Hi Howard, even though this MDS is the diagnosis you were expecting it’s still a shock to have the confirmation. As for treatment, it’s impossible to speculate on what the options will be. At this point, I think it’s just wise to wait and see what your doctor puts out there for you, for your particular myelodyplastic syndrome. There are several MDS types.

Each one is potentially treated differently depending on that type.
Some meds can increase the number of blood cells if that’s what’s needed. Other meds can suppress the immune system or stimulate blood cells to mature. Sometimes there are genetic components involved that will call for completely different meds. I’m not trying to be evasive but there is just no way to know for sure what your doctor will suggest for treatment without knowing the facts.

The only treatment option that offers the potential of a cure for myelodysplastic syndromes is a bone marrow transplant. This gives your body an entirely new immune system with a fresh start.
I’ll be waiting anxiously with you for Friday, to hear what your doctor has to offer by way of treatment. Then I can help connect you with others going through a similar experience. ☺️