On behalf of the Board of FightMND, it is with immense sadness that I advise the passing of our Foundation’s co-founder and inaugural Chairman, Dr. Ian Davis, from Motor Neurone Disease on Thursday, November 1.

In 2011, at the age of 33, Ian was diagnosed with MND and has dedicated his time since his diagnosis to growing greater awareness of the disease and fundraising critical dollars to commit to research and drug development to find a cure.

Ian played a pivotal role in the establishment of FightMND in 2014 following his retirement as a medical doctor due to his ailing health. He served as Chairman of the Foundation while also chairing the FightMND Cure subcommittee.

His medical background and experience enabled him to provide the Foundation with significant knowledge and expertise in the medical science environment, achieving positive progress and development in the quest to find a suitable treatment and cure for MND.

Since the Foundation’s inception, Ian’s tireless work, passion and commitment to finding a cure for MND has impacted and inspired people affected by MND worldwide.

Among his many achievements was the creation of the inaugural Australasian Motor Neurone Disease Symposium in March 2018, attracting over 400 delegates from around the world, who all assembled with the joint intent to create a world free from MND.

Ian’s dedication to the fight against MND continued until his final days, ensuring in his absence the same rigour will be applied to the pursuit of the most promising research.

The legacy Ian leaves behind will be profound and all the people affected by MND, be they patients, families, carers and researchers, have a great deal to thank Ian for.

Ian is survived by his wife Mel and son Archie and we extend our love and support to them and Ian’s extended family, friends and colleagues at this sad time.

Yours sincerely,

Bill Guest

Chairman, FightMND