Not much to report today. Second and final day of Melphalan. We will return to the cancer center tomorrow for labwork and fluids. She feels pretty good — using the “give me more” button on the DAB pump when she needs it. Reinfusion aka DAY 0 will be Thursday. I’ve read a few other blogs of MM patients who refer to reinfusion as a birthday. Maybe there will be cake? Let’s hope it’s chocolate.