Bottoms of feet sore
I have had 2 chemo treatments, A/C. The bottoms of my feet are really sore, I have 6 more treatments to go and I am thinking if my feet keep feeling this way I may not be able to walk by the time I am done. They burn and feel like I am walking on blisters although I cannot visibly see anything. I am wondering if anyone has found anything that helps with this. Anyone find any particular shoe or insole that helps? Has anyone found anything that gives their scalp relief from the itching and tenderness? Much appreciated.
Comments
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Sounds like neuropathy in your feet. There's meds that can help such as Amitriptyline and Neurontin. You should let your MO know as sometimes they have to adjust your chemo amount. You can also take the supplement L-Carnitine as its supposed to help too. My feet burned and felt like I had rocks in my shoes.
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I had this and posted some about it in the July 2011 chemo group thread. (I started chemo July 1st, so my postings on this may have been around the end of July or beginning of August.) My feet felt blistered. If I went for a walk, they would turn red and developed spots that looked like blisters healing (without the fluid). They did burn a lot as well. I found that it did not hurt to the same degree with each treatment. I did 4 A/C dose dense treatments. I think that it was around the 2nd that was the worst. Then the other treatments, it didn't hurt as bad. I found that when it was the worst, lotion on my feet with socks did not help, but putting my feet up above my heart on a giant pillow when I slept did help, not sure why - but it took the edge off the burning.
Eventually, when I went to 4 Taxol dose dense treatments, my feet started peeling in big pieces of skin. The largest was when more than my entire heel came off in one piece. Gross, I know! But I found when that was happening, it helped to wear socks when walking around my house, instead of barefoot. I also tried the lotion on my feet with socks on when I slept and that did help. Now I am struggling with neuropathy in my hands and feet from the Taxol, and it feels completely different. It does not burn, just feels tingly, numb and sometimes painful.
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My feet just started to do this. When it started it felt like I had walked around too long without shoes on. Then my feet turned really read and burned. I thought it may be from the Taxol as I had just had tx#1 when the burning started, but the onc nurse thought it might be from the AC. I found that putting Aquaphor or Neosporin on my feet with socks helped. Also a bag of ice when the burning got too bad.
Onc nurse also suggested taking benedryl, but that didn't seem to help me too much.
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JMULL: Mine started during A/C.
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martygra, I had really sore feet during chemo. The only shoes I could wear were adidas raziya. They had cushy gel insoles, oh so nice to walk on, and the mesh upper was easier on my tender toenails. For your itchy tender scalp, splurge on a satin pillowcase. It's ten bucks well-spent, so soothing. I use mine to this day. Best wishes!
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Hi
I'm having this problem with TAX. Crocs are the only shoes I can wear - cheap but effective and nice and bouncy.
I moisturise twice per day with emollient cream and keep my socks on and I've heard that cream with added urea can be good.
Laurie x
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Mine started feeling sore after chemo was done which was back in February. No improvement so far. I feel like I'm 80 years old when I get up from sitting or lying......hobble around for a few minutes. Feels like I am walking barefoot on pebbles. Some times one foot will be sorer than the other and other times both are sore. I just finished Herceptin Monday. I am hoping that Herceptin is the culprit and they get better.
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martygra, I had TC, and one thing that helped a lot with the neuropathy it caused was the vitamin supplement B6. I used Whole Foods own brand... 50 mg... and there was a noticeable difference when I started using it. Deanna
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Thank you all for your replies. My feet started feeling better a couple of days ago so hopefully it won't come back but if it does I will try some of your suggestions. I have noticed the last few days that the tips of my thumbs and fingers are kind of sore. I had a hard time unbuttoning my blouse the other night. Oh the joys of it all! Deanna did you take the B6 while you were having chemo or after? I have not been taking any vitamins or anything during this because I don't know if I am suppose to or not, I sure do not want anything to interfere with the treatment. I will ask the dr. when I see her on Friday. The best to you all, Mary
I
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martygra, I took it during chemo -- probably started after my 2nd or 3rd infusion, when I noticed the tingling, especially after I'd walked any distance.
As far as whether or not to take any supplements, what makes sense to me is that we not take supplements within the first 48 hrs. of an infusion -- just so that they don't potentially interfer with the circulating chemo. And I really think it's more Vitamin C and other antioxidants that could hypothetically protect cancer cells, although I don't think anyone really knows for sure. But since most of us certainly don't eat a balanced diet while on chemo, taking some basic supplements to ensure adequate nutrition might be a good idea, if your onc agrees. My docs were all on board with supplements throughout tx, but just cautioned about excessive Vitamin C or other antioxidants around infusion days. Deanna
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I also took a vitamin B6 supplement during treatment, along with CoQ10, 2,000 IU of vitamin D3 and a multi-vitamin.
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Ouch !! My feet are also sore they feel bruised !!! I get up like I'm 90 year old trying to find my balance , to find how won't hurt but after few minutes it eases , soon as I sit rest get back on them they ache , I finished Chemo in feb this year ...
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Hi, I will definitely be asking my onc about all this, anything I can do to minimize collateral damage sounds good to me! Wow Angelice you finished in February and you still have these problems with you feet, that is disheartening. Hope this goes away for you eventually. Thank you ladies.
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I had A/C then taxol from April thru Sep and there were days I could barely walk. I recently found the info below on the American Cancer Society message board. I have to say I think it has helped me and what woman can't use more calcium?
Researchers at Yale School of Medicine reported in a study published in the Proceeding of the National Academy of Sciences, a molecular basis for the peripheral pain or numbness caused by Taxol. It appears to be caused when the drug binds to a protein (neuronal calcium sensor or NCS-1) and initiates improper "calcium" signaling.
When Taxol binds to NCS-1, it makes the cell more sensitive to normal signals and increases the magnitude and frequency of changes in calcium. Over time, increased calcium levels activate an enzyme called calpain (no pun intended) that degrades proteins, especially NCS-1.
Calcium signals are needed for nerves to be stimulated and to respond and the loss of NCS-1 makes it more difficult to generate any calcium signals. While the loss of NCS-1 stops the protein interaction that is causing the inappropriate calcium signals, it also decreases the ability to have normal responses (PNAS 104: 11103-11108 June 20, 2007).
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Monirae, that's really interesting! Thanks for finding and posting it. I hope some of our BCO members who happen to be chemists or scientists or pharmacists can weigh in a bit on this info', which makes me wonder if the sequence of events in that explanation are all necessary for the Taxane to work properly and kill bc cells, or if adding a supplement or med to counteract some of the sequence would be safe and helpful. Deanna
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