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#FightLikeMaddie

against bone marrow failure syndromes

Maddie Riewoldt's Vision aims to raise funds to #FightlikeMaddie and find new treatments for Bone Marrow Failure. The Vision aims to ultimately find a cure for the syndromes that affect younger Australians each year. Maddie Riewoldt lived with Aplastic Anaemia for only 5 years. There are no words on a page that can do justice to Madeleine Riewoldt's life and it is her legacy that we wish to honour.

ABOUT US ABOUT BMFS

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All funds raised will help support research into treatments, prevention and trying to find a cure.

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LATEST NEWS

National Symposium on BMFS
New Partnership with BBL

National Symposium on BMFS The Maddie Riewoldt's Vision Centre of Research Excellence in Bone Marrow Biology was delighted to host the Inaugural National Symposium on Bone Marrow Failure Syndromes in May this year.

New Partnership with BBL The Melbourne Stars and Melbourne Renegades proudly announced a special joint partnership with Maddie Riewoldt’s Vision as official charity partner for the Melbourne based Big Bash clubs.

Aplastic anemia is most common in ages 15-25

UP TO 5 PEOPLE PER MILLION ARE DIAGNOSED GLOBALLY EACH YEAR WITH BMFS

EACH YEAR UP TO 140 AUSSIES ARE DIAGNOSED WITH BMFS

MRV NEWSLETTER

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#FightLikeMaddie

against bone marrow failure syndromes