no, I’m not going to do that. So of course, like most people, I got online and I looked around and I found the Walk On program in California. And I went on to some of those videos. which looked amazing because people were getting up and walking from those videos. And I went, that’s crazy. So I thought, how do I get in touch with these people I’d like to do? Not that I wanted to walk again, but I just wanted to get to do a physiotherapy program. And then on the, I think on the site, there was this little box in the corner saying, coming to Australia. And I went, what? So I contacted Sydney and I had an interview up there at the university where they’d just started the program and they said, guess what, we’re bringing it to Perth in a little while and I said, great, sign me up. So I did. And that’s how it happened.

    I didn’t have any major goals, I guess, thinking, oh yeah, I’m going to get up and walk, or, I did have some function still, but I wasn’t really sure of what I was going to expect. So I basically went in there with an open mind, thinking, we’ll see what they can provide, and been here ever since, especially with My transfers, that’s been a big deal for me to be able to be independent in that respect, that I’m not relying on someone or a sling to get me across from somewhere to another. So my independence in that is really important. I think if you’ve got other people in your group who are doing this for you, they can only do so much. But coming from yourself, exactly how you feel, what your body needs. Don’t rely on everybody else to be able to tell you what you think you should be doing. It’s more about travelling. It’s me being able to go to visit my kids, I think, and also continue to do trips overseas. I think I’m lucky that I’m in a reasonably healthy condition right now, so in my later stages of life. So I think that’s what I’m looking forward to. I mean every other part of my life is being made possible by what I do here and I will not stop doing this until I can’t ever get out of bed. Because I just think NeuroMoves is just amazing. I’m grateful for the fact that they’ve come here to Perth and that there is a NeuroMoves program still running.

    Want to learn more about NeuroMoves?

    NeuroMoves is a specialised exercise physiology and physiotherapy service for people with disability and neurological conditions. Find out more about how they can help you, or a loved one, by visiting the NeuroMoves website.

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