Support Liam's Lissencephaly Journey

Jasmine Marshall is organizing this fundraiser on behalf of Sarah Arambage.

Donation protected

This fundraiser is in support of the Arambage family, to provide the brightest possible future for their 2 year old son Liam.

Liam was born with a rare genetic condition called Lissencephaly. The life expectancy for Liam's condition is 10 years, and he is currently under palliative care. Despite this, Liam continues to defy the odds and his spirit continues to shine.

As Liam grows, the Arambages' really need a suitable vehicle to comfortably transport Liam and all of his specialised medical equipment. Unfortunately the NDIS is unable to provide funding towards a suitable vehicle for Liam. Additionally, the family has experienced significant financial stress ever since Sarah had to give up work to become Liam's full-time carer.

*The goal for this fundraiser is $100'000.

This money will assist the Arambages' to fund a suitable vehicle for Liam, whilst allowing the family to create lasting memories with their son Liam, through experiences they are not currently able to afford.

Many will already know the incredible generosity of the Arambage family. They are always the first to help others out, and now is our turn to rally behind them.