Walk 4 Duchenne – Melbourne, VIC.

28th February – 7th March 2020.

The Walk 4 Duchenne will be taking place in Melbourne Victoria.

A 186km walk visiting 11 schools of boys living with Duchenne, raising awareness and vital funds in our fight for a cure.

WALK EVERY STEP.

0km
Walking from Geelong to Epping, Victoria
0 days
Walking approximately 20km per day
0 schools
Visiting schools with kids living with Duchenne

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Registered Walkers

Romeo georges

Dear family and friends, Duchenne muscular dystrophy (a muscle wasting condition) affects young boys and in…

$0 of $10,000 raised

Romeo georges

$0 of $10,000 raised

Dear family and friends, Duchenne muscular dystrophy (a muscle wasting condition) affects young boys and in rare cases girls.

Currently there’s no cure and no one survives.

On the 28th of February 2020, Elie Eid, the founder of Save Our Sons, along with myself and a group of walkers will be walking  186 KMS over nine days across Melbourne, visiting schools of Kids with Duchenne to raise vital awareness and funds.No matter how tough this may be for me physically, it does not compare to the lifetime of hardship that kids and families living with this cruel condition have to endure.Your donation, no matter how big or small will go a long way in making a difference in their lives today.

Thank you in advance for your generosity.

$
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Donation Total: $1.00

{amount} donation plus {fee_amount} to help cover fees.

Sue Tantaro

Dear family and friends, Duchenne muscular dystrophy (a muscle wasting condition) affects young boys and in…

$0 of $10,000 raised

Sue Tantaro

$0 of $10,000 raised

Dear family and friends, Duchenne muscular dystrophy (a muscle wasting condition) affects young boys and in rare cases girls.

Currently there’s no cure and no one survives.

On the 28th of February 2020, Elie Eid, the founder of Save Our Sons, along with myself and a group of walkers will be walking 186 KMS over nine days across Melbourne, visiting schools of Kids with Duchenne to raise vital awareness and funds.No matter how tough this may be for me physically, it does not compare to the lifetime of hardship that Joshua, our family, other children and families living with this cruel condition have to endure.Your donation, no matter how big or small will go a long way in making a difference in their lives today.

Thank you in advance for your generosity.

$
Select Payment Method
Personal Info

Credit Card Info
This is a secure SSL encrypted payment.

Donation Total: $1.00

{amount} donation plus {fee_amount} to help cover fees.

Michelle Jones

Dear family and friends, Duchenne muscular dystrophy (a muscle wasting condition) affects young boys and in…

$0 of $10,000 raised

Michelle Jones

$0 of $10,000 raised

Dear family and friends, Duchenne muscular dystrophy (a muscle wasting condition) affects young boys and in rare cases girls.

Currently there’s no cure and no one survives.

On the 28th of February 2020, Elie Eid, the founder of Save Our Sons, along with myself and a group of walkers will be walking  186 KMS over nine days across Melbourne, visiting schools of Kids with Duchenne to raise vital awareness and funds.No matter how tough this may be for me physically, it does not compare to the lifetime of hardship that Joshua, our family, other children and families living with this cruel condition have to endure.Your donation, no matter how big or small will go a long way in making a difference in their lives today.

Thank you in advance for your generosity.

$
Select Payment Method
Personal Info

Credit Card Info
This is a secure SSL encrypted payment.

Donation Total: $1.00

{amount} donation plus {fee_amount} to help cover fees.

Vanessa Brown

Dear family and friends, Duchenne muscular dystrophy (a muscle wasting condition) affects young boys and in…

$70 of $10,000 raised

Vanessa Brown

$70 of $10,000 raised

Dear family and friends, Duchenne muscular dystrophy (a muscle wasting condition) affects young boys and in rare cases girls.
Currently there’s no cure and no one survives.

As many of you know, our two boys Riley and Tarek were diagnosed with this devastating disability in 2016. Since then our lives haven’t been the same. The doctors appointments, therapist appointments, grief and daily stresses have now become our new normal but no matter what we face we will do whatever we can to help find a cure for our boys.

On the 28th of February 2020, Elie Eid, the founder of Save Our Sons, along with myself and a group of walkers will be walking  186 KMS over nine days across Melbourne, visiting schools of Kids with Duchenne to raise vital awareness and funds.No matter how tough this may be for me physically, it does not compare to the lifetime of hardship that kids and families living with this cruel condition have to endure.Your donation, no matter how big or small will go a long way in making a difference in their lives today.

