CSN Login
Members Online: 10

Nuerontin/Gabapentin- Should I or Shouldn't I?

pluckey's picture
pluckey
Posts: 471
Joined: Jul 2009

Post folfox neuropathy- the more I walk or stand on me feet, the worse it gets.
Onc prescribed Gabapentin- from my internet research on patient reviews, everyone gained weight and it was a 50/50 relief

Anything else to keep the burning pain at bay when I walk ? I commute to work- drive to Train station, but being in the city, you want to walk around, leave the building, do errands etc....walking 4 blocks about did me in today. My first Zumba class in months was an epic FAIL! I can't imagine Yoga keeping the blubber away!

thanks

Peggy

Annabelle41415's picture
Annabelle41415
Posts: 4347
Joined: Feb 2009

I've been on it for years and it helps me and if I've gained weight it's only because of my diet. There is a big difference for me when the cold weather hits and when it does, even on the medicine, my feet and hands still ache but it's so much better being on it than not. You should at least try it and see how it makes you feel. If you don't like it or doesn't make much difference then don't use it again. Good luck.

Kim

ron50's picture
ron50
Posts: 1308
Joined: Nov 2001

My neuropathy was late onset ,around seven years after chemo. I have tried lyrica,neurontin and endep. None of them helped with the pain and burning at night. All the docs wanted to do was keep doubling the dose and thats when the side effects really start to kick in. I could not afford to keep on trying higher doses , In Australia these drugs are only on the pharmaceutical bebefits scheme when prescribed for epilepsy.Lyrica was costing me around $400.00 a month. Ron.

Doc_Hawk's picture
Doc_Hawk
Posts: 685
Joined: Jan 2012

Before I was diagnosed with cancer, I was told that I had neuropathy in my legs. I have two fractured vertebrae which were causing the burning and pain. So my doc started me on neurontin which stopped working after a couple of months. By time I was dx'd and started chemo, the neurontin was prescribed for every 4 hours, 3600 mg a day. We had to do that route before the insurance company would auth lyrica. It took about two weeks before the lyrica started to work and it's been absolutely amazing for me!

I really don't have much problems with my hands (other than my fingers splitting all the time) but the numbness in my feet is pretty limited and there's none of the burning or sensation of fire ants marching up and down my legs. I just cannot imagine how bad it would be without the lyrica.

smokeyjoe
Posts: 1428
Joined: Feb 2011

I pop over and read the Colon Club forums from time to time....a gal on there tried something called Bio Freeze. You can check out that discussion :)

Subscribe with RSS
About Cancer Society

The content on this site is for informational purposes only. It is not a substitute for professional medical advice. Do not use this information to diagnose or treat a health problem or disease without consulting with a qualified healthcare provider. Please consult your healthcare provider with any questions or concerns you may have regarding your condition. Use of this online service is subject to the disclaimer and the terms and conditions.

Copyright 2000-2014 © Cancer Survivors Network