Chemotherapy-induced neuropathy: What helps get rid of it?

I am curious to know if it helps… my oncologist has already prepared me for the effects and said if they become intolerable then we stop that part of treatment. I already have nerve issues, so I feel like it’s going to be a quick ride with that particular part of chemo. (Oxipalatin)

I'm sorry. I'm not sure I understand your question unless you didn't read my first post as well.

I had minimal symptoms during treatment. The oxaliplatin was causing some numbness in my feet. I had an allergic reaction to the 11th treatment and stopped, but the neuropathy got worse afterwards. It's now been four months and I feel the symptoms are stable. I got an excellent benefit from the chemo so it seems like a small price to pay. I am able to carry out all activities of daily living and drive. I don't regret the chemo.

This was for the trial that was mentioned. I am wondering if it is successful with helping the neuropathy issues.

I finished chemo last May and the neuropathy my mouth has resolved, but I still have it in my fingers and feet. The doctors I talk to say there is no cure. It should resolve on its own but can take a long time. Nerves grow back very slowly.

I discussed that in a prior post. The trial has not been completed as of yet as they are still recruiting volunteers. They are testing the supplement niagen which I believe is nicotinamide riboside. I myself did not see significant improvement, but I don't know if I received the supplement or the placebo. Two different oncologists told me at the time that they had other patients who were seeing good results. I just recently had to replace my oncologist who moved out of the area, and decided to go back to one of the oncologists involved in the trial even though she practices 50 miles away. We did not discuss the trial, but before I left, she suggested I try niagen. I did not question her further as I didn't want to ask questions she might not be allowed to answer with the trial ongoing. It's a double blind trial which means the doctors don't know who is getting the placebo. My best guess is that the doctor and I both think I was getting the placebo. Here's a link to the trial information.
https://clinicaltrials.gov/search?cond=Peripheral%20Neuropathy&term=Chemotherapy-Induced%20Peripheral%20Neuropathy&intr=Niagen&aggFilters=status:not%20rec

This was published last year. May be trading one cancer for another?
‘ The dietary supplement nicotinamide riboside (NR) may increase the risk of developing a specific type of breast cancer and subsequent metastasis to the brain, according to a study from the University of Missouri (MU). The study authors noted this finding is in contrast to prior research linking the supplement to benefits related to cardiovascular, metabolic, and neurological health.’

Do you have the link to this study? I note the word "may" increase the risk rather than "does". That implies conjecture rather than statistics.

This one only one of many things published about the risk of cancer with NR. If you do a google search for nicotinamide riboside and cancer risks you will find them.
This is one of the ones I read. (I didn’t save the link)
https://showme.missouri.edu/2022/insight-to-popular-supplements-potential-role-in-cancer-progression/

Thank you for the link. The information was intriguing. Still, the words could and potential. The study was not done on humans. The clinical trial I mentioned involves a lot of monitoring with blood work, skin biopsies, and ultrasounds keeping a close eye on the possibility of cancer reoccurring. Participants are screened carefully, and must be cancer free. Again, I'm not advocating for or against. I don't regret participating in the trial, and would do it again.