Thank you in advance for your generosity.

$
Select Payment Method
Personal Info

Credit Card Info
This is a secure SSL encrypted payment.

Donation Total: $1.00

{amount} donation plus {fee_amount} to help cover fees.

Icon Construction Group

Dear family and friends, Duchenne muscular dystrophy (a muscle wasting condition) affects young boys and in…

$0 of $10,000 raised

Icon Construction Group

$0 of $10,000 raised

Dear family and friends, Duchenne muscular dystrophy (a muscle wasting condition) affects young boys and in rare cases girls.

Currently there’s no cure and no one survives.

On the 28th of February 2020, Elie Eid, the founder of Save Our Sons, along with myself and a group of walkers will be walking  186 KMS over nine days across Melbourne, visiting schools of Kids with Duchenne to raise vital awareness and funds.No matter how tough this may be for me physically, it does not compare to the lifetime of hardship that kids and families living with this cruel condition have to endure.Your donation, no matter how big or small will go a long way in making a difference in their lives today.

Thank you in advance for your generosity.

$
Select Payment Method
Personal Info

Credit Card Info
This is a secure SSL encrypted payment.

Donation Total: $1.00

{amount} donation plus {fee_amount} to help cover fees.

Michael Zann

Dear family and friends, Duchenne muscular dystrophy (a muscle wasting condition) affects young boys and in…

$0 of $10,000 raised

Michael Zann

$0 of $10,000 raised

Dear family and friends, Duchenne muscular dystrophy (a muscle wasting condition) affects young boys and in rare cases girls.

Currently there’s no cure and no one survives.

On the 28th of February 2020, Elie Eid, the founder of Save Our Sons, along with myself and a group of walkers will be walking 186 KMS over nine days across Melbourne, visiting schools of Kids with Duchenne to raise vital awareness and funds.No matter how tough this may be for me physically, it does not compare to the lifetime of hardship that Joshua, our family, other children and families living with this cruel condition have to endure.Your donation, no matter how big or small will go a long way in making a difference in their lives today.

Thank you in advance for your generosity.

$
Select Payment Method
Personal Info

Credit Card Info
This is a secure SSL encrypted payment.

Donation Total: $1.00

{amount} donation plus {fee_amount} to help cover fees.

Nicola Malak

Dear family and friends, Duchenne muscular dystrophy (a muscle wasting condition) affects young boys and in…

$0 of $10,000 raised

Nicola Malak

$0 of $10,000 raised

Dear family and friends, Duchenne muscular dystrophy (a muscle wasting condition) affects young boys and in rare cases girls.

Currently there’s no cure and no one survives.

On the 28th of February 2020, Elie Eid, the founder of Save Our Sons, along with myself and a group of walkers will be walking  186 KMS over nine days across Melbourne, visiting schools of Kids with Duchenne to raise vital awareness and funds.No matter how tough this may be for me physically, it does not compare to the lifetime of hardship that kids and families living with this cruel condition have to endure.Your donation, no matter how big or small will go a long way in making a difference in their lives today.

Thank you in advance for your generosity.

$
Select Payment Method
Personal Info

Credit Card Info
This is a secure SSL encrypted payment.

Donation Total: $1.00

{amount} donation plus {fee_amount} to help cover fees.

Michael Malak

Dear family and friends, Duchenne muscular dystrophy (a muscle wasting condition) affects young boys and in…

$0 of $10,000 raised

Michael Malak

$0 of $10,000 raised

Dear family and friends, Duchenne muscular dystrophy (a muscle wasting condition) affects young boys and in rare cases girls.

Currently there’s no cure and no one survives.

On the 28th of February 2020, Elie Eid, the founder of Save Our Sons, along with myself and a group of walkers will be walking  186 KMS over nine days across Melbourne, visiting schools of Kids with Duchenne to raise vital awareness and funds.No matter how tough this may be for me physically, it does not compare to the lifetime of hardship that kids and families living with this cruel condition have to endure.Your donation, no matter how big or small will go a long way in making a difference in their lives today.

Thank you in advance for your generosity.

$
Select Payment Method
Personal Info

Credit Card Info
This is a secure SSL encrypted payment.

Donation Total: $1.00

{amount} donation plus {fee_amount} to help cover fees.

