News
Dr Phil interviews 17 year old Jake and his Mum about not letting Duchenne Muscular Dystrophy (DMD) get in the way of living a great life. A medical doctor also explains a little about DMD. Jake’s motto is “Don’t live the diagnosis, live the life”
Dive into our new Peer Connect Calendar for July-December and discover new ways to connect, learn and get involved. Plus, registrations for NIRD are now open, get a first look at Summer Break, and stay informed as changes to NDIS legislation continue to unfold.
This edition celebrates the incredible impact you made at the Big Red Roll + Stroll, and invites you to save the date for NIRD 2026. Read about how Peer Connect Local is helping people across regional NSW find connection, support and belonging closer to home.
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 […]
An annual online seminar that brings together the country’s leading experts to provide our community with the latest neuromuscular research.
A monthly virtual catch up for mothers in our community to share stories and connect in a casual environment.
Say hello & contact our friendly team today.
Email: info@mdnsw.org.au
Phone: (02) 9888 5711
Freecall: 1800 635 109
Muscular Dystrophy NSW
ABN 11 774 587 436
Phone: (02) 9888 5711
Freecall: 1800 635 109
Email: info@mdnsw.org.au
Postal Address: PO Box 3071, North Strathfield NSW 2137
Muscular Dystrophy NSW would like to acknowledge the Traditional Custodians of the land on which we live and work, and we pay our respects to their Elders past and present. We extend that respect to all Aboriginal and Torres Strait Islander peoples.
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