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 » Symptoms list - Lyme or Co-Infection?

 - UBBFriend: Email this page to someone!    
Author Topic: Symptoms list - Lyme or Co-Infection?
Roxxxy
Member
Member # 15297

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

I was treated for lyme (positive test) 5+ years ago. Dr. Sw in PA, then Dr. J (same area of PA). Symptoms never totally went away, but I couldn't afford to go any more after my 12yo son was diagnosed too (he was treated with Dr. J in CT).

For the last several years, I've been OK - some symptoms - like stiff neck, joint pain, all tolerable. But now, over the last 3 months, I'm having the following and wonder if I'm having a lyme relapse or co-infection:

Badly Burning Hands (for the last week, every day, almost can't stand the pain)
Stiff Neck, right side
Memory Loss
Extreme Mood Swings
Lump under armpit, not painful
Unexplained bruises on body, legs, arms, hands
Eye spasms & twiching, left side only
Extreme Fatigue
Head Pain, right side front by eye (like a sword stabbing me in the head)
Sore glands in my neck

The only time I ever felt "good" when being treated was on Levaquin/(another med I can't remember) combo.

Any thoughts would be appreciated!

Roxy

Posts: 31 | From PA | Registered: Apr 2008  |  IP: Logged | Report this post to a Moderator
CD57
Frequent Contributor (1K+ posts)
Member # 11749

Icon 1 posted      Profile for CD57     Send New Private Message       Edit/Delete Post   Reply With Quote 
Your symptoms sound like under-or un treated bartonella/BLO...plus the feeling better on Levaquin is a dead giveaway.

Can you start this again? Lyme is rarely alone, as we know, there are co-infections in 99% of us!

Posts: 3528 | From US | Registered: Apr 2007  |  IP: Logged | Report this post to a Moderator
Roxxxy
Member
Member # 15297

Icon 1 posted      Profile for Roxxxy     Send New Private Message       Edit/Delete Post   Reply With Quote 
Hi! Please excuse my ignorance but what does the BLO part stand for?

Roxy

Posts: 31 | From PA | Registered: Apr 2008  |  IP: Logged | Report this post to a Moderator
Roxxxy
Member
Member # 15297

Icon 1 posted      Profile for Roxxxy     Send New Private Message       Edit/Delete Post   Reply With Quote 
Thanks for the link!
Posts: 31 | From PA | Registered: Apr 2008  |  IP: Logged | Report this post to a Moderator
sixgoofykids
Moderator
Member # 11141

Icon 1 posted      Profile for sixgoofykids   Author's Homepage     Send New Private Message       Edit/Delete Post   Reply With Quote 
Improving on Levaquin is a dead-giveaway that you have bartonella.

I'd get back to an LLMD for treatment.

--------------------
sixgoofykids.blogspot.com

Posts: 13449 | From Ohio | Registered: Feb 2007  |  IP: Logged | Report this post to a Moderator
Alv
Unregistered


Icon 1 posted            Edit/Delete Post   Reply With Quote 
Big time Bartonella like organism-BLO!
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 
Wow, really does sound like you have bartonella as well.

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

Posts: 96223 | From Texas | Registered: Feb 2001  |  IP: Logged | Report this post to a Moderator
daise
Unregistered


Icon 1 posted            Edit/Delete Post   Reply With Quote 
Here's something called Presription Hope. They have Levaquin! If you have insurance and they won't pay for Levaquin, then as long as you qualify, they say, they can get it sent to you to you for $7.00 per month.

http://flash.lymenet.org/scripts/ultimatebb.cgi?ubb=get_topic;f=1;t=065398


daise [Smile]

IP: Logged | Report this post to a Moderator
Roxxxy
Member
Member # 15297

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

Saw the doctor today - agreed Bartonella likely!

Started treatment:

Cipro 500mg/Amoxicillin 500mg (will switch to Levaquin if the Cipro doesn't do the job) and Neuroatin/300mg for my burning hands (dx: neuropathy).

Last medicine I was on 5+ years ago was Levaquin 500mg/Amox 500mg, so we're going to start there.

Any thoughts about the combo with Neuroatin?

Thanks
Roxy

Daise, thanks too for the link, I'll try it if I need it. [Smile]

Posts: 31 | From PA | Registered: Apr 2008  |  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 
Neurontin?

Should be fine. You may have to up the dosage once you're able to tolerate it. You have to start out slowly with that one.

Congrats on getting started again! [Smile]

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

Posts: 96223 | From Texas | Registered: Feb 2001  |  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.