Topiramate neuropathic pain
Common Questions and Answers about Topiramate neuropathic pain
topamax
Has anyone had success with Topamax for neuropathic pain? Thanks in advance...
But its the pain in my chest i wanted to know about it was my doctor who prescribed the Amitriptyline tablets he said they where used years ago to treat depression but would do the same job for my pain and he said it sounds like i have damaged nerves in my chest they did take away the soreness but its comin back again i have it now about 7 months he also called it Neuropathic pain its like a burning ,stabbing ,aching pain very uncomfortable its even a worse pain tht the frozen shoulder please
Sometimes this causes me to have wake up with pain/tingling in my feet as a side effect. I find relief from this pain by using a "hidow" electronic massager that uses electricity on the bottoms of my feet. I'm not sure if that is relevant but that's what I had just started using when the pain in my feet was so intense.
Ive taken this for about a year now and its been SUCH a lifesaver. It prevents migraines.
How does Rolaids or tums help with the tingling sensations caused by taking topiramate?
I am currently on Keppra and Topiramate and have just been told my latest tests are showing major kidney damage from the topiramate. I have been on these two meds since 2002. I have to admit, reading all this is very scary. NO Other Meds have worked to control my seizures ! PERIOD!! Plus I have severe Migraines and Short term memory is almost gone in a matter of seconds. What is a girl to do?
Signed....
Tami....
You can call the pharmacist who filled your prescription. Often they are better able to answer these types of questions than your doctor because they have access to all the databases available that contain information about drug interactions and so on. They are also much easier to get a hold of than most doctors.
I'm day 5 into taking Topiramate 25mg at night for migraine prevention. My migraine is a daily pressure headache at the base of my skull. I have Chiari malformation type 1 but neurosurgeon says I don't need surgery, thankfully. He and my neurologist advised i try Topiramate as Amitriptyline didn't suit me (made me suicidal) and my asthma prevents them trying me on beta blockers.
Hi, and welcome to the forum. Neuropathic pain is difficult to treat and we were lucky enough to have a pain management doctor wrtie up to Health Pages on the subject. Please click on the two links below. the first one is explaining what neuropathic pain is and the second is describing how to treat it and explaining why you want (actually NEED) to go slow. No one WANTS to go slow, of course.
http://www.medhelp.org/health_pages/Multiple%20Sclerosis/Pain---A-Primer/show/371?
He learned that the MSIR, given for the cancer treatment pain, was able to manage the neuropathic pain. There has been no etiology determined for the neuropathy. His Lumbar puncture was normal except for elevated protein. His skin is very hot when his pain is bad, & he is lightheaded & unsteady.
Hello, I was looking for some treatment options for General Neuropathic Pain as the only diagnosis my dr can provide me after negative EMGs both upper and lower extremeties and complete work up including MRIs, bone scans, x-rays, and blood tests.
My pain is debilitating sciatica like in both legs and ulnar nerve pain in both arms from shoulder down to the pinky fingers which feels like tightness in so many muscle groups. Pain for 2 years without answer or any treatment to help.
I hope someone can shed light on this. I have been experiencing neuropathic pain for 8 months after taking vitamins and supplements. My initial symptom was twitching in my left calf. This progressed with pins and needles sensation in more of my left leg. A week or so later I had similar symptoms in my right leg as well as significant numbness in my right thigh. Next I experienced parenthesis across my mid back at about th mid-thoracic level.
It could be neuropathic, though an unlikely possibility. Neuropathic pain can be managed with medications or nerve destruction.
3. Likely possibilities include referred pain from other regions, infections, inflammations, chronic irritation etc.
It would be best to get this evaluated by a urologist or an internist for an accurate diagnosis and appropriate management.
Hope this is helpful.
Take care!
I had my first migraine when I was 12 and they became chronic and literally everyday after two car accidents. (Rear end and head on). I am soon going to b getting my nerves on my c3-6 burned to help with the headaches and neck pain. I'm only 23 yrs old. I had to quit my career (cosmetologist) I loved it and right before my migrianes randomly became daily I had an offer to become a redken color artist and do hair in big time hair shows up on stage with many famous hairstylist.
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