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October 27, 2012 - 1:00AM. Sullivans. ITS been two years since Scott Sullivan's world as he knew it fell apart. Two years since he was told he was going to die. Mr Sullivan, now 40, was shocked to the core to learn he had Motor Neurone Disease. It had snuck up on him without warning. Struck him in the prime of his life.
- Elissa Lawrence
Apr 29, 2014 · BRISBANE man Scott Sullivan, who became a tireless campaigner and fundraiser for research into motor neurone disease after he was diagnosed with the condition in 2010, has died. Mr Sullivan, who ...
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National. Queensland. Difficult milestone passes for Scott Sullivan, father of two with motor neurone disease. IT WAS marked on the calendar for months. An uneasy milestone that crept ever closer. Scott Sullivan put a cross through the date - January 22 - and put his affairs in order. Elissa Lawrence. 2 min read. January 26, 2013 - 1:00AM.
Diagnosed with ALS/MND (a terminal disease) Ian Davis & Scott Sullivan embark | Check out 'Legacy - A Ride To Conquer Motor Neurone Disease' on Indiegogo.
Apr 27, 2018 · Scott Sullivan’s legacy to support MND research continues - Queensland Brain Institute - University of Queensland. 27 Apr 2018. . The renewal of the Scott Sullivan Fellowship in motor neurone disease (MND) research has been announced on the fourth anniversary of campaigner and fundraiser Scott Sullivan’s passing.
Sarah, whose late husband Scott Sullivan set up the motor neurone disease foundation MND and Me, this week begins trekking to Everest Base Camp in Nepal in a major fundraising venture for the charity.
