This Is MS Multiple Sclerosis Community: Knowledge & Support

Welcome to the world's leading forum on Multiple Sclerosis research, support, and knowledge. For over 10 years, This is MS has provided an unbiased community dedicated to Multiple Sclerosis patients, caregivers, and affected loved ones.
It is currently Wed Jun 19, 2013 12:41 am


All times are UTC - 8 hours [ DST ]




Post new topic Reply to topic  [ 61 posts ]  Go to page 1, 2, 3, 4, 5  Next
Author Message
PostPosted: Fri Mar 14, 2008 9:09 pm 
Offline
Newbie
User avatar

Joined: Fri Mar 14, 2008 4:00 pm
Posts: 4
......................


Last edited by andrewjf on Wed Mar 27, 2013 9:07 am, edited 4 times in total.

Top
 Profile  
 
 Post subject:
PostPosted: Tue Mar 25, 2008 4:31 pm 
Offline
Family Member
User avatar

Joined: Wed Mar 19, 2008 4:00 pm
Posts: 26
Location: Florida
I will get tested for Lyme disease....it makes sense to me because all my symptoms of MS started again when I stopped taking antibiotics(for acne) and I have pulled to many ticks from my body to remember how many!


Top
 Profile  
 
 Post subject:
PostPosted: Tue Mar 25, 2008 5:15 pm 
Offline
Newbie
User avatar

Joined: Fri Mar 14, 2008 4:00 pm
Posts: 4
Hi Pegs!!!

You've pulled so many ticks from yourself that you cannot remember! That's scary!!! I was only bitten by one!!!

If you need any help or information please let me know! I will reply quicker if you email me!

andrewfacchin@hotmail.com

Thank you for reading my story and posting!

Andy :D


Top
 Profile  
 
 Post subject:
PostPosted: Wed Mar 26, 2008 4:46 pm 
Offline
Family Elder
User avatar

Joined: Tue Aug 01, 2006 3:00 pm
Posts: 169
Location: S. California
Hey there, what was the CA lab? I have been negative for Lyme 2x, but that does not mean much eh? It may be worth another test.
Plenty of ticks in my life....some even are the actual insects
G


Top
 Profile  
 
 Post subject:
PostPosted: Wed Mar 26, 2008 9:30 pm 
Offline
Newbie
User avatar

Joined: Fri Mar 14, 2008 4:00 pm
Posts: 4
Hi Grumpster, :P

The lab is called IGenex.

www.IGenex.com

1-800-832-3200

You can call that number and ask for Dr. Harris, you will have to leave him a message but he will get back to you!

It is true that those 2 Lyme tests you have had could be False Negatives. Your right it may be worth another test. However the test is not cheap it cost me about $380 Canadian! It was well worth it though! Especially if you know you have been bitten by ticks!

If you have anymore questions you can post here or email me,

andrewfacchin@hotmail.com

Thanks for reading my story, hope you are well.

Andy


Top
 Profile  
 
 Post subject:
PostPosted: Thu Mar 27, 2008 11:05 am 
Offline
Family Elder
User avatar

Joined: Mon May 24, 2004 3:00 pm
Posts: 300
Pegs--and others--as of now, there is NO DEFINITIVE test for LD! IgeneX comes about as close as it gets. But just keep in mind, if you test neg or pos that's no guarantee it is accurate. I started researching LD when my daughter first started having problems. If you go to the testing protocal as stated by the FDA for LD, the criteria ix EXACTLY the same as for MS!

My daughter had so many non-MS symptoms that I was convinced she had LD. She ended up taking a natural treatment for strep bacteria infection and has been MS-free ever since.

The antibitoic LD treatment is highly controversial. There is apparently a wonderful treatment by a Chinese doctor. Users say it works as well as the antibiotics.

The best place to contact is your local LD chapter. They can refer you to Lyme literate docs and provide you with all kinds of really helpful info.

Good luck to you ALL! Chris


Top
 Profile  
 
 Post subject:
PostPosted: Fri Mar 28, 2008 10:27 am 
Offline
Family Elder
User avatar

Joined: Tue Sep 25, 2007 3:00 pm
Posts: 140
Location: East Coast USA
I've been tested for Lyme 3-4 times(all negs) and I think they did two different tests. I've been bitten by a few ticks and I wonder if the test would be available in my area to do. I don't think I could travel to Canada for a test either.


Top
 Profile  
 
 Post subject:
PostPosted: Fri Mar 28, 2008 11:19 am 
Offline
Family Elder
User avatar

Joined: Sat Sep 22, 2007 3:00 pm
Posts: 344
Location: Lexington, KY
My neuro ruled out LD when my lesions were both brain and spinal cord. He told me LD only causes brain lesions. Has anyone else heard this? I really hate to get my hopes up that my MS diagnosis could be wrong.

Marcia

_________________
Marcia


Top
 Profile  
 
 Post subject:
PostPosted: Fri Mar 28, 2008 11:22 am 
Offline
Family Elder
User avatar

Joined: Sun Nov 07, 2004 4:00 pm
Posts: 1228
Location: Colorado
Chris -
You said in your post:

"My daughter had so many non-MS symptoms that I was convinced she had LD. She ended up taking a natural treatment for strep bacteria infection and has been MS-free ever since."

