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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
Spring Appeal 2025
Your Ticket = Real Support for Families Like Sue and David’s
Sue’s son David lives with a neuromuscular condition. Each day brings uncertainty - they don’t know when David might lose another ability, or how much more support he’ll need. The physical challenges are hard, but the emotional strain can be just as exhausting.
That’s why Muscular Dystrophy Queensland launched a free social work support program - to give families like Sue and David a safe place to talk, offload their fears and build the resilience they need to keep going.
“Having a safe, understanding place to talk, without guilt or fear, allowed my worries to finally spill out,” Sue says. “It made a world of difference.”
This vital program is funded through generous donations and supporters like you buying tickets in our Lucky 13 Lottery. Every ticket sold helps fund this lifeline - so families don’t have to face these dark moments alone.
The demand for support is growing faster than we can keep up - but your ticket can help close that gap.
Buy a ticket today - and make sure families like Sue and David’s get the care and support they can’t go without.
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.
