posted
Anyone else get this? I get muscle twitches but only a portion of the muscle twitches, something impossible to do voluntarily. Like my thigh muscle will twitch, but only a long thin band of the muscle.
Scary crap.
Posts: 743 | From New York | Registered: Apr 2009
| IP: Logged |
posted
Many many people have muscle twitching. It was just one of many scary symptoms I had before I was diagnosed. Now that I know it's just Lyme and co, it's simply a reminder that I'm still infected and not dying of ALS or something! I've been treating for a year and a half and the twitching has subsided tremendously.
-------------------- IV graduate. As of 1/10, oral Omnicef, Minocyline, Mycobutin, Levaquin, and Flagyl. Lyrica and a bunch of supplements. Posts: 123 | From Atlanta | Registered: Mar 2009
| IP: Logged |
posted
I have the muscle twitching too but with treatment, it's gone away almost completely.
I have read that it has something to do with low magnesium and supplementation can also help.
It is nice to know that it is not ALS garunner...I thought that I had that as well once.
Posts: 114 | From Atlanta, GA | Registered: May 2009
| IP: Logged |
posted
still twitching. Have been treating for 2,5 years. Better though, but still here.
Posts: 347 | From sweden | Registered: Feb 2008
| IP: Logged |
posted
magnesium will help I take 750-1000 mg per day and it has all but knocked the twitching out.
Posts: 294 | From sw chicago suburbs | Registered: Apr 2007
| IP: Logged |
posted
From Dr B's guide: BARTONELLA & ''BARTONELLA-LIKE ORGANISMS''- � Gradual onset of initial illness. � CNS symptoms are out of proportion to the musculoskeletal ones- if a patient has no or minimal joint complaints but is severely encephalopathic (see below), then think of Bartonella/BLO. � Obvious signs of CNS irritability can include muscle twitches, tremors, insomnia, seizures, agitation, anxiety, severe mood swings, outbursts and antisocial behavior.
Bartonella is causing this type of symptom Dr B recommends levaquin as first choice, the rifampin. Others having some success with clarithro and bactrim.
-------------------- Ideas not advice. Posts: 448 | From Downeast Maine | Registered: Jul 2009
| IP: Logged |
posted
I twitch all the time, regardless of how much Mg I consume. It is better with treatment, but still bothersome.
Posts: 747 | From Utah | Registered: Apr 2010
| 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/