What type of doctor(s) will I need to see?

What is an allogeneic transplant? Who is eligible for a transplant?

What does palliative care for MDS look like?

What are the different risk groups and what differentiates between them?

What are MDS treatment options?

How quickly does MDS progress?

How do I know treatment is working?

Do I need to start treatment right away?

What is the goal of treatment (manage symptoms or cure MDS)?

What testing should be done to confirm a myelodysplastic syndromes diagnosis?

What testing is most important to monitor your myelodysplastic syndromes over time?

What lab abnormalities will you normally see in a newly diagnosed myelodysplastic syndromes patient?

What is NGS (next generation sequencing)?

How often will I need to have a bone marrow biopsy?

How are high risk and low risk myelodysplastic syndromes defined?

Where in the body are myelodysplastic syndromes found?

What are myelodysplastic syndromes signs and symptoms?

What are myelodysplastic syndromes risk factors?

Are myelodysplastic syndromes more common in certain groups/demographics?

Are myelodysplastic syndromes genetic? Should my family be tested if I am diagnosed?