Help Zack Live His Best Life With Duchenne
Donation protected
Zack McCrea is a hilarious, loving, caring amazing 12 year old boy - who lights up his parents world.
Zack was born completely normal, but at just 2 years old, Zack's parents Danielle & Mat received devastating news no parent wants, that their beautiful boy had a fatal genetic disease called Duchenne Muscular Dystrophy.
Danielle & Mat were given a life expectancy for Zack of 16 years of age at this time.
Duchenne Muscular Dystrophy breaks down all muscle within the body, including the liver, lungs and heart, until you can no longer move or breathe. This disease takes takes away the ability to run, climb, walk and even cuddle. Eventually it will take away the ability to hold your hand, as a parent, you can only imagine that this has been the absolutely most painful experience for Zack's family.
The cost of simply living as a family of 6, as well as other costs involved for Zack, are just not attainable for their family, and its making it harder each day for them to cope with making Zack's remaining life as happy & as care free as possible, the way any child's life should be.
I'm asking for donations that go directly to Zack & his family, to make desperate modifications to the family car as well as making some of his own dreams possible, so Zack & his family are able to enjoy and treasure the time they have with him. Even the smallest donation can help, every dollar counts and so does every share. Whether you are able to donate or not, please SHARE this with your friends and family. The more you can share, the more people we will reach.
Donations will Go toward;
*Car modifications. To make outings easier for when Zack can no longer walk and need's the constant use of a wheelchair - unfortunately the NDIS are unable to fund this due to their car not meeting age and kilometres requirements.
*Experiences Zack would love to do and see before he leaves us, precious memories for his family.
Danielle & Mat are amazingly beautiful people, they're not people who ever ask for help, or anything for that matter, so I've made this GoFundMe to ask for them.
I know everyone's support would mean the world to them and they would be forever grateful to be able to stop worrying about how they're going to get everything they need, & instead be able to focus their time and energy on Zack, where it should be focused. Time is everything . Time is precious.
Below is a note from Danielle, Zack's Mother.
"If I could ask for anything, it would be for our son not to have this disease, but he does. Any help anyone can give would be greatly appreciated, in making Zack's life a happy one for everyone to remember him by."
Zack was born completely normal, but at just 2 years old, Zack's parents Danielle & Mat received devastating news no parent wants, that their beautiful boy had a fatal genetic disease called Duchenne Muscular Dystrophy.
Danielle & Mat were given a life expectancy for Zack of 16 years of age at this time.
Duchenne Muscular Dystrophy breaks down all muscle within the body, including the liver, lungs and heart, until you can no longer move or breathe. This disease takes takes away the ability to run, climb, walk and even cuddle. Eventually it will take away the ability to hold your hand, as a parent, you can only imagine that this has been the absolutely most painful experience for Zack's family.
The cost of simply living as a family of 6, as well as other costs involved for Zack, are just not attainable for their family, and its making it harder each day for them to cope with making Zack's remaining life as happy & as care free as possible, the way any child's life should be.
I'm asking for donations that go directly to Zack & his family, to make desperate modifications to the family car as well as making some of his own dreams possible, so Zack & his family are able to enjoy and treasure the time they have with him. Even the smallest donation can help, every dollar counts and so does every share. Whether you are able to donate or not, please SHARE this with your friends and family. The more you can share, the more people we will reach.
Donations will Go toward;
*Car modifications. To make outings easier for when Zack can no longer walk and need's the constant use of a wheelchair - unfortunately the NDIS are unable to fund this due to their car not meeting age and kilometres requirements.
*Experiences Zack would love to do and see before he leaves us, precious memories for his family.
Danielle & Mat are amazingly beautiful people, they're not people who ever ask for help, or anything for that matter, so I've made this GoFundMe to ask for them.
I know everyone's support would mean the world to them and they would be forever grateful to be able to stop worrying about how they're going to get everything they need, & instead be able to focus their time and energy on Zack, where it should be focused. Time is everything . Time is precious.
Below is a note from Danielle, Zack's Mother.
"If I could ask for anything, it would be for our son not to have this disease, but he does. Any help anyone can give would be greatly appreciated, in making Zack's life a happy one for everyone to remember him by."
Organizer and beneficiary
Nikki Newman
Organizer
The Entrance North, NSW
Danielle Savage
Beneficiary