LymeNet Home LymeNet Home Page LymeNet Flash Discussion LymeNet Support Group Database LymeNet Literature Library LymeNet Legal Resources LymeNet Medical & Scientific Abstract Database LymeNet Newsletter Home Page LymeNet Recommended Books LymeNet Tick Pictures Search The LymeNet Site LymeNet Links LymeNet Frequently Asked Questions About The Lyme Disease Network LymeNet Menu

LymeNet on Facebook

LymeNet on Twitter




The Lyme Disease Network receives a commission from Amazon.com for each purchase originating from this site.

When purchasing from Amazon.com, please
click here first.

Thank you.

LymeNet Flash Discussion
Dedicated to the Bachmann Family

LymeNet needs your help:
LymeNet 2020 fund drive


The Lyme Disease Network is a non-profit organization funded by individual donations.

LymeNet Flash Post New Topic  New Poll  Post A Reply
my profile | directory login | register | search | faq | forum home

  next oldest topic   next newest topic
» LymeNet Flash » Questions and Discussion » Medical Questions » ceftin question?

 - UBBFriend: Email this page to someone!    
Author Topic: ceftin question?
bv
LymeNet Contributor
Member # 9578

Icon 1 posted      Profile for bv     Send New Private Message       Edit/Delete Post   Reply With Quote 
LLMD switching me to ceftin in place of doxy. Curious as to what to expect. I have tolerated the doxy well. Occassional gi issues, but not severe.

Has anyone had good results with ceftin? How about side effects? thank you for responding.

Posts: 213 | From ohio | Registered: Jul 2006  |  IP: Logged | Report this post to a Moderator
caat
Frequent Contributor (1K+ posts)
Member # 2321

Icon 1 posted      Profile for caat     Send New Private Message       Edit/Delete Post   Reply With Quote 
ceftin is a good one- it's the only oral second (or third? I forget) generation cephalasporin that crosses the blood brain barrier.

I followed 1 month of rocephin and flagyl with ceftin and tinnidazole and I think it got rid of lyme!! Now I'm working on co-infections.

Flagyl and tinnidazole work on the cyst (egg) life stages of lyme while ceftin and rocephin work on the adult stages.

Posts: 1436 | From Humboldt county ca usa | Registered: Mar 2002  |  IP: Logged | Report this post to a Moderator
yourtroubl
LymeNet Contributor
Member # 11087

Icon 1 posted      Profile for yourtroubl     Send New Private Message       Edit/Delete Post   Reply With Quote 
I am on ceftin and omnicef and am feeling alot of pain the last few days and fever.....I have only been taking 1 1/2 weeks. However, I dont have gi upset and usually I do.
Posts: 347 | From WV | Registered: Jan 2007  |  IP: Logged | Report this post to a Moderator
Cobweb
Unregistered


Icon 1 posted            Edit/Delete Post   Reply With Quote 
I took oral ceftin , 1000 mg 2x a day, for 11 months, with Doxy added after a couple months, and flagyl pulsed a couple of times.
Interestingly I continued to get a monthly rash for about six months. they subsided.

Now I am on IV Rocephin, in same class of Ceftin, and I really think , at least at this point, it is doing some real good.
I may still feel physically like a rundown old horse, but I feel more "connected" in my head.

Carol

IP: Logged | Report this post to a Moderator
WildCondor
Unregistered


Icon 6 posted            Edit/Delete Post   Reply With Quote 
I took 3,000 mg Ceftin with 2,000 mg Biaxin and 3 shots of Bicillin per week and it worked great! Lots of herxing in the beginning, but very worthwhile. [Smile] Good luck!
IP: Logged | Report this post to a Moderator
jif
LymeNet Contributor
Member # 9215

Icon 1 posted      Profile for jif     Send New Private Message       Edit/Delete Post   Reply With Quote 
just an fyi , and i am apparently sensititive to everything

ceftin was great for me, in SOME ways, the three weeks i was on it, joint pain went away, neurpathies greatly reduced, but HAD rashiness , itchiness, anxiousness, and crazy pelvic pain and bleeding, actually my first lyme symptoms. ie, when i first new something was really wrong, --but i had these under control b4 dx

so weird, ceftin, worked on some stuff brought back the old and bad, clearly i could not remain on it, even if you would call it a herx there are certains types of pai nthat you jsut can't continue w/, really i think it was an allergic reaction

so, it looks like it i great for some folks but if for some reason if it is bad for you, know you are not alone

