'Justin Yerbury made a promise to his mother while she was dying of motor neurone disease (MND) that he would do everything he could to find a cure. MND had already taken several members of Justin’s family, and he learned that they carried a rare genetic form of the disease that gave them a fifty-fifty chance of inheritance.
'Desperate to help his loved ones, Justin went to university to study science, eventually becoming a professor of molecular biology at the University of Wollongong and one of the world’s leading experts on MND. While in New York, delivering a lecture on his groundbreaking research, Justin felt his thumb stop working – ‘the beast’ that had lurked so long in the shadows had caught up with him.
'Now 99 per cent paralysed and able to move only his eyeballs, Justin refuses to yield. With eye-tracking software, he has written his extraordinary memoir to shine light on this terrible disease and to show that, even in the bleakest of moments, there is always a reason to keep fighting.
'All proceeds from this book will be donated to Fight MND.' (Publication summary)
'When Justin and Rachel Yerbury met, they had no idea that he would become a world-leading scientist – studying a disease that would lead to his own tragic decline'
'When Justin and Rachel Yerbury met, they had no idea that he would become a world-leading scientist – studying a disease that would lead to his own tragic decline'
