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 » ~explosions in mouth~

 - UBBFriend: Email this page to someone!    
Author Topic: ~explosions in mouth~
foggedup
LymeNet Contributor
Member # 7415

Icon 1 posted      Profile for foggedup     Send New Private Message       Edit/Delete Post   Reply With Quote 
I have had 3 seperate 'explosions' in my mouth in the past 5 months. It feels as if tiny fireworks have exploded in one small place in my mouth. Feels electric, hot and painful in just that small area.

The first was in my cheek area(inside my mouth) and woke me from sleep. The 2nd one lower down but still in cheek area. The 3rd one was my bottom lip, just inside. I could feel my lip swelling, so I applied ice. Later that day I had a small bump (pea size) and it is purple/red, like a bruise.

I am being treated for Lyme from Dr C and it's been 1 year now. These explosions happen during sleep. I was on different antibiotics, but continuously on Cymbalta and Percocet. Don't know if it's medication related or what...any ideas??

The 4th of July is coming up soon and I don't want to be the one giving the fireworks display!

Thanks
Michele

Posts: 106 | From Texas | Registered: Jun 2005  |  IP: Logged | Report this post to a Moderator
dontlikeliver
Frequent Contributor (1K+ posts)
Member # 4749

Icon 1 posted      Profile for dontlikeliver     Send New Private Message       Edit/Delete Post   Reply With Quote 
Hi Foggedup,

I have no idea what that could be but sounds nerve related - could it be cranial nerve related?

Anyway, I was wonder how you are doing. Have you improved since starting treatment?

DLL

Posts: 2824 | From The Back of Beyond | Registered: Oct 2003  |  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 
OUCH!

Bringing this up for help.

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

Posts: 96223 | From Texas | Registered: Feb 2001  |  IP: Logged | Report this post to a Moderator
foggedup
LymeNet Contributor
Member # 7415

Icon 1 posted      Profile for foggedup     Send New Private Message       Edit/Delete Post   Reply With Quote 
Hi DLL.

I did not see much improvement with the orals so we are going to try IV antibiotics. Dr C is hoping this will help me, but he was disappointed that the orals didn't help much.

Of course I had been misdiagnosed for 20 years so we both knew it would not be a short recovery. I am detoxing right now, and then start the IV next week.

Thank you for asking...how are you doing?

Look forward to your reply.
M

Posts: 106 | From Texas | Registered: Jun 2005  |  IP: Logged | Report this post to a Moderator
foggedup
LymeNet Contributor
Member # 7415

Icon 1 posted      Profile for foggedup     Send New Private Message       Edit/Delete Post   Reply With Quote 
up...

anyone else have any ideas?

Posts: 106 | From Texas | Registered: Jun 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.