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100% of your donation goes toward funding research, with administrative costs covered by The Babich Family Foundation. 

RUNX1 FPD/AML is considered an 'orphan disease' and has had little attention given to it, up to now.  Current research is starting to shed light on how many individuals who have had AML actually had an inherited RUNX1 mutation which led to their developing AML. The RUNX1 Research Program aims to increase the awareness of RUNX1 FPD/AML both in the public and medical communities, gaining new information in the hope of ultimately finding a cure.  

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