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, fatigue, digestive stuff - is this a herx or a bad reaction?

 - UBBFriend: Email this page to someone!    
Author Topic: ceftin, fatigue, digestive stuff - is this a herx or a bad reaction?
BenRoss
Member
Member # 20227

Icon 1 posted      Profile for BenRoss     Send New Private Message       Edit/Delete Post   Reply With Quote 
Hi all,

Two weeks ago I switched my abx from Biaxin and Plaquenil to Ceftin. Since being on Ceftin, I've experienced periods of feeling hot, and have woken up about 5 times a night (as opposed to about 3 times a night before). The past few days I've started waking up less again, but my level of fatigue has really increased quite a bit. I've also been experiencing an increase in stomach upset.

Does this sound like a herx to anyone? I worry because my stomach is very very sensitive and I'm concerned that I could have leaky gut syndrome and that the fatigue and heat I'm experiencing is actually due to damaged stomach lining rather than a die-off reaction. Have other people had similar experiences with Ceftin. Did the fatigue lift and then people felt improvement?

I really appreciate anyone's thoughts! Thank you so much!!!

Ben Ross

Posts: 11 | From Florence, MA | Registered: May 2009  |  IP: Logged | Report this post to a Moderator
nenet
Frequent Contributor (1K+ posts)
Member # 13174

Icon 1 posted      Profile for nenet     Send New Private Message       Edit/Delete Post   Reply With Quote 
Hi Ben, welcome to lymenet!

I am currently on Ceftin, though on lower doses than most, as I am ramping up through heavy herxing. I had a huge Lyme load from over 20-30 years of untreated symptomatic Lyme.

Are you taking a probiotic along with your antibiotics?

The stomach issue sounds like a common side effect of many antibiotics, whatever they are being used to treat for. You might want to look into protective measures for your stomach, if you already had troubles in that area. I would definitely look into your diet if you haven't already, and begin a probiotic regimen if you have not.

If you haven't tried an elimination diet, that would be a good place to start. My stomach pains and GERD/Reflux did not completely subside until I removed gluten, dairy/lactose, nightshades, and fried foods, along with sugar and other items, from my diet.

If you have had Lyme-induced inflammation for a while you can develop food sensitivities, which can lead to more inflammation, and then cause leaky gut syndrome, stomach pain, and other GI problems. This might be a big part of your issue. An elimination diet coupled with probiotics and soem protective herbal regimens might help a great amount.


As for fatigue, that can be a very common Herx symptom, or it could be from leaky gut, as you mentioned, or from many different factors.

The best approach is to do an end-run around the possible downsides and improve your diet, take probiotics, and perhaps take a break from the Ceftin for a few days (my LLMD says this is safe when necessary, but check with your) and see if the stomach repairs.

I have an herbal stomach tea that I make to counteract my own stomach sensitivities - I had developed an ulcer before even going on antibiotics. It can really help your stomach heal over time, and protect it from damage, as well as your GI system. It's made of a few very safe herbs that you can find in many store-bought herbal teas. If you want that recipe I will be happy to share it.

Bottom line, it sounds to me, in my non-medical opinion, that you are experiencing herxing (I too get the overheating at night) and stomach pain as a result of the antibiotic side effects. These can be moderated or relieved with some protective measures.


As for Herxing, I hope you don't mind if I copy something for you that I posted yesterday (I only have so much brain energy per day):

Everyone experiences Lyme differently, and everyone experiences Herxing differently. Some people never Herx, some people never stop Herxing until they are in remission. Many seem to experience a cycle of Herxing, generally at the one-month mark, but this is not always the case.

Some begin to Herx a few hours after taking the new medicine or larger dose, and some won't Herx for a month, or anywhere in between. The reasons are many and complex.

In brief, Herxheimer reactions can bring about new Lyme symptoms, or increase old Lyme symptoms, and there can be just as varied and numerous Herxheimer symptoms as there are Lyme symptoms. Basically, you are turning up the volume on your Lyme by killing it off. The Lyme toxins that normally make you sick are increased when they die off.


I'm sorry this was such a long post - I find the more fatigued I get mentally, the less concise I become.

--------------------
Dr. C's Western Blot Explanation

Lymenet Success Stories

ILADS Treatment Guidelines

Medical & Scientific Literature on Lyme

"Long-Term Antibiotic Therapy Improves Persistent Symptoms Associated with Lyme Disease"

Posts: 1176 | From KY | Registered: Sep 2007  |  IP: Logged | Report this post to a Moderator
MorningSong
LymeNet Contributor
Member # 19989

Icon 1 posted      Profile for MorningSong     Send New Private Message       Edit/Delete Post   Reply With Quote 
Ben~

Welcome. At one time I was on Ceftin 500mg 2x a day and it made me very fatigued. In fact, I slept a lot on it.

Also, before taking it, my doctor advised me of taking a quality probiotic. I was informed to take the probiotics at a different time from the Ceftin to help ensure absorbing probiotics.

