Patient Video - Bill’s story: What advice do you have for other patients on their journey with MDS-related anemia?
Bill shares his advice about living with MDS-related anemia. He recommends learningas much as possible about the disease and doing research to find the best doctors and facilities in your area that specialize in treating your specific condition. Finally, Bill says that it’s very important to not dwell on the disease but rather to keep living your life as normally and as long as you possibly can.
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This educational activity has been developed by the Myelodysplastic Syndromes Foundation, Inc. and Mechanisms in Medicine Inc.
This activity is supported by an educational grant from Acceleron Pharma, Bristol-Myers Squibb, Celgene Corporation, Jazz Pharmaceuticals, Novartis, and Takeda Oncology.
This website is part of the Animated Patient™ series developed by Mechanisms in Medicine Inc., to provide highly visual formats of learning for patients to improve their understanding, make informed decisions, and partner with their healthcare professionals for optimal outcomes.