Hi, I'm having my nerve conduction tests tomorrow, can anyone tell me if they've been of help.? What info do they tell the neurologist? That kind of thing?
I've got my gabapentin at 400 a day which gives me about 90% relief and means I can mostly function normally, apart from dropping stuff because I'm getting arthritis in my hands.
Looking forward to hearing from you. :0)
Usually they want for you to be still while testing. You can chat a little between. For me at Neuro Science and Mayo, Hopkins, I had a tech, not the doctor doing the tests Never leave your appointment without a plan for breakthrough pain ( some sort of rescue plan as Mayo calls it) and also have a next step information sheet if the treatment that you are currently on fails to work....that way you will have your reading done, your mind made up and the doctor may start the treatment at that same appointment or at least get the ball rolling. Make sure that it's crystal clear who you need to call on weekends if it gets really bad (pain or other problems that come up) That first appointment is all about setting up how the two of you will take care of business - Always ask if you can increase the dose if it doesn't work well at your current dose... with you calling to let them know. You will be making yourself a partner with the doctor. They like this. =)
My wife had these tests which confirmed the type of neuropathy. We were disappointed that he did not offer any ideas as to treatment. My wife's condition has worsened and she is revisiting the neurologist next week.
Not sure this helps. But it is reality in our experience
My nerve test went ok. The doctor passed a comment saying that "something is irritating your nerves.." I just have to wait till I see my neurologist in June to find out what!
I hope you're all ok?
hi. i had the tests done a few years ago as my hands keep swelling up and getting pins and needles for no reason. they did the tests which said that they couldnt find anything. i do sincerely hope that they find something out for you, in the meantime ihave to make do with my swollen hands and tingles. good luck x
Hi, the tests went fine, they now think I have fibromyalgia, I still get the burning feet and swollen fingers and sore joints.... Fibro makes more sense with other issues I have too.... Hope you're ok?
Peripheral neuropathy
Chronic pain in both hands and feet. 
Baffled and 
Docs are trying to save my life
