Everything Else
The Loop Voices: Sarah adapts to the new normal
"Initially I sort of went, well, I won't be able to cope with this... and then I came to the realisation that I don't kn...
Everything Else
"Initially I sort of went, well, I won't be able to cope with this... and then I came to the realisation that I don't kn...
Everything Else
"When you're first diagnosed, the inclination is to wrap yourself in cotton wool, not to taken chances. But by taking ri...
Everything Else
Tristram explains how his Lego hobby is helping him maintain his finger strength.
Everything Else
Sarah shares some of the modifications she's made to her Kia Carnival.
Everything Else
Most neuromuscular conditions are progressive, which means they worsen with time. How do you deal with this?
Everything Else
Don't even get me started...! The Loop crew discuss the good, bad and ugly of disabled parking.
Everything Else
"Getting a diagnosis is a bit like being told you have to go to a foreign country you don't want to go to." Sarah shares...
Everything Else
"On bad days it's good to feel like I've got writing to turn to, that I can just escape for a while and not have to thin...
Everything Else
Tracey shows off her made-for-purpose adaptive clothing.
Everything Else
India shares her solution for storing and accessing her clean clothes after a shower.
Everything Else
The Loop crew discuss how they feel about living with their condition.
Everything Else
MC Wheels talks about the impact music has had on his life and coming to terms with his condition.
Everything Else
Sarah shares some of the modifications she's made to her Kia Carnival.
Everything Else
Being part of a community is vital for everyone. What does it mean to you?
Everything Else
How have you managed bullying and negative attention?
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Does your neuromuscular condition make you feel different?
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"If you get the opportunity to do something a little outside your comfort zone, just do it. Jump. Do it."
Everything Else
India shows off her tele-stick, which helps her pick things up from the ground.
To support and empower people living with a neuromuscular condition, their families and support network — created by Muscular Dystrophy Foundation Australia with the state-based MD organisations.
We acknowledge the Traditional Owners of Country throughout Australia and recognise their continuing connection to land, waters and culture. We pay respect to Elders past and present.