Runx1 Research Program
RUNX1 Research Program is the world's only foundation supporting patients with RUNX1 Familial Platelet Disorder (RUNX1-FPD), a rare hereditary disease that affects blood platelets and can lead to other health concerns. Most notably, individuals with RUNX1-FPD have a 30 times higher risk of developing blood cancer compared to the general population. We fund innovative research focused on blood cancer prevention, and provide educational initiatives as well as opportunities for patients and their families to share their voices with researchers and clinicians.
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Amanda Eggen
Director of Patient Engagement and Clinical Programs · Other
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Katie Korgan
Executive Assistant · General Business & Management
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Katrin Ericson
President and Executive Director · General Business & Management
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- 1director of patient engagement and clinical programs
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