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 » Tinnitus and lyme disease

 - UBBFriend: Email this page to someone!    
Author Topic: Tinnitus and lyme disease
dtaild
Junior Member
Member # 27253

Icon 1 posted      Profile for dtaild     Send New Private Message       Edit/Delete Post   Reply With Quote 
I've had ringing in my left ear for a while now and I've seen online tinnitus is a symptom of lyme disease, just wondering how common this is and if other people are experiencing it as well.

Thanks,
Tom

Posts: 3 | From Mt Laurel, NJ | Registered: Jul 2010  |  IP: Logged | Report this post to a Moderator
jarjar
LymeNet Contributor
Member # 8847

Icon 1 posted      Profile for jarjar     Send New Private Message       Edit/Delete Post   Reply With Quote 
Yes very common and often a symptom of bartonella. You can do a search on the board and find lots of post about it.
Posts: 805 | From Utopia | Registered: Feb 2006  |  IP: Logged | Report this post to a Moderator
Keebler
Honored Contributor (25K+ posts)
Member # 12673

Icon 1 posted      Profile for Keebler     Send New Private Message       Edit/Delete Post   Reply With Quote 
-
VERY common. There can be any number of reasons or causes. Noise damage is the number one thing people forget. And lyme, and other tick-borne infections can damage ears in many ways.

Ears MUST be protected when on antibiotics. Many drugs lower the decibel level at which sound can permanently damage ears.

First: ear plugs or decibel rated muffs even when around a hairdryer, blender, vacuum, lawn tools, etc. Avoid in-the-ear pods and be sure to keep volume low when around music, TV, concerts, in general.

Second: Liver support and attention to liver and kidney stress are also vital. The toxins from infections - and the stress of chemical treatment affect ears in various ways.

Even aspirin is toxic to the ears and a frequent cause of tinnitus but there are also many drugs (and some supplements) that are ototoxic.

All that is explained in the second link below.
------------

Ringing, hissing, roaring, pulsating sounds or sensations in the ears:

www.ata.org

AMERICAN TINNITUS ASSOCIATION

======================

Specifically for LYME patients - lots of details about ears and what can help:

3/4 of the way down page one, there are lots of LIVER LINKS:

http://flash.lymenet.org/scripts/ultimatebb.cgi?ubb=get_topic;f=1;t=065801

Topic: TINNITUS: Ringing Between The Ears; Vestibular, Balance, Hearing with compiled links - including HYPERACUSIS
-

Posts: 48021 | From Tree House | Registered: Jul 2007  |  IP: Logged | Report this post to a Moderator
BackinStOlaf
Frequent Contributor (1K+ posts)
Member # 23725

Icon 1 posted      Profile for BackinStOlaf     Send New Private Message       Edit/Delete Post   Reply With Quote 
Yes, I have tinnitus too at times

--------------------
First Symptom 9/09
Multiple docs, negative Labcorp test
LLMD: 1/10
Positive Igenex/CDC test
Treatment 2/10
2/10-8/10 Amox, ceftin, zith, flagyl
Currently: Bicillin, Minocycline, still dealing with severe breathing issues

 -

Posts: 1121 | From New York, New York | Registered: Dec 2009  |  IP: Logged | Report this post to a Moderator
dogmom2
LymeNet Contributor
Member # 23822

Icon 1 posted      Profile for dogmom2   Author's Homepage     Send New Private Message       Edit/Delete Post   Reply With Quote 
I got mine on short course of antibiotics( short because I stopped them), and then more noises showed up after trying a computer based rife.

diana

Posts: 857 | From northern california | Registered: Dec 2009  |  IP: Logged | Report this post to a Moderator
lululymemom
Frequent Contributor (1K+ posts)
Member # 26405

Icon 1 posted      Profile for lululymemom     Send New Private Message       Edit/Delete Post   Reply With Quote 
I've had mine even before going on treatment.. both ears..

--------------------
IGM 41 IND, 83-93+ IGG 31 IND,34 IND, 41++, 58+, 83-93 IND

31 Epitope test neg.

Bartonella henselae 1:100

Posts: 2027 | From British Columbia | 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 have it in both ears. Better now, but still there. At times one ear or the other will go quiet and ring loudly for a while.

Not sure if it is my Bart and / or Lyme.

Anyone have ear "fullness" too? I have that. constantly feels like I need to pop my ears.

--------------------
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
Keebler
Honored Contributor (25K+ posts)
Member # 12673

Icon 1 posted      Profile for Keebler     Send New Private Message       Edit/Delete Post   Reply With Quote 
-
ear "fullness" is very common and usually from inflammation. The Tinnitus thread addresses that, too.

Never pop ears with any amount of force. A gentle yawn, good swallow, etc. is okay but never blow pressure through nose to pop ears. That just sends all sorts of mucous to places it should not go. More detail about over in that other thread, too.
-

Posts: 48021 | From Tree House | Registered: Jul 2007  |  IP: Logged | Report this post to a Moderator
hadlyme
LymeNet Contributor
Member # 6364

Icon 1 posted      Profile for hadlyme     Send New Private Message       Edit/Delete Post   Reply With Quote 
There is a NP that treats lyme in CA, she has a facebook acct and on there you can get into her lecture notes on Tinnitus. You can pm if you want to read what she says.

