Patient resources
Materials help patients understand MDS and navigate care.
For over 30 years, the MDS Foundation has supported patients, families, and healthcare providers affected by myelodysplastic syndromes and related diseases. It is a global nonprofit advocacy organization focused on improving the lives of people impacted by MDS, a rare blood cancer. Patient support is central to its work. The Foundation provides resources to help people understand diagnoses and treatment options, and connects patients and caregivers with information for navigating care. It also offers education for healthcare professionals, supports research, and advocates for the MDS community. Its materials include Building Blocks of Hope, newsletters, and myMDS resources about MDS-related anemia. The MDS Exchange invites people to share personal stories to raise awareness and connect with others. The organization is based in New York City.
Disclosure: Profile information has been compiled from publicly available sources and has not yet been verified by the business.
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Materials help patients understand MDS and navigate care.
Education supports healthcare providers working in MDS.
Advocacy and research support the MDS community.
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