posted
Thank you Meg for the link!! The nurse that was maintaining my PICC line actually told me about that support group. I am still looking for a LLMD to be able to contact if anyone knows of one. I was diagnosed with Lyme in 2008 and it was found in my spinal fluid in Sept. 09. I was put on 30 days of Rocephin (spelling?) in Oct. and it was a waist of time and money as I feel like total crap and all of my previous symptoms have returned to include cognitive deficits. Right now I feel terrible and I do not want to waist any more time seeing an ID MD. Thanks!
Diagnosed 2009, Infected lonnng time ago---- Posts: 17 | From NC | Registered: Feb 2010
| IP: Logged |
Siciliano
Frequent Contributor (1K+ posts)
Member # 15920
posted
Hi, Tomiss and WELCOME to our lyme site. We're glad you came to us for help.
I have sent you a private message (pm), click on the flashing envelope.
Also, check out our great "Medical Questions" forum where you can ask all the questions you might have and our wonderful, knowledgeable members will answer them. Just read some of the threads and you'll see just how informative they are!
-------------------- I'm sorry but I am no longer accepting any private messages due to my own battle with lyme. Posts: 3897 | From New Hampshire | Registered: Jun 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/