The Myelodysplastic Syndromes (MDS) Foundation, Inc. is a global non-profit advocacy organization that for over 25 years has supported patients and their families as well as healthcare providers in the fields of MDS and its related diseases. Our Vision is for every MDS patient to benefit from our initiatives and research as early as possible.
The MDS Foundation supports and educates patients, their communities, and healthcare providers, and contributes to innovative research in the fields of MDS and its related continuum of diseases to better diagnose, control and ultimately cure these diseases.