I've been on one chemo or another since my diagnosis of MM in 2011. SCT in 2016. Now in 2026 food tastes awful and I have no appetite. Is anyone else having this problem with food? I've lost 25 lbs. over the past year. My Dr. doesn't seem concerned. Peanut butter is the most recent casualty. Right up until a few weeks ago It was one of the few things left I liked, but now it just tastes off. Horseradish sauce, butterscotch pudding and cinnamon rolls are still good.

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Playlist: Starting Treatment -Induction, Consolidation, Maintenance
What drugs are available in the induction setting? Is there an optimal induction therapy?
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Playlist: Nutrition and Diet as a Biologically-Based Therapy
What recommendations do you have for myeloma patients that do not want to try a whole food plant based diet?
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Playlist: Cytogenetic (Genetic) Testing in Myeloma- Updated
Should plasmacytomas be biopsied and tested genetically?
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