Members of the Media
Every day, at least 50 people in the United States are diagnosed with a bone marrow failure disease. Yet when someone is stricken, it is likely that they have never even heard of their disease. Because these are such rare diseases, it is vital that patients receive up-to-date medical information, expert treatment, and emotional support.
The Aplastic Anemia & MDS International Foundation (AA&MDSIF) is an independent nonprofit organization whose mission is to support patients, families, and caregivers coping with aplastic anemia, myelodysplastic syndromes (MDS), paroxysmal nocturnal hemoglobinuria (PNH), and related bone marrow failure diseases.
AA&MDSIF:
- Provides educational materials, medical information, and access to peer support via a global network of volunteers who offer hope to those struggling with bone marrow failure diseases
- Builds awareness and knowledge of bone marrow failure diseases among medical and healthcare professionals and the general public
- Raises public and private support for research to improve patient treatments, restore patients to health, and ultimately, to find cures for bone marrow failure diseases
The foundation's ongoing commitment and dedication to this mission is based on our core values of fairness, integrity, transparency, respect, and responsibility.
- About Bone Marrow Failure
- Support & Community
- Contact a Patient Educator
- Conferences
- Peer Support Network
- Standing Up for Your Health
- Communities of Hope
- Community Calendar
- Stories of Hope
- Calendar of Hope
- Marrowforums
- AA&MDSIF Scholarships
- Frequently Asked Questions
- Research & Grants
- Get Involved
Members of the Media
Online Learning Center
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Find out how you can further research and treatment. Act now!
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Media Inquiries
If you need more information, need to speak to medical experts, or have any questions, please contact John Huber, Executive Director at (301) 279-7202 x100 or by email at huber@aamds.org.
Contact MDS patients willing to share their story.



