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 » sharp bone pain not joints

 - UBBFriend: Email this page to someone!    
Author Topic: sharp bone pain not joints
stymielymie
Frequent Contributor (1K+ posts)
Member # 10044

Icon 1 posted      Profile for stymielymie     Send New Private Message       Edit/Delete Post   Reply With Quote 
i now have a new symptom, when i thought i was in remission.

severe stabbing bone in shin and ball of one foot.
feels like nail is in foot, can't walk even with
metatarsal pads, but htey do help somewhat.

any ideas?
docdave

Posts: 1820 | From Boone and Southport, NC | Registered: Sep 2006  |  IP: Logged | Report this post to a Moderator
Carol B
Unregistered


Icon 1 posted            Edit/Delete Post   Reply With Quote 
yeah- sit back relax and this too shall pass
IP: Logged | Report this post to a Moderator
valymemom
Frequent Contributor (1K+ posts)
Member # 7076

Icon 1 posted      Profile for valymemom     Send New Private Message       Edit/Delete Post   Reply With Quote 
Shin bone pain is bartonella. Rifampin/doxy/zith is what my son is doing.

I did levaquin/ceftin 9 weeks at the beginning of treatment and then again 9 weeks at the end.

Have you been treated for bart?

Posts: 1240 | From Centreville,VA | Registered: Mar 2005  |  IP: Logged | Report this post to a Moderator
CaliforniaLyme
Frequent Contributor (5K+ posts)
Member # 7136

Icon 1 posted      Profile for CaliforniaLyme     Send New Private Message       Edit/Delete Post   Reply With Quote 
Stabbing pains in hands and feet tend to be Babs

Yup, as was said already, calve & shin pain tends to be Bart

Deep BONE pain interior pain is often Ehrlichiosis/Anaplasmosis

but it can all be cross-over and remember, everything is not Lyme, could also be separate issue- so I would first go to regular doc & check if it is somethign simple- then go to LLMD!!

Too bad, Stymie!!!

--------------------
There is no wealth but life.
-John Ruskin

All truth goes through 3 stages: first it is ridiculed: then it is violently opposed: finally it is accepted as self evident. - Schopenhauer

Posts: 5639 | From Aptos CA USA | Registered: Apr 2005  |  IP: Logged | Report this post to a Moderator
AliG
Frequent Contributor (1K+ posts)
Member # 9734

Icon 1 posted      Profile for AliG     Send New Private Message       Edit/Delete Post   Reply With Quote 
I'm sorry you have a new one, Stymie. [Frown]
I hope you get it figured out & fixed quickly. [Smile]

I think I remember complaining about something like this early on. I tested neg for Bart, pos for Babs.

[group hug]
Ali

--------------------
Note: I'm NOT a medical professional. The information I share is from my own personal research and experience. Please do not construe anything I share as medical advice, which should only be obtained from a licensed medical practitioner.

Posts: 4881 | From Middlesex County, NJ | Registered: Jul 2006  |  IP: Logged | Report this post to a Moderator
Jill E.
Frequent Contributor (1K+ posts)
Member # 9121

Icon 1 posted      Profile for Jill E.     Send New Private Message       Edit/Delete Post   Reply With Quote 
Hi DocDave,

Good to see you back posting again, but I'm sorry it's because of a symptom.

I had shin splint pain in both legs when I first became symptomatic with Lyme & Co, but it went away with Doxy.

It has come roaring back, along with some bone pain, now that I'm on Rifampin for Bart.

As you know, sore soles are usually symptoms of Bart, which I also first got when on Levaquin for Bart. But I also get stabbing pains in my arches, but they are very nerve-oriented for me - electrical shocks that make my legs recoil. It sounds different from what you are experiencing.

I did see a podiatrist several months ago for Achilles Tendon pain from Levaquin, just to rule out something mechanical. He knew nothing of Lyme, but said there was no way it was plantar fascitis because my symptoms were so symmetrical. He just knew it was something systemic based on my symptoms.

He also said that tarsal tunnel is like carpal tunnel, but it's in the feet, and it can some times cause pain in the feet.

Please let us know what happens.

Jill

--------------------
If laughter is the best medicine, why hasn't stand-up comedy cured me?

Posts: 1773 | From San Diego | Registered: Apr 2006  |  IP: Logged | Report this post to a Moderator
Lymeblue
LymeNet Contributor
Member # 6897

Icon 1 posted      Profile for Lymeblue     Send New Private Message       Edit/Delete Post   Reply With Quote 
Sorry Docdave..no clue...but my daughter used to complain about a similar pain and those went away with bart/babs treatment.
She used to describe them as "sensation of having blisters on her soles"
I was told those pain are nerve pains originated in the brain.

Posts: 983 | From The sky | Registered: Feb 2005  |  IP: Logged | Report this post to a Moderator
Allison Smith
Member
Member # 11631

Icon 1 posted      Profile for Allison Smith     Send New Private Message       Edit/Delete Post   Reply With Quote 
[confused]

So what if you have the stabbing bone pain everywhere. I get them in my hands, my under forearms, my legs, shins, and feet?

It's horrible!!! I jump and yell "OWWWWW!" and scare the crud out of my husband. They are very painful!!!

Posts: 94 | From Greenville, Tx | Registered: Apr 2007  |  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.