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Tips for Managing Fatigue

Cancer-related fatigue is a common challenge. If you've faced it, we'd like to hear your tips:

-How do you manage cancer-related fatigue?
-Share strategies or resources that have helped.
-Any lifestyle changes or treatments you've found effective?

Your insights can support others on this journey. Thanks for sharing!

  1. I have been surviving CLL since 2015. Fatigue is definitely a constant challenge which is made worse by chemo.


    I have found it easiest to manage by literally taking it day by day. Keeping a positive mindset and embracing life for what it is has helped me. Some days I can do more than others. I do try to maintain protein in some form in my diet, even if it is in liquid form. And staying hydrated helps. The biggest tip I give anyone (and still have to tell myself) is to listen to your body! When your body says "Rest"... listen! It knows what it needs. Fatigue is not "Tired or Sleepy." When your body can't do any more for the time being it's okay.


    My biggest lifestyle change was asking for help and allowing people to help. I also don't drive right now. But accepting that my loved ones are there when I need them and want to be has been wonderful. It's brought us closer.

    1. that’s a good routine. I would give anything to be able to sleep that long at night! I suffer from insomnia. I have been prescribed sleeping pills but that’s counterproductive for me because it just puts me in a deep sleep and I still feel exhausted when I wake up. I do think maintaining a regular daily routine is helpful and I am just not that girl lol! I believe in my daytime naps! I got married last year and my husband had to adjust to that. When I don’t get to nap or rest I feel horrible.

    2. I am a BIG routine guy. I like my daily routines and I like them a lot. I try to stick to it whenever I can and when they are disrupted it throws my whole day, if not a few days, out of whack! You are not alone in that! Keep on keepin' on, DPM

  2. I have SLL and was diagnosed in Jan 2022. The fatigue is like nothing I’ve ever felt and a constant challenge as well. I’m not in treatment yet but I’ll find out in March how close I am to needing it. I’m not good at asking for help but I’m getting better! I think for me, the hardest thing is realizing I can’t do some of the things I want to do when i want to do them. It’s especially hard in the summer when all I want to do is walk the beach and sit by the water. Sometimes I’m just too tired to do it although some exercise if I can manage it can help. One day at a time!

    1. So agree - keeping active is important as is connecting with folks - Dennis(Blood-Cancer.net TEAM)

    2. why aren't you in treatment yet?

  3. I push through it until I can't anymore ten I lay down several times sometimes a day

    1. finding the balance of when to push and when to stop and rest can be a challenge. It sounds like you've learned your limitations.

  4. I finally got to remission with my AML but I’m still taking an oral chemo for maintenance. Both AML & the chemo gang up on me to give me fatigue almost everyday. When it’s not too bad, I do things in 30 min. - 1 hour increments. Then I rest.

    1. congratulations on your remission! It's good that you are honoring what you feel and resting when needed, I know that's not always easy. Thanks for sharing!

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