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 » Advice on U of Michagan for lyme tx...

 - UBBFriend: Email this page to someone!    
Author Topic: Advice on U of Michagan for lyme tx...
msariess
Member
Member # 7713

Icon 1 posted      Profile for msariess     Send New Private Message       Edit/Delete Post   Reply With Quote 
HI All, after getting a CDC positive on the Western Blot (Igm & Igg).. my HMO wants to send me to university of Michigan for testing and treatment plan...

Any one have experience with U of M??? This would be with an ID doc. I'm really, really leery of this appointment! I'm afraid they will test me with a sub-standard lab and then refuse to tx me.

Give me your opinions & experiences, please!!!!

TIA,

Posts: 21 | From Midwest, USA | Registered: Aug 2005  |  IP: Logged | Report this post to a Moderator
vitch
LymeNet Contributor
Member # 8094

Icon 1 posted      Profile for vitch     Send New Private Message       Edit/Delete Post   Reply With Quote 
I don't know about U of M but universities, in general, are bad on Lyme. ID docs are bad on Lyme. I'd contact the Michigan support groups to ask for help. If possible, I'd also get a LL lawyer.

--------------------
[email protected]

www.lymediseaseassociation.org/Conflicts.doc

Worthless tests & labs, a dangerous vaccine, insurance companies refuse to pay, undertreatment the norm, all about money. MO.

Posts: 281 | From CT | Registered: Oct 2005  |  IP: Logged | Report this post to a Moderator
Lymetoo
Moderator
Member # 743

Icon 1 posted      Profile for Lymetoo     Send New Private Message       Edit/Delete Post   Reply With Quote 
If you have a positive test, it would be best to not let any dr re-test you. It could mean denial by insurance and, as you said, denial of treatment by an ID. [Most ID's are ducks, so that wouldn't be a great loss.....Forget about HMO's too. UGH!]

I would NOT suggest ANY university for treatment of Lyme. Most, if not ALL universities go by the theory that Lyme is easily treated with 4 wks of abx. Forget it!!

Many folks in the Midwest go to Dr C in Missouri. Go for the best if you want to get well!

--------------------
--Lymetutu--
Opinions, not medical advice!

Posts: 96239 | From Texas | Registered: Feb 2001  |  IP: Logged | Report this post to a Moderator
msariess
Member
Member # 7713

Icon 1 posted      Profile for msariess     Send New Private Message       Edit/Delete Post   Reply With Quote 
Thanks for the imput, I cancelled the ID appt today.

(Told them I was going to find another doctor closer to home)

Posts: 21 | From Midwest, USA | Registered: Aug 2005  |  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.