Neuropathy and Walking

markatger
markatger Member Posts: 314
edited March 2014 in Colorectal Cancer #1
Hi Everyone,

I posted about neuropathy a couple weeks ago. If you happened to read, I was debating whether to do the final 12th round of FOLFOX because I had finally developed neuropathy in my feet.

Well I went ahead and did the final round at the urging of my oncologist. Now I'm done...Woohoo!

My neuorpathy isn't too bad..only in my feet. It consists of mild pins and needles and the feeling that my feet are cold. It really is more annoying than painful. I bought a foot warmer today.

I am wondering if staying off your feet is recomended? Does walking a lot make the neuorpathy worse and lengthen the healing time?

The first time the nueropathy bothered me was after we went for an early spring long-ish walk. I asked my onocologist if walking was bad for nueorpathy. All he would say was that trauma was bad for it. Does being on your feet a lot count as trauma?

Its frustrating to me because I am healed up from my surgery in January and finally all done with chemo. I'm ready to get going on some projects and fun, but I feel a little limited still.

Thanks as always for any input,
: ) Maria

Comments

  • CAMaura
    CAMaura Member Posts: 719 Member
    Hi There - I am wondering if your neuropathy is becoming worse. Mine did after chemo ended; my feet had not been involved during chemo. Anyway, to anser your question about staying off of them, I would say no because xercise will help circulation. If I were you, I would think about two different supplements: Vit B6 and Alpha Lipoic Acid - both help with nerve function. It is important to think about this as a wave....it will be heavier and then it will, in time, subside. I am coming up to a year after chemo ended in May, and my hands and feet are still affected, but to a much lower amount; the first fews months after chemo were much more difficult. I hope you receive a few more posts to give other opinions, but I would still try to remain active. You might also try some sports which are not as hard on you feet, but which will still be healthy for you - like swimming or cycling. Give it a thought. All the best to you and I also hope you are feeling well and gaining strenth post-chemo! - Maura
  • DK2006
    DK2006 Member Posts: 126
    Hi Maria!

    WOW!! Done with chemo...let the healing begin!!

    I'm half way thrrough the folfox. How bad was the second half compared to the first half? What did your oncologist say to convice you to do all 12 treatments? I'm thinking of maybe stopping at treatment 10 or 11. I'm concerned about the long term effects of the oxaliplatin. Best wishes! Donna
  • KathiM
    KathiM Member Posts: 8,028 Member
    CONGRATS!!!!! I will be done with chemo for 2nd cancer on Wed this week.....I know what you are feeling!!!! Dancing!!!!
    My cancer #2 (1 was rectal) involves Taxol, a know neuropathy causer. I find that keeping SUPER hydrated (I drink water constantly...only bad thing is I have to use the restroom alot) AND B6 helps greatly.
    YEAAAAAAAA for NO MORE CHEMO!!!!
    Hugs,
    Kathi
  • mwomack
    mwomack Member Posts: 78
    CAMaura said:

    Hi There - I am wondering if your neuropathy is becoming worse. Mine did after chemo ended; my feet had not been involved during chemo. Anyway, to anser your question about staying off of them, I would say no because xercise will help circulation. If I were you, I would think about two different supplements: Vit B6 and Alpha Lipoic Acid - both help with nerve function. It is important to think about this as a wave....it will be heavier and then it will, in time, subside. I am coming up to a year after chemo ended in May, and my hands and feet are still affected, but to a much lower amount; the first fews months after chemo were much more difficult. I hope you receive a few more posts to give other opinions, but I would still try to remain active. You might also try some sports which are not as hard on you feet, but which will still be healthy for you - like swimming or cycling. Give it a thought. All the best to you and I also hope you are feeling well and gaining strenth post-chemo! - Maura

    My husband's onc. recommended the B-complex. Also, he was being treated for neuropathy by a neurologist years before chemo and he had recommended the ALA. This was after trying several prescriptions drugs for it. The ALA is the only thing that had really helped his non-chemo related neuropathy. He did struggle with chemo neuropathy at the end but it may have been because he did not take the B-complex or ALA consistently during treatments because of nausea.

    I was doing some research this morning and found the following:

    Many of the B vitamins have been found to help with symptoms of peripheral
    neuropathy, although high levels of B6 may worsen symptoms. The ones that are
    helpful are B1, B12 and folate. Try taking a multivitamin with vitamin E in it,
    and a B complex to help with symptoms of peripheral neuropathy. Make sure the B
    complex, sometimes called a vitamin B stress complex, has folate in it. Vitamin
    B12 can also be given by shots into a muscle every couple of weeks, and this
    probably gets more vitamin B12 into the body than vitamin pills. Drinking
    alcohol can block how your body uses folate and vitamin B12.

