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 » 1st Lyme, then Fms, then Lyme now FMS

 - UBBFriend: Email this page to someone!    
Author Topic: 1st Lyme, then Fms, then Lyme now FMS
mrdsmom
Member
Member # 5630

Icon 8 posted      Profile for mrdsmom     Send New Private Message       Edit/Delete Post   Reply With Quote 
I don't know whether I should scream or cry. Over the past 5 years I've been dx'd with both Lyme and Fibromyalgia...different docs dx'd me differently.

Just went to a doctor who "specializes in Lyme Disease" and was told that I have Fibromyalgia...definately not Lyme...most likely never had it.

I've had positive Elisa, Western Blot and PCR test but "most likely" never had Lyme.

I had a high fever which lasted over a week and might have had Babesia, but my immune system would have gotten rid of it on it's own and does not need to be treated for it now. I was told Lyme disease does not cause high fever.

My head is spinning...thanks everyone, for just listening....I really need to vent!!!!!


Posts: 56 | From Belvidere,NJ USA | Registered: May 2004  |  IP: Logged | Report this post to a Moderator
bg
Junior Member
Member # 46416

Icon 1 posted      Profile for bg     Send New Private Message       Edit/Delete Post   Reply With Quote 
what specific LYME blood test did you have?

elisa you said but what about western blot IGM & IGG?

more important, WHAT LAB did this? Igenex or MDL? If they didn't test all 16 protein bands, you were screwed by them.

We do have FM with our lyme; that's why we have so much pain. Betty G.


Posts: 1 | From US | Registered: Aug 2015  |  IP: Logged | Report this post to a Moderator
kam
Honored Contributor (10K+ posts)
Member # 3410

Icon 1 posted      Profile for kam     Send New Private Message       Edit/Delete Post   Reply With Quote 
I was just scanning this article today. It is called lyme wars. It mentions fibromalgia. I think it will help you.
[URL=http://www.wildernetwork.org/Lyme_Wars.html]


The second thing that popped in my mind is who is this lyme specialist? Is he a member of ILADS? Was he referred by the Lyme Disease Association or by someone here on lymenet or ILADS?

I, too, saw so called lyme specialist only to have to tell them how to read the Igenex Lab results. He also said I only needed a few weeks of abx. HE knew because he was an ivy league doctor! I wondered about that doc and didn't go back.

I also was given a dx of fibro then not fibro, then fibro.

The bottom line for me is not what it is labeled, but what is going to be done to help me regain my health.

Scott Taylor, DVM has written excellent report/summary of his research regarding his dx of fibromalgia and traveling out of state for help from a lyme doc.

It is called Lyme Disease: the disease of ignorance. I think his web site is myremedi.com

[This message has been edited by kam (edited 07 February 2005).]


Posts: 15927 | From Became too sick to work or do household chores in 2001. | Registered: Dec 2002  |  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 
quote:
Originally posted by mrdsmom:

Just went to a doctor who "specializes in Lyme Disease" and was told that I have Fibromyalgia...definately not Lyme...most likely never had it.

I've had positive Elisa, Western Blot and PCR test but "most likely" never had Lyme.



Where did you find this bird brain of a duck? Good gosh!

Do you have an LLMD??? Guess not?!

Forget what this duck said, and move on. Find a dr with a brain and get proper treatment.

Sure, you probably have fibromyalgia....from Lyme and babs.

------------------
oops!
Lymetutu


Posts: 96227 | From Texas | Registered: Feb 2001  |  IP: Logged | Report this post to a Moderator
Lymetoo
Moderator
Member # 743

Icon 6 posted      Profile for Lymetoo     Send New Private Message       Edit/Delete Post   Reply With Quote 

Posts: 96227 | From Texas | Registered: Feb 2001  |  IP: Logged | Report this post to a Moderator
TheCrimeOfLyme
Frequent Contributor (1K+ posts)
Member # 4019

Icon 1 posted      Profile for TheCrimeOfLyme     Send New Private Message       Edit/Delete Post   Reply With Quote 
What in the world lyme doctor did you see?

I hope it was a doc recommended by a lyme patient?

P.S. The doctor DOES NOT have to be a member of ILADS to be a LLMD.


Posts: 3169 | From Greensburg, Pennsylvania | Registered: Jun 2003  |  IP: Logged | Report this post to a Moderator
mrdsmom
Member
Member # 5630

Icon 1 posted      Profile for mrdsmom     Send New Private Message       Edit/Delete Post   Reply With Quote 
Thanks everyone, like I said, I just need to vent. With positive tests on and off during the last 5 or so years, I know it's Lyme and probably Babesia (never treated for Babs. This doc doesn't even understand why I felt better during treatment (since it's not Lyme, you know).

I haven't seen my regular LLMD in a couple of months due to $$$ issues and hoped this other doc was a doctor and not a duck...guess I was wrong.

Lymetoo, thanks for the "Wacky Dux"...I needed the laugh.

Tonight I have a sleep study scheduled and Thursday I see an attorney to help me with disablity. After that, I'll start my search for a LLMD.

Thanks Again!

Carol


Posts: 56 | From Belvidere,NJ USA | Registered: May 2004  |  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.