Worse Neuropathy After EMG Test?

Posted by joslyn @joslyn, Jan 8, 2022

I had an EMG test done four days ago, and my neuropathy pain has been MUCH MUCH worse the last three days. Anyone else? Suddenly, none of my creams, meds, and devices work to reduce the burning and tingling. What can I do???

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Profile picture for arcuri24 @arcuri24

I share your sentiments about doctors. Also, today I asked my primary care doctor if research was being undertaken to find a cure for neuropathy and he said yes it is being done. Then, why do we never hear about it? We do learn of other areas of research for other diseases. Are we a forgotten group? It sure seems that today's doctors have almost zero bedside manners. If anything, I come out of these doctors visits more troubled than before I went in. I seem to get better support and info from this support group.

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Yes, research has proven that there is absolutely no cure for PN and its effects. All we can do is adjust our lives and deal with it. PN made me retire early as my weak feet couldn’t get the brakes down properly and when you’re landing on a 6000 ft runway at 110kts, you need to get the plane stopped. Hang in there people.

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Profile picture for cit10jetjockey @cit10jetjockey

Yes, research has proven that there is absolutely no cure for PN and its effects. All we can do is adjust our lives and deal with it. PN made me retire early as my weak feet couldn’t get the brakes down properly and when you’re landing on a 6000 ft runway at 110kts, you need to get the plane stopped. Hang in there people.

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We all have a tendency to say "...there is absolutely no cure..."
Ivig, however, has proven to be quite effective in the treatment of certain types of neuropathy.
It is absolutely crucial that we are properly diagnosed.

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I had an EMG performed last summer with no apparent side effects. Since it is non-invasive, I can't imagine any long-term problems. However, I tried to have a trial of a SCS last Fall. About two months after that, I began to feel all kinds of neuropathic symptoms develop in my legs and feet. Was it that invasive procedure that caused all the new symptoms? Who know?(Only the Shadow knows)

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My NCS and EMG left me in terrible pain for about 4 days. I could barley walk.
This confirmed my suspicions i should never have been given a SCS, and it strengthend my resolve to remove it...didnt have much choice my body was rejecting hardware plus I couldn't ever use Stimulator again. Hope you feel better.

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