Talk to your doctor about new MDS symptoms and side effects

Meet Your Guide
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Maureen Ratliff
Advocate

Maureen Ratliff was diagnosed with myelodysplastic syndromes (MDS) in 2018, after some issues with her bone marrow. Soon after that, she started traveling from her home in Georgia to Nashville to hear talks from the MDS Foundation. She did some networking with health care professionals and joined clinical trials for 3 years. Maureen has a career in social work, so she was a natural to start a support group to help others who have MDS. She's awaiting a transplant.

Show Sources

SOURCES:

Maureen Ratliff, myelodysplastic syndromes patient and advocate, Ball Ground, GA.

National Cancer Institute: “Myelodysplastic Syndromes Treatment.”