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 » Thoughts/opinions on Ceres' Nanotrap Lyme test?

 - UBBFriend: Email this page to someone!    
Author Topic: Thoughts/opinions on Ceres' Nanotrap Lyme test?
missday
Member
Member # 44591

Icon 1 posted      Profile for missday     Send New Private Message       Edit/Delete Post   Reply With Quote 
Hi Everybody,

What have folks heard about Ceres new urine based lyme test?
My LLMD thinks it's a big deal. He said "we're literally coming out of the dark ages with this." It's supposedly much more accurate than blood based western blots.

I wonder what other folks have heard?

Thanks!
Day

Posts: 12 | From New York | Registered: Sep 2014  |  IP: Logged | Report this post to a Moderator
Told you I was sick
LymeNet Contributor
Member # 35068

Icon 1 posted      Profile for Told you I was sick     Send New Private Message       Edit/Delete Post   Reply With Quote 
Asking on behalf of a friend in New England. Anyone have anything to chime in on this test?

Many thanks, in advance. [Smile]

Told you...

Posts: 315 | From Negative (-) to positive (+) | Registered: Nov 2011  |  IP: Logged | Report this post to a Moderator
Jordana
Frequent Contributor (1K+ posts)
Member # 45305

Icon 1 posted      Profile for Jordana     Send New Private Message       Edit/Delete Post   Reply With Quote 
I believe that too. They're making it a little hard to get to since you need to have your doctor call. But if your LLMD wants to do it, and you can afford it -- it's a game changer.
Posts: 2057 | From Florida | Registered: Feb 2015  |  IP: Logged | Report this post to a Moderator
Told you I was sick
LymeNet Contributor
Member # 35068

Icon 1 posted      Profile for Told you I was sick     Send New Private Message       Edit/Delete Post   Reply With Quote 
Jordana-

Thanks for responding. My friend's test is positive. You think that that's a game changer? She treated her tbd for 4 years but then stopped. She fell very ill about a year and a half ago off of treatment...clearly a relapse. That's what I told her, anyways. I guess that this test was suggested to her, so she did it.

I hope that she resumes treatment following this positive.

Thanks so much for sharing your wisdom. [Smile]

Posts: 315 | From Negative (-) to positive (+) | Registered: Nov 2011  |  IP: Logged | Report this post to a Moderator
Jordana
Frequent Contributor (1K+ posts)
Member # 45305

Icon 1 posted      Profile for Jordana     Send New Private Message       Edit/Delete Post   Reply With Quote 
Yes, the nanotrap indicates when Lyme is *active*. That's the game changing part. It's not auotoimmune or candida or anything else. It's active Lyme.
Posts: 2057 | From Florida | Registered: Feb 2015  |  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.