I would be interested in what the natural treatment for the strep bacteria infection was. I suffered with strep throat for many years (haven't had it recently), but my daughters who are in their late thirties get it at least once a year sometimes twice. And, of course anytime they are sick or stressed I say silent prayers to keep the MS away from them. Since the strep seems to "run in the family", I have had a major concern that it might be, or have been in my case, the MS trigger.

You may have posted the treatment on the site before, but I could not find.

Thanks,
Sharon


Top
 Profile  
 
 Post subject:
PostPosted: Fri Mar 28, 2008 11:28 am 
Offline
Newbie
User avatar

Joined: Fri Mar 14, 2008 4:00 pm
Posts: 4
Hi MattB,

You can get tested from where ever you live. They send you the package through the mail, you get your blood taken at a clinic and then send it back.

Marcia, I am sorry I am not aware of lesions on both brain and spinal cord with Lyme Disease. It may be possible I just don't know.

Thanks everyone,

Andy


Top
 Profile  
 
 Post subject:
PostPosted: Fri Mar 28, 2008 1:04 pm 
Offline
Family Member
User avatar

Joined: Wed May 03, 2006 3:00 pm
Posts: 56
Location: TN
Marcia,


After researching this it does cause brain lesions. With it being the cns. I would assume that regardless if it states it or not i would bet that if it can do it in the brain it can do it in the spinal cord. Its all the cns. This is a disease where they don't know much about. It can cause an array of similiar symptoms in other diseases..Gues what. Its more prevelant in the north. Anyway..Google lyme disease in canada. It will bring up a site called canlyme i believe. Click on symptoms. Look at all the symptoms they have associated with lyme..Kinda Scary..


Top
 Profile  
 
 Post subject:
PostPosted: Fri Mar 28, 2008 1:22 pm 
Offline
Family Member
User avatar

Joined: Wed May 03, 2006 3:00 pm
Posts: 56
Location: TN
here ya go marcia.

There are multipel lesions in the spinal cord. This is another typical feature of MS .
By the way did you notice the lesion in the brainstem?
A spinal cord lesion together with a lesion in the cerebellum or brainstem is very suggestive of MS.
Spinal cord lesions are uncommon in most other CNS diseases, with exception of ADEM, Sarcoid, Lyme and SLE.



if i am reading this right it is stating that lesions in the spinal cord can happen with lyme. Or have i been up too long and it doesn't state that.

[/b]


Top
 Profile  
 
 Post subject:
PostPosted: Fri Mar 28, 2008 1:32 pm 
Offline
Family Elder

Joined: Wed May 03, 2006 3:00 pm
Posts: 6063
.


Last edited by Lyon on Mon Nov 28, 2011 5:25 pm, edited 1 time in total.

Top
 Profile  
 
 Post subject:
PostPosted: Fri Mar 28, 2008 1:49 pm 
Offline
Family Member
User avatar

Joined: Wed May 03, 2006 3:00 pm
Posts: 56
Location: TN
no lyon..it was a very informative site..it had mri brain and spinal..i couldn't link the site..here is what i could find www.radiologyassistant.nl

i typed in "lyme disease and spinal cord lesions" and clicked images. finally found this site...i hope this helps...let me know what you think. i don't intrepret everything as good as you..


Top
 Profile  
 
 Post subject:
PostPosted: Fri Mar 28, 2008 1:58 pm 
Offline
Family Elder

Joined: Wed May 03, 2006 3:00 pm
Posts: 6063
.


Last edited by Lyon on Mon Nov 28, 2011 5:24 pm, edited 1 time in total.

Top
 Profile  
 
Display posts from previous:  Sort by  
Post new topic Reply to topic  [ 61 posts ]  Go to page 1, 2, 3, 4, 5  Next

All times are UTC - 8 hours [ DST ]


Related topics
 Topics   Author   Replies   Views   Last post 
There are no new unread posts for this topic. Does anyone read these?!?!?

[ Go to pageGo to page: 1, 2 ]

conandcait

17

3075

Sat Nov 03, 2007 2:48 pm

conandcait View the latest post

There are no new unread posts for this topic. Like to read

011201104

2

815

Mon Feb 15, 2010 10:52 am

Loobie View the latest post

There are no new unread posts for this topic. have you read this book ?

robbie

4

1234

Sat Feb 25, 2006 5:55 pm

robbie View the latest post

There are no new unread posts for this topic. Everyone should read this link...

[ Go to pageGo to page: 1, 2, 3, 4, 5 ]

viper498

70

6688

Thu Oct 19, 2006 4:35 pm

robbie View the latest post

There are no new unread posts for this topic. Is it MS or Porphyria? This is a must read for all with MS

Bethr

14

3954

Sat Jun 01, 2013 1:33 am

Bethr View the latest post

 


Who is online

Users browsing this forum: No registered users


You cannot post new topics in this forum
You cannot reply to topics in this forum
You cannot edit your posts in this forum
You cannot delete your posts in this forum

Search for:
Jump to:  


News News Site map Site map SitemapIndex SitemapIndex RSS Feed RSS Feed Channel list Channel list
Read hundreds of personal Multiple Sclerosis stories on Experience Project. Experience Project is an anonymous community where people connect through their life experiences, made by the same people who built This is MS. With over 30 million personal stories about every possible life experience, you can quickly find people like you!


Interesting: Secret Confessions | Dream Meanings | Ask Questions, Get Answers

Advertise on the premier multiple sclerosis forum