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 » First post (Bart symptoms?)

 - UBBFriend: Email this page to someone!    
Author Topic: First post (Bart symptoms?)
CSS
Member
Member # 34634

Icon 1 posted      Profile for CSS     Send New Private Message       Edit/Delete Post   Reply With Quote 
First post with a question.

My LLMD recently diagnosed me with hemobartonella confirmed by Fry labs (blood smear). I believe I have had the bug for many years and it just now surfaced after going thru a very stressful period.

Approx. a year ago I felt a small marble in size type pressure, tingling, burning, and sometimes cool flowing sensation in the ball of my left foot. Over the last year it has spread into both feet. Sometimes the symptoms are really strong and other times they are very weak. Getting off my feet helps immensely.

I am even getting a grabbing pressure , tingling, type feeling in my back now that comes and goes. A few burning areas in my left leg and right arm also. Occasional tingling in my left finger tips. Do these sound like Bart symptoms? I am assuming my nerves are inflammed?

Started on rifampin, tindamax, and doxy approx. a 1 1/2 months ago. Taking mag, b12, and numerous other supplements. I have felt no change at all.

I am starting to wonder if this is something else? Thinking about seeing a neurologist? Any thoughts, suggestions, or advise would be greatly appreciated.

Thanks

Posts: 22 | From California | Registered: Oct 2011  |  IP: Logged | Report this post to a Moderator
Kramberry
LymeNet Contributor
Member # 34032

Icon 1 posted      Profile for Kramberry     Send New Private Message       Edit/Delete Post   Reply With Quote 
Who is treating you?

Im on my 3rd month treating bart no improvememt either. Sad but true some folks here doesnt see improvement also but continue to take abx for years.

--------------------
 -

Posts: 215 | From California | Registered: Sep 2011  |  IP: Logged | Report this post to a Moderator
CSS
Member
Member # 34634

Icon 1 posted      Profile for CSS     Send New Private Message       Edit/Delete Post   Reply With Quote 
Dr Y in the San Diego area.
Posts: 22 | From California | Registered: Oct 2011  |  IP: Logged | Report this post to a Moderator
lucky8711
Member
Member # 26221

Icon 1 posted      Profile for lucky8711     Send New Private Message       Edit/Delete Post   Reply With Quote 
I have that same sensation in my foot but never tied the two together...I lways just though it was some sort of bone chip or omething in there causing it, but now as I hear you describe the same thing I don't know why I would think I even had a bone chip in there with no injury to cause it. Funny how we try and rationalize and find caues to explain it away. I have been being reated for 2 years now for Lyme but starting to attack the bart which flared up horribly after the birth or my son in August. Between the stress on my body and then some emtional stress unrelated to the birth or baby It has been a very uncomfortable flare. I am only 3 weeks into treatment and not finding much change other then some mild herxing. Stick with it for a while. My plan is to give it 6 moonths to a year wth ABX but if Im not getting the improvement I need I am planning to try the Byron White Formulas. My mother is having very good luck with them and I have heard my other positive things about them. Good luck!
Posts: 80 | From RI | Registered: Jun 2010  |  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.