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Muscular Dystrophy Queensland is committed to a future where people living with neuromuscular conditions have the support, opportunities and connections they need to live the lives they choose.
People living with neuromuscular conditions often face complex challenges that can impact their independence, wellbeing and participation in everyday life. Our purpose is to ensure no individual or family faces these challenges alone.
Today, Muscular Dystrophy Queensland provides vital services and support to people living with neuromuscular conditions and their families across Queensland, at every stage of life.
Alongside NDIS plan management, support coordination and allied health services, we deliver a range of free charitable programs including advocacy, information and referral services, family connection events, equipment support, peer support and community programs. These services are made possible through the generosity of donors, partners and supporters who help us create stronger, more connected communities.
Where The Proceeds Go
Spring Appeal 2026
This Spring Appeal, your ticket can help families like Sandra's stay strong, supported and connected.
Sandra is raising two boys with Duchenne muscular dystrophy, a progressive condition that impacts every aspect of family life.
Despite the daily challenges, Sandra is focused on giving her boys every opportunity to thrive. When families like hers connect with Muscular Dystrophy Queensland, they find trusted guidance, allied health supports, family programs and a community that understands their journey.
This Spring Appeal is about ensuring no family faces muscular dystrophy alone. Each ticket you buy in the Lucky 13 Lottery helps fund vital services, support programs and connections for Queenslanders living with neuromuscular conditions.
This spring, help ensure families like Sandra's have the support, connection and hope they need. Buy your ticket or make a donation today.
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.
