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Team Poults Power Cars 53 & 61
Team Poults Power Cars 53 & 61
Team Poults Power Cars 53 & 61
Story
10 years ago MND took our beloved Dad Neil Poultney (aka Poults) from us at the age of only 61. My siblings Jeff, Brad and I have been participating in this amazing event since losing our Dad and this marks our 10th Drive for MND adventure. Our Poults Power crew has expanded over the years as our friends have joined the fight against MND. It is a cruel bastard of a disease that currently has no known cause, treatment or cure. Watching our strong workhorse of a father slowly wither away broke our hearts and will forever haunt us. Dad described having MND as having to watch himself slowly die and being trapped inside himself. He wanted us to share his story and be his voice when he no longer had one. No one deserves to suffer with MND, and we will continue to fundraise and raise awareness for MND year after year until one day there is a cure. The only way to fight this insidious disease is to raise money for research, which brings hope to those living with MND. This event supports a WA based MND Research Consortium and also MNDAWA to help care for those living with MND in WA.
This year Team Poults Power will hit the road with the boys car #53 (Jeff, Misho, Joey and Brownie) and the girls car #61 (Jodie, Kate, Amanda, Caroline, Andi and making her drive debut - Isabella!)
A massive shout out to the Canning Football Club family who will once again help us kick start our fundraising by hosting the Annual MND Cup and Quiz Night!
We would appreciate any contribution you could make to help this amazing cause.
All donations over $2 are tax deducatible.
Thank you for your support and help us do Poults Proud! #mndsux
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Care Cure Support Ltd
CCS is a fundraising health promotion organisation that contributes 100% of the funds it raises towards the Care for people living with Motor Neurone Disease (MND), whilst investing in research to find a Cure for MND and providing Support to the families of people living with MND. Our simple purpose is to make a beneficial difference to others.
Our Long term aim is to contribute to a world where MND is no longer 100% terminal, by helping to uncover what causes MND and eventually finding a cure. We are currently doing this via the Motor Neurone Disease association of WA (MNDAWA) and funding research such as the US drug trial Tecfidera conducted by the Perron Institute (here in WA) currently underway.
In the short term, we will provide funding to improve the care and support for people living with MND and their families whilst contributing to research to find a cure.
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