Neuropathy and Caffeine?

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Has anyone noticed and increase of neuropathy with caffeine consumption?

I've had intermittent neuropathy that I have noticed seems to correlate with my tea consumption and I'm wondering if it's coincidence or causation.

Comments

  • Vslush
    Vslush Member Posts: 183
    edited September 2018

    Thank you for this, as I've got lingering neuropathy (slight), and the one thing I haven't given up is Mt Dew (I know, Soo bad!). Never thought about the possible connection. Hope someone comes along with some insight on this.

    Vickki

  • WC3
    WC3 Member Posts: 1,540
    edited September 2018

    Vickki:

    There is surprisingly little information out there on the subject. But I am two weeks out from my last infusion and yesterday I had no neuropathy yesterday. I had some unsweetened green tea that afternoon though and woke up with neuropathy today.

  • Vslush
    Vslush Member Posts: 183
    edited September 2018

    I think I will try to drink only water this weekend and see if it goes away. Bring on the caffeine withdrawal headache! Lol. I'll let you know if it makes a difference!

  • Vslush
    Vslush Member Posts: 183
    edited September 2018

    Almost forgot... Congratulations on finishing chemo!!!

    Vickki

  • WC3
    WC3 Member Posts: 1,540
    edited September 2018

    Vickki:

    I worded that poorly. I am two weeks out from the infusion I just had. But my infusion next week will be my last infusion so I will take an early congratulations :-)

  • Vslush
    Vslush Member Posts: 183
    edited October 2018

    WC3,

    Wishing you well on your final chemo this week. May it be uneventful with minimal SEs. Ring that bell...you did it! ☺️🎉

    Vickki

  • L8Blmr
    L8Blmr Member Posts: 133
    edited October 2018

    WC3, I don't know if there is a correlation between caffeine & neuropathy, but here is my experience.. I did not drink caffeine during chemo and I had severe neuropathy in my feet. MO wanted me to take gabapentin, but I didn't want any more drugs. It was suggested by an orthopedic doctor to take 500mg Vit. C and 500mg B-Complex for nerve regeneration. Within 3 days of starting the C and B, the burning in my feet was completely gone. It has been 3 months since I started taking the Vit C and B-Complex and the neuropathy is about 95% gone. Last week, I started drinking one cup of coffee 3x/week and still no neuropathy.

    And YAY - you're done with chemo this week!! Congrats!!

  • Spookiesmom
    Spookiesmom Member Posts: 9,568
    edited October 2018

    green tea is higher in caffeine than black tea. I had some neuropathy before chemo from diabetes. Now I have CIPN. I don’t notice any difference in it with my caffeine intake.

  • WC3
    WC3 Member Posts: 1,540
    edited October 2018

    Plot twist!

    My dad says he gets neuropathy when he takes caffeine pills.

    I guess it's maybe something in my family.


    L8Blmr, Vickkig

    Thanks for the congrats :-)

    L8Blmr:

    Thanks for the tip. I've just been for going my morning tea but I would like to have my cake and eat it too so I will give the vitamins a try.

    Spookiesmom:

    Thanks for the input. Sorry you developed CIPN. Did it happen during thr chemo?



  • Spookiesmom
    Spookiesmom Member Posts: 9,568
    edited October 2018

    Yes, I had a severe reaction to taxotere. Was horrible. It’s also in my hands.

  • Vslush
    Vslush Member Posts: 183
    edited October 2018
  • Spookiesmom
    Spookiesmom Member Posts: 9,568
    edited October 2018

    chemo induced peripheral neuropathy.

  • Vslush
    Vslush Member Posts: 183
    edited October 2018

    Oooh! Should have known that one, just hadn't seen it acronym'd before. Duh! 😲

  • Spookiesmom
    Spookiesmom Member Posts: 9,568
    edited October 2018

    That’s ok, live and learn😄😄

  • CaliKelly
    CaliKelly Member Posts: 474
    edited October 2018

    Hi all! My cipn is still aggravating me, 3 years post TAC chemo and 1 year post Xeloda chemo. Tried all mentioned vitamins, otc topical pain rubs, Gabapentin (helpful about 50%) Cymbalta, (Not very helpful) and CBD oil( helpful, for short amounts of time). Don't drink coffee so that's not a factor. Since I'm a former fitness trainer, and workout every day, it's a real drag😜Has anyone tried BAK? Baclofen, Amitriptyline, Ketamine topical lotion? I've only read about it recently, going to ask my oncologist, be good if I could quote some other's experience. Cipn really sucks! Btw, CBD oil actually kills the pain and jumpy, tingly feeling,is relaxing ,esp.at night, but wears off after an hour or 2. Not the one from hemp, though, that didn't work. And I was against legalizing It!

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