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 » those who had tendon pain with cipro-levaquin

 - UBBFriend: Email this page to someone!    
Author Topic: those who had tendon pain with cipro-levaquin
Laura_W
LymeNet Contributor
Member # 31491

Icon 1 posted      Profile for Laura_W     Send New Private Message       Edit/Delete Post   Reply With Quote 
I'm on cipro. Ive been trying to differentiate between HERX reactions and adverse reactions. Hard to do.

And have leg pain, muscle spasms, vision issues and much much more. I have decreased my dose to only once a day. I have been on it for 5 days this time.

For those of you that have had previous tendon issues... Can you describe what it feels like?

What did it feel like in the beginning before it got bad?

Was it both sides of the body? Or can it occur in just one site?


Thank you

--------------------
10/10 EIA 1.4+, 41 (IGG), 23 (IGM)
Bitten over 20 years ago.
Currently not treating, looking for a Dr who will work with my insurance lol.

More muscular, cognitive, nerve issues than joints. Facial droop and blurred vision.

Posts: 323 | From Michigan | Registered: Apr 2011  |  IP: Logged | Report this post to a Moderator
kadee
LymeNet Contributor
Member # 21199

Icon 1 posted      Profile for kadee     Send New Private Message       Edit/Delete Post   Reply With Quote 
It's hard to tell the difference. I pushed through for 4 weeks until I was floxed.

quote:
And have leg pain, muscle spasms, vision issues and much much more
"Much more" makes me very suspicious. My flox-reactions felt like ALL my bodysystems were affected.
Posts: 269 | From Germany | Registered: Jul 2009  |  IP: Logged | Report this post to a Moderator
lymeinhell
Frequent Contributor (1K+ posts)
Member # 4622

Icon 1 posted      Profile for lymeinhell     Send New Private Message       Edit/Delete Post   Reply With Quote 
Mine started as sciatic pain (lower back), then progressed to wrap around and down my thigh, then down my calf, all the way to my toes. It was a pulling type of pain, that increased in severity over time.

(This was pre-Lyme dx, and I had spent 4 mos on Levaquin for an incurable 'sinus infection', and the morons had me exercising).

It got so bad that they sent me to physical therapy (never once considering it was from the Levaquin they had put me on). I Had no idea it was from the Levaquin until many months later when I came here. I wish I could have sued....

--------------------
Julie
_ _ ___ _ _
lymeinhell

Blessed are those who expect nothing, for they shall not be disappointed.

Posts: 2258 | From a better place than I was 11 yrs ago | Registered: Sep 2003  |  IP: Logged | Report this post to a Moderator
Laura_W
LymeNet Contributor
Member # 31491

Icon 1 posted      Profile for Laura_W     Send New Private Message       Edit/Delete Post   Reply With Quote 
Thank you for responding

--------------------
10/10 EIA 1.4+, 41 (IGG), 23 (IGM)
Bitten over 20 years ago.
Currently not treating, looking for a Dr who will work with my insurance lol.

More muscular, cognitive, nerve issues than joints. Facial droop and blurred vision.

Posts: 323 | From Michigan | Registered: Apr 2011  |  IP: Logged | Report this post to a Moderator
LymeMECFSMCS
LymeNet Contributor
Member # 13573

Icon 1 posted      Profile for LymeMECFSMCS   Author's Homepage     Send New Private Message       Edit/Delete Post   Reply With Quote 
For me it started off aching, but then quickly got VERY painful, to the point that putting any weight on my legs was excruciating -- standing up was hell.

I was worried I had waited too late to stop. My tendon pain did reverse but it took some time and it was pretty worrisome.

Posts: 929 | From Massachusetts | Registered: Oct 2007  |  IP: Logged | Report this post to a Moderator
annxyzz
Frequent Contributor (1K+ posts)
Member # 20404

Icon 1 posted      Profile for annxyzz     Send New Private Message       Edit/Delete Post   Reply With Quote 
I just had to stop it for a UTI infection. My left knee becme so tight and stiff that I could not walk normally . I stpped it and will not risk permanent damage . It happens more commonly in folks 50 plus years age . It can cause serious damage needing surgery to repair tendons .

--------------------
annxyzz

Posts: 1178 | From East Texas | Registered: May 2009  |  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 
Suggest you read what this webpage says to do and follow its advice:

http://www.lymebook.com/antibiotic-treatment-for-babesia-bartonella-ehrlichia-co-infections

Posts: 9931 | From Maryland | Registered: Dec 2007  |  IP: Logged | Report this post to a Moderator
Laura_W
LymeNet Contributor
Member # 31491

Icon 1 posted      Profile for Laura_W     Send New Private Message       Edit/Delete Post   Reply With Quote 
TF, I read it and found it useful, thanks for the link.

I appreciate everyone sharing their first hand experiences

[group hug]

--------------------
10/10 EIA 1.4+, 41 (IGG), 23 (IGM)
Bitten over 20 years ago.
Currently not treating, looking for a Dr who will work with my insurance lol.

More muscular, cognitive, nerve issues than joints. Facial droop and blurred vision.

Posts: 323 | From Michigan | Registered: Apr 2011  |  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.