Posts: 208 | From Santa Fe | Registered: May 2006  |  IP: Logged | Report this post to a Moderator
aiden424
LymeNet Contributor
Member # 7633

Icon 1 posted      Profile for aiden424     Send New Private Message       Edit/Delete Post   Reply With Quote 
I was on Ceftin for 8 months. It is one of the few antibiotics that I tolerate really well. I didn't get sick from it, but I also didn't see much improvements either. Everyone is different, so it could work great for you.

Kathy

--------------------
You never know how strong you are until being strong is the only choice you have.

Posts: 807 | From South Dakota | Registered: Jul 2005  |  IP: Logged | Report this post to a Moderator
Andie333
Frequent Contributor (1K+ posts)
Member # 7370

Icon 1 posted      Profile for Andie333     Send New Private Message       Edit/Delete Post   Reply With Quote 
Ceftin has been my primary abx for treating Lyme (in combo with rifampin and tindi).

I also herxed badly on the ceftin, but I'd gone undiagnosed for about 9 years and had a high high bacterial load.

I'm back at work finally (after being treated for 1.5 years). Still on ceftin, too.

For me, this has been a great abx.

Feel free to pm me if you want to know anything else.

Andie

Posts: 2549 | From never never land | Registered: May 2005  |  IP: Logged | Report this post to a Moderator
Health
Frequent Contributor (1K+ posts)
Member # 6034

Icon 1 posted      Profile for Health     Send New Private Message       Edit/Delete Post   Reply With Quote 
Caat,

I never read that the cyst was an egg. I read that the spirochete, went into a cyst to avoid the antibiotics, to hide from it.

that is why you are given an antibiotic to kill the spirochete, and then the flagyl to break open the cyst.

Then there is the L-form, which has no cell wall. I read in Dr B's guidelines that they are not sure if the Cyst form is actually the

L-form. Which would make sense, as the spirochete can loose its cell wall from what I read, and this may be the L-form, or the Cyst.

Trish

Posts: 1250 | From Canada | Registered: Aug 2004  |  IP: Logged | Report this post to a Moderator
caat
Frequent Contributor (1K+ posts)
Member # 2321

Icon 1 posted      Profile for caat     Send New Private Message       Edit/Delete Post   Reply With Quote 
check out the pictures on the first page of my website- the link is below. One is a cyst with spirochetes inside, the other is an adult spirochete with cyst attatched by what looks like slime. Also, if you look around the site there is a collection of studies/observations on cyst forms.

Yep, the correct word is cyst. I use the word "egg" as it's easier to understand. It serves the function of an egg. Baby spirochetes come out of them.

It is also possible that some of them could be hibernation chambers for adults. There are a couple observations that note cysts of 2 different sizes. I don't think there is any definite clear information on that, but it does look possible.

"Reverted to cyst form" could mean 2 different things- that the original spirochetes reverted OR that the spirochetes as a group reverted- they reproduced and the cysts survived while the adults did not.

The L-forms seem to be juvenile spirochetes. Not sure if anyone knows, but they might not be very different from adults. Yes, when they loose the "cyst wall" they are "hatching" and are juveniles or L-forms.

Posts: 1436 | From Humboldt county ca usa | Registered: Mar 2002  |  IP: Logged | Report this post to a Moderator
   

Quick Reply
Message:

HTML is not enabled.
UBB Code� is enabled.

Instant Graemlins
   


Post New Topic  New Poll  Post A Reply Close Topic   Feature Topic   Move Topic   Delete Topic next oldest topic   next newest topic
 - Printer-friendly view of this topic
Hop To:


Contact Us | LymeNet home page | Privacy Statement

Powered by UBB.classic™ 6.7.3


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, NJ 08534 USA


| Flash Discussion | Support Groups | On-Line Library
Legal Resources | Medical Abstracts | Newsletter | Books
Pictures | Site Search | Links | Help/Questions
About LymeNet | Contact Us

© 1993-2020 The Lyme Disease Network of New Jersey, Inc.
All Rights Reserved.
Use of the LymeNet Site is subject to Terms and Conditions.