Philip Iacovou

Dear family and friends, Duchenne muscular dystrophy (a muscle wasting condition) affects young boys and in…

$0 of $10,000 raised

Philip Iacovou

$0 of $10,000 raised

Dear family and friends, Duchenne muscular dystrophy (a muscle wasting condition) affects young boys and in rare cases girls.

Currently there’s no cure and no one survives.

On the 28th of February 2020, Elie Eid, the founder of Save Our Sons, along with myself and a group of walkers will be walking  172 KMS over six days across Melbourne, visiting schools of Kids with Duchenne to raise vital awareness and funds.No matter how tough this may be for me physically, it does not compare to the lifetime of hardship that kids and families living with this cruel condition have to endure.Your donation, no matter how big or small will go a long way in making a difference in their lives today.

Thank you in advance for your generosity.

$
Select Payment Method
Personal Info

Credit Card Info
This is a secure SSL encrypted payment.

Donation Total: $1.00

{amount} donation plus {fee_amount} to help cover fees.

Team Sasha

Dear family and friends, Duchenne muscular dystrophy (a muscle wasting condition) affects young boys and in…

$0 of $10,000 raised

Team Sasha

$0 of $10,000 raised

Dear family and friends, Duchenne muscular dystrophy (a muscle wasting condition) affects young boys and in rare cases girls.

Currently there’s no cure and no one survives.

On the 28th of February 2020, Elie Eid, the founder of Save Our Sons, along with myself and a group of walkers will be walking  186 KMS over nine days across Melbourne, visiting schools of Kids with Duchenne to raise vital awareness and funds.No matter how tough this may be for me physically, it does not compare to the lifetime of hardship that kids and families living with this cruel condition have to endure.Your donation, no matter how big or small will go a long way in making a difference in their lives today.

Thank you in advance for your generosity.

$
Select Payment Method
Personal Info

Credit Card Info
This is a secure SSL encrypted payment.

Donation Total: $1.00

{amount} donation plus {fee_amount} to help cover fees.

Sasha Robertson

Dear family and friends, Duchenne muscular dystrophy (a muscle wasting condition) affects young boys and in…

$0 of $10,000 raised

Sasha Robertson

$0 of $10,000 raised

Dear family and friends, Duchenne muscular dystrophy (a muscle wasting condition) affects young boys and in rare cases girls.

Currently there’s no cure and no one survives.

On the 28th of February 2020, Elie Eid, the founder of Save Our Sons, along with myself and a group of walkers will be walking  186 KMS over nine days across Melbourne, visiting schools of Kids with Duchenne to raise vital awareness and funds.No matter how tough this may be for me physically, it does not compare to the lifetime of hardship that kids and families living with this cruel condition have to endure.Your donation, no matter how big or small will go a long way in making a difference in their lives today.

Thank you in advance for your generosity.

$
Select Payment Method
Personal Info

Credit Card Info
This is a secure SSL encrypted payment.

Donation Total: $1.00

{amount} donation plus {fee_amount} to help cover fees.

Anthony Mariniello

Dear family and friends, Our 9 year old son James has a terminal genetic muscle-wasting disease…

$1,023 of $10,000 raised

Anthony Mariniello

$1,023 of $10,000 raised

Dear family and friends,

Our 9 year old son James has a terminal genetic muscle-wasting disease called Duchenne Muscular Dystrophy

Currently, there’s no cure and no one survives.

This cruel disease will most likely see him confined to a wheelchair from around 10-12 years old, require a respirator in his teens and ultimately due to heart or respiratory failure will pass away before his 25th birthday.

James already suffers with 5 spinal compression fractures and we’ve recently discovered his heart has begun to fail.

As any father would, I refuse to watch my son slowly die before my eyes.

That’s why on the 28th of February 2020, Elie Eid, the founder of Save Our Sons, along with myself and a group of walkers will be walking  172 KMS over six days across Melbourne, visiting schools of Kids with Duchenne to raise vital awareness and funds for life-saving research and support services.

At 120 Kg’s No matter how tough this may be for me physically, it does not compare to the lifetime of hardship that James and other kids have to endure.

Your donation, no matter how big or small will go a long way in making a difference in saving James.

Please help save my son.

$
Select Payment Method
Personal Info

Credit Card Info
This is a secure SSL encrypted payment.

Donation Total: $1.00

{amount} donation plus {fee_amount} to help cover fees.