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 » Tingling more dispersed now. Is this significant?

 - UBBFriend: Email this page to someone!    
Author Topic: Tingling more dispersed now. Is this significant?
Friend PAM
Member
Member # 10051

Icon 1 posted      Profile for Friend PAM     Send New Private Message       Edit/Delete Post   Reply With Quote 
I have few symptoms, compared to so many who post here. Mostly I'm concerned about an increase in neuropathy, with pins and needles suddenly not just being in my feet anymore, but all over my body, mostly left side, including head and face. My memory and balance has been better, even as this has gotten worse. Have never had a positive blood test for anything! My doctor was treating me for Babs., though I've never had headaches or fevers. (Have had night sweats in the past and do get a hot flash when I wake up frequently.) Have had constant eye dryness and frequent blurred vision. Any ideas about what's going on? I'm on Doxy again now and Flaggl and I take Artemisin, 2 weeks on and 2 weeks off. Thanks!
Posts: 40 | From Cincinnati, Ohio | Registered: Sep 2006  |  IP: Logged | Report this post to a Moderator
karenl
Frequent Contributor (1K+ posts)
Member # 17753

Icon 1 posted      Profile for karenl     Send New Private Message       Edit/Delete Post   Reply With Quote 
No idea. Dry eye could be immune problem. Arte can flare lupus first.
Probably toxins. Detox to meds??

Posts: 1834 | From US | Registered: Oct 2008  |  IP: Logged | Report this post to a Moderator
psano2
LymeNet Contributor
Member # 11711

Icon 1 posted      Profile for psano2     Send New Private Message       Edit/Delete Post   Reply With Quote 
it sounds like you have Lyme disease to me. Lyme causes the pins and needle pain in the feet that you describe. You can't rely on blood tests to determine if you have Lyme.

It's good that you're back on Doxy and Flagyl,

Posts: 975 | From California | Registered: Apr 2007  |  IP: Logged | Report this post to a Moderator
middlesizedpanda
Member
Member # 20676

Icon 1 posted      Profile for middlesizedpanda     Send New Private Message       Edit/Delete Post   Reply With Quote 
Hi Pam,
Your symptoms sound very similar to mine, Constant tingling / pins & needles in both hands & feet for about 8 months now. Also dry eyes & blurred vision & a tingling on my head. I also have numbness on my back & left foot & extreme fatigue.

I also have had no positive tests & do not get night sweats or head aches.

I do think I was bitten by a tick last Dec.

Although these symptoms do sound like lyme, there are other things that can cause similar symptoms. I have had so many tests now & am waiting for nerve conduction studies.

My doctor thinks im over obsessed with lyme & that it is probably something else. Im trying to stay open minded about it.

Take Care
Panda

Posts: 69 | From UK | Registered: Jun 2009  |  IP: Logged | Report this post to a Moderator
Haley
Frequent Contributor (1K+ posts)
Member # 22008

Icon 1 posted      Profile for Haley     Send New Private Message       Edit/Delete Post   Reply With Quote 
This can be a side effect of Flagyl. I would tell your doctor about it. Flagyl can effect the nerve endings.
Posts: 2232 | From USA | Registered: Aug 2009  |  IP: Logged | Report this post to a Moderator
Deep in 'tis pear
LymeNet Contributor
Member # 10427

Icon 1 posted      Profile for Deep in 'tis pear     Send New Private Message       Edit/Delete Post   Reply With Quote 
I have been on Flagyl for two months now and feet and hands started tingling. I am glad I found your post, because it is something that I suspected. Thank you for the info, [woohoo]
Posts: 123 | From Los Angeles | Registered: Oct 2006  |  IP: Logged | Report this post to a Moderator
Deep in 'tis pear
LymeNet Contributor
Member # 10427

Icon 1 posted      Profile for Deep in 'tis pear     Send New Private Message       Edit/Delete Post   Reply With Quote 
I have been on Flagyl for two months now and feet and hands started tingling. I am glad I found your post, because it is something that I suspected. Thank you for the info, [woohoo]
Posts: 123 | From Los Angeles | Registered: Oct 2006  |  IP: Logged | Report this post to a Moderator
Deep in 'tis pear
LymeNet Contributor
Member # 10427

