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 » question about babs

 - UBBFriend: Email this page to someone!    
Author Topic: question about babs
suexi
Member
Member # 10822

Icon 1 posted      Profile for suexi   Author's Homepage     Send New Private Message       Edit/Delete Post   Reply With Quote 
My dr. recently told me that it sounds like i have babesia along with lyme. I'm just wondering if anyone who HAS Babs, DOES NOT get sweats at night. For that matter i don't HARDLY get sweaty at all.

After getting on the biaxin; about 5 weeks into it, i was getting hot/cold flashes for about a week. And that was IT. I think the dr. made his conclusion PARTIALLY from that episode.

I'm NOT questioning his analysis, because i know he's good, just wondering if there is anyone that does not have this common symptom of babs?

thanks
sue

Posts: 30 | From LV, so. calie | Registered: Dec 2006  |  IP: Logged | Report this post to a Moderator
luvs2ride
Frequent Contributor (1K+ posts)
Member # 8090

Icon 1 posted      Profile for luvs2ride     Send New Private Message       Edit/Delete Post   Reply With Quote 
I have several positive tests for Babs WA-1 and I hardly ever sweat. Before I became sick, I used to sweat profusely.

Go figure!

--------------------
When the Power of Love overcomes the Love of Power, there will be Peace.

Posts: 3038 | From america | Registered: Oct 2005  |  IP: Logged | Report this post to a Moderator
daise
Unregistered


Icon 1 posted            Edit/Delete Post   Reply With Quote 
Hi,

I don't have sweats. Not everyone with babs does and no one knows why.

With Lyme, babs and bart, the signs and symptoms lists do not mean that you have to have all the signs and symptoms. We are individuls.

daise [Smile]

IP: Logged | Report this post to a Moderator
hokie
LymeNet Contributor
Member # 14720

Icon 1 posted      Profile for hokie     Send New Private Message       Edit/Delete Post   Reply With Quote 
I tested extremely high for babs microti (1:320) when normal range is 1:10 or less. My LLMD feels that I certainly have it with that high of a ratio. I am being treated for it.

No sweats, ever, unless working out.

Posts: 129 | From Virginia | Registered: Feb 2008  |  IP: Logged | Report this post to a Moderator
Hides1
LymeNet Contributor
Member # 6348

Icon 1 posted      Profile for Hides1     Send New Private Message       Edit/Delete Post   Reply With Quote 
I had more chills than sweats. Mine level was 1:1280 when finally found. Not until I got into treatment in 2005 did I finally get the sweats and air hunger everyone talks about. To this day I battle the Babesia as my last recent test was 1:1280 even though my FSH was neg. My Babs was missed for a while because I didn't have the classic sweats in fact for some reason I wasn't sweating much at all even in the summer back then.
Posts: 238 | From Bethlehem, PA | Registered: Oct 2004  |  IP: Logged | Report this post to a Moderator
Cass A
Frequent Contributor (1K+ posts)
Member # 11134

Icon 1 posted      Profile for Cass A     Send New Private Message       Edit/Delete Post   Reply With Quote 
I didn't have sweats either--just would heat up and cool down sometimes for no apparent reason. I did get an out-of-balance feeling sometimes, and sometimes got true vertigo.

I decided to treat for Babs just in case--and got the best results of anything I'd tried to date!! Some particularly bothersome problems went away and haven't come back, including the two I mentioned.

After self-treating with artemisinin and cryptolepsis, I got the Fry Labs test done--smear and titers. The smear was clean, but the titers showed positive, so it wasn't gone. Drat.

I've been treating for Babs for about two months now with an herbal formula from my LLMD, and just started Mepron/Zith today.

Best,

Cass A

Posts: 1245 | From Thousand Oaks, CA | Registered: Feb 2007  |  IP: Logged | Report this post to a Moderator
trish4
LymeNet Contributor
Member # 14156

Icon 1 posted      Profile for trish4     Send New Private Message       Edit/Delete Post   Reply With Quote 
I am positive for babesia and never had night sweats.
Posts: 370 | From NJ | Registered: Dec 2007  |  IP: Logged | Report this post to a Moderator
realist
Member
Member # 15105

Icon 1 posted      Profile for realist     Send New Private Message       Edit/Delete Post   Reply With Quote 
I don't have night sweats and also tested positively for Babesia.
Posts: 31 | From Leesburg, VA | Registered: Apr 2008  |  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 Hides1:
I had more chills than sweats.

Me too. Even the chills were rather minimal. My worst babs issues were extreme fatigue, headaches, dizziness, and pain.

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

Posts: 96239 | From Texas | Registered: Feb 2001  |  IP: Logged | Report this post to a Moderator
Lauralyme
Frequent Contributor (1K+ posts)
Member # 15021

Icon 1 posted      Profile for Lauralyme     Send New Private Message       Edit/Delete Post   Reply With Quote 
No sweats for me either. Very strong positive Babesia result. Alot of chills though. I have awaken from a deep sleep shivering cold.

