Internal vibrations: Anyone else experiencing this?

Hello- yes it’s a year and i am still having inner tremors occasional buzzing in soles of my feet . All diagnostic tests normal …. Had EMG last week and told its normal .., so i said most be long COVID effects md replied back or could be anxiety .. i felt so broken after hearing that… i know my body it’s not anxiety ….not sure at this point what i will do from here
Hang in everyone …. Keep fighting

Hi.
I to have been dealing with this since my first infection 02/22 and when I explained it to my doctor he had no idea what to say. This internal running causes me to loose sleep which bring on the migraine and vertigo. It's a horrible cycle and the only thing that helps a little bit is deep breathing. I wish I had more answers for you, this is such a horrible unexplained illness that we are living with. My life is slipping by.

Hi there..
The buzzing in my feet is now severe pain that keeps me awake with everything else! I seriously feel like I'm going to loose my mind with all this . I just got over a second infection and all the inflammation has returned. There has to be something the Doctors can do for us!!

I’m so sorry you’re going through this as well. I feel the same way, my life just feels like I’m just existing, not living. Most of the time I don’t go anywhere because of these symptoms (experiencing more than just the internal tremors). Can’t believe this is my life now.
I hope you find some relief and healing.

I have something similar. I describe it as adrenaline rush. It wakes me in the morning (early) and continues periodically through the day. I too have had the “anxiety” diagnosis. Well yes, I am anxious about my health. But that is a symptom, not the root of my many issues. There are not many answers out there.
I am in treatment. Mostly working to get inflammation down with antihistamine and vitamin C (amongst other things). I don’t really feel any better and like other posters, I mostly stay home with my life passing me by.

I had covid 19 in mid December 2019 for the first time. I picked it up on a mission trip to Belize. I left Florida healthy on Saturday, but by Wednesday I had a nasty cough with lots of clear mucous. No fever or fatigue at that time. When I returned to Florida I went to urgent care on 12/24 morning. Diagnosed with lower respiratory infection and put on antibiotic. I went back to Urgent Care the following week because the cough was horrific affecting my sleep. A chest X-ray was done, revealing pneumonia in the lower left lobe. I was prescribed levaquin and a cough medicine. I completed the prescription, but the cough continued with fatigue. I saw my primary care doc a few weeks later for the ongoing fatigue. I had that shaky feeling on the inside that I had never experienced before. I would fall asleep at night, but wake up and couldn’t go back to sleep. Hours of laying in bed unable to sleep.

Autonomic Nervous System Dysfunction or Central Sensitization Syndrome, stuck in fight or flight. I had the Stellate Ganglion Block procedure done. Game changer....it is what started me on my path to getting better. I flew out of state to have it done on my own, no referral needed. Vagus Nerve disruption, also comes to mind. Calm the ANS. Sound bowls or tuning fork vibration therapy is another slower route to fix in my opinion, TENS unit, NAD+/NADH, NAC, LDN also needed.

Sorry to hear what you have been going through. Yea this has been really tough managing symptoms and just getting through the day.
I really hope you find some resolve soon and completely recovered.

So glad to hear you’re feeling better. I have been doing some research on the vagus nerve and found some really interesting information. I’m going to talk to my doctor to see if it a possible cause of my symptoms which include; heart palpitations, digestive issues etc. And I see that acupuncture might reset the vagus nerve.

Continued good health to you.

I am curious too. I have something similar. I initially thought it was anxiety, but I had panic attacks in 1999 and it’s not like that. It’s more pervasive. It feels like a high intensity internally. An adrenaline rush is a good description of it. Like high pressure in my body. I’ve read some describe it as vibrations, but I wouldn’t describe mine like that. It’s severe intensity. I have checked my blood pressure during an episode before and it has always been normal! Odd. Blood sugar normal too. I have T1 diabetes. Well controlled.

I’m debating if I should start taking an SSRI and see if that helps. Neurologist prescribed it. I’m not sure what to do next. I also have taste/smell disorder, tingling/numbess in hands and feet. Not neuropathy, according to neurologist.