Neuroblastoma is an insidious cancer which took the life of one of our own. A little 3 year old boy. Committee asked members to support a determined effort to raise at least $5,000 for the work of Neuroblastoma Australia.


Amazing Prizes ... Amazing Organisation

Amazing Promotion ... Amazing Response


Stunning Outcome ... Total = $5029



 1st ... Garage Hoist (2ยท8 ton) ... Bev Riddell
Value $2300

hoist YL 628
Donated by a generous Moke Owner


2nd ... Daydream Hanging Chair

Jill Whatmore ... Value $599
hoist YL 628Donated by BBQs R Us Mitcham

3rd ... Art by Andra

Andy Preston ... Value $225
hoist YL 628Donated by Andra Bacon of Andy's Artistry


To see more of Andra's work log in here with Instagram or Facebook:

4th ... Ryobi Pressure Washer

Rod Grist ... Value $100
hoist YL 628
Donated by a generous Moke Owner

5th ... Bunnings Vouchers

Greg Twaits ... Value $100

 hoist YL 628
Donated by a generous Moke Owner






The constitution of our club requires that we be of some good in the community. This raffle is one of the ways we are fulfilling that obligation.


 ethan sm


We want to sincerely thank the MOA for raising funds for Neuroblastoma Australia through the 2022 Easter raffle.Unfortunately we are the family that lost our son Ethan to this horrible disease.We just wanted to put some words together about Ethan and what he went through trying to beat this under researched childhood cancer.

In mid February 2021, Ethan at just 22 months old contracted a urinary tract infection.After being in and out of hospital over a 2 week period and not getting anywhere, we insisted Ethan have more scans to investigate further, to our surprise we were informed he had a mass on his adrenal gland and we would need to go to Sydney Kids Hospital Randwick for more tests.

The following day our world changed, after a number of scans and tests we were informed Ethan had High Risk Neuroblastoma something we had never heard of before, but the most shocking part was he had a 50% chance of survival.Neuroblastoma is a cancer that starts in nerves and develops into tumours and then can quickly spread up and down the nerves within the spinal system.Ethan had a large tumour on his adrenal gland, a secondary tumour in his lower spine and cancer in every bone in his body

Due to the aggressive nature and lack of research into High Risk Neuroblastoma the only way to treat it is with some extremely putrid chemotherapy that made Ethan extremely sick and has some very hard long term side effects, unfortunately after 3 months of treatment we were informed the chemo didn't work and we would need to move him to a clinical trial treatment to try and get on top of the cancer.

After 3 months of the trial we had a breakthrough.The treatment was working and we quickly moved to the next phases of treatment that included a double bone marrow transplant and a major operation to remove his tumour in January this year.The operation was an amazing success and we went home to recover before moving to the final stage of treatment.

3 weeks into the recovery Ethan was not feeling great and we took him back to hospital, after some scans we were sadly informed the cancer had returned, and unfortunately with Neuroblastoma there is a 0% chance of survival if you relapse.

Ethan had 6 spots of cancer on his lungs, and the doctors told us that we may have 6 to 12 months with him.4 days later Ethan's health deteriorated rapidly, the cancer was extremely aggressive and had taken over his entire lungs and he passed away the next day.After an intense 12 month battle his body had enough!

So why are we so passionate about Neuroblastoma Australia? It's a tiny charity ran by a mum who also lost a child to NB and all funds raised go directly into research of this underfunded disease.Most of all because the original research which resulted in the 1 treatment that worked for Ethan (the clinical trial) was funded and lobbied for by Neuroblastoma Australia; this charity gave us 1 last Christmas together.

Australia is in many ways leading the research into this disease, but the funding isn't there to take the research to the next level.Every dollar helps take 'thoughts and ideas' to research then onto treatment.

No child should have to go through what Ethan did.

It is amazing to be a part of an organisation / club that not only shows great care for its members but also the wider community.

If you would like to hear more of Ethan's story please see this link for an interview we did with The Project on channel 10:

Ryan and Kate Paterson MOA #1052