Eating well with multiple myeloma can feel complicated. Treatment side effects that lead to eating challenges — including loss of appetite, nausea, and changes in taste — can shift what, and how, you eat. Extreme fatigue can make meal prep feel harder, too.
At the same time, good nutrition can help heal and strengthen your body.
To better understand what works in real life, we looked at conversations from MyMyelomaTeam like this one titled “Have your eating habits changed since your myeloma diagnosis?”
MyMyelomaTeam members have shared how they adjust their diets, what helps them feel better, and how they manage challenges like low appetite or digestive issues.
Bear in mind that not every diet is right for everyone. Working with an oncology doctor or healthcare provider and a registered nutritionist can help you craft a diet plan that's best suited to your individual needs.
If you’ve tried any of these strategies, let others know whether you’ve found them helpful.
Many MyMyelomaTeam members describe shifting toward more plant-based foods, along with fish or lean proteins.

Many members say they eat less processed foods and sugary drinks, but they also make those changes in ways that feel realistic.
“I have switched… Read more
Appetite shifts and taste changes are common during treatment. Some people lose interest in food, while others find that familiar foods taste… Read more
Digestive side effects can make full meals feel like too much. Constipation, diarrhea, nausea, and taste changes are all common nutrition-related… Read more
What did we miss? We'd love to hear what diet changes you've made to improve symptoms or feel better.
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