Read our Annual Report

The Maddie’s Vision 2022/23 Annual Report is now available!

A brighter future for patients living with Bone Marrow Failure Syndromes

Since Maddie’s Vision was founded in 2015, we’ve made an extraordinary impact into research and patient and family support.

Our Impact
$8.8m

committed to research

36

research projects funded

100

patients supported by our Telehealth Nurse

$23.3m

of leveraged funding

Maddie Riewoldt

Maddie Riewoldt was just 26 years old when she died of complications from Aplastic Anaemia, a Bone Marrow Failure Syndrome. Maddie wanted to ensure nobody else went through what she did. Maddie Riewoldt’s Vision is her legacy.

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Latest News

Keep up to date with the latest Maddie Reiwoldt’s Vision news, upcoming events and Bone Marrow Failure Syndromes research.

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World Rare Disease Day 2024

Rare Disease Day, held this year on February 29, is a global movement that aims to recognise and raise awareness for the 300 million people worldwide who are living with a rare disease, …

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Join the Maddie’s Vision Cents2Bills Fundraising Program

At Maddie Vision, we’re making regular giving easier than ever, and we want you to be a part of it! Now you can support Maddie’s Vision through Cents2Bills, which will enable you …

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Carter & Skye

Carter and Skye’s mum Karen shares her family’s story — from searching for answers to her children’s illness to diagnosis of Shwachman-Diamond Syndrome, an inherited Bone Marrow Failure Syndrome.

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Matty & Cheryll

Meet Matt and his grandmother Cheryll who he affectionately calls Honey. Cheryll talks about Matty’s journey with Fanconi Anaemia — an inherited Bone Marrow Failure Syndrome — and her hopes of a cure.

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Evgenia’s Story

Undergoing a bone marrow transplant can be a lonely experience. Here, Evgenia shares her story in the hope that it will help others going down this road.

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