One thing I wish more people understood about Motor Neurone Disease is that right now, despite all the hope, fundraising and research, THERE IS STILL NO CURE. We all desperately wish for that to change one day. We need it to. There are a small number of medications that have shown limited success...
I completely missed this one when I was interstate last week for work. Great work fundraising Finn! We are all very proud of your efforts. backdating this post to the date the article was released. We are incredibly grateful to the Pakenham Gazette for recently sharing Shane’s story and helping...
Today Alexandra Newspapers shared Shane Lewis’s story, and while it’s incredibly hard to see your family’s journey laid out on a newspaper page, I’m also grateful for the opportunity to help shine a light on what living with MND really looks like behind closed doors. This article talks...