Every drive helps fund life-saving research and vital support for patients and families.
Since Maddie’s Vision was founded in 2015, we’ve made an extraordinary impact into research and patient and family support.
Our Impactcommitted to research
research projects funded
patients supported by our Tele-Support Service and Peer Support Program
of leveraged funding
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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We embrace bold science, technology and new ideas, fostering creativity and breakthroughs that have the power to inspire hope and change lives.
We face challenges with strength and determination, pushing boundaries in research and advocating fiercely for patients and families who deserve a louder voice.
We show empathy, kindness, and respect, ensuring everyone who turns to Maddie’s Vision feels seen, heard, and supported.
We empower patients and families through education, resources, and guidance to be informed advocates in their own care and equip researchers to pursue groundbreaking ideas.
As the trusted national leader in Bone Marrow Failure Syndromes, we honour Maddie’s spirit by turning her vision into lasting impact, carrying forward her bravery and determination in everything we do.
Keep up to date with the latest Maddie Riewoldt’s Vision news, upcoming events and Bone Marrow Failure Syndromes research.
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Read more30 September 2026 Could you, a family member or one of your patients help shape the future of Bone Marrow Failure Syndrome research in Australia? The Aplastic Anaemia and Other Bone …
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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.
View all research projects