Getting electric, buzzing feeling in head, (brain), and eyes!!

Your experience is the closest to mine at this thread. Last time i had this buzzing feeling was 13 years ago. I was generally having this feeling while thinking on stuff extremely nonsensical.

For example one day i leave the house without telling anyone and come back two years later as if I was at home yesterday. And my family don't even think of asking where i was. My mom tells me breakfast is almost ready like we have seen each other the other night.

I was occasionally thinking on that kind of totally nonsense stuff on purpose and trigger this buzz.

Last time i had this buzzing feeling was 13 years ago. I was generally having this feeling while thinking on stuff extremely nonsensical.

For example one day i leave the house without telling anyone and come back two years later as if I was at home yesterday. And my family don't even think of asking where i was. My mom tells me breakfast is almost ready like we have seen each other the other night.

I was occasionally thinking on that kind of totally nonsense stuff on purpose and trigger this buzz.

My BP was high but heart rate low as well.
Electric buzzing in head flash in eyes & feeling some faint.
73 yrs. Old. ??

I've been off Prozac for a couple weeks now and the brain zaps are really creepy. Every 30 seconds or so if I'm standing up or sitting. If I lay down I'm fine. I hope it goes away eventually. I have 2 young children to care for. :(

Most insurances will not let you see a doctor out of network. If doctors in your insurance network have ever performed under the pineal surgery code you are at that Neurosurgeon's mercy as to whether or not they will perform the procedure. Even if you do get a doctor willing to do it chances are slim that he has the experience and knowledge that would fascilitate confidence on the part of the patient in the doctor's ability to perform surgery in almost the exact center of your brain. Most likely it will require fundraisers. I struggle with idea of reaching out to my community for financial help with surgery because I am not terminal. It can be very frustrating and a long time waiting to figure out a plan.
I have been dealing with a symptomatic pineal gland tumor for almost a year. It has severely depleated my quality of life. I am totally over medicated with synthetic neurological chemicals and have days I cannot get out of bed. Sadly it's completely curable but having two children and limitted income I am stuck filling prescriptions and being treated like a lunatic when I talk to doctors. In fact, when I first started having near syncope (a dizziness unlike anything most people will ever experience) I lost feeling in my arm and became nervous at the odd reaction my body was having I went to the local small town emergency room, I insisted that I was having something neurological going on as I have a strong grasp on my mind and body. I avoid doctors' offices if I can. The doctor at the ER insinuated that I was experiencing symtoms of hysteria and fed me an aderol. I was simply nervous because I thought I might be having a stroke. I, by no means, was overly excited if anything I had a sunserviant and submissive behavior until he was going to send me home with the diagnosis of "crazy". I insisted that a scan be taken of my brain and wouldn't you know it- 12mm pineal gland cystic tumor. I was told that they are never syptomatic and that finding was incidental. After my initial visit I continued to have escalating and life altering issues while the "hysterica"l lable followed me around on my patient chart from doctor to doctor. I never even thought that it was the "cyst' so I started to fear the unknown until I decided to inform myself and look up symptomatic pineal gland tumors/cysts in scholarly documents. Time and time again I read about people, just like me, with unbearable headaches, light and sound sensitivity, intercranial pressure, imbalance, numb or falty limbs, decreased mental clarity, spike in clumsiness, ringing ears, and depression. I was diagnosed with epilepsy before I took an EEG but The EEG showed no signs of epilepsy. I have seen many neuro-doctors. It has been insane. I advocate for myself with the very part of my body that is making me feel like c**p almost every day. I get tired of the judging condescention from medical professionals and the tests. I get sick of the medication. I am sick of explaining or readdressing my discomfort every day. But I know that I am not the only one who goes through this. The medical world needs to change. This issue is rare, but it is curable. I'm sick, like many of you, of listening to doctors tell me the world is flat.
I literally had one doctor address his views on the doctors in Houston and California who perform the surgery with great success by saying, "some doctors will do anything for money". This was to suggest that they are like cult leaders and people with these "incidental" pineal tumors are not really sick but looking for a cult leader in the form of experienced neurosurgeons and that these neurosurgeons are just taking advantage of a large group of hypochondriacs.
Eyes need to be opened and the way this condition is viewed, diagnosed, and dealt with needs to change. 

 

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Your description best describes the sensation I feel. I also think I can hear it but not through my ears which is hard to explain but you nailed it. I have had this happen for as long as I can remember, maybe since I was 4 or 5 years old. I am now 39. It doesn't hurt or make me dizzy but almost feels good. Sometimes just one or two clicks sometimes a few seconds long and at different frequencies and intensities. I have never brought it up with a doctor since it just seemed normal to me. However I have been working long hours where I may sleep 3 hours a day for as long as a month or for a few days in the week. I started to have more frequent and longer lasting clicks at a higher intensity than ever before and it started to scare me. I have since backed off from the crazy marathons of work and they did stop happening so frequently and at such intensity. But since then I notice them more and have been curious if anyone else has the same sensation. Seems to be normal and hasn't killed me yet but I have a feeling it has something to do with endorphin and serotonin levels in the brain and is some kind of electrical discharge.

I have the feeling threw many actions including speech when I get excited feels good almost when ideas come by specially when I describe ideas. It seems that when I am exploring electric charge I can keep it and transmit it. It seems that I can charge and let it go like a battery it turns on higher while publicly speaking .

I have this and I hate the feeling. It also coinsides with my fibromyalgia flare up. I don't know if the two are linked or not. I don't sleep of a night when I get this sensation as its almost like it put me into a too deep sleep. Now that does really make me sound crazy

PLEASE TELL ME THE ANSWER!

What should I do? Should I keep taking the meds or should I just of off it completely?

I have the "electric" feeling in my brain for a few years now. I went to the doctor and he said "dehydrated". I don't think so. However, another doctor stated it could be anxiety. So, not sure what it is, but..............

I also "hear electricity". I wonder if its the old electric connections in the building, or people's hearing aids, or if its all in my head. It seems like the tone changes in different rooms of my apt. I think it is in my head, no one else seems to hear it. I wonder if it is tinnitus, or the beginning stage of hearing loss. Only once it stopped for one second as I was falling asleep and I thought- "ah quiet, that must be what it will be like when I die". I would love to know the cause of this phenomenon, and if its internal electricity that I hear or from the environment.

Bog off, your comments though funny are not at all helpful

Hang in there, I am a fellow sufferer and have no idea where to turn to
for an answer.

I don't know if this will be much help, but have you looked into Exploding Brain syndrome? It's harmless and common in migraine sufferers