Icon 1 posted      Profile for Deep in 'tis pear     Send New Private Message       Edit/Delete Post   Reply With Quote 
I have been on Flagyl for two months now and feet and hands started tingling. I am glad I found your post, because it is something that I suspected. Thank you for the info, [woohoo]
Posts: 123 | From Los Angeles | Registered: Oct 2006  |  IP: Logged | Report this post to a Moderator
kgg
Frequent Contributor (1K+ posts)
Member # 5867

Icon 1 posted      Profile for kgg   Author's Homepage     Send New Private Message       Edit/Delete Post   Reply With Quote 
I second Haley's comment. Please contact your lyme doc.
Posts: 1856 | From Maine | Registered: Jun 2004  |  IP: Logged | Report this post to a Moderator
glm1111
Frequent Contributor (5K+ posts)
Member # 16556

Icon 1 posted      Profile for glm1111     Send New Private Message       Edit/Delete Post   Reply With Quote 
Everyone, PLEASE look into treating for parasites. Parasites/worms are now being considered the number one co-infection of Lyme. Look at the symptom list at Humaworm and also check the current PARASITE WARRIORS SUPPORT THREAD.

Gael

--------------------
PARASITES/WORMS ARE NOW
RECOGNIZED AS THE NUMBER 1 CO-INFECTION IN LYME DISEASE BY ILADS*

Posts: 6418 | From philadelphia pa | Registered: Jul 2008  |  IP: Logged | Report this post to a Moderator
didogs
LymeNet Contributor
Member # 40101

Icon 1 posted      Profile for didogs     Send New Private Message       Edit/Delete Post   Reply With Quote 
I know many symptoms overlap but what about bart? I had increased tingling and dry, itchy eyes a few days after starting bart meds. Just my experience but may be worth discussing with your doctor. Never had a positive bloodtest. Good luck
Posts: 238 | From new england | Registered: Feb 2013  |  IP: Logged | Report this post to a Moderator
amk33
LymeNet Contributor
Member # 13206

Icon 1 posted      Profile for amk33     Send New Private Message       Edit/Delete Post   Reply With Quote 
I was thinking bart, too. Since you have been treating babs, maybe the bart is coming out. Babs helps suppress bart. This happened with my son. His bart streaks go so much worse after treating babs.
Posts: 418 | From NJ | Registered: Sep 2007  |  IP: Logged | Report this post to a Moderator
didogs
LymeNet Contributor
Member # 40101

Icon 1 posted      Profile for didogs     Send New Private Message       Edit/Delete Post   Reply With Quote 
That was my experience as well-after treating babs my bart symptoms came on with a vengeance. Good luck
Posts: 238 | From new england | Registered: Feb 2013  |  IP: Logged | Report this post to a Moderator
tick battler
Frequent Contributor (1K+ posts)
Member # 21113

Icon 1 posted      Profile for tick battler     Send New Private Message       Edit/Delete Post   Reply With Quote 
I have had the same experience with tingling and pins and needles starting in the feet and then moving to my whole body. I am 95% sure it is from parasites since it happened after drinking contaminated well water and getting very ill from that. I did take several courses of flagyl and tindamax and I think that aggravated the symptoms and my nervous system but couldn't get rid of the parasites. It would help temporarily.

I do not have lyme any longer, but did last year. I'm not saying you don't have it - you may very well have it since normally these other things like EBV and parasites don't bother people to the extent that they affect people with lyme.

What has helped me is salt/C and herbal parasite cleanses since the parasite drugs would help for a short time but couldn't cure me. I am slowly getting rid of the tingling. I do have an increase right after I take the salt/C so I know it is doing something.

EBV can also cause peripheral neuropathy, as my kids have had that when their EBV was bad. But this normally happens when your immune system is down from lyme and coinfections.

The good thing about salt/C is that it hits a lot of things so if you don't know exactly what you have, that is OK.

I would recommend getting some energetic testing done so you can find out which infections you have. EDS testing or good muscle testing (ART) would be great.

tickbattler

Posts: 1763 | From Malvern, PA | Registered: Jul 2009  |  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.