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Over the years, I have learnt to ride these episodes out. I calm myself by acknowledging what I believe is happening, that it's just the natural transition between sleep stages, when my brainwaves are changing frequency, into REM. It happens to everybody while they sleep, but they are not consciously aware of it during their normal night's sleep. Being narcoleptic, it tends to be during the transition to REM when the conscious part of me wakes up and so I become consciously aware of it. Its just the electrical circuits in the brain doing the work it needs to.
I've discussed this with my neurologist, who was very interested in my theory, as I have proved him right on other aspects, such as the whole appetite link with narcolepsy, which I said for years before it was officially discovered.
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The "buzz" is neurological in nature, and can be an effect of SSRI withdrawal
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Hi, so I too experience these "brain buzzes", which luckily have not been life threatening, but have become a problem as of writing this on a daily basis.
Essentially one day out of no where (no anxiety/depression symptoms up to this point) I had a MAJOR one. It was on both sides of the head, and it caused tremors all over my body, and vertigo and disorientation. This happened once every week for three weeks, and triggered a long run of anxiety and depression. I initially began to see recovery when they doctors put me on Klonopin (for the "anxiety attacks" or possible seizures. and Trazodone (For sleep). While I struggled with anxiety and depression, the brain buzzes went away. Eventually I found that no antidepression meds were working on me, so I was only taking Trazodone, until I wasnt able to see a doctor to replenish it. Recently, they happened again, but much more frequently. I had been on a rather stressful week, but instead of happening once, they happen regularly while I am awake. Since picking up on trazodone and klonopin, the intensity has generally gone down, but the frequency stays. How I describe this sensation:
It is an inner buzzing, NOT on the surface muscles, but deeper within, on my right temple above that ear. The larger ones will extend the electric sensation to my entire head and cause higher amounts of accompanying symptoms. The small ones can sometimes just be buzzes, while others are tiny dizzy spells.
As was with the first one, they seem to be semi-random. I find that being more active/stressed causes them to happen a bit more frequently, but we shall see.
While I think the MAIN cause is an improper balance of sleep, I was hoping if anyone had this condition and was able to resolve it. When I go to my doctor next, I will mention serotonin levels and BVVP, as it is from one side of my head. I think its also safe to say each buzz is the same frequency, around 21 hz (or possibly the octave lower) (I have perfect pitch, and ive had enough of these lately I can determine its an F)
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I have Myalgia Encephalitis, Fibro Myalgia and Borderline Personality Disorder.
I get these "Buzzes or Zaps" in my head, in my teeth and when they're bad they literally zap from head to toe! I personally think they are nerve related because I've ground my teeth for years and think I have some nerve damage in my teeth which is why I get them so bad in my teeth!!
I hope this helps with your own research xx
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Have a nice day
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I see these messages were left over a yr ago but putting in my 2 cents for what that's worth anyway. I was struggling with the same thing also and I too thought I was losing it or imagining it when sleeping or something. I did tell doctors but this was so hard to put into words ( "yea rite lady buzzing") mmmhmmm lol. so seeing your post helped me a lot. I take Zoloft also along with a couple other medications and noticed it much more when I ran out. anyway just wanted to say thank u to yall's posts. so far this site is the only place I could find where ppl were going through same thing. helped a lot
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MRI and CT scans ruled out tumors; the Neuro at first was stumped, until he ordered an ENT visit. ENT diagnosed as Stapedius Myoclonus (aka Tensor Tympani). Very rare, but diagnosis confirmed by a 2nd ENT with a audio machine exam.
Treatment is a minor surgery that goes into the ear and severs the tensor muscle; takes about 5 minutes. I've been putting it off, as I don't like surgeries. I am intensely relieved now that I know what is causing it, and find that it doesn't bother me much anymore except when it flares (once every 6 months, for a few weeks). Also, the neuro prescribed Flexeril, a muscle relaxer, to help sleep when it's flaring. Good luck to all.
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