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 » Rapid fire information/dry cough and done in

 - UBBFriend: Email this page to someone!    
Author Topic: Rapid fire information/dry cough and done in
kam
Honored Contributor (10K+ posts)
Member # 3410

Icon 1 posted      Profile for kam     Send New Private Message       Edit/Delete Post   Reply With Quote 
People will talk at me and my brain will try and take in what they are saying.

I can take in one, two, maybe 3 bits of information then it becomes too much.

For awile now the dry coughing starts in and I feel like i am going to throw up.

If they leave and I lay quiet for a while it goes away.


Any ideas on what to do to get the brain to work better??

I don't have a LLMD due to lack of funds and health to get to an LLMD out of state.

[ 08-08-2011, 10:16 AM: Message edited by: kam ]

Posts: 15927 | From Became too sick to work or do household chores in 2001. | Registered: Dec 2002  |  IP: Logged | Report this post to a Moderator
AZURE WISH
Frequent Contributor (1K+ posts)
Member # 804

Icon 1 posted      Profile for AZURE WISH     Send New Private Message       Edit/Delete Post   Reply With Quote 
Do you think that if the person said one sentence at a time at a slower pace and took a 20-30 second break (or whatever you need) in between sentences it would help.

I am sound sensitive and sometimes i can only physically handle so much noise. If it is too overwhelming it flares my nervous sytem symptoms which includes nausea.

Also does the rapid fire info stress you out? my nervous system symptoms can flare if i get too stressed. (especailly if my mcs or food senstivities was recently triggered because they both hit my nervous system)

if it is stress related the pauses may help calm down the stress.

Hopefully people would be kind enough to accomidate you.

I know you have said you have mcs. Do you know if foods are also a trigger?

I am reactive to what seems like almost everything but one thing that has helped me determine at least some of my problemed foods is a food and symptom diary. I write down everything i consume and if symptoms change i note that.

I eat 4 meals a day. if symptoms flared inbetween meal 2 and 3 thats where i would note it on m y page.

if you are not sure what chemicals you react to you could also note if you started using a new product on that day.

I know this is alot of work and I understand you may not be up to it but I just wanted to tell you what has helped me reduce my being triggered.

It is also alot of work to go through the notebook (after you have been keeping the diary awhile)and determine a list of things that seem to be triggers. (I was hoping maybe someone would be kind enough to help you with this)

--------------------
multiple chemical sensitvity group:
http://www.lymefriends.com/group/multiplechemicalsensitivities

Group for artists. All media welcome:
http://www.lymefriends.com/group/creativecorner


http://groups.yahoo.com/group/Lyme_Artist

Posts: 3860 | From nj,usa | Registered: Mar 2001  |  IP: Logged | Report this post to a Moderator
kam
Honored Contributor (10K+ posts)
Member # 3410

Icon 1 posted      Profile for kam     Send New Private Message       Edit/Delete Post   Reply With Quote 
Not able to take in all that you wrote.

but, the part about the sound of the person's voice hit home.

I have the other caregive/housekeeper this week for an hour.

She talked all the way from the front door of the apartment building to my apartment door.

I was coming from my car to my door.

I could barely walk from the car to the door once she started talking.

And the heart was beating over time.

Got the coughing thing too.

Also not able to write on the white board on what things to do as that part of the brain that writes was not working.

I told her about sound...even teh sound of a person's voice sets me back.

She needs to talk

Posts: 15927 | From Became too sick to work or do household chores in 2001. | Registered: Dec 2002  |  IP: Logged | Report this post to a Moderator
MattH
LymeNet Contributor
Member # 30846

Icon 1 posted      Profile for MattH     Send New Private Message       Edit/Delete Post   Reply With Quote 
Kam,

I may have Lyme from 30 years ago but I tested positive for CP. www.cphelp.org The treatment is abx and partially similar to treating Lyme so I am sort of doing both.

My cough has decreased from say 100% to 20% and is not as deep. I think I got CP because my immune system was ineffective, CD 57 at 59. I have been on ABX for about 6 weeks and just added a second ABX two weeks ago. I also am doing the Buhner protocol.

So if you haven't taken a look at CP you might to make sure that is not an issue for you. Also note that as your immune system gets hammered you are become a virus and bacteria magnet but you could also be experiencing a mold issue.

All the Best, MattH

Posts: 607 | From Houston Texas | Registered: Mar 2011  |  IP: Logged | Report this post to a Moderator
kam
Honored Contributor (10K+ posts)
Member # 3410

Icon 1 posted      Profile for kam     Send New Private Message       Edit/Delete Post   Reply With Quote 
Tried going to the web site to learn what CP was but pulled up something with symbols...no text

also tried typing URL in and got the same thing

Posts: 15927 | From Became too sick to work or do household chores in 2001. | Registered: Dec 2002  |  IP: Logged | Report this post to a Moderator
skigal
LymeNet Contributor
Member # 7443

Icon 1 posted      Profile for skigal     Send New Private Message       Edit/Delete Post   Reply With Quote 
cpnhelp.org
Posts: 269 | From VA | Registered: Jun 2005  |  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 
Let's make it even easier.

www.cpnhelp.org

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

Posts: 96239 | From Texas | Registered: Feb 2001  |  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.