Hope this helps.

Posts: 515 | From In His Loving Care | Registered: Apr 2009  |  IP: Logged | Report this post to a Moderator
bettyg
Unregistered


Icon 1 posted            Edit/Delete Post   Reply With Quote 
welcome ben!! [Smile]

never been on ceftin; no experience to share.

have you been tested for FOOD ALLERGIES? many times that is effecting your stomach.

Welcome; i'm so glad you found us!! You've come to the right place for education and support!


Dr. Burrascano's most recent "Diagnostic Hints and 2008 Treatment Guidelines for Lyme and Other Tick Borne Illnesses" .

PAGES 17-19 discuss ADULT & KIDS MED TREATMENTS!

http://www.ilads.org/lyme_disease/treatment_guidelines.html


Dr. B's Supplement List
http://www.lymepa.org/Nutritional_Supplements.pdf


this link, making the most of your LLMD visit, may help you also.
http://flash.lymenet.org/scripts/ultimatebb.cgi?ubb=get_topic&f=1&t=020605#000005

http://flash.lymenet.org/ubb/ultimatebb.php/topic/1/77378

***************

TREEPATROL'S NEWBIE LEARNING LINKS ... over 1000 links of good info and guidelines galore!! MUST SKIM & READ !!

http://flash.lymenet.org/ubb/ultimatebb.php/topic/1/29917
************************************************************************


Betty's suggested POSTING GUIDELINES . many of us have neuro lyme where we can NOT read long solid block text and be able to comprehend and read it as is.

please edit your post by CLICKING PAPER/PENCIL ICON to right of your name. that opens up BOTH subject line and body text.

now please break up your WORDY SENTENCES into one sentence paragraphs. Then hit ENTER KEY ``TWICE`` after each paragraph; we need that space for comprehension.

then go to left hand corner and mark box to receive ALL REPLIES, and click EDIT SEND

we thank you for helping us; [Wink] otherwise, we will SOB, SCROLL ON BY, since we can't read to help you. If I see posts like this, I SOB them; to hard on me.
------------------------------------------------------

People seeking doctors might be able to get help from their state online information and support group. Nearly 3,400 people belong to state groups. Some of the groups are small but more than 20 of them have 50 or more people and seven have over 100.

To find your state group, go to
http://health.groups.yahoo.com/group/statenamelyme

Type your state name and lyme as one word, like this -
http://health.groups.yahoo.com/group/newyorklyme

South Carolina is the only state that needs a hyphen between the statename
and lyme, e.g. http://health.groups.yahoo.com/group/southcarolina-lyme

The groups are moderated and you have to apply. Most don't allow doctor names, but once on the group, you can ask for doctors in a certain area and ask people to email you privately.
*******************************************

This explains the medical politics around lyme WHY you need an ILADS-educated or ILADS-member LLMD (and there are also some ILADS-member LL NDs (naturopathic doctors):

www.clinicaladvisor.com/Controversy-continues-to-fuel-the-Lyme-War/article/117160/


TESTING

You should also be evaluated for coinfections. Not all tests are great in that regard, either, but a good LLMD can evaluate you and then guide you in testing. One of the top labs is:

www.igenex.com IGENEX

-----
There are a couple other good labs for certain tests: Fry; Clognen; Focus. Your LLMD will know.
========================

VERY important to read - even BEFORE testing:

Dr C's Western Blot explanation is discussed here:

http://flash.lymenet.org/ubb/ultimatebb.php?ubb=get_topic;f=1;t=042077

"With most infections, your immune system first forms IgM antibodies, then in about 2 to 4 weeks, you see IgG antibodies. In some infections, IgG antibodies may be detectable for years.

Because Borrelia burgdorferi is a chronic persistent infection that may last for decades, you would think patients with chronic symptoms would have positive IgG Western blots.

But actually, more IgM blots are positive in chronic borreliosis than IgG. Every time Borrelia burgdorferi reproduces itself, it may stimulate the immune system to form new IgM antibodies.

Some patients have both IgG and IgM blots positive. But if either the IgG or IgM blot is positive, overall it is a positive result.

Response to antibiotics is the same if either is positive, or both. Some antibodies against the borrelia are given more significance if they are IgG versus IgM, or vice versa.

Since this is a chronic persistent infection, this does not make a lot of sense to me. A newly formed Borrelia burgdorferi should have the same antigen parts as the previous bacteria that produced it.

But anyway, from my clinical experience, these borrelia associated bands usually predict a clinical change in symptoms with antibiotics, regardless of whether they are IgG or IgM."
===========

TREATMENT *** www.ilads.org

ILADS
The International Lyme and Associated Diseases Society (ILADS) provides a forum for health science professionals to share their wealth of knowledge regarding the management of Lyme and associated diseases.
===========
i'm going to try to post a link here with info on SUCCESSFUL LAWSUITS WON ON LYME DISEASE from www.lymenet.org site!
look on LEFT side :legal resources" !! all WINNERS!

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.