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Real members of MyMyelomaTeam have posted questions and answers that support our community guidelines, and should not be taken as medical advice. Looking for the latest medically reviewed content by doctors and experts? Visit our resource section.
December 15, 2025
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A MyMyelomaTeam Member

I work several jobs and am not particularly tired. Just get rest whenever you can and enjoy the days when you do absolutely nothing!! Eat a healthy diet and take your Vitamin D and maybe a multi vitamin. I do take small naps whenever I can.

December 15, 2025
A MyMyelomaTeam Member

Yes, we could start a club if we had the energy🤣. I'm 9 years in. I still get so tired. I've got a cold sinus infection which makes me more tired. So the IVIG I'm getting might not be doing it's job. Plus, I got a big old cold sore, so I'm calling to see if I need to up my dose of Valtrex. I've had shingles before and I sure don't want them again. Anyway, it's not just you. Big hugs to you.🥰 Walking and eating right does help. I usually restrict all sugar, but being the Holidays, I have eaten some. I don't think surgery food help my immune system at all.

December 15, 2025
A MyMyelomaTeam Member

Hi Clara - I sm 8 years post sct. Still on my initial response, taking 5mg revlimid, IVIG monthly and Zometa quarterly. I do have fatigue, some days more than others. This disease is complex as are the drugs we take. I have been told that Revlimid has an accumulative effect over the years. The other side effects of lower Gi issues, (lately) a lot of cramps and muscle spasms, disrupted sleep, a bit of so-called chemo fog, etc. , I think, also contribute to fatigue issues. I stay very active and try to ignore it but sometimes it catches up. I guess this is a small price to pay compared to the issues of so many others. Happy Holidays!

December 15, 2025
A MyMyelomaTeam Member

Absolutely, Yea ! I’m also in remission but feel fatigued every single day. My life and energy levels are not the same. It’s my new normal that I’m trying to accommodate.

December 15, 2025
MyMyelomaTeam

Are you experiencing fatigue even while in remission from myeloma?

Yes, fatigue can definitely linger even during remission. A MyMyelomaTeam member shared that they've been in remission for 17 years and still experienced fatigue during their journey. This is a common experience that many people with myeloma face.

Fatigue Show Full Answer

Are you experiencing fatigue even while in remission from myeloma?

Yes, fatigue can definitely linger even during remission. A MyMyelomaTeam member shared that they've been in remission for 17 years and still experienced fatigue during their journey. This is a common experience that many people with myeloma face.

Fatigue related to myeloma is different from regular tiredness—it doesn't always go away with rest and can persist even when the disease is under control. Unfortunately, fatigue can be difficult to completely resolve and may remain part of the experience for some time.

Why might you still feel fatigued in remission?

Several factors can contribute:
- Lingering effects from previous treatments
- Low blood counts that haven't fully recovered
- Thyroid or hormonal imbalances from past steroid use
- Emotional stress and anxiety about your health
- Poor sleep quality
- Reduced physical activity during treatment

What can help manage fatigue?

- Stay as active as possible with gentle, regular exercise
- Prioritize important activities when you have the most energy
- Practice self-compassion and don't push yourself too hard
- Address any reversible causes with your doctor (like anemia or thyroid issues)
- Maintain good nutrition and hydration

Many members find that gradually increasing activity levels helps reduce fatigue over time.

December 15, 2025

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A MyMyelomaTeam Member asked a question 💭
want to share a little update about my journey. Recently I went for a CT scan of my lungs, and today the doctor explained the results to me. They found some changes in my left lung compared to before. There are areas where the lung lining looks thicker, and a small mass in the lower part of the left lung has grown a bit since my last scan. Because of these changes, the doctors want to do another test called a bronchoscopy, where they use a small camera to look inside the airways and take samples to understand it better. Hearing all this was not easy for me. It made me emotional because it feels like one thing after another. But at the same time, I am thankful that I am already under medical care and the doctors are taking steps to find out exactly what