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 News24 February, 2026 Returning for its second year, the 2026 National Bone Marrow Failure Syndrome Awareness Week will take place from 2–8 March, aiming to build national awareness of Bone …
Read more15 December 2025 Maddie Riewoldt’s Vision is proud to announce a major milestone for Maddie’s Month — $1 million raised since the campaign began in 2016, including another $100,000 …
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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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