posted
Does anyone feel like they are virating on the inside. You can't see it only feel it. I have been getting them in my chest and my feet,they come and go.
Posts: 49 | From philadelphia | Registered: Sep 2008
| IP: Logged |
posted
yes, whole body feels electric, like a low current is always flowing, I take ativan to calm it down....
Posts: 208 | From Hudson Valley, New York | Registered: Mar 2008
| IP: Logged |
karenl
Frequent Contributor (1K+ posts)
Member # 17753
posted
I have this vibrating in my big bones on the left leg. It can get very bad during the nights. It gets worse when I take killers like My Oil, Tea tree oil, enzymes. I can get it better by rifing 3 minutes every day. I think it is not from the brain but there is bacteria/ fungi/ viruses actually in the leg. It was gone when I was on 15 HH a day, but is back when I take only 10.
Posts: 1834 | From US | Registered: Oct 2008
| IP: Logged |
Seems to be a pretty common symptom. Thanks for the links
Posts: 49 | From philadelphia | Registered: Sep 2008
| IP: Logged |
Keebler
Honored Contributor (25K+ posts)
Member # 12673
posted
-
Yes, indeed.
Magnesium is the best help when this happens for me. Also being sure that my blood sugar is not too low helps.
What is likely happening (in addition or due to infection) is that the NMDA receptors in the brain are too excited. The calming receptors need help. Magnesium is the number one thing for that.
You can take it to bowel tolerance. B-6 helps it get into cells. B-vitamins during the day time can help strengthen the nerves.
Liver support can help the liver move toxins out. Toxins are most of what causes the NMDA nerve receptors to be so "wired"
Nutritional Supplements in Disseminated Lyme Disease
J.J. Burrascano, Jr., MD (2008)
Four pages
=================
This book, by an ILADS member LLMD, holds great information about treatments options and support measures (including adrenal support and calming a "wired" body:
Boomerang
Frequent Contributor (1K+ posts)
Member # 7979
posted
Yes, DH complains of this quite often. He is currently on IV Vanco and the tremor/vibrating sensation seems to be worse right now.
Posts: 1366 | From Southeast | Registered: Sep 2005
| IP: Logged |
posted
Yes, and hate it! When mine is on high I tremor too. One of my worst symptoms, as someone said above, I feel like I'm plugged into an electrical outlet.
Actually, when this symptom was at its worst, everything I touched (in the warm summer months) I would get static shocked, it was crazy; I felt like a live wire; I was really a mess. I actually read some obscure paper online about a year later talking about Lyme disease patients - that many had a propensity to static shock. That was when I finally got serious, looked for an LLMD to try to get figured out.
This symptom is still there, pretty much constantly; but, after 10 months of tx so far, I will say it's very slowly improving (did I say VERY SLOWLY?)
Anyway, you're definitely not alone! TS
Posts: 566 | From West Coast | Registered: May 2008
| 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/