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Our Families
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Team Thomson
Montana suffered a traumatic brain injury in 2002 and at 8 years old continues to need considerable therapy, medical treatment, equipment and aids. We are grateful for the encouragement and support that we receive … more
Team Matthew
"Courage doesn't always roar. Sometimes courage is the little voice at the end of the day that says I'll try again tomorrow." Mary Anne Radmacher Imagine you are an independent, active, outgoing pers … more
Team Flynn
Flynn’s Story Flynn and his twin brother, Jack arrived in this world 16 weeks early giving us all a big shock! Flynn weighed 720 grams and Jack only 630 grams. As the boys required intensive medical attent … more
Team Jakob
When I grow up, I want to dance and sing on stage in front of everyone. Hi, my name is Jakob, I am 4 years old and I have cerebal palsy. I love music and when I grow up I want to be able to dance and sing on … more
Team Swan
My name is Quentin and I am currently 13yrs old. I have multiple disabilities and as my dad says this is what makes me one special kid. I have Cerebral Palsy, Epilepsy, Autism and I am vision impaired. I have a s … more
Team Calem
Hi, my name is Calem McDavid and I am 9 years old. My parents are Mum Summer and Dad Shane and they have a vision for me, it is my wish also and that is ‘To live life to my full potential and that I will be able to … more
Lachlan to America
Hi my name is Lachlan Stretton. I am 3 and have Cerebral Palsy - Spastic Triplegia. I was fortunate enough to win an Intense Therapy in Florida, USA for use during October 22 - November 9, 2012, to give me the c … more
Team Daniel
Hi, my name is Daniel and I am 5 years old. I live on the Far North Coast of NSW with my Mum & Dad (Michelle & Grant). I have Ataxic Cerebral Palsy (CP) which means my balance is poor and my muscle tone is l … more
Blaise
Our vision for Blaise is that he will continue to shoot for the stars with whatever challenges come his way. Hi! My name is Blaise, and I am 3 years old. I have Spastic Quadraplegic Cerebral Palsy, which means I … more
Sophie Hastie
REACH FOR THE SKY - TO MAINTAIN A GOOD QUALITY OF LIFE Hi, my name is Sophie Hastie. I am 10 years old and I have RETT SYNDROME, a rare neurodevelopmental disorder. I absolutely love to be taken out to access the c … more
