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@loribmt

Hi @janetlen. It’s interesting that you had 2 questionable bone marrow biopsies and the 3rd was clear. That would be good news. From my understanding (and I’ve had 13 of them) a bone marrow biopsy is basically a point check…looking at a single point in your marrow. So there may be differences if biopsies were taking from other areas. It can take a while for conditions such as MDS to proliferate so not every area may be involved at one time.

The samples taken are a core specimen of the marrow and an aspirated sample of the peripheral blood also from the marrow. When analyzed, these detailed results give your doctor a picture of the condition of your marrow and its ability to produce healthy blood products. But again, it is from a single area.
A better barometer is the overall condition of your peripheral blood…blood taken from a routine blood draw. The reason being is that blood changes come from within your bone marrow. When there are an excess of defective cells within the marrow they begin to spill out into the peripheral blood. If the peripheral blood is normal, blood numbers are stable, and the biopsies look good, then this condition most likely isn’t proliferating very fast which warrants the watchful waiting/active surveillance mode. The fact that your doctor has lengthened the leash between visits says that they’re confident that this isn’t developing very quickly. So you may not require a transplant any time soon unless things change.

Just keep up with your routine blood work and in the meantime live life like you did before the diagnosis. What led you to the diagnosis? Were you experiencing symptoms or was this from a followup to routine blood work?

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Replies to "Hi @janetlen. It’s interesting that you had 2 questionable bone marrow biopsies and the 3rd was..."

The 1st 2 biopsies showed 5-10 blasts. The Drs thought they did not make sense with my relatively good blood work. Since 2020 I had low neutrophils and high blood volume, but nothing was being done about it. Then this year along with low white blood cells and high blood volume I had low red blood cells and the investigation began. I was referred to a stem cell specialist after the 2nd biopsy. I was preparing to make that choice and then had the 3rd biopsy which had blasts in the "normal" range. It's been a challenging year. I hope to remain Watch and wait for a while but will request another biopsy at least yearly. I do not want to get beyond the window for a transplant. As I understand it, the 5 year survivability for transplants is 30%. Quality of life is more important to me than quantity. Before I had the diagnosis, I was experiencing fatigue and did not know why. Now I experience some shortness of breath. So things are not the same. The oncologists think I should not have the symptoms, but I do.