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Secondary MDS
I am looking for information on secondary MDS. My partner was diagnosed after 14 years of remission from non-hodgkins lymphoma and a stem cell transplant at Beth Israel in Boston.
She just had a donor transplant at City Of Hope. I dont see a lot of data out there, i understand that the transplant is the only chance for a cure. But is there more data about how patients do with secondary MDS? I am trying to be opitmistic.........but have not seen a lot that looks good.
Thanks for any feedback.
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