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The MDS Foundation is a global nonprofit advocacy organization dedicated to raising awareness and providing support for individuals affected by Myelodysplastic Syndromes (MDS), a rare blood cancer. With over 30 years of experience, the foundation assists patients, families, and healthcare providers in navigating the complexities of MDS and related diseases.
Through comprehensive resources, educational materials, and community-building initiatives, the MDS Foundation empowers patients and caregivers to make informed decisions regarding treatment and care. Their commitment to advocacy and support fosters a sense of community, ensuring that no one faces MDS alone.
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