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 » Just started Mepron; would love to hear your experiences

 - UBBFriend: Email this page to someone!    
Author Topic: Just started Mepron; would love to hear your experiences
mmcmann
LymeNet Contributor
Member # 21872

Icon 1 posted      Profile for mmcmann     Send New Private Message       Edit/Delete Post   Reply With Quote 
Although I tested negative for Babesia, after 7 months of treatment with abx for Lyme -
including Doxy, Zith, Rifampin, Tindamax -

my LLMD is not happy with my lack of progress.

So, decided to add Mepron into the mix.

I have heard of it but do not know anyone who has taken it. I would love to hear your experiences, good and bad.

Also, is it supposed to be that thick?

I won't be at my computer again until later this afternoon, but I will review and answer any questions then!

Thanks in advance.

Posts: 104 | From No. VA | Registered: Aug 2009  |  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 sure to read this:

Mepron Blues
http://flash.lymenet.org/scripts/ultimatebb.cgi/topic/1/89042?

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

Posts: 96222 | From Texas | Registered: Feb 2001  |  IP: Logged | Report this post to a Moderator
mmcmann
LymeNet Contributor
Member # 21872

Icon 1 posted      Profile for mmcmann     Send New Private Message       Edit/Delete Post   Reply With Quote 
Thanks
Posts: 104 | From No. VA | Registered: Aug 2009  |  IP: Logged | Report this post to a Moderator
sammy
Frequent Contributor (5K+ posts)
Member # 13952

Icon 1 posted      Profile for sammy     Send New Private Message       Edit/Delete Post   Reply With Quote 
Mepron is supposed to be thick. Texture is kinda like paint. Taste is not too good or bad.

I didn't have a problem with side effects. Just be careful when you measure it out, it spills easily.

And remember to use a measuring spoon (not a regular kitchen spoon that you eat cereal with) to get the accurate dose.

Posts: 5237 | From here | Registered: Nov 2007  |  IP: Logged | Report this post to a Moderator
asummers
LymeNet Contributor
Member # 18068

Icon 1 posted      Profile for asummers     Send New Private Message       Edit/Delete Post   Reply With Quote 
I LOVE Mepron. I know why they call it 'liquid gold.' Like you, I had made great progress getting my lyme load down, but was stuck at 85% better.

Then my new LLND stated that she didn't think I hit Babs hard enough and put me on Flagyl, Zith, Mepron, Art & Larium. Within 3 weeks, my severe fatigue lifted.

I have not had to worry about depression which is a side effect of Mepron & Larium.

Good Luck!

Posts: 379 | From Sydney, Australia | Registered: Nov 2008  |  IP: Logged | Report this post to a Moderator
Sammi
Frequent Contributor (1K+ posts)
Member # 110

Icon 1 posted      Profile for Sammi     Send New Private Message       Edit/Delete Post   Reply With Quote 
Some people experience a herx on day three and every three weeks or so when taking Mepron. I did.

Which antibiotic are you taking with it?

Make sure you eat something fatty when you take Mepron or it will not be absorbed properly.

Good luck!

Posts: 4681 | Registered: Oct 2000  |  IP: Logged | Report this post to a Moderator
Haley
Frequent Contributor (1K+ posts)
Member # 22008

Icon 1 posted      Profile for Haley     Send New Private Message       Edit/Delete Post   Reply With Quote 
Since I have been on Mepron I am experiencing Tinnitus. I have never heard of that as a side effect of Mepron. I also take Zith but it's a low dose that I have taken for a long time.

Has anyone experienced Tinnitus (ringing in the ears) from Mepron?

I also have nausea and headaches occasionally.

asummers - How long did you take Mepron?

Posts: 2232 | From USA | Registered: Aug 2009  |  IP: Logged | Report this post to a Moderator
lymebytes
Frequent Contributor (1K+ posts)
Member # 11830

Icon 1 posted      Profile for lymebytes   Author's Homepage     Send New Private Message       Edit/Delete Post   Reply With Quote 
Haley,
Ringing in the ears is a side of effect of Zith. You may want to tell your LLMd and switching to Biaxin might be better for you.

--------------------
www.truthaboutlymedisease.com

Posts: 2003 | From endemic area | Registered: May 2007  |  IP: Logged | Report this post to a Moderator
asummers
LymeNet Contributor
Member # 18068

Icon 1 posted      Profile for asummers     Send New Private Message       Edit/Delete Post   Reply With Quote 
Haley -- I have been taking Zith & Mepron since middle of Jan 2010. My LLND thinks I will be on it 6 - 12 months.

I don't have the Tinnitus, but I do have a heartbeat that I can hear in my right ear. I think it is from the Zith.

I am currently using rife and I am thinking about the Salt/C protocol b/c I would like to transition off of abx at the end of the yr. That will be the 2yr mark for me being on abx.

Posts: 379 | From Sydney, Australia | Registered: Nov 2008  |  IP: Logged | Report this post to a Moderator
Sammi
Frequent Contributor (1K+ posts)
Member # 110

Icon 1 posted      Profile for Sammi     Send New Private Message       Edit/Delete Post   Reply With Quote 
Haley, I had nausea and severe headaches from Babesiosis.

I agree the tinnitus could be from Zithromax.

Check out bettyg's Babesiosis symptom list at http://flash.lymenet.org/ubb/ultimatebb.php/topic/1/81386

Posts: 4681 | Registered: Oct 2000  |  IP: Logged | Report this post to a Moderator
mmcmann
LymeNet Contributor
Member # 21872

Icon 1 posted      Profile for mmcmann     Send New Private Message       Edit/Delete Post   Reply With Quote 
Thanks everyone. Sorry just now responding, been a rough 24 hours.

sammi - I am taking Doxy and Zith daily and pulsing Tindamax every 4th week. Thanks for the warning on herx..I enter day 3 tomorrow.

sammy - thanks for the analogy - it fits perfectly and now my DH may not be so concerned that the pharm didn't mix it right [Smile]

asummers "but I do have a heartbeat that I can hear in my right ear." That is EXactly what has been happening to me. I didn't know how to describe it before. Such an odd feeling.

I really hope the mepron works and that I do not have issues with worsening depression as I already struggle with it.

so tired of it all.

good luck to you all.

Posts: 104 | From No. VA | Registered: Aug 2009  |  IP: Logged | Report this post to a Moderator
Wolfed Out
LymeNet Contributor
Member # 23727

Icon 1 posted      Profile for Wolfed Out     Send New Private Message       Edit/Delete Post   Reply With Quote 
Good luck mmcmann,

I hope it works for you, please keep us updated.

I may be taking Mepron in the near future.

Wolf

Posts: 829 | From MD | Registered: Dec 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.