Has anyone experienced internal vibrations?
I started having the only way I can explain it is internal vibrations. I've had them for 3 months now, I went to t hihe ER and they told me it was anxiety. A doctor diagnosed me at a clinic as having Lyme disease I've started a 21-day prescription of Doxycycline I'm on day 7. I went to a psychiatrist a week ago to get something because of my nerves are just over the brink. He prescribed me Gabapentin and Valium I've only been on them a few days.
Has anyone experienced these internal vibrations?I have them almost 24/7 chest neck stomach from the hips down. I have more lab tests that should be in today, but the doctor's office said that they would not call unless there was some abnormality in the lab work.
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Welcome @honey0425, @novajeff shared his BFS diagnosis earlier in this discussion here - https://connect.mayoclinic.org/comment/231012/. There is another discussion that you also might be interested in:
-- Benign fasciculation syndrome (BFS): https://connect.mayoclinic.org/discussion/benign-muscular-fasciculation/
Have you been diagnosed with BFS? Do you mind sharing what you were searching for when you found Connect?
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1 ReactionI know this is a very old thread but I was just wondering how things are now? My internal tremors started a year ago but for the last two weeks every muscle is on fire. All my tests come back normal. The pain is killing me. Getting a referral to Mayo now.
Hello John, and thank you for welcoming me to the group!
I have not been diagnosed with BFS, or anything else for that matter. Like so many others, my doctors are baffled when I initiate a conversation about my situation. A few years ago, I began having what I always refer to as an internal vibration. It starts at about my neck level, and runs down the center of my torso, stopping at about the end of my tailbone area. I visualize it being in the center of my spinal column. I did suffer a lower back sprain in the late 1970's, and throughout the years, have basically maintained the same level of damage, excepting age related deterioration. In 2013, I began seeing a pain management doctor, who did series of lumbar injections, 2 per year, for a few years. They were helpful for my back pain. This was prior to the onset of the internal vibration. I just automatically assumed the vibration was somehow related to the spine issues. I am a self avowed detail maniac, and have a high level of self awareness regarding my body. I also watch for patterns and document timelines. So when I talk to doctors about it, I share specific and detailed information about what I experience. Usually, they stare at me with an eyes wide open look and puzzled expression. I've had 3 neurologists, an internal medicine doctor and an osteopathic doctor tell me they've never had a patient present with an internal vibration, nor have they ever heard of it. I always share with them that should they decide to google it, they will find hundreds of forums with thousands of people discussing very similar symptoms to mine.
Here are the specifics of my issue: It is NOT tremors. It is NOT twitching. It IS vibration, like you would expect if you were lying on a bed that has a massage feature that is turned to low. It is NOT constant. It is ALWAYS engaged when I wake up each and every morning. I sleep in zero gravity, and primarily stay on my back for 7 - 8 1/2 hours, unless my back is out of whack, at which time I may lower my bed and sleep on one of my sides. I have severe sleep apnea and sleep with a CPAP device. I generally do not have trouble sleeping; only on occasion will the vibration be strong enough to wake me up. As I begin my daily routine, the vibration usually is not noticeable. There are times, specifically when I'm stressed or when I drink too much caffeine, that it revs up significantly, and literally feels and sounds like a small motor running inside my body. Occasionally, it is so strong that I become nauseated and can even feel my body becoming anxious, with weakness and tension. I practice deep breathing faithfully, and do muscle relaxation exercises as needed.
The only 3 factors that I can determine are consistent are: the vibration is always present when I awaken; is strongest when I drink too much caffeine and when I am unusually stressed.
I have had nerve tests, and multiple MRIs, from my brain to my tailbone. Nothing stands out that can explain the vibration. Only every once in a blue moon do I become concerned that it is something dangerous. Practically speaking, if it were, I think I would have died by now.
