This post is super old but I have multiple sclerosis and when you say it starts from your head and goes to your feet, that was something I had years before I was diagnosed with MS by an ER doctor and an MRI. I did not notice the buzzing/electric feeling all the time. I told doctors too and got no suggestions. It is called Lhermitte's sign. It is closely paired with MS but general cervical spine issues as well. I felt the first one at 21 years old. Was told to get MRI but did not so...Then along with other issues, ended up in the ER, age 32 or 33 years old. That was when I was diagnosed. Your post says you felt it in your teens and on through to 28, last year. It could be spinal issues or who knows. But if you have not, maybe ask a doctor about MRI, if it is still an issue or bothers you.
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I have the same thing its like I need to unplug something. The electric buzzing isnt in my ears either, its in my brain it feels like. It comes and goes.
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This was me until finally I got an Occipital Neuralgia diagnosis. Stimulated needles every couple weeks have been helping!
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It took almost 2 years of brain buzzing and other symptoms until I was diagnosed with OCCIPITAL NEURALGIA. I had seen my doctor and an ENT, neither found anything wrong. I am now almost completely free of symptoms. Treatments that have worked are acupuncture (including stim needles) and manual muscle release.
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Why isn't anybody thinking about our devices or 5G, is being ignored and blamed on medication really?
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How do you know when they turn it up or surge? Is there a website? I feel lit strong today after the gov test.
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