Moving Forward
You're so right about asking the questions to the folks who know the answers. I have an appointment with my doc at the end of this cylce of Vidaza. I have a nice list of questions for him and the transplant folks as well. I am a "controller" by nature, and really have to keep myself in check, as I know this is a one-day-at-a-time process, and a long process at that. For me there seems to be a fine line between being educated and aware of my disease and being scared out of my wits! Thanks for all your input and advice.
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Sherry Baby 62 Diagnosed 2/11/12 MDS to AML-6; del 20q and trisomy 21; Vidaza 3 month trial unsuccessful; ALLO BMT 7/2/12; Sister Donor 10/10 match; Chronic GVHD mucous membranes, otherwise all's well :0)
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