Our 8 yr old grandson has aml, he had a bone marrow transplant last fall, and now has graft vs host. The Drs. are not giving us much hope, any hope really. The only thing my step daughter is telling me about what to expect is that the Drs. say "it's not pretty". I have searched the internet, and can not find anything. Our grandson was diagnosed with aml last May, spent most of last year in Strong Mem. Hospital. I don't know, anything, does anyone know how bad this is going to get? time frame? My heart breaks for our grand son and my step daughter. Any one have any answers?