Has anyone used Cymbalta for nerve pain?
I just started Cymbalta wondering if anyone else has had sucess with it for pain in my feet and hands.
Interested in more discussions like this? Go to the Chronic Pain Support Group.
I just started Cymbalta wondering if anyone else has had sucess with it for pain in my feet and hands.
Interested in more discussions like this? Go to the Chronic Pain Support Group.
I can’t find confirmation for the nasal spray you were commenting on it
Can u please include the name
All I heard was they didn’t work
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1 ReactionYes I am.. and gabapentin but to be honest I don't think it helps me.
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1 ReactionI have been on it for about 3 years for neuropathy and stabbing pain in my legs and burning pain in my feet. Previously was on gabapentin and before that amytriptyline. It has worked well for the stabbing pains but I now also take topiramate which has helped with the burning pain. When the numbness set in and started escalating none on them seemed to help. I only had the numbness for a couple of years before it started affecting almost all of my toes and the bottoms of both feet. Heard about lipoic acid and that has returned almost all of the feeling in my feet except for a couple of toes.
Had started having neuropathy symptoms in my hands and forearms but this has improved n the lipoic acid.
For the past 3 years I have had a weird type of muscle cramps which migrate from one Muscle to nearby muscles causing each one to start cramping. Affect my feet, ankles, lower legs, knee area, hands wrists and forearms. Anyone have anything similar?
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1 ReactionJust started Cymbalta and Humira. BP went up. Thought it was the Humira but may be Cymbalta. Thank you.
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1 ReactionIt would be nice if Drs educated themselves about these drugs before prescribing them.
Do you take medication to help with your CRPS? Have you had any digestive or motility problems many years after the CRPS or heart abnormalities?
I agree about the medication deal. I was prescribed 7x the dosage for Fosamax during worst times during CRPS flares or fentanyl patches and I didn’t use these things. This was over 15 years ago. I was scared
I find it so sad that the medical community is aware of these side effects and the withdrawal problem but to support the drug companies still promote these kind of drugs. I was prescribed Cymbalta and absolutely could not take it. My doctors continued to prescribe anti-depressants for my FM, I always had terrible side effects including vision loss. I am not a depressed person nor have I ever been so my reactions are extreme. I continue to live with terrible pain because fear of addiction stops me from taking the opioids I would need.
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2 ReactionsI cannot tell if my weight gain is from Cymbalta, as I’ve gained weight in the last year and half. I’ve had a C5-6 discectomy and fusion with hardware. Since then I’ve been on so many medications. My current regimen includes Gabapentin, Nurtec, and Cymbalta. It’s terrible that we have to deal with this side effect when we already have so much else to struggle with.
Best of luck to you all!
Kat
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1 ReactionWhat do you mean by emotional stunting? And how does it affect your conversations? I do have brain fog at night mostly, but it could be a number of things for me. I’m just curious how it affects you.
Thank you.
Mainly conversational, I seemed to be late in contributing to day to day interaction with people, usually pretty engaging and humorous however on this drug I feel a little zombiesh.
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