    I found this on nih.gov:

    Anyone taking large doses of vitamin B6 supplements for carpal tunnel syndrome
    needs to be aware that the Institute of Medicine recently established an upper
    tolerable limit of 100 mg per day for adults [12]. There are documented cases in
    the literature of neuropathy caused by excessive vitamin B6 taken for treatment
    of carpal tunnel syndrome [22].

    Too much vitamin B6 can result in nerve damage to the arms and legs. This
    neuropathy is usually related to high intake of vitamin B6 from supplements,
    [28] and is reversible when supplementation is stopped. According to the
    Institute of Medicine, "Several reports show sensory neuropathy at doses lower
    than 500 mg per day" [12]. As previously mentioned, the Food and Nutrition Board
    of the Institute of Medicine has established an upper tolerable intake level
    (UL) for vitamin B6 of 100 mg per day for all adults [12]. "As intake increases
    above the UL, the risk of adverse effects increases [12]."
  • lfondots63
    lfondots63 Member Posts: 818 Member
    Hi Maria,

    I agree with all the below but I have some things that alternative treatments I am doing also. I figure something should help. I am going to an accupuncturist for this so it doesn't get too bad. I only have only done 2 treatments but it just started after the second. The other thing is something that I am doing through my son's Tangsodo Karate Dojang. It is a very easy exercise program to help circulation call QiGong or also you can do T'ai Chi. These are both low impact but good for the circulation.

    By the way, WHOO HOO that you are done chemo. I can't wait to say that and yes you need to start having FUN! Take care.

    Lisa
  • markatger
    markatger Member Posts: 314
    DK2006 said:

    Hi Maria!

    WOW!! Done with chemo...let the healing begin!!

    I'm half way thrrough the folfox. How bad was the second half compared to the first half? What did your oncologist say to convice you to do all 12 treatments? I'm thinking of maybe stopping at treatment 10 or 11. I'm concerned about the long term effects of the oxaliplatin. Best wishes! Donna

    Hi Donna,

    My 12 rounds of chemo were interupted by surgeries so I think that might have made them easier. I did notice that the sick feeling lasted a little longer each time. But all in all it really wasn't too bad.

    I hope yours goes well : )
    Maria
  • markatger
    markatger Member Posts: 314
    CAMaura said:

    Hi There - I am wondering if your neuropathy is becoming worse. Mine did after chemo ended; my feet had not been involved during chemo. Anyway, to anser your question about staying off of them, I would say no because xercise will help circulation. If I were you, I would think about two different supplements: Vit B6 and Alpha Lipoic Acid - both help with nerve function. It is important to think about this as a wave....it will be heavier and then it will, in time, subside. I am coming up to a year after chemo ended in May, and my hands and feet are still affected, but to a much lower amount; the first fews months after chemo were much more difficult. I hope you receive a few more posts to give other opinions, but I would still try to remain active. You might also try some sports which are not as hard on you feet, but which will still be healthy for you - like swimming or cycling. Give it a thought. All the best to you and I also hope you are feeling well and gaining strenth post-chemo! - Maura

    Hi Maura!

    Thanks so much for your reply. They are always so helpful to me.

    I can't tell if my nueropathy is getting worse or better.

    I think I am going to try biking on a recumbent at the club. Thanks for the idea!!

    Maria
  • bonanza48
    bonanza48 Member Posts: 1
    neuropathy

    I had my 12 chemos for stage 4 Colon Cancer, then my second surgery to remove lymph node that shrunk from chemo. I have had neuropathy beginning  after last chemo too. Go ahead and walk, your feet will tell you when you need to stop as it is more annoying and yo wont want to walk any more. I never heard walking was bad. I hope your neuropathy goes away in about 3 months like I was told usually happens, mine didnt , been since end of May. I take Gabapentin, no side effects may help a little, but weaning off now as I have had diahrea symptoms since surgery and getting off certain medications may be helpful fo me. Good luck.

  • DD3
    DD3 Member Posts: 136 Member
    My wife has neuropathy from

    My wife has neuropathy from FulFox...  Her is her daily regimen.

    Gapapentin (prescription)

    Alpha-lipoic acid (600 mg)

    Vitamin D

    B complex

    And here is one her neurologist recommended.  Capzasin creme.  It's for arthritis.  However, helps with neuropathy.  Trust me when I say a little goes a long way. Tongue Out 

    By the way these are all approved by her neurologist.  Seems to help her and she is back to running 3-5 miles a day. 

     

  • wts
    wts Member Posts: 40 Member
    After my chemo with Folfox,

    After my chemo with Folfox, the neuropathy bothered me a lot but I still played soccer best I could having no energy. I found that the more I walked, ran, etc the better it got. Or maybe I just got used to it. Been little over a year since I finished chemo anf the nueropathy is 95% gone. Still notice it but more in the mornings.