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Bridget, Blake and Angela took on the Larapinta Adventure for different reasons, but with one shared purpose – to support the next generation of young people living with neuromuscular conditions. […]

Every year, we run a Community Survey to give you the chance to tell us what’s working, what needs work, what we should be prioritising and how our programs are serving you and […]

By Jaxon Taylor Living with a disability can change your entire outlook on life. For many, adapting is just a part of life. Yet for some, such as Chris and […]

By Jaxon Taylor Growing up with spinal muscular atrophy (SMA) looks different for everyone. For Sam and Jamieson, both young adults living with SMA, one factor shaped their experience more […]

By Jaxon Taylor Sometimes the most fascinating subjects can become more than just a passion. They can become your whole world.  Chris is an MDNSW community member who is currently undertaking a […]

By Jaxon Taylor Last month, several MDNSW participants took part in the 2026 Australian Powerchair Football Association (APFA) Club Championship, Australia’s elite powerchair football competition.  This national competition, held yearly, saw 10 teams face off to take home the title of Club Champions for 2026.   Powerchair […]

There are some life moments many parents remember vividly. The days or weeks after their child is diagnosed with a neuromuscular condition is often one of them.   Life suddenly fills with unfamiliar words, […]

Best friends Mitch and Julie have always shared a love of adventure and creativity, which shines through their debut children’s book A Dash of Adventure. It’s a story that celebrates […]

We’re aware of the recent NDIS changes to short term respite (STR), previously known as short term accommodation (STA). We understand these changes may affect some members of our community […]