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 » Tindamax

 - UBBFriend: Email this page to someone!    
Author Topic: Tindamax
VV
LymeNet Contributor
Member # 38828

Icon 1 posted      Profile for VV     Send New Private Message       Edit/Delete Post   Reply With Quote 
I'm about to try Tindamax. Who has some good stories on this one? I'm hoping this can put a real dent in the Lyme. I've seen the Eva Sapi research on it and have high hopes.
Posts: 922 | From Philadelphia | Registered: Sep 2012  |  IP: Logged | Report this post to a Moderator
Judie
Frequent Contributor (1K+ posts)
Member # 38323

Icon 1 posted      Profile for Judie     Send New Private Message       Edit/Delete Post   Reply With Quote 
It helped the first month I took it (I felt better, not worse). It unclogged something. I took a break, tried it again because I had such a good reaction the first time (the doc said it wasn't necessary, but since I did well, I wanted to try it again). The 2nd time it didn't work (I had an allergic reaction).

My doc said you don't need to treat with it for very long.

Tindamax can also cause peripheral neuropathy, I'd stop it at the first sign of problems like that (burning, pain, numbness in feel/hand/ankles, etc...)

Don't mistake a herx for an adverse drug reaction.

Posts: 2839 | From California | Registered: Jul 2012  |  IP: Logged | Report this post to a Moderator
surprise
Frequent Contributor (1K+ posts)
Member # 34987

Icon 1 posted      Profile for surprise     Send New Private Message       Edit/Delete Post   Reply With Quote 
Start very slow! Like a sliver. It was extremely powerful to me. But needed to build up, for sure.

My LLMD recommended same days off as on- pulsing. Got up to 2 weeks on/ off.

--------------------
Lyme positive PCR blood, and
positive Bartonella henselae Igenex, 2011.
low positive Fry biofilm test, 2012.
Update 7/16- After extensive treatments,
doing okay!

Posts: 2518 | From USA | Registered: Nov 2011  |  IP: Logged | Report this post to a Moderator
GretaM
Frequent Contributor (1K+ posts)
Member # 40917

Icon 1 posted      Profile for GretaM     Send New Private Message       Edit/Delete Post   Reply With Quote 
One of my favorite!

Tinidazole always always makes me feel better.

Action against all forms of lyme, action against protozoas, bart and babs.

It is important to pulse it.
My doc and another doc start one week on, one week off. Then when the worst of the herxing is over, two weeks on two weeks off.

VV your lyme reminds me a lot of mine.

I sure hope you feel good on tinidazole also.

It makes my energy seem "clearer" if that helps. I can't describe it.

Just better.

Posts: 4358 | From British Columbia, Canada | Registered: Jun 2013  |  IP: Logged | Report this post to a Moderator
rowingmom
LymeNet Contributor
Member # 41213

Icon 1 posted      Profile for rowingmom     Send New Private Message       Edit/Delete Post   Reply With Quote 
Our daughter used it 3 days on / 4 off. The first couple of herxes were hard, but subsequent ones were better, with resolution to a better baseline each time.

When she was barely herxing with each pulse we weaned to herbal protocols and haven't looked back. She's doing great!

--------------------
13 yo DX PANS/Tourette's/Asperger's/ADHD treated for Igenex positive bartonella/IND lyme with 2 years of abx treatment. Weaned off abx April 2013 at 80% improvement. Continuing with Buhner bartonella/babesia protocols. Aug 2014 99% improvement.

Posts: 265 | From Canada, Ontario | Registered: Jul 2013  |  IP: Logged | Report this post to a Moderator
Judie
Frequent Contributor (1K+ posts)
Member # 38323

Icon 1 posted      Profile for Judie     Send New Private Message       Edit/Delete Post   Reply With Quote 
I just took it straight through. No ramping, no pulsing. No herxing either, I just felt better.

I was on doxy and bicillin shots at the time.

I guess doctors prescribe it differently for different people. It did the trick it needed to do the first time and I was done.

Posts: 2839 | From California | Registered: Jul 2012  |  IP: Logged | Report this post to a Moderator
MTMT
Member
Member # 40756

Icon 1 posted      Profile for MTMT     Send New Private Message       Edit/Delete Post   Reply With Quote 
I saw great improvements with my knee pain when I started that. I had to start slow. It made me feel squeazy and a feeling similar to a cold coming on. Once I got full bore into it knee pain got much worse but then much better.

I did that for a couple months and then switch to Flagyl and that made the knee pain much worse and then much better after.

Posts: 35 | From Western, MD | Registered: May 2013  |  IP: Logged | Report this post to a Moderator
VV
LymeNet Contributor
Member # 38828

Icon 1 posted      Profile for VV     Send New Private Message       Edit/Delete Post   Reply With Quote 
It looks like there are some positive experiences here!

I'll be starting at 1/2 pill (125mg) as a pulse to see if I notice any reactions. What's the top dose on this one? 1 or 2 grams a day?

Greta, are you still on the Tinidazole? If you feel better on it, have you tried full time/full dose?

Does everyone take it with other abx?
I am taking mino and omnicef.

Posts: 922 | From Philadelphia | Registered: Sep 2012  |  IP: Logged | Report this post to a Moderator
gz
LymeNet Contributor
Member # 43818

Icon 1 posted      Profile for gz     Send New Private Message       Edit/Delete Post   Reply With Quote 
I've been taking a couple doses daily since I began solid tx this past July. I started it paired with doxy and later added bactrim.

