Living with Multiple Myeloma
Receiving a diagnosis of multiple myeloma can be overwhelming and isolating. With many treatment options available, it is important to discuss the latest therapies with your oncologist and develop a care plan.1 This plan should take into account your goals and preferences. It is also essential to clearly understand what to expect from treatment—including possible side effects, how often you will need assessments and treatments, and what future treatment options might involve.1 Here are some helpful questions to ask your physician1:
What is the stage of my multiple myeloma and what does that mean?
Are there tests that I might need to help me understand how best to treat my myeloma?
How frequently might I need to come in for these tests?
What other professionals should I turn to for additional support?
Are there clinical trial opportunities we might consider?
Joining a support community may also be a consideration for people living with multiple myeloma. These communities can provide emotional support, information, and perspectives from other patients.
There are additional ways to support your physical and mental health and wellbeing through lifestyle choices and everyday activities.2 These include eating healthy foods, adjusting meal size and frequency due to appetite changes, resting, exercising, and informing your healthcare team about any depression or anxiety throughout your myeloma journey. All of these steps can make a positive impact on your quality of life.2
References
- American Cancer Society. Questions to Ask About Multiple Myeloma. Revised February 28, 2025. https://www.cancer.org/cancer/types/multiple-myeloma/detection-diagnosis-staging/talking-with-doctor.html
- Cleveland Clinic. Multiple Myeloma. Revised August 18, 2025. https://my.clevelandclinic.org/health/diseases/6178-multiple-myeloma
ALL URLs accessed April 18, 2026
