posted
just started on flagyl yeaterday after being on doxy. anybody here have experience with that ? Its suppose to have excellent CNS penetration.
Posts: 41 | From new york | Registered: Mar 2006
| IP: Logged |
cantgiveupyet
Frequent Contributor (1K+ posts)
Member # 8165
posted
There is a post on Flagyl started by heatherkiss.
I just brought it back up for you. There are more posts too if you do a search on Flagyl.
-------------------- "Say it straight simple and with a smile."
"Thus the task is, not so much to see what no one has seen yet, But to think what nobody has thought yet, About what everybody sees."
-Schopenhauer
pos babs, bart, igenex WB igm/igg Posts: 3156 | From Lyme limbo | Registered: Oct 2005
| IP: Logged |
Carol in PA
Frequent Contributor (5K+ posts)
Member # 5338
posted
Patti, I don't have experience with this, but I'm bringing this back up, for more comments.
Carol
Posts: 6956 | From Lancaster, PA | Registered: Feb 2004
| IP: Logged |
HEATHERKISS
Frequent Contributor (1K+ posts)
Member # 6789
posted
ER,
I love flagyl! I herxed pretty good on it.
Ramp up slowly. It is worth the herx.
I've been working more, doing more around the house and thinking much clearer.
Now I'm waiting for my memory to return.
Hopefully soon,
-------------------- HEATHER
Posts: 1974 | From ABERDEEN, NJ 07747 | Registered: Jan 2005
| IP: Logged |
posted
All I can tell you is that my LLMD took me off the 1500 mg daily I was on plus the IV Rocephin, because after 3+ months on it I developed peripheral neuropathy in my feet. From what I've read, it could very well have been caused by the Flagyl, and I could be very well disabled permanently from it.
All I know is that I told them for almost 2 weeks my feet were burning, and all the symptoms, but I guess they fell on deaf ears. Now I'm in terrible pain, can barely walk, and on no abx for Lyme, wondering what's next. He's referring me to a neuro, and wants to see me back in 2 months.
I had no other problems with it other than this. I wish you the very best of luck, and healthy healing,
Jill
Posts: 203 | From Jacksonville, FLorida | Registered: Oct 2005
| 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!
Printer-friendly view of this topic