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 » Is anyone on Tindamax?

 - UBBFriend: Email this page to someone!    
Author Topic: Is anyone on Tindamax?
Mariel25
Member
Member # 45205

Icon 1 posted      Profile for Mariel25     Send New Private Message       Edit/Delete Post   Reply With Quote 
Is there anyone that takes Tindamax and if so do you take it every day or pulse it? Thanks. It's a horrible drug for me.
Posts: 61 | From Connecticut | Registered: Jan 2015  |  IP: Logged | Report this post to a Moderator
TF
Frequent Contributor (5K+ posts)
Member # 14183

Icon 1 posted      Profile for TF     Send New Private Message       Edit/Delete Post   Reply With Quote 
I took flagyl (metronidazole) many years ago when I was treating lyme. I took it every day for 60 days. It operates the same as Tindamax--they both kill the cyst form of lyme. This is how I got rid of lyme over 10 years ago.

Many people take flagyl/Tindamax so many days and then take a break. Generally, the doctor wants you to take it or try to take it for 2 weeks straight. That is when it is the most effective. So, maybe you were told to work up to that.

Those who have a hard time with it have to slowly work up to the full 2 weeks.

I suggest you drink a lot of water with fresh lemons squeezed into it throughout the day every day to help detoxify yourself. Then the Tindamax may not be so difficult to take.

When I was treating lyme, I made lemon water my only drink. You can also drink Alka Seltzer Gold with lemon squeezed into it to help you feel better when the Tindamax makes you feel horrible.

People are really surprised at how well these things work. They flush out all of the dead germs that are the result of the Tindamax. Those dead germs are what make us feel awful.

My doctor told me to eat 4 lemons per day this way, but I never got up to 4 per day. I ate about 2 per day. He said that lemons are a natural cleanser and water flushes out the body. So, drink up and feel better.

Posts: 9931 | From Maryland | Registered: Dec 2007  |  IP: Logged | Report this post to a Moderator
Lymetoo
Moderator
Member # 743

Icon 1 posted      Profile for Lymetoo     Send New Private Message       Edit/Delete Post   Reply With Quote 
Be careful if you get symptoms of nerve damage.

--------------------
--Lymetutu--
Opinions, not medical advice!

Posts: 96222 | From Texas | Registered: Feb 2001  |  IP: Logged | Report this post to a Moderator
MichaelTampa
Frequent Contributor (1K+ posts)
Member # 24868

Icon 1 posted      Profile for MichaelTampa     Send New Private Message       Edit/Delete Post   Reply With Quote 
I pulse it
Posts: 1927 | From se usa | Registered: Mar 2010  |  IP: Logged | Report this post to a Moderator
still winning
Member
Member # 44439

Icon 1 posted      Profile for still winning     Send New Private Message       Edit/Delete Post   Reply With Quote 
It's been a real important med for me, in combination with another antibiotic, such as omniceff. Gets into the brain. But it does cause headaches. My doc puts me on tindamax only 3 days a week. I wish it was more.

If offered take it. Keep fighting. Try to keep smiling.

Still Winning

Posts: 55 | From Maryland | Registered: Aug 2014  |  IP: Logged | Report this post to a Moderator
me
Frequent Contributor (1K+ posts)
Member # 45475

Icon 1 posted      Profile for me     Send New Private Message       Edit/Delete Post   Reply With Quote 
I take it along with other stuff for Lyme, so it's hard to tell what makes me herx the worst. I take it daily.

I pulse coartem, and that has really nasty effects on me.

I know it's awful. Keep reaching out and keep fighting. If you ever need to unload, please feel free to PM me. Best wishes.

Posts: 1431 | From USA | Registered: Mar 2015  |  IP: Logged | Report this post to a Moderator
duncan
LymeNet Contributor
Member # 46242

Icon 1 posted      Profile for duncan     Send New Private Message       Edit/Delete Post   Reply With Quote 
I took tinidazole and mino for about five or six months, no pulsing.

It didn't help, but to me research seemed to suggest it was a combo that might benefit some. That's why I embraced it. It just didn't work for me.

Based on the Lewis/Zhang/Embers studies, I'd give consideration to pulsing, if I were to try that tandem again any time soon. Finding the right schedule, though, would be important.

Posts: 228 | From Unitied States | Registered: Jul 2015  |  IP: Logged | Report this post to a Moderator
Mariel25
Member
Member # 45205

Icon 1 posted      Profile for Mariel25     Send New Private Message       Edit/Delete Post   Reply With Quote 
Thank you so much. I am on Rocephin and will try to take it as many days in the week as possible. Horrible drug but if it works it is worth it.
Posts: 61 | From Connecticut | Registered: Jan 2015  |  IP: Logged | Report this post to a Moderator
me
Frequent Contributor (1K+ posts)
Member # 45475

Icon 1 posted      Profile for me     Send New Private Message       Edit/Delete Post   Reply With Quote 
I had awful, awful, awful herxes on Rocepherin, but it helped me make progress . . .
Posts: 1431 | From USA | Registered: Mar 2015  |  IP: Logged | Report this post to a Moderator
goose
Member
Member # 45410

Icon 1 posted      Profile for goose     Send New Private Message       Edit/Delete Post   Reply With Quote 
I'm on it and I feel a little skeletal/spine discomfort. I don't know if this is herxing or not. I have had these problems though as long as I can remember. I've only been on it a week though. My doc just tells me to take it every day so far. I was told if I start to herx and I can't handle it...stop until it subsides and then restart. I took flagyl for a month and I didn't herx at all.
Posts: 44 | From Owatonna | Registered: Feb 2015  |  IP: Logged | Report this post to a Moderator
Mariel25
Member
Member # 45205

Icon 1 posted      Profile for Mariel25     Send New Private Message       Edit/Delete Post   Reply With Quote 
What dosage is everyone taking?- I'm on 1000 mg. per day. Awful drug.
Posts: 61 | From Connecticut | Registered: Jan 2015  |  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.