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Has Anyone Had Hand Pain?
I have a question , my stem cell transplant was Oct 2018, in remission . Recently my hands have become painful, I’m still active and working but it’s frustrating and worried it will get worse .My oncologist said I need to stop the Revlimid and think about “quality of life”, with no other alternatives , has anyone else experienced this? Are you familiar with other treatments?
I think this is an example of the reason patients are encouraged to get second opinions.
I do have some pain but it's mainly in my fingers. But I would think they could give you something..not just stop the revlimid and that's it. Do you think it's neuropathy? Good luck sugar..but I am so impressed with you for continue working. I don't work anymore..hope you feel better soon. Hugs
Hi Peter,
He is a MM specialist down at Emory, hematologist and researcher as well , that’s why I was so shocked he was just throwing in the towel with that minor issue
Nora....you really need a MM specialist, I think.
Yes, members of MyMyelomaTeam have shared their experiences with hand pain. One member mentioned, "The most pain is neuropathy in hands (oh my!!!!) and feet." This indicates that neuropathy, a common issue in multiple myeloma, can cause significant pain in the hands.
This AI-generated response comes from MyMyelomaTeam and other selected sources. It is not a substitute for medical advice. Always ask your doctor about specific health concerns.
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