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

Please ensure you have read the terms and conditions below, before completing the registration.

* Conditions apply

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Registered Walkers

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  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.

$
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Donation Total: $1.00

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

Elizabeth Ibrahim

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

$0 of $10,000 raised

Elizabeth Ibrahim

$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.

Anthony Mariniello

$0 of $10,000 raised

Anthony Mariniello

$0 of $10,000 raised
$
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Donation Total: $1.00

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

Evette Makari

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

$0 of $10,000 raised

Evette Makari

$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.

Eva Herzog

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

$0 of $10,000 raised

Eva Herzog

$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.

Citywide

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

$0 of $20,000 raised

Citywide

$0 of $20,000 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.

Carolyn Josephson

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

$0 of $10,000 raised

Carolyn Josephson

$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.

Team Victoria

Raising funds so we can find a cure for Duchenne Muscular Dystrophy and help improve the…

$0 of $180 raised

Team Victoria

$0 of $180 raised

Raising funds so we can find a cure for Duchenne Muscular Dystrophy and help improve the lives of those who are currently affected by DMD.

$
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Donation Total: $1.00

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

Voula Allimonos

1566

$0 of $500 raised

Voula Allimonos

$0 of $500 raised

Please provide a couple paragraphs describing why you want to support Walk 4 Duchenne. This will be posted directly on your donation form for others to see and help them want to support you.

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Donation Total: $1.00

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

Mia Timotheou

I am walking in honor of my little brother Lucas and all boys diagnosed with Duchenne.…

$0 of $100 raised

Mia Timotheou

$0 of $100 raised

I am walking in honor of my little brother Lucas and all boys diagnosed with Duchenne.
Lucas is not able to walk long distances anymore. ❤️

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This is a secure SSL encrypted payment.

Donation Total: $1.00

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

Riley and Cooper’s family

In May 2019, the twins, Riley and Cooper were diagnosed with Duchenne Muscular Dystrophy. We want…

$0 of $1,000 raised

Riley and Cooper’s family

$0 of $1,000 raised

In May 2019, the twins, Riley and Cooper were diagnosed with Duchenne Muscular Dystrophy. We want to raise funds to help find a cure for Riley and Cooper and other boys (and rare girls) like them.

$
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.