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 » When would someone get IV antibiotics?

 - UBBFriend: Email this page to someone!    
Author Topic: When would someone get IV antibiotics?
MysteryGirl44
LymeNet Contributor
Member # 10201

Icon 1 posted      Profile for MysteryGirl44     Send New Private Message       Edit/Delete Post   Reply With Quote 
Hi!

I was wondering what would make a Lyme patient need IV antibiotics vs oral.

I know that the very severe cases might start with it off the bat, but I've been treated for a year with oral antibiotics and I still feel pretty much the same and I'm having seizures and a lot of neurological symptoms.

I would like to try IV antibiotics, if my LLMD feels I need it, but I'm not sure how to bring it up.

Any thoughts would be greatly appreciated. [group hug]

--------------------
"Life doesn't have to be perfect to be wonderful."

www.myspace.com/lymediseaseawareness

Posts: 514 | From New Jersey | Registered: Sep 2006  |  IP: Logged | Report this post to a Moderator
sonicbmx
LymeNet Contributor
Member # 12949

Icon 1 posted      Profile for sonicbmx     Send New Private Message       Edit/Delete Post   Reply With Quote 
my LLMD said there were 3 levels..

1. Doxycycline if positive for Borrelia

2. Zithromax/Mepron combo if co-infection present

3. IV Rocephin if neuro issues found (abnormal Brain SPECT)

i wanted IV on day one but i had to go through the process so he didn't get heat from medical board (i believe).

my suggestion is to do ALL the testing you can up front. this process delayed my IV treatment approx 4 months.

i am 100% better than i was prior to IV treatment. i'm 80-85% recovered and i feel like i'm damn near fully recovered.

will post more on the subject of my road to recovery very soon.. waiting on latest lab results at the moment.

hope this helps.. all the best.
--
sonicbmx

--------------------
"The hell with Drs.. we have each other!"
My story began here:

http://forums.wrongdiagnosis.com/showthread.php?t=16210
http://forums.wrongdiagnosis.com/showthread.php?t=7833
http://forums.wrongdiagnosis.com/showthread.php?t=6873

Posts: 127 | From Van Nuys, CA | Registered: Aug 2007  |  IP: Logged | Report this post to a Moderator
MysteryGirl44
LymeNet Contributor
Member # 10201

Icon 1 posted      Profile for MysteryGirl44     Send New Private Message       Edit/Delete Post   Reply With Quote 
Thanks! [Smile]

--------------------
"Life doesn't have to be perfect to be wonderful."

www.myspace.com/lymediseaseawareness

Posts: 514 | From New Jersey | Registered: Sep 2006  |  IP: Logged | Report this post to a Moderator
tdtid
Frequent Contributor (1K+ posts)
Member # 10276

Icon 1 posted      Profile for tdtid     Send New Private Message       Edit/Delete Post   Reply With Quote 
Also with a lot of doctors still trying to fly under the radar, they only treat with orals.

I did 20 months of orals and I was getting better but then wham, got hit hard, so my "under the radar" LLMD referred me to Dr. R who isn't under that radar in the same way.

He felt that after 20 months of orals and still fighting, it was time for IV.

Insurance wants nothing to do with it, so it's out of pocket and I feel like crap from it, but if it works, it will be very worth it.

Cathy

--------------------
"To Dream The Impossible Dream" Man of La Mancha

Posts: 2638 | From New Hampshire | Registered: Oct 2006  |  IP: Logged | Report this post to a Moderator
gemofnj
Frequent Contributor (1K+ posts)
Member # 15551

Icon 1 posted      Profile for gemofnj     Send New Private Message       Edit/Delete Post   Reply With Quote 
I believe according to Dr. Burrasacano's guidelines under iv antibiotic treatment is only used in certain chronic conditions:

CHRONIC LYME DISEASE (PERSISTENT/RECURRENT INFECTION)

"By definition, this category consists of patients with active infection, of a more prolonged duration, who are more likely have higher spirochete loads, weaker defense mechanisms, possibly more virulent or resistant strains, and probably are significantly co-infected.

Neurotoxins may also be significant in these patients. Search for and treat for all of these, and search for concurrent infections including viruses, chlamydias, and
mycoplasmas.

Be sure to do an endocrine workup if indicated. These patients require a full evaluation for all of these problems, and each abnormality must be addressed.

This group will most likely need parenteral therapy, especially high dose, pulsed therapy, and antibiotic combinations, including metronidazole.

Antibiotic therapy will need to continue for many months, and the antibiotics may have to be changed periodically to break plateaus in recovery.

Be vigilant for treatment related
problems such as antibiotic-associated colitis, yeast overgrowth, intravenous catheter complications, and abnormalities in blood counts and chemistries."

Taken from: http://www.ilads.org/files/burrascano_0905.pdf

Posts: 1127 | From atlantic city, nj | Registered: May 2008  |  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.