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Elizabeth's Legacy
Elizabeth's Legacy
Story
Donate to help Elizabeth's light shine on ...
In late June 2023, Elizabeth received the devastating news that she had Neurofibromatosis (NF) related brain cancer. After a short and brutal battle, she sadly passed away on October 14, 2023.
Elizabeth was diagnosed with NF in late 2019. She inherited NF from her mother Faye, who also passed away from NF only a few weeks after Elizabeth.
Elizabeth was married to Nick, and they have two adorable energetic children. Coincidentally, Nick's sister Zoe also has NF.
Elizabeth's Legacy was established as an opportunity for Elizabeth to bring hope to others, to allow her light to continue to shine and to help make a difference - now and in the future - by raising funds to support NF medical research.
Flicker of Hope has partnered with The Brain Cancer Centre to fund a world leading NF2 research project, to be known as "Elizabeth's Legacy - Deciphering the Molecular Mosaic of NF2".
Your support will help make Elizabeth's Legacy a reality - bringing hope to all those impacted by NF. 100% of your donation to Elizabeth's Legacy will be directed to NF medical research.
All donations over $2 receive a tax receipt.
Thank you for your generous support.
Donations made through this platform are secure and will be remitted directly through to The Flicker of Hope Foundation
Thanks so much for your support!
Donate to make a difference
Flicker of Hope Foundation Limited
The Flicker of Hope Foundation was inspired by Zoe – who was diagnosed with NF at four months of age.
Zoe loves to dream big … and she dreams of a bright future for all those affected by NF. In 2018 Zoe and her family established Flicker of Hope to raise much needed funds to support researchers in their quest to find positive treatments and improve the quality of life for those impacted by NF.
Thanks to the generous support of individuals, businesses, community and school groups Flicker of Hope has raised over $2.5 million in five years. 100% of this amount has been donated to fund essential research into NF.
Please join us on this journey – a journey that may be life changing for those impacted by NF.