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 » Excess Saliva Anyone?

 - UBBFriend: Email this page to someone!    
Author Topic: Excess Saliva Anyone?
tickssuck
LymeNet Contributor
Member # 15388

Icon 1 posted      Profile for tickssuck     Send New Private Message       Edit/Delete Post   Reply With Quote 
I did a search on this and saw a few posts from 2005-2006. Just wondering if anyone shares this symptom? I get excess saliva very randomly, comes and goes.


When I was first acutely sick it was so bad I had to spit in a cup to keep from getting nauseous. Now it's more of an off and on nuisance. LD or Co's messing with glands? Any thoughts? This is by far not one of my worst symptoms by any stretch...guess it's just the misery loves company thing. Thanks. TS

Posts: 566 | From West Coast | Registered: May 2008  |  IP: Logged | Report this post to a Moderator
joysie
LymeNet Contributor
Member # 11063

Icon 1 posted      Profile for joysie     Send New Private Message       Edit/Delete Post   Reply With Quote 
[QUOTE]Originally posted by tickssuck:
[QB] I did a search on this and saw a few posts from 2005-2006. Just wondering if anyone shares this symptom? I get excess saliva very randomly, comes and goes.

Yes! This was one of my first symptoms. It came and went monthly. For me, it was just a gush of saliva at random points in the day, so much that I felt I couldn't swallow. It went away about 6 months into treatment. My LLMD thought Bartonella. You're the only other person I've seen make reference to this. Misery loves company, even after the fact [Smile]

Posts: 520 | From Maryland | Registered: Jan 2007  |  IP: Logged | Report this post to a Moderator
JudyEric
Member
Member # 4070

Icon 1 posted      Profile for JudyEric     Send New Private Message       Edit/Delete Post   Reply With Quote 
My son has had this happen a few times over the summer. He said he also feels nauseous when this happens. The other day he said he ran out on the deck and spit out a "puddle" of saliva.

Now that school has started again he is concerned that he will have this happen in school. I was thinking it could be related to a food he ate but maybe it is more Lyme related.

--Judy

Posts: 67 | From Maryland | Registered: Jun 2003  |  IP: Logged | Report this post to a Moderator
h8lyme
LymeNet Contributor
Member # 11765

Icon 1 posted      Profile for h8lyme     Send New Private Message       Edit/Delete Post   Reply With Quote 
I get this too. I'm not sure what causes it, but I have been diagnosed with Lyme, Bart, Babs.

It hasn't been bad as of late, but there are times when it gets pretty nasty.

Posts: 158 | From Santa Monica | Registered: May 2007  |  IP: Logged | Report this post to a Moderator
0624sm
Member
Member # 15591

Icon 1 posted      Profile for 0624sm   Author's Homepage     Send New Private Message       Edit/Delete Post   Reply With Quote 
This symptom is continuous for my husband and has been for many years.

He gets strangled on his own saliva several times a day, drools on his pillow, and drools when he doesn't remember to swallow.

Heavy salivation is a symptom of elevated mercury levels, so I've been hoping it would resolve when he has more chelation.

Joyce/cypriane

--------------------
Dallas caregiver for husband Steve who has Bb, Cpn, Mpn, EBV, CMV, other Herpes family viruses

Posts: 51 | From Dallas, TX | Registered: May 2008  |  IP: Logged | Report this post to a Moderator
antsettler
LymeNet Contributor
Member # 7236

Icon 1 posted      Profile for antsettler     Send New Private Message       Edit/Delete Post   Reply With Quote 
i too, autonomic nervous system
Posts: 108 | From spain eur | Registered: Apr 2005  |  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.