This Christmas, children with neuromuscular conditions need to know they're not alone.
Living with a neuromuscular condition can be isolating, especially at this time of year. Families rely on vital programs and services to help children thrive and feel supported.
Your gift funds the programs and support services that bring connection, hope, and community to kids like Emma.
• 41,000+ Australians live with a neuromuscular condition
• Programs include camps, peer support, and family services
• Every gift helps ensure no child faces the festive season alone
Thanks to a generous group of supporters, today every dollar you donate will be MATCHED, dollar-for-dollar.
That means your $50 becomes $100.
Your $100 becomes $200.
Your $500 becomes $1,000.
But here's the catch: The matching funds are LIMITED.
Once they run out, they're gone.
Your donation is secure and protected.
-37779fa4-eb99-49d1-93e1-80e6bc7cbc86.jpg)
Emma found a community, support and connection.
Emma was diagnosed with Charcot-Marie-Tooth disease (CMT) at age 12 after years of uncertainty. Her condition affects her muscles and movement, meaning everyday activities and school can be a challenge.
With support from Muscular Dystrophy Australia, Emma has been able to access vital programs like Camp MDA, where she makes friends, builds confidence, and participates in activities tailored to her needs. Debbie, her mum, says:
“Emma loved spending time at Camp MDA. She grew in confidence and plans to attend again next year. The camp was fantastic, with carers and medical staff ensuring every child was well supported.”
Emma’s journey shows just how much difference the right support can make. From programs for young children to initiatives like MDA InnovAITe, which helps teens and young adults connect, build skills, and explore new technology, MDA ensures children and families have the resources to live fuller, more independent lives.
Your gift helps children like Emma access life-changing support and programs, from camps and peer networks to InnovAITe programs for teens and young adults. Every donation helps MDA provide care, connection, and opportunities for children to thrive — and ensures no child has to face a neuromuscular condition alone this festive season.
Your gift supports
Camp MDA
Connecting children with others who share their journey, building confidence and lasting friendships in a supportive environment.
MDA InnovAITe
Empowering young people through a 12-month program designed to build confidence and prepare them for adulthood.
MDA Connect
Our client services hub is the first place families turn after diagnosis - providing crucial information, support, and connections to resources.
‘When I think of what the future will bring. My goal for Emma, is not just about maintaining the daily routine but giving Emma opportunities for her to develop and keep her independence.’
- Debbie, Emma's mother
Children need your support
41,000+
Australians living with muscular dystrophy
32,505
People reached by MDA
programs in 2024
1 in 2,500
Children affected by neuromuscular conditions
-46c5bc35-2375-4ef8-ab8c-2ad22a98c756.png)
"With donor support, MDA can continue to build an impactful program where young people living with neuromuscular diseases can learn more about themselves physically and emotionally, in a safe space – a place where they can make friends and are accepted for who they are."
– Mary Orgill, Head of Programs & Impact
Thank you to our amazing supporters, together we are building a brighter future for people with muscular dystrophy.
This Christmas, Give Connection & Support
No child should face a neuromuscular condition alone. Your gift funds the programs and support services
that bring hope, community, and confidence to children and families when they need it most.
Thanks to a generous group of supporters, today every dollar you donate will be MATCHED, dollar-for-dollar
That means your $50 becomes $100.
Your $100 becomes $200.
Your $500 becomes $1,000.
But here's the catch: The matching funds are LIMITED.
Once they run out, they're gone.
Your donation is secure and protected.
This Christmas, children with neuromuscular conditions need to know they're not alone.
Living with a neuromuscular condition can be isolating, especially at this time of year. Families rely on vital programs and services to help children thrive and feel supported.
Your gift funds the programs and support services that bring connection, hope, and community to kids like Emma.
• 41,000+ Australians live with a neuromuscular condition
• Programs include camps, peer support, and family services
• Every gift helps ensure no child faces the festive season alone
Give today to provide essential care, connection, and opportunities for children like Emma to participate fully in life.
This Christmas, children with neuromuscular conditions need to know they're not alone.
Living with a neuromuscular condition can be isolating, especially at this time of year. Families rely on vital programs and services to help children thrive and feel supported.
Your gift funds the programs and support services that bring connection, hope, and community to kids like Emma.
• 41,000+ Australians live with a neuromuscular condition
• Programs include camps, peer support, and family services
• Every gift helps ensure no child faces the festive season alone
Thanks to a generous group of supporters, today every dollar you donate will be MATCHED, dollar-for-dollar.
That means your $50 becomes $100.
Your $100 becomes $200.
Your $500 becomes $1,000.
But here's the catch: The matching funds are LIMITED.
Once they run out, they're gone.
Emma found a community, support and connection.
Emma was diagnosed with Charcot-Marie-Tooth disease (CMT) at age 12 after years of uncertainty. Her condition affects her muscles and movement, meaning everyday activities and school can be a challenge.
With support from Muscular Dystrophy Australia, Emma has been able to access vital programs like Camp MDA, where she makes friends, builds confidence, and participates in activities tailored to her needs. Debbie, her mum, says:
“Emma loved spending time at Camp MDA. She grew in confidence and plans to attend again next year. The camp was fantastic, with carers and medical staff ensuring every child was well supported.”
Emma’s journey shows just how much difference the right support can make. From programs for young children to initiatives like MDA InnovAITe, which helps teens and young adults connect, build skills, and explore new technology, MDA ensures children and families have the resources to live fuller, more independent lives.
Your gift helps children like Emma access life-changing support and programs, from camps and peer networks to InnovAITe programs for teens and young adults. Every donation helps MDA provide care, connection, and opportunities for children to thrive — and ensures no child has to face a neuromuscular condition alone this festive season.
Your gift supports
Camp MDA
Connecting children with others who share their journey, building confidence and lasting friendships in a supportive environment.
MDA InnovAITe
Empowering young people through a 12-month program designed to build confidence and prepare them for adulthood.
MDA Connect
Our client services hub is the first place families turn after diagnosis - providing crucial information, support, and connections to resources.
‘When I think of what the future will bring. My goal for Emma, is not just about maintaining the daily routine but giving Emma opportunities for her to develop and keep her independence.’
- Debbie, Emma's mother
‘When I think of what the future will bring. My goal for Emma, is not just about maintaining the daily routine but giving Emma opportunities for her to develop and keep her independence.’
- Debbie, Emma's mother
Children need your support
41,000+
Australians living with muscular dystrophy
41,000+
Australians living with muscular dystrophy
32,505
People reached by MDA
programs in 2024
1 in 2,500
Children affected by neuromuscular conditions
32,505
People reached by MDA
programs in 2024
1 in 2,500
Children affected by neuromuscular conditions
"With donor support, MDA can continue to build an impactful program where young people living with neuromuscular diseases can learn more about themselves physically and emotionally, in a safe space – a place where they can make friends and are accepted for who they are."
– Mary Orgill, Head of Programs & Impact
Thank you to our amazing supporters, together we are building a brighter future for people with muscular dystrophy.
This Christmas, Give Connection & Support
No child should face a neuromuscular condition alone. Your gift funds the programs and support services
that bring hope, community, and confidence to children and families when they need it most.
This Christmas, Give Connection & Support
No child should face a neuromuscular condition alone. Your gift funds the programs and support services
that bring hope, community, and confidence to children and families when they need it most.
