People that use derogatory terms when talking of cancer, any type of cancer, are indeed showing their ignorance and perhaps their naivety in thinking there is no way they are going to be a sufferer or a carer for a loved one, in their lifetime.
The people that say this are not worth a second thought. Things have a habit of biting one on the bum ( pardon pun ) when we least expect it, then education on such matters involves a very sharp, steep learning curve. Its your support team that are important.
So... hand and foot, keep them nice and warm, nice thick socks, thermal gloves are good, avoid standing on cold tiles in bare feet like bathrooms etc use a moisturiser to prevent dry skin, get one of the family to do feet, very gently though, its easier for someone else to do your feet and more relaxing.
Every night, we would set aside one hour and I would sit down with my wife and gently massage her feet with Sorbalene, a good moisturiser. We did this for 2 years.
Peripheral neuropathy and dry skin was never an issue with her feet, some slight pn in her hands and that was after 8 rounds of folfox.
Keep your hands out of fridges / freezers etc, even loading frozens into bags at the checkout and unloading them at home, all these little things assist in minimising side effects of the treatment.
Take care
Wombat4
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