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 » anyone tried ivig?

 - UBBFriend: Email this page to someone!    
Author Topic: anyone tried ivig?
2young2dieMom
LymeNet Contributor
Member # 25434

Icon 1 posted      Profile for 2young2dieMom     Send New Private Message       Edit/Delete Post   Reply With Quote 
My drs aren't sure if I have ALS but I have tested positive for fl1953. My latest EMG shows significant nerve loss but isn't entirely consistant with ALS.

My neuro refuses to prescribe ivig for me. He ordered some genetic tests (probably looking for the als gene) but if that comes back positive I'll never get ivig.

Has anyone tried ivig and gotten better?

--------------------
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
joalo
Frequent Contributor (1K+ posts)
Member # 12752

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

--------------------
Sick since January 1985. Misdiagnosed for 20 years. Tested CDC positive October 2005. Treating since April 2006.

Posts: 3228 | From Somewhere west of the Mississippi | Registered: Aug 2007  |  IP: Logged | Report this post to a Moderator
karenl
Frequent Contributor (1K+ posts)
Member # 17753

Icon 1 posted      Profile for karenl     Send New Private Message       Edit/Delete Post   Reply With Quote 
sent two pms
Posts: 1834 | From US | Registered: Oct 2008  |  IP: Logged | Report this post to a Moderator
showmemom
Member
Member # 34213

Icon 1 posted      Profile for showmemom     Send New Private Message       Edit/Delete Post   Reply With Quote 
You would probably need to see an immunologist for IVIg. They would probably need to run you Ig subclasses and CD3, CD4, CD8, CD19 and natural killer cells to see if they are within range. If your b cells and t cells are out of whack, you will not be able to fight off any infection, including Lyme.
Posts: 55 | From Missouri | Registered: Sep 2011  |  IP: Logged | Report this post to a Moderator
jwall
LymeNet Contributor
Member # 22999

Icon 1 posted      Profile for jwall     Send New Private Message       Edit/Delete Post   Reply With Quote 
So would one qualify for IVIG with low natural killer cell counts, low cd4, cd8, etc counts? An immunologist prescribes this or can an LLMD? Does IVIG help with nerve loss?
Posts: 618 | From NC | Registered: Oct 2009  |  IP: Logged | Report this post to a Moderator
Sammi
Frequent Contributor (1K+ posts)
Member # 110

Icon 1 posted      Profile for Sammi     Send New Private Message       Edit/Delete Post   Reply With Quote 
I believe you do need to see an immunologist and/or have thorough testing done to get IVIG prescribed.

My Lyme doctor ran some basic immune function tests. When they were abnormal, I then saw an immunologist who did much more extensive testing over a couple of months.

I was found to have an immune deficiency, and I get IVIG once a month. From what I understand, you must be deficient to be considered for IVIG. It is extremely expensive and not without risks.

Posts: 4681 | Registered: Oct 2000  |  IP: Logged | Report this post to a Moderator
Rumigirl
Frequent Contributor (1K+ posts)
Member # 15091

Icon 1 posted      Profile for Rumigirl     Send New Private Message       Edit/Delete Post   Reply With Quote 
Actually, you would be better off to see a LL neuro to test you to see if you qualify for IVIG for neuropathy, which you likely would.

The protocol of small-fiber neuropathy, or CDIP (Chronic Demyelinating Inflammatory Polyneuropathy) is higher dosage and more given more frequently, which you would surely need.

There is a sort of LL neuro in your state who evaluates for this and rx's it. You would definitely have to have insurance to cover it, however, as it is insanely expensive otherwise.

Posts: 3771 | From around | Registered: Mar 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.