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 » Severe burning-what is it? Somebody has to know

 - UBBFriend: Email this page to someone!    
Author Topic: Severe burning-what is it? Somebody has to know
amkdiaries
LymeNet Contributor
Member # 7035

Icon 1 posted      Profile for amkdiaries   Author's Homepage     Send New Private Message       Edit/Delete Post   Reply With Quote 
I have severe burning of my scalp, neck spine and abdomen. I know this is called neuropathy but where is it coming from? Is the Lyme in these areas and inflaming the nerves? Is it neurotoxins if there is such a thing? Is it Bartonella or Babesia. Every time I take antibiotics, escpecially I.V. ones the burning gets so bad it feels like I have third degree burns in these areas. Nothing helps these symptoms. I tried B-12 shots but it got worse. I know it can't be the antibiotics because the burning is only in certain areas that hurt me before. Please help-it's making me insane!
Posts: 425 | From NY, United States | Registered: Mar 2005  |  IP: Logged | Report this post to a Moderator
Laurie
LymeNet Contributor
Member # 159

Icon 1 posted      Profile for Laurie   Author's Homepage     Send New Private Message       Edit/Delete Post   Reply With Quote 
Inflammation of the many, many various nervous systems of the body is a hallmark of neurological Lyme. I know it's driving you crazy because I have burning neuropathic pain in my calves and feet, controlled symptomatically by Neurontin and Elavil.
Posts: 459 | From Connecticut - just across the river from the Lymes (Old Lyme, Hadlyme, East Lyme, South Lyme & Lyme) | Registered: Oct 2000  |  IP: Logged | Report this post to a Moderator
timaca
Frequent Contributor (1K+ posts)
Member # 6911

Icon 1 posted      Profile for timaca     Send New Private Message       Edit/Delete Post   Reply With Quote 
amkdiaries~

I have no advice as to how to relieve your pain. I can only tell you that I am in the same boat.

I have burning, sparking, creeping, crawling nerves all over my body. It was one of my first lyme symptoms, and got much worse after one dose of IV vancomycin during my knee surgery. I had no idea what was going on at the time, but now know that it was probably a herx.

I am hoping that in time, and with treatment, it will go away. I am considering trying some of the supplements that Dr. B recommends in his guidelines for nerve pain.

[group hug]

Posts: 2872 | From above 7,000 ft in a pine forest | Registered: Feb 2005  |  IP: Logged | Report this post to a Moderator
bpeck
Frequent Contributor (1K+ posts)
Member # 3235

Icon 1 posted      Profile for bpeck     Send New Private Message       Edit/Delete Post   Reply With Quote 
If it's pain from neuropathy ask your Doc. to try hydroxyzine. That's the parent formulation of an over the counter H2 blocker called Clariton.. but clariton doesn't cross the BBB the way Hydroxyzine does.

Barb

Posts: 1875 | From VT | Registered: Oct 2002  |  IP: Logged | Report this post to a Moderator
SForsgren
Frequent Contributor (1K+ posts)
Member # 7686

Icon 1 posted      Profile for SForsgren         Edit/Delete Post   Reply With Quote 
I also get significant increase in my burning sensations when I change ABX. Just happened again for about 5 days last week when I changed to Levaquin.

--------------------
Be well,
Scott

Posts: 4617 | From San Jose, CA | Registered: Jul 2005  |  IP: Logged | Report this post to a Moderator
Rubicon
Member
Member # 7919

Icon 1 posted      Profile for Rubicon     Send New Private Message       Edit/Delete Post   Reply With Quote 
I feel your pain!! I had all of the same feelings of burning and stabbing, which increases upon switching meds. The pain is mostly in hands, feet, back. In fact, the pain was so bad the past few days, i ask my LLMD to switch my meds.

Had lyme since 1993 and this is my 2nd relapse. I never had neuro symptoms the frist 2 times. Why is this happening this time? Any one know??

--------------------
I'm in the tunnel and I still don't see any light!!

Posts: 42 | From RI tick capitol of the world | Registered: Sep 2005  |  IP: Logged | Report this post to a Moderator
painted turtle
LymeNet Contributor
Member # 7801

Icon 1 posted      Profile for painted turtle   Author's Homepage     Send New Private Message       Edit/Delete Post   Reply With Quote 
Robicon I don't know why this is happening are you sure you don't have coinfection??? It sounds like maybe your treatment was not effective if it continued to progress in neuro, but I am sure I don't know. I am learning.

YES! I can relate to the severe burning in my spine...the last 3 days my leg felt like it was gonna fall off it hurt so bad. And numbness in my face ear chin spine everywhere. Not sure what all that amounts to except a lot of pain and I am still only on the oral treatments until I first rule out that babesia nuissance thing.

I noticed something interesting though during this last neuro herx. It starts from my mid spine and burns like crazy in pain not wanting to be touched then it radiates down all the way through my left leg. Then one day after two days of that, my leg started to get better but it moved into my neck and head which got swollen and a migraine was coming on. I took a zomig. Even though it made my heart skip beats, then the next day...not in head anymore! BUT back down to leg. Sneaky little critters. It is interesting to document.

--------------------
www.lymefire.blogspot.com

Posts: 855 | From United States of Mind | Registered: Aug 2005  |  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.