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 » CD57 Test or Not?

 - UBBFriend: Email this page to someone!    
Author Topic: CD57 Test or Not?
catdog
Member
Member # 26365

Icon 1 posted      Profile for catdog     Send New Private Message       Edit/Delete Post   Reply With Quote 
i was just diagnosed a few weeks ago so i'm a newbie to all of this.

another lymie insisted that i get a CD57 test. in fact that if my doc didn't order one, i should consider another doc.

do you agree? is there a lot of weight put on this test? should i consider another doc?

Posts: 95 | From IL | Registered: Jun 2010  |  IP: Logged | Report this post to a Moderator
bcb1200
Frequent Contributor (1K+ posts)
Member # 25745

Icon 1 posted      Profile for bcb1200     Send New Private Message       Edit/Delete Post   Reply With Quote 
I don't know if I would leave my LLMD over this. But Dr. B considers it a valuable "barometer" re lyme. Check out the link below.

http://flash.lymenet.org/ubb/ultimatebb.php/topic/1/96841

--------------------
Bite date ?
2/10 symptoms began
5/10 dx'd, after 3 months numerous test and doctors

IgM Igenex +/CDC +
+ 23/25, 30, 31, 34, 41, 83/93

Currently on:

Currently at around 95% +/- most days.

Posts: 3139 | From Massachusetts | Registered: May 2010  |  IP: Logged | Report this post to a Moderator
'Kete-tracker
Frequent Contributor (1K+ posts)
Member # 17189

Icon 1 posted      Profile for 'Kete-tracker     Send New Private Message       Edit/Delete Post   Reply With Quote 
If your doc's not "Lyme-Literate" it's doutbtful he/ she even knows what a CD-57 blood count IS.
It's fairly specialized test & is done by only 1 or 2 labs, to my knowledge.

Some LLMDs consider (changing) CD-57 counts over time an important measure of how effective a particular treatment is. Others find it somewhat useful, but don't rely on the results.

Go over your treatment parameters with us (i.e: what you're taking & for how long) & we'll be better able to tell if you're under appropriate care... or are atleast being sufficiently treated.

Give your doc a chance. He diagNOSED you with Lyme... That's a good starting point! [Smile]

Posts: 1233 | From Dover, NH | Registered: Sep 2008  |  IP: Logged | Report this post to a Moderator
catdog
Member
Member # 26365

Icon 1 posted      Profile for catdog     Send New Private Message       Edit/Delete Post   Reply With Quote 
kete, i went undiagnosed for 5 yrs and was just diagnosed by an LLMD late last month.

i just started treatment 2 wks ago on 500mg biaxin/day. i bump up to 1000mg biaxin on monday. i'm also on a most of the supplements/herbs on Dr. B's list on my own accord, LLMD didn't advise to do this.

my LLMD didn't inform me about CD57 and what the other lymie said kind of worried me that i wasn't seeing the best doc!

is it reliable? is in necessary??

Posts: 95 | From IL | Registered: Jun 2010  |  IP: Logged | Report this post to a Moderator
'Kete-tracker
Frequent Contributor (1K+ posts)
Member # 17189

Icon 1 posted      Profile for 'Kete-tracker     Send New Private Message       Edit/Delete Post   Reply With Quote 
My LLMD didn't bring up the CD-57 test until the 2nd visit. Don't know why.
It's not neccessary, but as far as "reliability", it's more a question of whether the doctor feels it's useful in his/her desire to know how current therapy is proceeding.

You can bring it up at your next appointment... if he doesn't mention it first.
The abx you're on- Biaxin- is a good one for Lyme.
You May find he'll add in either Plaquenil (hydroxychloroquine) or Symmetrel (amantadine), to boost it's effectiveness, later on.

LLMDs know to start late-stage Lyme patients out slow on the drugs, & add 1 at a time to be able to discriminate drug reactions from the "Jarsch-Herxheimer" reactions ("herxing") that spirochete-infected patients experience, esp. at the onset of antibiotic ("abx") therapy.

Hang in there. Those supplements recommended in Dr. B's guidelines are good ones... so continue on those... & keep the capsules organized.

Also, review what you're taking, & how Often, with the Doc next time. A FEW herbs can conflict with certain types of drugs. Do the research, or ask a knowledgable pharmacist.
Also, mineral supplements can sometimes "tie up" some of certain medications, so keep those doses seperated.

Good luck in your recovery!
2 weeks "in" is just beginning. It's a long journey, but you'll get there.

Posts: 1233 | From Dover, NH | Registered: Sep 2008  |  IP: Logged | Report this post to a Moderator
catdog
Member
Member # 26365

Icon 10 posted      Profile for catdog     Send New Private Message       Edit/Delete Post   Reply With Quote 
thx kete, that makes me feel better! [Big Grin] i was going to ask him about the CD57 the next time i see him in sept.

i haven't started the herbs yet because of money but i was going to start maitake & reishi mushrooms, ginsing, and astragalus which i read are supposed to help support the immune system. are these any of the ones you were referring to?

i know, i'm just a newbie at this! there's so much to learn!! [dizzy]

Posts: 95 | From IL | Registered: Jun 2010  |  IP: Logged | Report this post to a Moderator
ailat
Member
Member # 26113

Icon 1 posted      Profile for ailat     Send New Private Message       Edit/Delete Post   Reply With Quote 
does anyone know if the dx for this test would only be "lyme"?
Also, does the doctor write "cd-57 panel" for his order of this test?
thanks a lot
Ann

Posts: 21 | From NE | Registered: May 2010  |  IP: Logged | Report this post to a Moderator
4Seasons
LymeNet Contributor
Member # 14601

Icon 1 posted      Profile for 4Seasons     Send New Private Message       Edit/Delete Post   Reply With Quote 
My LLMD and many others often don't order a CD57 until later in treatment or not at all, as they don't think it very reliable.

I have a friend whose LLMD orders it regularly.

My daughter and I have been in treatment for over two years and just had our first CD57 tests.

--------------------
"Life isn't about waiting for the storm to pass, it's about learning to dance in the rain."
Anonymous

Posts: 450 | From California | Registered: Feb 2008  |  IP: Logged | Report this post to a Moderator
catdog
Member
Member # 26365

Icon 1 posted      Profile for catdog     Send New Private Message       Edit/Delete Post   Reply With Quote 
thanks 4seasons, that makes me feel much much better about my doc! [Smile]

i didn't want to get farther along into treatment and find out he should have been doing this test the whole time!

Posts: 95 | From IL | Registered: Jun 2010  |  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.