--------------------
Lyme, Babs, Fry Bug..... Whatever it is, may a treatment be discovered to make us all whole again!

Posts: 941 | From AZ-MT | Registered: Oct 2004  |  IP: Logged | Report this post to a Moderator
elizzza811
LymeNet Contributor
Member # 24713

Icon 1 posted      Profile for elizzza811     Send New Private Message       Edit/Delete Post   Reply With Quote 
Do you use a cell phone or cordless phone?

Regular mobile phone use linked to tinnitus: research
http://tinyurl.com/3y9dyqt

Regular use of a mobile phone for more than four years almost doubles the chance of developing tinnitus - the debilitating condition that causes constant ringing or buzzing in the ears.

A study has found that people who used their mobile phone for an average of ten minutes a day were more than 70 per cent more likely to have tinnitus.

But those who used their phones on both ears, and those who had used a mobile for four years or more were twice as likely to have tinnitus.

The findings area published in the journal Occupational and Environmental Medicine and may help to explain why the number of people reporting tinnitus is increasing.

It is thought the microwave energy produced by the phones might be the cause of the problem.

Dr Hans-Peter Hutter, Institute of Environmental Health, at, University of Vienna, in Austria compared 100 people with tinnitus to 100 similar people without the condition.

He said that although they relied on people reporting their own mobile phone use and could not be sure if this was accurate, the results were 'unlikely to be spurious'.

Tinnitus affects around five million people in Britain and is considered a debilitating condition as sufferers may constantly hear a rushing, roaring or high pitched tone in one or both ears most of the time.

The most common cause is damage to the hearing through trauma or exposure to loud noise, however some mental or physical changes can trigger it such as depression, redundancy and illness.

Dr Hutter added: "Tinnitus strongly interferes with the daily lives of people. There are very few interventions available that effectively reduce tinnitus loudness and annoyance. Therefore, all measures should be taken to avoid any further increase in tinnitus prevalence.

"Our results indicate that high intensity and long duration of mobile phone use might be associated with tinnitus. This possibility should be explored further by assessing mobile phone usage history in studies of tinnitus aetiology (cause) in the future."

Posts: 495 | From USA | Registered: Mar 2010  |  IP: Logged | Report this post to a Moderator
dtaild
Junior Member
Member # 27253

Icon 1 posted      Profile for dtaild     Send New Private Message       Edit/Delete Post   Reply With Quote 
With my tinnitus in regards to lyme disease, this was my very first symptom..I've always figured this was due to hearing loss, as I spent four years in the Marines and 3 in the Army and figured it was due to that..

Is it common for tinnitus to be a early symptom, or is that something that occurs later?

Posts: 3 | From Mt Laurel, NJ | Registered: Jul 2010  |  IP: Logged | Report this post to a Moderator
mbdq
LymeNet Contributor
Member # 26277

Icon 1 posted      Profile for mbdq     Send New Private Message       Edit/Delete Post   Reply With Quote 
I have tinnitus every morning and every night and sometimes throughout the day.

Once in a while I will suddenly lose hearing in one ear.

I did not know it was a bart symptom, and I have many other bart symptoms and I am currently treating with Rifampin.

Hopefully it will all work out. good luck

Posts: 233 | From Hudson Valley | Registered: Jun 2010  |  IP: Logged | Report this post to a Moderator
Keebler
Honored Contributor (25K+ posts)
Member # 12673

Icon 1 posted      Profile for Keebler     Send New Private Message       Edit/Delete Post   Reply With Quote 
-
Never assume any hearing problem is just lyme or just the medicine. Please see a hearing specialist. Be sure to protect ears.

Even if hearing changes occur now, they could have been caused by damage in the past. But there are still things that can help. Many things.
-

Posts: 48021 | From Tree House | Registered: Jul 2007  |  IP: Logged | Report this post to a Moderator
Robin123
Moderator
Member # 9197

Icon 1 posted      Profile for Robin123     Send New Private Message       Edit/Delete Post   Reply With Quote 
dtaild, it was an early symptom for me.

I did several sessions with a Magnapulse PEMF machine - stands for pulsed electromagnetic machine. It's a small box with a white coil that we hold as it clicks away.

I started with 20 seconds worth, and by the 10th session was up to an hour. After the longer sessions, I noticed that my tinnitus went away for 6 hours. The person with the machine left so I didn't get to do more. I asked an LLMD about it and he said it may have calmed the nerves to the ears.

We're electromagnetic creatures and the PEMF machine can reboost the electromagnetic charge of the nerves. They treat injured race horses with it to get them back on the racetrack more quickly.

Posts: 13171 | From San Francisco | Registered: May 2006  |  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.