The possible links that I've discussed with my doctors are: during one of my lumbar injections, while under sedation, my doctor called out my name and told me I was going to have to be still. After reading something related to misses during lumbar injections, I've wondered if there is any connection to a possible miss during that injection. In late 2018, I suffered a sudden onset hearing loss, as in overnight, I went from perfect hearing, to a moderate loss in one ear and mild in the other. I now wear hearing aids in both ears. My ENT was concerned that I may have Meniere's Disease. I have 3 of the 4 symptoms...sudden onset hearing loss, tinnitus and "full" or "plugged" feeling in only one ear. The only symptom I have not experienced is vertigo. There is no test to confirm Meniere's, so they have to eliminate other diseases that may involve same or similar symptoms. All tests have good results. Because I do not have the dreaded vertigo, my doctor has suggested we do the "wait and see". Lastly, I have read comments on other forums, regarding pinched nerves in the neck. I have had minor neck issues, so I wonder.
I will conclude with something my sister told me just last night. She has a friend who has something she describes as similar to what I describe. Someone has suggested to her that it may be related to being in close proximity to a 4G or 5G cell tower. I personally have read about people who have high levels of sensitivity to electromagnetic fields. I don't have a specific reason to suspect this is related to my internal vibration, but I also have no reason to believe it is not.
I appreciate the opportunity to share my experience with this issue.
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2 Reactions@honey0425, Thank you for sharing more details. Since you mentioned at one time you thought it might be spine related after an injury and some thoughts you had following what the doctor said while doing a lumbar injection, I thought about another discussion started by @jenniferhunter that may be helpful -- Myofascial Release Therapy (MFR) for treating compression and pain: https://connect.mayoclinic.org/discussion/myofascial-release-therapy-mfr-for-treating-compression-and-pain/
Have you heard of Myofascial Release Therapy (MFR)?
Welcome @manxkats, I'm not sure @crankyunicorn68 is still following Connect since she last posted 2 years ago. I'm sure @sallie70, @lcristobal, @honey0425 and others still following the dicscussion can relate to your symptoms and share their experience with you.
It's good to hear you are in the process of getting a referral to Mayo Clinic and part of a multidisciplinary team where hopefully you will get some answers and a treatment that helps. Do you know how soon it will be before you get an appointment?
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1 ReactionWell apparently my insurance will not cover anything at The Mayo Clinic, so I guess I am off to my 4th neurologist. None of my doctors have even heard of internal vibrations so I do not hold out hope. I do not have anxiety. I vibrate all day long, even my eyes which does not help to go to sleep. They feel less intense if I am standing, when I touch my arm or sit/lie down they are magnified. I have a pajama shirt that shows the vibrations so I wear it to each appointment. When you touch me you feel nothing. Within the last two weeks my leg and arm muscles feel like I swam across the ocean after running across the country All Day Long.
Has anyone on this message board received an answer for the vibrations???
@honey0425 Hello. I'm wondering if you would ever consider Mayo Clinic Pain Rehabilitation Center (PRC)? They offer a 3 week program that I believe may be of great benefit to you. PRC tackles much of what you describe. Have you heard of Central Sensitization Syndrome (CSS)?
CSS explains the sometimes unexplainable.
Here's a video about it in case you are curious:
How long have you been dealing with your symptoms?
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1 Reaction@manxkats What you experience must not be fun for you and very frustrating to say the least. I'm sorry. Are you presently taking nerve medication?
Do you not have out of network insurance coverage in order to attend Mayo? Is that why you were denied?
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1 Reaction@novajeff I know I'm responding to your post from last year but I was inspired by you and just had to give you a shout out!
What an impactful account of what you went through with BFS/CBFS and how you managed to come out on the other side through perseverance, a little luck, and positivity. I like that you say your mind and body improved, and you recognized you weren't dying from your symptoms or sacrificing degeneration. This is a huge revelation to pull strength from, and be able to manage existing symptoms in a more productive manor. Good for you!
Are you still able to maintain the activity level you mentioned last year at this time?
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2 ReactionsThank you!
I try to help people here and on the Reddit BFS group (things can get a little fishy over there, as fair warning) because I’m hoping I can give some comfort to some of the (probably MANY) undiagnosed patients suffering with these symptoms and when they google, thinking the worst.
To answer your question, yes, I am able to have the same if not better physical activity. Still ups and downs. Still bad nights and bad days.
Last night I had aching feet from it, and restless sleep, and when I woke, my calves were crampy and popping more than usual. Still, I hopped in the car and ski’d hard for 4 hours, and after some rest, I plan on paddle ball this evening. I’d say that’s pretty active!
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4 Reactions