I think it did a lot to knock back whatever was causing my babs sx. The first six weeks were rough, but after that I noticed an increase in energy and the constant air hunger abated to flares.

Tinidazole is often prescribed as a single dose 2 gram tx for giardia, for daily use the dosages are lower, and some people can't take but a small dose. It appears that many pulse it.

I had some instances in my first couple months of tx where I had partial hearing loss and/or increased tinnitus. I have a lot of that with lyme+co's anyway, so I don't know if it was side effect, toxicity, or herx. I put a lot into detox now and my tinnitus is immensely improved. Good luck with the tindamax!

Posts: 474 | From US | Registered: May 2014  |  IP: Logged | Report this post to a Moderator
ukcarry
Frequent Contributor (1K+ posts)
Member # 18147

Icon 1 posted      Profile for ukcarry     Send New Private Message       Edit/Delete Post   Reply With Quote 
I am allergic to it, but hopefully, you will not be!
Posts: 1647 | From UK | Registered: Nov 2008  |  IP: Logged | Report this post to a Moderator
LilaLee*
Member
Member # 43649

Icon 1 posted      Profile for LilaLee*     Send New Private Message       Edit/Delete Post   Reply With Quote 
my apologies in advance if this post is seen somewhere else, i have tried to post 3 times

and for some reason it appears to have gone to post heaven. I have been on Tindamax for 5 months, 500mg twice daily with pulsed IV Rocephin.

Aside from some managable Herxing i have done fine on it. Early on i took it with Doxy and then later Mino (and now the IV R).

Hard to tell in the mix of it all what helps what but i am very def better and feeling remarkably good so i would say it has worked

for me, i hope it helps you as well:)

--------------------
LL

Posts: 79 | From Rocky Mountains | Registered: Apr 2014  |  IP: Logged | Report this post to a Moderator
LilaLee*
Member
Member # 43649

Icon 1 posted      Profile for LilaLee*     Send New Private Message       Edit/Delete Post   Reply With Quote 
one more thing, are you taking LD Naltrexone? i think this might be why the Herxing has been managable for me. As i understand it, it helps get rid of the toxic yuck, the same stuff that makes you feel gross.

--------------------
LL

Posts: 79 | From Rocky Mountains | Registered: Apr 2014  |  IP: Logged | Report this post to a Moderator
yanivnaced
LymeNet Contributor
Member # 13212

Icon 1 posted      Profile for yanivnaced     Send New Private Message       Edit/Delete Post   Reply With Quote 
My kid did several rounds of Flagyl without any effect.

He could do Tindamax now that he is above the age threshold.

Both drugs are in the same class but is it possible for Tindamax to work for somebody when Flagyl had no effect?

Posts: 655 | From USA | Registered: Sep 2007  |  IP: Logged | Report this post to a Moderator
VV
LymeNet Contributor
Member # 38828

Icon 1 posted      Profile for VV     Send New Private Message       Edit/Delete Post   Reply With Quote 
Took 1/2 of a 250mg pill.
Feeling horrible.

Posts: 922 | From Philadelphia | Registered: Sep 2012  |  IP: Logged | Report this post to a Moderator
VV
LymeNet Contributor
Member # 38828

Icon 1 posted      Profile for VV     Send New Private Message       Edit/Delete Post   Reply With Quote 
!!!

I feel like I want to take all the Tinidazole now and nuke these spirochetes in one go !!!

I know I can't, but the thought of it just made me laugh.

Posts: 922 | From Philadelphia | Registered: Sep 2012  |  IP: Logged | Report this post to a Moderator
GretaM
Frequent Contributor (1K+ posts)
Member # 40917

Icon 1 posted      Profile for GretaM     Send New Private Message       Edit/Delete Post   Reply With Quote 
Haha VV! That made me chuckle too!

I think along the same lines when I take my bart med.

"die suckers die" is one I use quite often.

Also some unprintable words.

I picture myself with the Dirty Harry look. An antibiotic and antimicrobial gun slinger.

Posts: 4358 | From British Columbia, Canada | Registered: Jun 2013  |  IP: Logged | Report this post to a Moderator
VV
LymeNet Contributor
Member # 38828

Icon 1 posted      Profile for VV     Send New Private Message       Edit/Delete Post   Reply With Quote 
Ha! I remember watching the Alien(s) trilogy last year to get in the mood. I felt like most of the action in those movies is what's going on in my body.
Posts: 922 | From Philadelphia | Registered: Sep 2012  |  IP: Logged | Report this post to a Moderator
VV
LymeNet Contributor
Member # 38828

Icon 1 posted      Profile for VV     Send New Private Message       Edit/Delete Post   Reply With Quote 
quote:
Originally posted by LilaLee*:
one more thing, are you taking LD Naltrexone? i think this might be why the Herxing has been managable for me. As i understand it, it helps get rid of the toxic yuck, the same stuff that makes you feel gross.

I have some but I have yet to try it.

I have too many sleep issues and I don't want to risk the insomnia that LDN is known for.

Posts: 922 | From Philadelphia | Registered: Sep 2012  |  IP: Logged | Report this post to a Moderator
Judie
Frequent Contributor (1K+ posts)
Member # 38323

Icon 1 posted      Profile for Judie     Send New Private Message       Edit/Delete Post   Reply With Quote 
LDN made me insane. It doesn't work for everyone even at low doses.
Posts: 2839 | From California | Registered: Jul 2012  |  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.