We would walk 500 miles for Gary!

We are doing this challenge to become part of the solution to ensure no Queenslander has to face Motor Neurone Disease alone, like my family had to. Life is short and we need to make the most of it, and support those less fortunate. This is our chance to help them make a positive difference is the lives of people impacted by MND!

I know that the MND and Me Foundation does great work supporting both people with MND and their families while also funding critical research.

No donation is too small and any support you can provide is greatly appreciated.

What is Motor Neurone Disease?

You have nerves in your brain and spinal cord that control how your muscles work. These are called motor neurones. MND is a disease that affects the motor neurones. With MND, motor neurones gradually stop telling your muscles how to move. When muscles no longer move, they become weak, which can also lead to stiffness and loss of muscle mass (wasting). MND is a life-shortening illness that can affect how you walk, talk, eat, drink and breathe. This is usually different for each individual. You may not get all of the symptoms and there is no set order in which they happen. The disease will progress, which means symptoms will get worse over time. For some people this can be rapid, for others it is slower. There is currently no cure for MND.