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6 months agoThis is my first post, Hello everyone . I had my right kidney removed October 30th 2024. I then started ketruda infusion every 6 weeks. The side effects are not to bad, but some are very uncomfortable. I get tired very fast, nauseous, joint pain, and eyes are either dry or running all the time. I was wondering if anyone else has had this, and how they coped with it.
Accepted Answer
Welcome to the community! Managing side effects from treatment can be challenging, and many members here have found helpful strategies for dealing with fatigue, nausea, joint discomfort, and eye issues. Consider sharing specific symptoms you're experiencing so others who've been through similar situations can offer their practical tips and coping methods.
3+ patients found this helpful
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6 months agoPrayers! 🙏
Community Member
6 months agoThank you. I am going for an ultrasound tomorrow.
Community Member
3 months agoHi Colleen. I also get Keytruda (200 mg every 3 weeks) with manageable side effects. My oncologist tried me on the 400 mg 6 week dose for 2 rounds and my side effects were greatly magnified. So I went back to the lower dose and am doing well. A long way of saying, ask your oncologist about getting your Keytruda in the lower dose. Let us know if that works for you. Good luck!
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3 months agoThank you so very much. I will ask my doctor, and keep you posted. Some of my friends want me to stop treatments, they say they're not good for me. I want to follow my doctor. I have faith in him. They are entitled to their opinion, but I'm the one going through it. I will see my doctor on the 10th of September for another treatment, I will see what he says about the lower dose. I will post what he says. Again thank you for responding. Have a wonderful day. And I wish you well
Community Member
3 months agoColleen- please listen to your oncologist, not to your friends unless they’re oncologists! I was diagnosed over 7(!) years ago with incurable stage 4 kidney cancer. Although my cancer is still there it is much smaller and I am stable. Unless somebody comes up with a cure I will be in treatment for the rest of my life. I trust my oncologist and the treatment he prescribes. After all he’s kept me alive a lot longer than originally predicted (2years at most). If you haven’t realized it yet, cancer is the scariest game of Whack-a-Mole you’ll ever play. Trust in your oncologist to tweak and or change treatment as needed (I’m on my 4th med regime). S/he should work with you to not only prolong life but to give you quality of life. I hope you have an awesome day!
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3 months agoThank you for your input, I appreciate it more than you know. I decided I am going with what the doctor ordered. I am so glad you are doing what yours said. They brought you this far. I will pray for you. Have a wonderful day.
Community Member
3 months agoSorry took so Long to reach out, I'm also in the process of moving, that alone is a stressful event
Community Member
3 months agoMoving is super stressful. And I imagine having treatment makes it doubly hard. Make sure you make time to rest and eat protein! When I fail to eat enough (75grams) of protein I feel dragged out. Wishing you a good week ahead!
Community Member
3 months agoThank you, you as well
Community Member
2 months agoWelcome to the community! Managing side effects from treatment can be challenging, and many members here have found helpful strategies for dealing with fatigue, nausea, joint discomfort, and eye issues. Consider sharing specific symptoms you're experiencing so others who've been through similar situations can offer their practical tips and coping methods.
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