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Muscular Dystrophy Queensland has built on the dedicated efforts of these early volunteers towards a future where neuromuscular conditions no longer limit choice and control. People living with such conditions, like many living with a disability, are often excluded from participating in many areas of life. Our aim is to support our community members to make the most of opportunities and fulfil their potential to live the lives they choose.
Today, Muscular Dystrophy Queensland provides vital services and support for local people living with neuromuscular conditions and their families, throughout every life stage. As well as NDIS plan management, support coordination, and allied health services Muscular Dystrophy Queensland provides free charitable services – including an Infoline, advocacy, social support, equipment loans, extended care, and more – that rely entirely on the generous support of donors and philanthropic partners.
Where The Proceeds Go
Red Bow Appeal 2026
Red Bow Appeal 2026
This Red Bow Appeal, your ticket can help families like Leona’s stay strong, supported and connected.
Leona is raising two children while living with a progressive neuromuscular condition that affects her balance, strength and mobility. Each year brings new challenges and uncertainty, but like many parents we support, she is determined to keep showing up for the moments that matter most.
When Leona reached out to Muscular Dystrophy Queensland, she found more than information. She found a team who helped her navigate the health system, access orthotics and connect with physiotherapy and occupational therapy supports that improve her daily life. Just as importantly, she found a community that understands her journey.
Red Bow is about making sure no family walks this road alone. With the right support, Leona can focus on what matters most, being present for her children and building a future filled with possibility.
Each ticket you buy in the Lucky 13 Lottery helps fund vital services like this, ensuring Queenslanders with neuromuscular conditions receive guidance, therapy connections and community when they need it most.
This March, help us make sure families like Leona’s are never left to face these challenges alone.
Buy your ticket or make a donation today and give the gift of strength, belonging and hope.
1978
A group of families whose children had muscular dystrophy joined forces to raise awareness and funds. The first executive board members of “The Muscular Dystrophy Family Support Association of Queensland” were appointed on 25 June 1978.
1991
MDQ’s first Executive Director, Mr Peter Denham is appointed. Mr Denham lead the organisation until 2007.
1992
The organisation became incorporated and known as ‘South East Queensland Muscular Dystrophy Assoc. Inc.’ The newly incorporated organisation also achieved charitable status as per the Collections Act. Equipment loans including electric beds, ventilators and wheelchairs are provided to families with muscular dystrophy in addition to counselling and support services.
1994
All Hallows’ School Year 11 students collect donations for Muscular Dystrophy Queensland on the streets of Brisbane for Red Bow Day. This annual tradition still continues more than 25 years on.
Andrew, Greg and James Bell from Ray White Surfers Paradise host an inaugural Ball raising funds for muscular dystrophy. The annual Ball has now raised millions of dollars over the past 25+ years.
1995
The Brisbane Harley Owners Group host their first charity ride, raising funds for people with muscular dystrophy. More than 20 years later, this annual ride is a highlight on the MDQ calendar.
1999
The organisation moves from premises at Rocklea Markets to inner city Wharf Street.
2017
MDQ becomes an Australian Public Company limited by guarantee in preparation for the introduction of the NDIS which will allow the organisation to provide chargeable services to clients who’s supports will be funded through the new scheme. Charitable services continue for those not eligible for NDIS funding.
2018
MDQ celebrates its 40th birthday.
2019
NDIS rolls out across Queensland and MDQ employ specialised Allied Health therapists to provide services to clients.
Our Annual Reports
In May each year, Muscular Dystrophy Queensland publishes an annual report for presentation to our members at our Annual General Meeting.
Our Board
Muscular Dystrophy Queensland is fortunate to boast a dedicated Board, who ensure the organisation remains focused on achieving our vision.
Our Leadership Team
Meet the Muscular Dystrophy Queensland Leadership Team and staff.
Our Vision
Life without limits for people with neuromuscular conditions.
Life without limits for people with neuromuscular conditions.
Our Mission
Muscular Dystrophy Queensland empowers people living with muscular dystrophy and similar neuromuscular conditions to make the most of opportunities and live the lives they choose.
Muscular Dystrophy Queensland empowers people living with muscular dystrophy and similar neuromuscular conditions to make the most of opportunities and live the lives they choose.
Our Values
KNOWLEDGE
We grow our knowledge: listening and adapting to meet the changing needs of our neuromuscular community. We amplify the voice of the neuromuscular community for their benefit and wellbeing.
SERVICE
We work with care, dedication and excellence to serve our neuromuscular community.
COMMUNITY
We are a diverse group: people living with neuromuscular conditions and those who support them. We value inclusion, connection, respect and shared experience.
