Any updates on taking Gabapentin? I was on it starting off with 300 mg 3 times per day. I noted the nerve pain was not as bad, but I was like a walking zombie.

My doctor wanted to continue but with a much lower dose. 100 mg 1 times per day. Well I'm stopping it as it's not helping at all, but the fatigue is there.

Would like to hear other opinions on the results of taking Gabapentin for nerve damage?

tia ~Becca

I have been taking it for a few weeks. The great news is that I am experiencing no side effects, the bad news is that it is not helping my atypical facial pain. Best of luck.

Hi there, I have ulner nerve damage in my right elbow and severe osteoarthritis in my right elbow, I've was on on 3600 of gaba and 400 mg of morphine er before I had another arthroscopy, I'm now down to 160 morphine and 2100 of gaba but now I'm badly struggling with fatigue, today I've been in bed all day and I've been like this for months, up and down, if a get a reasonable day I seem to pay for it for the next few days, does this ring any bells with anyone ?

In my other reply I was confused .. anyway Neurontin is bad for your teeth so take extra special care of them ...

Yup...I suffer from the same... Pain double the vengeance n flairs for one day earned of slightest mobility...

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I take 1800 MG a day. It makes me dizzy and the memory loss is a bad side effect. I am hoping that CBD can help me lower the dose. My DR seems to think it could to the point of removing gaba from the picture. Fingers crossed, should find out in the next month or so. Will report back.

Good Evening / Morning All,
I just joined tonight, so please forgive improprities on my part.
Diagnosed with PN 7+ yrs ago that began as symmetrical numbness in soles of both feet that has progressed to severe PN in both legs.
Been on gababentine, 3200 MG daily, since initial diagnosis .
Stated baclofen 10+ yrs ago for c4-c7 injuries, 90 MG daily. Dr. started me on ropinirol 1 yr ago for related leg cramping, recently increased from 2 MG to 6 MG daily Very difficult for me to separate effects of combined meds from PN / spinal injuries. Balance is a problem now which I'm told goes with PN. Other than initial fatigue, none of these 3 meds have been problematic. Had meds others in the past that did give me trouble which I had to stop. The PN pain is constant but tolerable. Opiates were ineffective unless taken in such quantity that the sedation became worse than the disease. I'm still reasonably active but experience "severe cramping" when I've over - exerted .
I'm glad to be a part of your group and look forward to your insights.
Good night!