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Hi Marie. Thought I would just tell you what my Dr told me (I have secondary MDS too from my Aplastic Anemia treatment). He said that transplant is a good option for me. And that when it starts to evolve more, it may do it quite quickly and will be more aggressive. But for now I am living ok. The waiting is the hardest part. Take care and all the best, Marie. Jules
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Julie (38yrs); dx AA 1996 & treated w/ATG, cyclosporine & G-CSF; 2010 dx int-1 secondary MDS, low platelets, on prevention antibiotics, fevers of unknown origin, MUD found for BMT when the time is right, which is now! MDS transformed to AML after many infections.
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