Jordana
Frequent Contributor (1K+ posts)
Member # 45305
posted
For about two years now I've had shakes and vibrations in my head and shoulders, especially when I lie down.
Lots of other stuff of course but this was my initiating long term symptom and I wonder if it's going to stick around no matter how long I treat it. I've always tried to use it it s a gauge to see how I'm doing but I'm wondering if I should just get used to it and not consider this one of the symptoms that need to be gone for me to be "symptom free."
Thoughts?
Posts: 2057 | From Florida | Registered: Feb 2015
| IP: Logged |
me
Frequent Contributor (1K+ posts)
Member # 45475
posted
Where's my Magic 8 Ball when I need it?
I wish I had the answer. What I can say is that there is hope. I went from beyond hopeless to having some hope. Hang in there, k?
Maybe someone will have a better answer.
-------------------- Just sharing my experiences, opinions, and what I've read and learned. Not medical advice. Posts: 1431 | From USA | Registered: Mar 2015
| IP: Logged |
Phoiph
Frequent Contributor (1K+ posts)
Member # 41238
posted
I had internal vibrations constantly for 8 years. They were one of my initial symptoms, and the intensity grew as I became more ill.
Occasionally, during my recovery with mHBOT, they would return at a lower intensity when I had overtaxed myself, but eventually they disappeared completely.
It may have something to do (in part) with low adrenal function.
Posts: 1880 | From Earth | Registered: Jul 2013
| IP: Logged |
Jordana
Frequent Contributor (1K+ posts)
Member # 45305
posted
Thanks guys... Posts: 2057 | From Florida | Registered: Feb 2015
| IP: Logged |
bluelyme
Frequent Contributor (1K+ posts)
Member # 47170
posted
My vibrations just about stopped with roceph ,bvt 3x a week and iv magnesium .....also did ala and phosphatylcholine iv ?...recently pure mag oil topically has helped
-------------------- Blue Posts: 1539 | From southwest | Registered: Dec 2015
| IP: Logged |
The Lyme Disease Network is a non-profit organization funded by individual donations. If you would like to support the Network and the LymeNet system of Web services, please send your donations to:
The
Lyme Disease Network of New Jersey 907 Pebble Creek Court,
Pennington,
NJ08534USA http://www.lymenet.org/
UBBFriend: Email this page to someone!
![[group hug]](graemlins/grouphug.gif)
![[Smile]](smile.gif)
Printer-friendly view of this topic