MDS and minorities
I have been trying to find information on MDS and minorities - incidence, genetically-driven treatment issues, etc. I am African American and dealing the the myriad barriers to finding a suitable match for a BMT. Is anyone aware of any research on bone marrow failure diseases within specific ethnic groups?
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Leslie, 53, diagnosed MDS July 2007, RAEB II, 20q and 13 q del, currently taking Revlimid.
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