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Zoe Petropoulos
Zoe Petropoulos
Zoe Petropoulos
Story
Hello!
My Name is Zoe and I have Neurofibromatosis. With my family we run a charity called The Flicker Of Hope Foundation, where we shine a light on the condition and raise funds for research.
Since May is fast approaching, and also happens to be neurofibromatosis awareness month, I wanted to do something special. So I’m introducing a series called Dare, Donate, Do.
Here’s how it will work. I have set up a GoFundraise page, and if you want to dare me to do something you can send me a message on Instagram @chronicallyzoe_ or our Flicker Of Hope Facebook page and then you have to donate to get me to do it.
I will be taking on and advertising one dare at a time and whoever’s dare makes the most money will receive a flicker of hope gift pack and a $100 gift card and all money raised will go directly to research into neurofibromatosis.
If for whatever reason I am unable to accept and complete your dare you can still make a general donation to show your support.
All dares that I do accept & complete will have to be family friendly as all of them will be filmed and posted on our YouTube over the month of May.
So if you want to see me potentially tackle some fears, maybe get my hands a bit dirty, or just see me make a complete fool of myself make sure you tune in and welcome to Dare, Donate, Do.
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 $3 million in six 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.
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