neuropathy in hands
Comments
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Here is what they give me
I'm on FOLFOX and before they give me my Oxi. I get an hour of Magnesium and Calcium via IV then Chemo then another hour on the Mag & Calcium. So far the neuropathy has been bearable, I just have to remove my fingers from cold things and I'm good to go.
Don1 -
neuropathycoolvdub said:Here is what they give me
I'm on FOLFOX and before they give me my Oxi. I get an hour of Magnesium and Calcium via IV then Chemo then another hour on the Mag & Calcium. So far the neuropathy has been bearable, I just have to remove my fingers from cold things and I'm good to go.
Don
Thanks for the info. I had heard there was something they give you via IV but since I'm taking pills and only see the doctor once a month, I don't know how this would work. I see my doctor on Friday and I'll ask her. Thanks again.
Carolyn0 -
Worse after chemo ended
Carolyn, I've kept my hands busy, knitting and other crafts, all during chemo and the 7 weeks since it ended. My neuropathy in my hands has steadily gotten worse. I've taken vitamins and calcium daily since my DX and cannot say it helped.
Nerve regeneration can take a very long time. It took over 5 years for the nerves in my leg to regrow after I was mauled by a dog. Hopefully this won't take half that time. ]0 -
Hi, Carolyn,
My partner
Hi, Carolyn,
My partner (johnsfo) had neuropathy pretty bad in both his hands and feet while doing Xeloda with Oxalyplatin. I'll see about getting him to respond also, but one thing he did was to keep our neoprene kayaking gloves (the same kind that go with a wetsuit) next to the fridge for the times when he needed to reach in there. They have rubberized palms that made easier to grip and they're sufficiently insulated that the cold didn't bother him. When he finished that round of chemo his hands got better first, then his feet. I know this isn't exactly what you were asking for, but hopefully it will help.
Adrian0
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