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 » Success/Experiences with IV Ceftriaxone?

 - UBBFriend: Email this page to someone!    
Author Topic: Success/Experiences with IV Ceftriaxone?
ecr1
Member
Member # 18660

Icon 1 posted      Profile for ecr1     Send New Private Message       Edit/Delete Post   Reply With Quote 
Has anybody had success with IV Ceftriaxone?

I've been on oral antibiotics for 13 months and about to start 4 weeks of IV Ceftriaxone. Experiences and suggestions welcome.

Thanks!

[ 04-12-2010, 11:37 PM: Message edited by: ecr1 ]

Posts: 31 | From Boston, MA | Registered: Jan 2009  |  IP: Logged | Report this post to a Moderator
azdaisy
Member
Member # 25357

Icon 1 posted      Profile for azdaisy     Send New Private Message       Edit/Delete Post   Reply With Quote 
well hello there!
I did about 100 IM Ceftriaxone before I caved and got my PICC put in last September.
From the first injection the ringing in my ears took off. which told me the bugs don't like it! So I LOVE it!! KILL THE BUGS!! I have been low and slow and incredibly weak, low stamina.
this is NORMAL for IV ABX!! you must expect to be worse first. NO SUGAR NO FLOUR is crucial if you are at this step! Or beware the Thrush monster!!! besides bugs love sugar and I will be damned if Im going to feed them!!!
I also take Metronidizole to open cysts so ABX can work better. and Questran or Cholestyrimine is also really necessary to help clean up the neurotoxins that this level of bug warfare brings!!! check out shoemaker's site http://www.chronicneurotoxins.com/
otherwise my brain turns to sludge- when I take brakes from it I get really foggy! like misspell my name.... Let everyone that is in your support circle that you will be needing more help for a while.
I was really afraid of the PICC line and it's nothing compared to the injectables! really easy. Are your meds covered by insurance? if not I am happy to help you find out sources.
Breathe and trust the process. Have you seen the under our skin movie? it helps to see other people and thier recovery processes. Best to you!!!

--------------------
AzDaisy
life requires action

Posts: 58 | From Tucson, AZ | Registered: Apr 2010  |  IP: Logged | Report this post to a Moderator
KS
LymeNet Contributor
Member # 12549

Icon 1 posted      Profile for KS     Send New Private Message       Edit/Delete Post   Reply With Quote 
IV ceftriaxone was a good drug for me...some of my symptoms (i.e. internal vibrations) completely disappeared. Unfortunately my liver enzymes climbed to almost 900 so be sure someone is monitoring you liver.

Anyway, it didn't cure me...I did another 18 months of a variety of oral antibiotics to get me well.

Posts: 561 | From mass | Registered: Jul 2007  |  IP: Logged | Report this post to a Moderator
gatorade girl
LymeNet Contributor
Member # 24896

Icon 1 posted      Profile for gatorade girl   Author's Homepage     Send New Private Message       Edit/Delete Post   Reply With Quote 
Could someone please pm me resources bc my iv antibiotics are not being paid for by insurance ? I am on uv rocephin and is helping me.

--------------------
gatorade girl

"I still have Mt.Everest to climb, but I have traveled across the world and arrived at the mountain".

Posts: 633 | From baltimore | Registered: Mar 2010  |  IP: Logged | Report this post to a Moderator
ecr1
Member
Member # 18660

Icon 1 posted      Profile for ecr1     Send New Private Message       Edit/Delete Post   Reply With Quote 
Thank you for the notes!

azdaisy, my meds should be covered by insurance but if not, I will PM you. Thank you for your advice and offer to help. I am looking forward to doing some form of IV for even just a short while. I have responded well to oral abx over the past year but not completely better. So hoping the IV will make one final push to knock it all out. I have seen under our skin. I think it is a good documentary for sure.

KS, thanks for advice on watching liver carefully... I will do so.

More experiences welcome!!!

Posts: 31 | From Boston, MA | Registered: Jan 2009  |  IP: Logged | Report this post to a Moderator
ecr1
Member
Member # 18660

Icon 1 posted      Profile for ecr1     Send New Private Message       Edit/Delete Post   Reply With Quote 
up
Posts: 31 | From Boston, MA | Registered: Jan 2009  |  IP: Logged | Report this post to a Moderator
sammy
Frequent Contributor (5K+ posts)
Member # 13952

Icon 1 posted      Profile for sammy     Send New Private Message       Edit/Delete Post   Reply With Quote 
If insurance stops covering you IV meds, give Infuserve a call. They have fair prices (better than local pharmacies) and good customer service.

http://www.infuserveamerica.com/

Posts: 5237 | From here | Registered: Nov 2007  |  IP: Logged | Report this post to a Moderator
2young2dieMom
LymeNet Contributor
Member # 25434

Icon 1 posted      Profile for 2young2dieMom     Send New Private Message       Edit/Delete Post   Reply With Quote 
Has anyone with ALS been cured with Ceftriaxone?

--------------------
Dxd ALS 3/2010
Dxd cllinical Lyme 4/2010
Positive for Protomyxzoa but absolutely nothing else in Igenex

Posts: 417 | From central ct | Registered: Apr 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.