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 » pulsing antibiotics - are we aggressive enough?

 - UBBFriend: Email this page to someone!    
Author Topic: pulsing antibiotics - are we aggressive enough?
karawhite
Member
Member # 41374

Icon 1 posted      Profile for karawhite     Send New Private Message       Edit/Delete Post   Reply With Quote 
I am in treatment for a little more than a month. We started on Doxy 200 mg daily, increased to Doxy 400 mg daily. Added Levaquin 500 mg 5 days/week (which insurance is now denying). When I have my remission period (when I simply feel bad, not like im dying) I am to take Flagyl 500mg 2 x daily until I have my "dying" period, at which point I am to resume Doxy 400 mg daily. Does this make sense? I feel that my LLMD may be undertreating me. The LLMD does not have much experience, so I am concerned. What do people who have had success with antibiotics think?

I am also taking many supplements etc...

In his guidelines, Dr. B writes about IV ABX - is this the ultimate? Are orals not the best route to go?

If you've had success with ABX, did you build them up gradually, did you rotate them and pulse them? MY LLMD says its good to pulse to confuse the lyme, is this really true?

Would appreciate all feedback....:-)

Posts: 47 | From new york | Registered: Jul 2013  |  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 
Some doctors do pulse, others do not.

You may find it hard to know when the "remission" period is. I know I just felt horrible for 18-24 months.

Not everyone has to have IV. Some can get well without it. I did, but it took a long time. But then again, I had had it a LONG time. Took 4 yrs to get well.

But I am THERE!

I'll let others chime in, as I am signing off for the evening. Hope you get the help you need!

[Smile]

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

Posts: 96222 | From Texas | Registered: Feb 2001  |  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 
Hi,

Doxy gets rid of 90% of spirochetes in the blood. But it doubles the amount of cyst forms.

Flagyl, or Tinidazole (Tindimax), kills all forms of the lyme. But Flagyl and Tindimax, to a lesser degree, are hard on the body, liver and kidneys, so that is why they are pulsed.

Doxy is also good for some coinfections.

I started with 400mg daily Doxy, for one month.
I think the idea was to reduce the spirochete load, get rid of RMSF.

After a month I started Tindimax, pulsing one week on, one week off.

I had a doxy burn with the sun, so my doc switched me to Mino.

I then was given Biaxin. I took Biaxin, Mino and Tindi.

Then I had diareaha,stopped mino and biaxin and continued with Tindimax, full time, double dose.

After the c diff tests came back negative, I returned to mino, tinidazole pulsing and cryptolepsis.

I feel better not taking the biaxin. I don't feel like it did much for me except give me diareha.

I think your doc is making sure you don't herx so badly.

I am relieved not to be doing IV. Mino really helps me.

Posts: 4358 | From British Columbia, Canada | Registered: Jun 2013  |  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 
Your doctor sounds pretty good so far, IMO.

Probably seeing how you react to neurotoxins from die off, treating the dominant coinfection, and making sure you don't overwhelm your detox pathways by doing too much too soon.

I felt the same way, (wanted to blast the infections with abx, and wondering why my doc was conservatively treating), until starting cryptolepsis. I already feel improvement by treating babesia.

Now I am so grateful my doc is making sure I don't get worse before getting better.
Now I feel it's more about finding the right treatment for the right infection, rather than blasting the infections (and my body).


Hang in there, be patient, with your doc and yourself.

Many best wishes [Smile]

Posts: 4358 | From British Columbia, Canada | Registered: Jun 2013  |  IP: Logged | Report this post to a Moderator
kgg
Frequent Contributor (1K+ posts)
Member # 5867

Icon 1 posted      Profile for kgg   Author's Homepage     Send New Private Message       Edit/Delete Post   Reply With Quote 
Since you are just starting treatment, I would think this is a good approach. Warning, there are those who will disagree. But, this is a good way to find out how you react to treatment. Some people tolerate higher doses and some require baby doses, we are all different.

If after a while you don't feel like you are getting better this way, talk with your health care provider. But I personally like pulsing.

Posts: 1685 | From Maine | Registered: Jun 2004  |  IP: Logged | Report this post to a Moderator
sutherngrl
Frequent Contributor (1K+ posts)
Member # 16270

Icon 1 posted      Profile for sutherngrl     Send New Private Message       Edit/Delete Post   Reply With Quote 
I got over Lyme by taking low dose Doxycycline for several years; I took it everyday. This was after trying other antibiotics prior to. I have been off all meds for 10 months. I now think I have an underlying infection that needs attention; possibly something other than tick borne; but the Lyme is gone due to Doxy.

SG

Posts: 4035 | From Mississippi | Registered: Jul 2008  |  IP: Logged | Report this post to a Moderator
karawhite
Member
Member # 41374

Icon 1 posted      Profile for karawhite     Send New Private Message       Edit/Delete Post   Reply With Quote 
sutherngrl - I am quite a novice to this, but doesn't the doxy just hide the bacteria in cyst form? can it truly eradicate lyme?
Posts: 47 | From new york | Registered: Jul 2013  |  IP: Logged | Report this post to a Moderator
faithful777
Moderator
Member # 22872

Icon 1 posted      Profile for faithful777     Send New Private Message       Edit/Delete Post   Reply With Quote 
Many can do fine with orals. I did not do well with pulsing but many do okay.

I never took doxy at all during my treatment.

Remission by my LLMD's definition, is two months of little or no symptoms. I am there with no symptoms and my husband is just about there. He has gone 6 weeks with no symptoms and is about to get off abx.

I have been off abx for 4 weeks and am doing fine. I don't feel sick at all. Working on getting my stamina back to where I was before I got sick. I am seeing improvements in that every week.

--------------------
Faithful

Just sharing my experience, I am not a doctor.

Posts: 2682 | From Colorado | Registered: Oct 2009  |  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.