Sorry about the Lyme disease n yes I agree some Drs don’t have an idea what my vibrations are all about Except, on my MRI it does show a cyst n the spine about 3 inches long that may be preventing fluid to flow through properly. And he’s a Neurosurgeon who should know better n study more instead of telling me I need to follow up w a Neurologist. Well the one he had sent me to in the beginning only ran tests n didn’t want to get his hands dirty the way I feel. Just wants to sit back run the scans n then say sorry n not even evaluate or look over my back or neck. You can clearly see I’m hunch back from this. Meaning I have chronic back pain in 2 areas. Lower n mid back. When will Drs pay more attention to us? I just can’t understand it. It’s like they don’t have the time to study up on issues or talk w other Drs or Specialists to see if they’ve encountered such a thing. I can’t believe we’re the only ones with this problem. I’ve had this nearly 2 1/2 yrs now. I’m goin to Ann Arbor U of M next week n I Pray after their tests they know what my symptoms are all about. These vibrations r miserable at times. I’ve cried on my Dear Husband of 44 yrs shoulders since these started. My family is very patient of me. My lower half from mid back down to my feet. It’s like sitting on a rough motorcycle for hours but 10 times that amount. Some days like now it’s really angry. They’re rumbling to hard where I can just about hear it. I’m sure it’s spinal which explains my spondylitis or occipital nerves cause occasionally I can almost feel it at my chest n arms a few times. Not often just few times but they never seem to rest and I have to go to sleep this way. And when I wake up yep, they’re still w me. Only once I didn’t feel it for a day. And that’s when I had my total knee replacement n Nov. 21’ but I’m thinking that was due to maybe the nerve block or extremes plus the fentanyl that put me out. But 2nd day later they gradually built back up. We’re the only ones that knows how our Bodies work. I’m gonna have to be more voice full to get the needed attention. I know 1 Neurologist said last yr that might be next thing to go see Mayo Clinic. But I’m not sure how that works. My husband is retired but I do have good insurance (blue cross) darn these r Angry right now. I know after these started back in 20’ I was freaking out. My hands n arms was swinging like PD. Most people I’d imagine couldn’t handle this. I’m so grateful for my family and friends plus you Folks here. Knowing that I’m Not the only one. Our Drs need to follow up more n not get to over whelmed w getting more new patients. They should study up more on things I believe. There’s more diseases etc out there to understand. It can’t be just making another buck. I really appreciate responses to this. I’m so glad but sorry that I’m not imagining this. I just wish my Drs could feel this for 30 seconds n maybe it’ll dawn on them “yes, does feel like spine problems or how can anyone live w this? “ Thank you so much for your support n hopefully someone knows more about this. God Bless us All!

I too have had internal vibrations but my lyme disease test came back negative.
Over three years of this and seeing every specialist under the Sun and a million different tests too and last week my new Arrhythmia doctor told me my symptoms sound exactly like Vagus Nerve damage and problems with my Autonomic Nervous System. Vagus nerve malfunctioning falls under the Dysautonomia umbrella of symptoms affecting the Autonomic Nervous System.

The malfunctioning of your Vagus nerve can negatively affect every part of your body from brain, breathing, BP, pulse, bowels, vision and sensory issues