Has anyone experienced internal vibrations?

The 4th day after my covid vaccine I started with head tremors. They may not be related at all but yesterday, I started feeling internal lower abdomen vibrations/ sensations. I was thinking it was my bladder? Either way, I'm perplexed as to what it might be. Should I be worried?

Hello , a few weeks after my 2nd covid vaccine, I started having internal vibrations, tingling and more pronounced tremors from head to toe. This last week, I just started having a ringing or buzzing in my ears, that is constant. I have had a lumbar puncture that was normal, except protein was slightly elevated. All my other blood tests were normal. I am also a sufferer of migraines and have had some essential tremors half my life. I'm at a loss on what to do, but I am glad to have found this forum.

Do you still have the tremor? I'm a physician with similar issue that started after the vaccine. Trying to connect the dots...

Yes, I still have the tremors, and feelings of internal vibrations. It kinda feels as if my arms and legs have pins and needles in them, without the pain, as if they were falling asleep almost. I have had a long histiry of some essential tremors, but nothing like this, and this all happened several weeks post vaccine. My neurologist doesnt know what is wrong and wanted to treat my tremors with a low dose phenobarbital to seeif it helps, but I dont like the possible side effects. I want to know what is causing my issue. Could it have been my covid vaccine, that worsened my tremors? They were nothing like this before.

Are you still having these "tremors?" I'm trying to get a cohort of patients who have had this develop to then connect with and compare notes. I'm a physician and have had issues with this.

I have been reading all the talk on the internal tremors, which I have also experienced. I haven't been vaccinated for Covid, but will not get into why, it is a very lengthy discussion on its own. I have a few things to add to this that I have discovered in my last week's research. Symptom describing can make a HUGE difference in the area the doctor looks first. For example, I thought saying that "I felt a electrical sensation running up and down my spine" was the right way to describe one on my symptoms. I found that to be inadequate when using that terminology in a Google search and a Mayo search. What I found out I needed to say was "a vibration" the two ways of saying just one symptom made a major difference in what I was given to look up. Okay I'll get to my point. I have appointment with Doctor at Post Covid clinic on March 19th, 2022. Three months waiting for this appointment. The symptoms I started noticing after CV19, some of which I still have, some have stopped, new ones have begun to become a daily routine. I have been a fighter over every obstacle I have been thrown for years, but this time it's been different. This struggle has left me damaged in a way I didn't know was possible. I got to the point of questioning my own sanity. I ended up having to start seeing a therapist after years of not needing one. The pain and lack of sleep have placed an enormous burden on my mental health and overwhelmed my body, to the point of putting me on my back in bed. If not for friends and family I would not be here today. I have several autoimmune diseases, but I have learned so much in one week regarding one of them I have become overwhelmed. I typed this into a search engine just days ago "difficulty breathing while standing" okay I have what's called "Sjogrens Syndrome" my neurologist never made it seem all that big of a deal compared to my other diseases, so I didn't give it much research. The search on breathing brought me to a point on the Sjogrens International site with a warning to those who have it to study information that most doctors don't know about to tell us. I'm trying to make this shorter, doing my best. The Vagus Nerve is mentioned during the information, which is what grabbed my attention to this site as well as Sjogrens. Only specialized doctors even know what tests to run, so if you don't start with a doctor specializing with Dysautonomia, which Vagus Nerve also is attributed to, you may just be lost before you begin. Mayo Clinic has doctors that specialize in "Dysautonomia" of which there are 15 different types. This all has to do with the Nervous System and is quite overwhelming as there Soo much that can be wrong here. I'm just trying to give information to everyone with these out of the normal symptoms as much help as I have been able to find. If you want you can connect with me here and I will also try to put updates on what I find. I am on several groups of Mayo Connect. God bless!!

Yes yes yes. My psych nurse said it could be my medication. I have not seen the doctor yet but have a physical coming up. I call them internal tremors or quivers. Mine comes in spurts. I'll get them for a few weeks then go months without them then they come back again. I was worried it was a seizure thing. Because it happens so little I never think to ask my doctor when I see her. I hope you get it figured out.

I also have the internal vibrations pretty much 24/7. Calm mind, but body won’t quit vibrating! The vibrations are coming from my chest area. They make my head shake. I still feel them upon waking up from sleep sometimes. Can feel them in my tailbone if sitting on a hard chair. Feels like a phone buzzing in my pocket when there’s no phone in my pocket! Mine started after a low dose (10 mg) of Fluoxetine for a total of 13 days (not in a row) in January 2021. Persisting as of May 2022.