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Michael Murgolo
Michael Murgolo
Story
I am fundraising for the Flicker of Hope Foundation, a cause close to my heart. This foundation has been instrumental in funding research for Neurofibromatosis (NF)—a condition that has impacted my family, with our son Giorgio diagnosed at just six weeks old.
After a long journey, Giorgio has completed his treatment, a milestone that fills us with gratitude. To mark this moment and give back, I will be shaving my hair—not only to raise funds but to donate it for a wig to help another child.
We are incredibly fortunate to have received exceptional medical care, ensuring Giorgio’s quality of life is better than many others facing similar challenges. This is something we do not take for granted. Through this fundraiser, I hope to support those still fighting, just as Flicker of Hope has supported families like ours.
“Fear not, for I am with you; be not dismayed, for I am your God; I will strengthen you, I will help you, I will uphold you with my righteous right hand.” — Isaiah 41:10
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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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