--------------------
Fall down seven times, get up eight
~Japanese proverb

Posts: 1146 | From west coast | Registered: Mar 2008  |  IP: Logged | Report this post to a Moderator
painted turtle
LymeNet Contributor
Member # 7801

Icon 1 posted      Profile for painted turtle   Author's Homepage     Send New Private Message       Edit/Delete Post   Reply With Quote 
I tested positive for the babesia on the Fry smear (4 out of 5 density).

Didn't have the sweats problem at all and still don't.

But do have chills a LOT.

As well as a very frequent off balance feeling and constriction of breath.

--------------------
www.lymefire.blogspot.com

Posts: 855 | From United States of Mind | Registered: Aug 2005  |  IP: Logged | Report this post to a Moderator
SoSublyme
LymeNet Contributor
Member # 15185

Icon 1 posted      Profile for SoSublyme     Send New Private Message       Edit/Delete Post   Reply With Quote 
I'm just starting my Babs treatment (have Lyme and Bart too).

I haven't really have night sweats, just an all-around elevation in body temperature, I guess.

I spent this past winter dressed in short-sleeved or sleeveless shirts.

I couldn't bear the thought of putting on a sweater. But I don't have excessive sweating, day or night.

My other Babs symptoms seem to be fatigue, general "wooziness", migraines and huge itchy rashes popping up all over that my dr thinks are Babs-related.

Good luck!

Posts: 345 | From East Coast | Registered: Apr 2008  |  IP: Logged | Report this post to a Moderator
Bugg
Frequent Contributor (1K+ posts)
Member # 8095

Icon 1 posted      Profile for Bugg     Send New Private Message       Edit/Delete Post   Reply With Quote 
I, too, had babs with no significant night sweats...Only had a few, light nighsweats once I started Mepron, zith, and art...Before treating for babs, I had extreme fatigue and my legs felt like lead weights...During treatment, I got a very stiff neck and stiff muscles along my spinal column...Now, post-babs, no more heavy legs!!! Also, (as you'll see from a post I put on this board earlier today), make sure you keep up with your magnesium intake...If not, it can cause severe muscle tightness and cramping and exacerbate fatigue.....With babs treatment, I developed hypomagnesemia from an extreme mag deficiency....
Posts: 1155 | From Southeast | Registered: Oct 2005  |  IP: Logged | Report this post to a Moderator
daise
Unregistered


Icon 1 posted            Edit/Delete Post   Reply With Quote 
Thank you Bugg,

After taking good doses of magnesium for two 1/2 years, I just stopped because I couldn't fit it in anywhere in my list of meds/supplements, due to starting on cipro.

My pharmacy instructions for cipro say: Take at the same time every day 6 hours before or 2 hours after magnesium, a,luminum, calcium, (and iron or Zinc. )

Avoid milk products, unless it's part of a full meal.

Good grief!

Gotta get it on my list again ... somehow ... because I just started Mepron this morning.

daise [Smile]

IP: Logged | Report this post to a Moderator
christinelyme2
Member
Member # 15028

Icon 1 posted      Profile for christinelyme2     Send New Private Message       Edit/Delete Post   Reply With Quote 
[bonk] hello everyone! i was wondering if

anyone else has twitching in their eye and face?

also how do you know if you have co-infections

from lyme? what is given to treat them? any

info. would be great, thanks! [confused]

Posts: 27 | From pa | Registered: Mar 2008  |  IP: Logged | Report this post to a Moderator
daise
Unregistered


Icon 1 posted            Edit/Delete Post   Reply With Quote 
H E L L O ChristineLyme 2,

WELCOME! [hi]

We need to roll out the red carpet for you.

We can do that best if you could please start a new thread. All sorts of folks--maybe even from foreign countries--will jump into your thread to help you.

To do this, please go to near the top of this page and click "Post New Topic."

Tips: Please let us know a bit about your history. How long have you had signs and symptoms and what are they?

You can copy your post here, to the new thread.

Lymeland is information overload, so are you ready?

daise [Smile]

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 
Yes, please open a new thread. We'll help you all we can, Christine!

I hope you have an LLMD.

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

Posts: 96239 | From Texas | Registered: Feb 2001  |  IP: Logged | Report this post to a Moderator
CherylSue
Frequent Contributor (1K+ posts)
Member # 13077

Icon 1 posted      Profile for CherylSue     Send New Private Message       Edit/Delete Post   Reply With Quote 
Do you have to have headaches for it to be babesia?

My initial illness was high, prolonged fever, drenching sweats, extreme fatigue and malaise.

I'm in a relapse of something now with mild fever, chest tightness, burning skin, fatigue, etc.

Could this be babs even though I don't get headaches?

CherylSue

Posts: 1954 | From Illinois | Registered: Aug 2007  |  IP: Logged | Report this post to a Moderator
sixgoofykids
Honored Contributor (10K+ posts)
Member # 11141

Icon 1 posted      Profile for sixgoofykids   Author's Homepage     Send New Private Message       Edit/Delete Post   Reply With Quote 
I have babs and never had headaches. I did have profuse night sweats.

--------------------
sixgoofykids.blogspot.com

Posts: 13449 | From Ohio | Registered: Feb 2007  |  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.