June 2025: Talking Point
Get ready to dive into the latest update on what’s new in the world of MDNSW! Read the September issue of Talking Point here!
News, Fundraising
On Sunday, March 23, we were honoured to welcome partners, donors and friends – both longstanding and new – to our inaugural Sunday Soiree. Graciously hosted by the Montrone family in their elegant Glebe courtyard, the afternoon buzzed with warmth, connection and a shared purpose: supporting young people living with neuromuscular conditions.
The afternoon included fundraising activities, including a raffle, silent auction and our ever-popular ‘wine wall.’ Thanks to the generosity of our guests, we’re delighted to share that the event raised an incredible $70,000 in support of our work!
Our Senior Community Support Specialist, Carolyn Campbell-McClean, expertly MC’d the event, infusing humour and heart into every moment. Among the afternoon’s highlights was a special address from Her Excellency the Honourable Margaret Beazley AC KC, Governor of New South Wales and Patron of Muscular Dystrophy NSW (MDNSW). Her Excellency spoke with sincerity about MDNSW’s longstanding role in the neuromuscular community and her hopes for our future.
The event was designed to showcase our work with young people, especially during life’s transitions. From Young Adults Retreats, NDIS Support Coordination, Duke of Edinburgh Award support and a host of other social events throughout the year, our programs give young people the tools and resources to thrive.
To bring this to life, four powerful stories were shared:
Carolyn also shared a moving testimony from 25-year-old Scott Green who lives with Duchenne muscular dystrophy. He has been involved with MDNSW since 2011. In that time, he has attended countless MDNSW camps and participated in MDNSW’s Duke of Edinburgh program. He also took part in the Surf Life Saving Training Program at Coogee Surf Lifesaving Club, designed for individuals living with neuromuscular conditions.
Their stories reminded everyone in the courtyard of why we gathered – to ensure this kind of support continues to be available to all who need it.
As Robert so eloquently put it: “At Muscular Dystrophy NSW, we are more than just an organisation; we are a lifeline for individuals and families navigating life with a neuromuscular condition. Our vision is simple yet powerful: that every person with a neuromuscular condition can live a life they choose”
To everyone who attended, supported and made this special afternoon possible – thank you. You’ve helped bring our vision to life.
Special thanks to:
Get ready to dive into the latest update on what’s new in the world of MDNSW! Read the September issue of Talking Point here!
Get ready to dive into the latest update on what’s new in the world of MDNSW! Read the September issue of Talking Point here!
Say hello & contact our friendly team today.
Email: info@mdnsw.org.au
Phone: (02) 9888 5711
Freecall: 1800 635 109
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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