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.

Are you representing a company looking to walk as a relay? 2 or more walkers?

Register as a team

* Conditions apply

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Registered Walkers

Leanne James

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

$0 of $10,000 raised

Leanne James

$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.

$
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Donation Total: $1.00

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

Team Lucas

On September 5, 2011 3 days prior to Lucas Turning 5yo our little Superman Lucas was…

$150 of $10,000 raised

Team Lucas

$150 of $10,000 raised
On September 5, 2011 3 days prior to Lucas Turning 5yo our little Superman Lucas was diagnosed with Duchenne muscular dystrophy.
On this day 6 years ago our dreams for our son were ripped from under our feet, our life was turned upside down and inside out we have since lived with fear, anxiety, uncertainty and heartbreak all whilst trying to lead a ‘normal’ family life.
Lucas is a spontaneous case in our family.  The journey has been extremely difficult however with the support of our loved ones we find the strength to keep moving forward.
The fabulous five which make up ‘Team Lucas’ consists of Lucas’s parents, Mary & Harry, auntie Demmi and uncles Andy & Jason.
Lucas has so much zest for life, his smile lights up every room, his heart is full of love and the fire in his belly makes him a true fighter!  He has touched the life of so many people and leaves footprints in the hearts of those he meets.
We are walking for Lucas and all boys diagnosed with DMD.
The pain we will experience in our legs does not compare to the pain the boys experience everyday.  The everyday struggle to walk and run and keep up with their peers, the want to play soccer or any sport only becomes more challenging until it is taken away from them!
We will do whatever it takes to support the organisation supporting Lucas and all boys- Save Our Sons Duchenne Australia gives us hope and support like no other organisation around the world.
Hope that one day a diagnosis of Duchenne does not mean the loss of a beloved family member!
$
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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…

$190 of $10,000 raised

Michelle Jones

$190 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…

$7,220 of $10,000 raised

Vanessa Brown

$7,220 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…

$1,310 of $10,000 raised

Nicola Malak

$1,310 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.