Chemotherapy-induced neuropathy: What helps get rid of it?
I finished chemo April of 2022
I have neuropathy in my fingers and feet. It doesn’t seem to be going away. What are treatments I can do to help get rid of it.
Interested in more discussions like this? Go to the Cancer: Managing Symptoms Support Group.
One more thing. I don’t know if you are on curative or palliative chemo. My mother had a different type of cancer, had palliative chemo and also had some neuropathy. If you are in that situation, I want to encourage you that my mom was very glad she got the palliative chemo and we, her family, treasured the extra time we had with her. I will be praying for you.
Hi @susan159, this must be disappointing. You probably thought you were out of the woods during treatment and getting neuropathy. Unfortunately neuropathy can sometimes appear as a late term side effect after treatment. It can take a while to see improvement and sometimes the neuropathy doesn't go away completely.
To help you discover what others are doing, I moved your message to this existing discussion:
– Chemotherapy-induced neuropathy: What helps get rid of it?https://connect.mayoclinic.org/discussion/chemotherapy-induced-neuropathy/
Like @nbkod7b mentioned, there is an entire support group dedicated to Neuropathy here: https://connect.mayoclinic.org/group/neuropathy/
You may also be interested in these discussions:
– Chemo-related Neuropathy https://connect.mayoclinic.org/discussion/1st-time-at-mayo-for-neuropathy/
– Need hope: Neuropathy from chemo https://connect.mayoclinic.org/discussion/needshope/
No one will want to hear this but as for me I am totally do not like the medical field any longer as to me it is a game with them and they don't really have a clue what is wrong and the diagnosis I think are just guessing. Mystery illnesses they don't know how to fix.
For the neuropathy in my hands, I found that wearing comfortably loose soft leather gloves, (I'm using dress, not work gloves), somehow provides immediate relief. Not sure how it works but I wonder if it may be as simple as the gloves insulating my hands from even slight air movement (I have hypersensitivity). The gloves also keep my hands warm which I find soothing.
I found that cold aggravates the numbness and hypersensitivity in my feet and that using toasty warm Epsom salt foot baths for a half hour in the evening provides an hour or so of relief. Also, I started using toe warmers. They are thin, adhesive backed pads you apply to the outside of your socks. They are air activated (I believe oxygen is the catalyst), and the brand I have are made by Sport Temp. They provide gentle heat for up to ten hours. I put them on about 1:00pm and remove them before turning in for the evening.
Curcumin may help.
https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9227889/
https://www.sciencedirect.com/science/article/abs/pii/S0944711318301454
https://www.frontiersin.org/articles/10.3389/fphar.2018.01374/full
https://www.sciencedirect.com/science/article/abs/pii/S096522991830966X
https://www.mdpi.com/2076-3921/9/10/950
https://www.mdpi.com/1422-0067/23/22/14058
https://www.mdpi.com/1424-8247/13/9/212
https://www.jstage.jst.go.jp/article/bpb/43/2/43_b19-00862/_article/-char/ja/
Be sure to talk to your oncologist about Curcumin. My oncologist doesn’t want me using it right now because of negative interaction with temozolomide chemo I’m on.
You may try acupuncture, and physical therapy, but of course speak with your doctor first.
You might want to look at research being done on this:
https://pubmed.ncbi.nlm.nih.gov/25050915/
https://pubmed.ncbi.nlm.nih.gov/30974966/