posted
I'm new to this world of Lyme. I've been infected for over a year but was just recently diagnosed in June and started treatment.
My primary symptoms are achy joins & pain. However, my problem areas are limited to the LEFT side of my body (left wrist, fingers, elbow, shoulder, ankle...) Is this typical of Lyme to only impact 1 side of the body? I haven't read about other people with such focused areas so I'm looking for feedback. Are there any explanations why symptoms would be focused in certain areas? Common to spread over time?
Thanks, -K
Posts: 44 | From Midwest | Registered: May 2010
| IP: Logged |
Tricky Tickey
Frequent Contributor (1K+ posts)
Member # 26546
posted
I read somewhere on this forum, I don't remember where, that it seems to affect the left side. I may be wrong, but I'm sure I read it somewhere.
-------------------- Early Disseminated LD- 2010. Currently doing acupuncture and yoga. Negative Igenex (IND & Pos Bands) ISSUES AFTER: Tendonitis, letter reversal, Low immune system. PREVENTION:SaltC,Iodine,Humaworm, Chiropractic. Posts: 1013 | From In a van down by the river. | Registered: Jun 2010
| IP: Logged |
posted
Since my Lyme symptoms started in 12/09, all have been on the left side except for tremors and ticks, which happen on both sides.
Posts: 319 | From Mass | Registered: Feb 2010
| IP: Logged |
nefferdun
Frequent Contributor (1K+ posts)
Member # 20157
posted
Lyme usually affects one side of the body while babesia and bart affect both sides.
-------------------- old joke: idiopathic means the patient is pathological and the the doctor is an idiot Posts: 4676 | From western Montana | Registered: Apr 2009
| IP: Logged |
posted
When my sx first started, they were all over the place. All areas would be affected on one side then theyd hop to the other. It was misery. I made some drastic changes and now they seem to affect the right side. But NOTHING like it was, and only lasts about 3 days on average. Im a recent diagnosis as well. Its definitely confusing and frustrating. A club i wish none of us belonged to.
Posts: 624 | From Oklahoma | Registered: Jun 2010
| IP: Logged |
canefan17
Frequent Contributor (5K+ posts)
Member # 22149
posted
All left for me
Posts: 5394 | From Houston, Tx | Registered: Aug 2009
| IP: Logged |
Tammy N.
Frequent Contributor (1K+ posts)
Member # 26835
posted
I'm very left-sided also. A lot of my symptoms are very neurological is nature, so when my symptoms started over 14 years ago, several docs thought I had MS (big surprise) (one-sided symptoms are common for MS). Just wanted to mention this so if a doc tells you possible MS, don't be scared.... Another reason to stay with a LLMD, because they will know better. I think it's fairly common to be one-sided with Lyme. Wishing you well, Tammy
Posts: 2238 | From East Coast | Registered: Jul 2010
| IP: Logged |
BoxerMom
Frequent Contributor (1K+ posts)
Member # 25251
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/