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.
Interested in more discussions like this? Go to the Brain & Nervous System Support Group.
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?
Well 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?
@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?
@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?
Thank 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!
Have you been tested for HyperPOTS
@novajeff Awesome news, you're able to stay active! Thanks for being real regarding your symptoms and acknowledging they still exist despite your activity..
Thank you for supporting the Connect community. Comfort in connecting with others is so important. No doubt you have made a difference in someone's life.
You mention having bad nights. How do you handle those?
No magic secret for the worse nights unfortunately…basically just feel cruddy when I wake up the next day from tired muscles and poor sleep.
I saw a neurologist today about my internal tremors that have been going on for 2 months now. He did a few physical tests on me and said I was ok. But I explained to him that I'm in constant pain from internal tremors, head tremors, hands/feet going numb, restlessness/akinisia, and more. He looked at me and said there's no way I could be experiencing all that. I can't believe the situation I'm in. I'm waiting to see another neurologist on April 8. It's really long to wait, but I have no choice.