
About Us

The MDS Foundation is a global non-profit advocacy organization building critical awareness of myelodysplastic syndromes (MDS) - a rare, often undetected blood cancer. The MDS Foundation has supported patients and their families, as well as healthcare providers, in the fields of MDS, AML and other related cancers for over 30 years.
Vision: We envision a world where every MDS patient has access to the best possible care, treatments, and support—driving advancements in research, increasing awareness, and ultimately improving outcomes for all those impacted by MDS.
Mission: The MDS Foundation is committed to improving the lives of everyone affected by myelodysplastic syndromes (MDS) and its related diseases through comprehensive support, education, research, and advocacy. We empower patients, caregivers, and healthcare professionals with the knowledge, resources, and community they need to face MDS with strength, understanding, and hope.
Resources
Contact Us
228 Park Ave S, PMB 118983
New York, NY 10003-1502
Ashley Moncrief, Director of Patient Care | support@mds-foundation.org
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