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We’re supporting the Australian Neuromuscular Disease Registry

…our community. We encourage all MDNSW members living with a neuromuscular condition to find out more by visiting the website and to register your interest. Find out more at www.australiannmdregistry.org.au…

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Covid-19 Hub from People with Disability Australia

…Australia has collected resources for people with disability and disability service providers on important COVID-19 information. Visit their website for new information and resources as they become available at www.pwd.org.au/covid-19-hub….

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Emergency COVID-19 Appeal

…types of complex, progressive Neuromuscular Conditions (NMCs) that affect 1 in every 1000 Australians. People living with neuromuscular conditions are one of the most vulnerable groups in our community during…

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Living Independently

…make it possible for people with high support needs to live independently if they choose to. Accommodation options are limited at the moment, but growing. Read the story here: www.abc.net.au/news/2020-07-15/new-disability-housing-giving-people-more-options…

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MDNSW Big Red Roll & Stroll Press Release

…with common symptoms being loss of muscle strength and function, loss of mobility, pain and fatigue. To promote this year’s campaign, MDNSW has rallied ambassadors from within the neuromuscular community,…

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Sugar Free September registration is now open!

…MD in NSW? Why not do something nice for your health whilst supporting our MD community? So, sign up at www.sugarfreeseptember.org.au and get ready to kick sugar’s butt this September!…

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Hundreds to gather at Parramatta Park to raise awareness for rare genetic disorder effecting 13,000 people in NSW

…is why events like this are so special. When we unite, we develop friendships, comradery, support and strength. To feel like you’re not alone, and part of a community that…

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Team MD legends going the extra mile

…and for raising awareness and vital funds for the Muscular Dystrophy NSW community! The 2022 Blackmores Sydney Running Festival is an iconic event with a spectacular course that includes a…

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FSHD Global Research Foundation’s “FSHD Medical Education Portal”

…they are encouraging the neuromuscular community to join the FSHD Global registry, to enable them to connect people living with FSHD to medical research institutions and biotechs researching and/or recruiting…

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Medical Info

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Help kids with Muscular Dystrophy by simply going Sugar Free!

…a tribe of others who knew exactly what we were going through. The community are so generous, not only with their advice but in their actions, with one family even…

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We need a treatment for adults with SMA

…needed by the community wanting access to treatment. Consumer comments are open till the 26th May at the Department of Health website. Even if you have submitted before or would…

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