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
$9.3m

committed to research

36

research projects funded

130

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

$23.6m

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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Tim takes on a mammoth Ultraman Challenge for a cause close to his heart

This May, Tim Belstead is set to face the Ultraman in Noosa, one of the toughest endurance events around, to support a cause very close to his heart. Tim is the cousin of the late Alex …

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A historic day at the final Maddie’s Match – Thank you for your generosity and support!

We are so grateful to everyone who joined us for the final Maddie’s Match, your support, energy, and generosity made this event truly unforgettable. The day was filled with countless …

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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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