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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
$10m

committed to research

37

research projects funded

170

patients supported by our Tele-Support Service and Peer Support Program

$37.9m

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 Riewoldt’s Vision news, upcoming events and Bone Marrow Failure Syndromes research.

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The Table for Change Gala 2026 raises over $340,000! Thank you for your generosity and support

Maddie Riewoldt’s Vision is proud to announce that the 2026 Table for Change Gala has raised more than $340,000 in support of patients and families affected by Bone Marrow Failure …

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Thank you for supporting National Bone Marrow Failure Syndrome Awareness Week 2026

In March, we proudly delivered our second National Bone Marrow Failure Syndrome Awareness Week, uniting patients, families, partners and supporters across Australia to raise awareness …

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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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