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Hi, Otter.
Welcome to Marrowforums! I'm in Los Angeles, too, and had my transplant for MDS at City of Hope. Are the doctors saying your MDS is secondary to your treatment for CLL? Do you know what subtype of MDS you have?
Needless to say, I am a big fan of City of Hope. I'd be happy to answer any questions you might have and share my experiences.
Regards,
Ruth Cuadra
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Diagnosed AA 10/96, MDS/RA 6/98, MUD/BMT 10/6/98
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