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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Since Maddie’s Vision was founded in 2015, we’ve made an extraordinary impact into research and patient and family support.
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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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Keep up to date with the latest Maddie Riewoldt’s Vision news, upcoming events and Bone Marrow Failure Syndromes research.
Read More NewsMaddie 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 …
Read moreIn 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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Thanks to our incredible community, we’re funding the projects and researchers we believe will lead to breakthroughs. Since 2015, we’ve supported 36 research projects.
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