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NIH transplantee looking for others
I had my transplant in October and I'm out but staying in the area till further notice. I'm on tacrolimus and prednisone (tapering). I was just looking for anyone else who may have also gone to nih for a transplant, or who was on tacrolimus? I am just looking for other peoples stories/opinions/experiences.
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27 year old female diagnosed MDS RCUD 2012, GATA2, multiple carcinomas in-situ, SCT 10/03/2013 @NIH, chronic GVHD starting 11/2015
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