Joanna
Anne
Janet
Muza
Marisa
Beres
Susan

ABOUT US

The WANTZ Committee was estabished in 2003 by several friends from very diverse backgrounds who decided to fundraise to purchase equipment for a different charity annually. The name WANTZ is an acronym of the names of the five original committee members - W for Sally Warriner, A for Anne Spooner, N for Janet Nathanson, T for Joanna Tait and Z for Muza Ulasowski. It also represents what the committee does - every year the WANTZ Committee chooses a charity organization to support and fundraises for equipment the chosen charity has on its 'WANTZ Wish List'

In 2020-21 the WANTZ Committee is proudly supporting MND and Me Foundation which supports people and their families living with Motor Neurone Disease (MND) in Queensland. The Foundation delivers support programs and funds research into treatments and a cure for MND.

Motor Neurone Disease is the name used to describe a group of diseases in which the nerve cells (neurones) in the brain and spinal cord that control the way we walk, talk, eat, swallow, and breathe progressively die. In some countries, MND is known as Amyotrophic Lateral Sclerosis (ALS), and in the US, it is also called Lou Gehrig’s disease.

When the neurones begin to die, the muscles that they control can no longer receive messages from the brain. The muscles become weaker and weaker, and eventually stop working, leaving people motionless, unable to talk, and trapped in their bodies. In most cases the mind is left intact, but some patients have MND and a form of dementia known as Frontotemporal Dementia (FTD)1.

In MND, no one person is the same – where the weakness first starts, how the weakness progresses, and the rate at which the weakness progresses is different from person to person. Although some people can live a long time with MND, the average life expectancy is 27 months following diagnosis

With your help MND and Me Foundation are continually improving the level of care to Queenslanders impacted by MND and contributing to research so one day we can live in a world without Motor Neurone Disease.

LINKS:

MND and Me Foundation

Donations Reply Slip

Purchase tickets to WANTZ Gala Dinner

CURRENT COMMITTEE MEMBERS:

For more info, please click onto the photos below........