Is there hidden defibrillator inside my body giving me shock?

Posted by nickm @nickm, May 29, 2023

The electric shock I am experiencing is in the form of a violent convulsion. The best visual description I can provide is my whole body jerks similar to a patient who has been applied a voltage via a defibrillator.
The story gets even more interesting. I can release the electric charge in my body "on command." This I discovered accidentally when I started practicing meditation. When I go deep into a certain meditational state, the electric currents get discharged. At the present time, I am not looking at my condition as an ailment requiring treatment. I am looking at it more like a mystery that needs to be solved. Whoever can help me in any way or even point me in the right direction, will be a recipient of my gratitude.

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This is really interesting. I have experienced the “electric shock” as well. I have been told that it is related to energy.

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First, it sounds like you need to talk to a medical person about this. Then see where it takes you...good luck !

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Thank you @Ladybeintes and everyone else who responded to my post. As far as seeing a Neurologist, here is the rest of my story. Seeing a Neurologist (with Medicare) is not as easy as you might imagine. I attempted to find a decent Board certified Neurologist. Our scripted medical vending system in the USA goes something like this. It is like buying a burger online.
This Neurologist I found on the Internet has a practice attached to a major hospital. So I called to set up an appointment. The receptionist wanted to know why I wanted to see the doctor. I was taken aback. Seemed strange for a receptionist to ask such a question. I said I needed a Neurological Consult. The answer was not enough for her. She wanted to know what exactly was the problem I was calling about. So I elaborated on my concern to her satisfaction. She replied, "Oh we don't do that. We only do neck ache and backache and that kind of stuff" I said, of course under my breath, "The greatest health care system in the world"

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@casey1329

First, it sounds like you need to talk to a medical person about this. Then see where it takes you...good luck !

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Thank you, Casey, I am going to do just that. Tomorrow I am going to see my Primary Care Physician in order to get a referral to see a Neurologist.

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@mitfit

This is really interesting. I have experienced the “electric shock” as well. I have been told that it is related to energy.

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This sure is interesting. Tomorrow I have an appointment with my Primary Care. I hope to get a referral to see a Neurologist. If you stay tuned @mitfit I will keep all of y'all posted.

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@nickm

This sure is interesting. Tomorrow I have an appointment with my Primary Care. I hope to get a referral to see a Neurologist. If you stay tuned @mitfit I will keep all of y'all posted.

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Yes, please keep us posted. Thank you.

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Have you checked out if you have Lyme?

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Wow! I just recently started complaining of something very similar! I told my husband that it was an electrical shock feeling or like being tazed, even though I've never been electrocuted or tazed. I believe it would feel something like this horrible & very painful zap that I experience occasionally. I am not in control of this issue like you are. Maybe because I haven't done the meditating??? But it comes on like a freight train. One day I was home alone in the bathroom when it happened. I was relieved no one was home. I screamed out like someone had physically assaulted me. This is new for me. It started in February or March of 2023, I think. I have memory issues so my time may be off. I vaguely remember this happening once or twice last year but it was different. It was more subtle. It's now very strong & severe, almost violent! It scares me. I literally shake and spaz out like I'm being electrocuted or tazed. If you learn what this is, please let me know.

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@ladybenites

Tou need to see a neurologist.

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I saw a few different neurologists and none of them could agree or even name what is going on in my body. This is why I am here. I'm trying to find medical studies or at least some pioneers who are open to learning what is going on with the CRPS community and help us solve our problems cooperatively instead of a bunch of know-it-all doctors with their own agendas. It's unfortunate, but not every doctor has their patient's best interests in mind.

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