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    Your central hub for information, support tools, and practical advice.

    We have a wealth of knowledge to share with you about living with a spinal cord injury (SCI), and have pulled this together in this section to help you access the information you need, when you need it.

    Discover our resources

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    Carers Support
    Disability Advocacy
    Disability Awareness

    World MS Day 2026 – Mark and Marvin

    World MS Day is held each year on May 30th to raise awareness and share the lived experience of those...
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    Disability Awareness
    Education
    Life Stories

    Can You Ask That? Any Questions That You Wouldn’t Answer If Asked?

    What questions would our Peer and Family Support team have trouble answering?
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    Accessible Travel
    Disability Awareness
    Exercise and Rehabilitation

    How a Pacemaker Set The Course for a Trip of A Lifetime

    In this episode meet Luke Spencer and Kat Yee. At age 12, Luke was diagnosed with Fredrich’s Ataxia, and in...
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    Disability Awareness
    Education
    Life Stories

    Can You Ask That? How Much Did Your Wheelchair Cost?

    Depending on your needs, Dan, Heidz and Rob from SCIA's Peer and Family Support Team explain that it can get...
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    Life Stories

    Gary’s Story – Parkinson’s Awareness Month 2026

    For this year’s Parkinson’s Awareness month, we sat down with Gary, a NeuroMoves St Peters client, who shares his 14-year...
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    Disability Awareness
    Education
    Life Stories

    Can You Ask That? Can I Have a Go in Your Wheelchair?

    Have your mates had a go at your wheelchair? What did they think about it? Did they fall out?
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    World MS Day is held each year on May 30th to raise awareness and share the lived experience of those living with Multiple Sclerosis (MS).

    To recognise this important day, SCIA, in collaboration with our exercise service NeuroMoves, recently caught up with NeuroMoves Liverpool client Mark Elisha and his support worker Marvin Jaurigue. Diagnosed at just 24 years old, Mark candidly shares his journey with MS from his initial diagnosis, through to finding his community through Boccia.

    Reflecting on his last 13-years living with MS, Mark credits the NDIS and his support workers on the positive impact they have had in helping him along the way.

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