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 » General Support » Is it okay that Dr. H in WI doesn't use IGENEX after all?

- UBBFriend: Email this page to someone!    
Author Topic: Is it okay that Dr. H in WI doesn't use IGENEX after all?
Jessibell777
Member
Member # 18235

Icon 1 posted      Profile for Jessibell777     Send New Private Message       Edit/Delete Post   Reply With Quote 
Thank you ALL so much for all the information, it's making a HUGE differece in what I say to my son's Infectious Disease MD. I have 2 questions.


I talked to Dr. H in WI yesterday. He sounds GREAT!

1. It turns out he DOES NOT use IGENEX. I told him IGENEX had some special equipment. He said his local University Lab has the same equipment.


Is that okay? Should I kind of INSIST that he use an IGENEX lab or TRUST that he knows what lab to use?


2.)BettyG says he's a ILADs MD, I don't know what that is YET. Is that good?
Posts: 43 | From Austin, TX | Registered: Nov 2008  |  IP: Logged | Report this post to a Moderator
Robin123
Moderator
Member # 9197

Icon 1 posted      Profile for Robin123     Send New Private Message       Edit/Delete Post   Reply With Quote 
Hi - you could check in with your state Lyme support groups. They are listed under SupportGroups/UnitedStates/Wisconsin.

ILADS stands for International Lyme and Associated Diseases Society. They are the most experienced group of doctors treating Lyme and coinfections. You can go read their website (ILADS.org). Famous treating guidelines there are the Burrascano guidelines.

All the best - Robin
Posts: 13171 | From San Francisco | Registered: May 2006  |  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.