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 » imig vs. ivig

 - UBBFriend: Email this page to someone!    
Author Topic: imig vs. ivig
ihavelyme
Member
Member # 30170

Icon 1 posted      Profile for ihavelyme     Send New Private Message       Edit/Delete Post   Reply With Quote 
Hi All! I'm new to this site and have a Question.

My LLMD recommended imig (intramuscular injection instead of iv) It is VERY expensive.

Just wondering if anyone has tried imig and if it was helpful.

--------------------
lyme, bart, myco, EBV, yada, yada, yada...

Posts: 40 | From nc | Registered: Jan 2011  |  IP: Logged | Report this post to a Moderator
lou
Frequent Contributor (5K+ posts)
Member # 81

Icon 1 posted      Profile for lou     Send New Private Message       Edit/Delete Post   Reply With Quote 
I don't know anything about this and will be interested to see what kind of replies you get. Do you mean that IVIG is very expensive, or IMIG is (or both)?
Posts: 8430 | From Not available | Registered: Oct 2000  |  IP: Logged | Report this post to a Moderator
dmc
Frequent Contributor (1K+ posts)
Member # 5102

Icon 1 posted      Profile for dmc     Send New Private Message       Edit/Delete Post   Reply With Quote 
Do you mean Bicillin shots (or another abx shot)verses IV antibiotics?
Posts: 2675 | From ct, usa | Registered: Jan 2004  |  IP: Logged | Report this post to a Moderator
lou
Frequent Contributor (5K+ posts)
Member # 81

Icon 1 posted      Profile for lou     Send New Private Message       Edit/Delete Post   Reply With Quote 
I think ihavelyme means immune globulins, which is a blood product composed of antibodies, and is asking the question about whether to administer it by intravenous or intramuscular method. I had no idea it could be given in a shot form.

http://en.wikipedia.org/wiki/Intravenous_immunoglobulin

Posts: 8430 | From Not available | Registered: Oct 2000  |  IP: Logged | Report this post to a Moderator
ihavelyme
Member
Member # 30170

Icon 1 posted      Profile for ihavelyme     Send New Private Message       Edit/Delete Post   Reply With Quote 
yes, lou, that is exactly what I mean.

I have been off all abx since early Nov. in order to deal with yeast and to detox. As soon as my liver panel comes back (assuming all is well) I will begin 100 straight days of oral abx at higher doses.

Previously was on abx from Feb. 2010- Nov. 2010. It did a decent job of clearing up Bart as well as late stage Lyme. I took Plaquenil, Rifampin, doxy, flagyl and cefdinir

Currently doing weekly B-12 shots and LOTS of detox...brushing, magnesium baths, herbs such as milk thistle, oil of oregano, clove and other supplements.

LLMD suggested begining weekly intramuscular shots of immuno globulininalong with very large doses of abx and antivirals in order to assist my immune system in fighting off lyme and epstein barr.

The problem is cost. Each shot is $100...which adds an extra $400 per month on top of what I already spend on abx and supplements.

I was wondering if anyone else on this forum had experience with intramuscular shots of immuno-globulin.

--------------------
lyme, bart, myco, EBV, yada, yada, yada...

Posts: 40 | From nc | Registered: Jan 2011  |  IP: Logged | Report this post to a Moderator
ihavelyme
Member
Member # 30170

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

--------------------
lyme, bart, myco, EBV, yada, yada, yada...

Posts: 40 | From nc | Registered: Jan 2011  |  IP: Logged | Report this post to a Moderator
imagine2
LymeNet Contributor
Member # 3136

Icon 1 posted      Profile for imagine2     Send New Private Message       Edit/Delete Post   Reply With Quote 
Subcutaneous IGG is fairly new. It is not a shot but an iv put just under the skin instead of directly into the blood stream like IVIG.

The risk of side effects is much lower. When placed under the skin, it takes the body a lot longer to metabolize it.

Could this be what you mean?

Posts: 677 | From Virginia | Registered: Sep 2002  |  IP: Logged | Report this post to a Moderator
mookie333
LymeNet Contributor
Member # 26021

Icon 1 posted      Profile for mookie333     Send New Private Message       Edit/Delete Post   Reply With Quote 
I have spent a small fortune on gamma globulin im injections since last april.

I can not feel a thing from these...I have continued though. I have never done IV gammaglobulin.

Only thing I know is that my NK cell level has dropped and now my white cell count is at an all time low of 2.

Thank God I have not been getting sick...but I do the IM Bicillin shots as well..too tell you the truth I know I need to add a cyst buster to this...but can't really do anything until the white cells go up.

Posts: 151 | From south east | Registered: May 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.