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04/25/2012 07:41 AM

Need LLMD in Canada, Minnesota or Wisconsin

nikki2060
 
Posts: 5
New Member

My wife 38 yrs old has being going to our doctor since last summer and getting all the tests done that showed nothing until January she was tested for Lyme

ELISA+reactive western blot IGM-reactive tested in Kingston Public Health Lab. She finished the 3 week treatment about a month ago

now waiting for a MRI that is scheduled next month.

We would really appreciate any help anyone can give us to find a LLMD in our area or close by.

Post edited by: nikki2060, at: 04/25/2012 04:41 PM

Post edited by: nikki2060, at: 04/25/2012 05:54 PM

Post edited by: nikki2060, at: 04/26/2012 04:02 AM

Post edited by: nikki2060, at: 04/26/2012 04:03 AM

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04/25/2012 08:01 AM
littlegirlbigdream
littlegirlbigdream  
Posts: 643
Member

Hello, can you please edit your post to 1-2 lines max, for the people with neuro lyme.

One of the leaders will be by soon to help with this. But they may require more info not sure.

But are you in MB?

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04/25/2012 08:28 AM
nikki2060
 
Posts: 5
New Member

We live in Ontario
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04/25/2012 09:01 AM
littlegirlbigdream
littlegirlbigdream  
Posts: 643
Member

oh man I was hopefull haha, a lot of the Canadians on here are from Ontario or BC, or some where on the east coast.

I have only met one from where I live.

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04/25/2012 10:06 AM
lymeontario
 
Posts: 104
Member

Hi Nikki, I'm from Ontario. I can help, however BettyG, the group leader will need to collect some information from you first...
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04/25/2012 10:07 AM
lymeontario
 
Posts: 104
Member

Also Nikki, sorry there are no LLMD's in Ontario...
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04/25/2012 10:47 AM
nikki2060
 
Posts: 5
New Member

We are just starting this battle and appreciate any help and I will gladly supply any more info that is needed.
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04/25/2012 12:04 PM
lymeontario
 
Posts: 104
Member

Hi Nikki, Where in Ontario are you from?
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04/25/2012 01:18 PM
nikki2060
 
Posts: 5
New Member

North Western Ontario

Post edited by: nikki2060, at: 04/26/2012 07:06 PM

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04/25/2012 03:07 PM
Bettyg
 
Posts: 32269
VIP Member
I'm an Advocate

hi nikki,

please answer all questions below using my posting guidelines and breaking up your solid block text.

i'll be happy to help you after you've provided all i need first!

hugs/prayers, bettyg, leader

************

Welcome to MD JUNCTION! I'm so glad you found us! You've come to the right place for education and support!

Private messages DELETED in 30 days!

ARCHIVE, upper right!

My WELCOME LETTER is posted at the top of SUPPORT FORUM in sticky pin full of good info and HYPERLINKS ready to be read.

http://www.mdjunction.com/forums/lyme-disease-support- forums/general-support/2356916-bettygs-welcome-letter-wgood- beginner-links-

The most important things are at the top; MUST READ and print off as mentioned there already to start your lyme/co-infection journey with us all.

The 1st things to do are:

• JOIN LYME BOARD;

• Post in LLMD REQUEST FORUM for a LYME LITERATE md; see my welcome letter and the INSTRUCTIONS there if you are SPECIALLY FROM CALIF. Where it's broken down into 8 NAMED AREAS.

• You'll need to give me my calif. NAMED area where you live in the areas shown there in SUBJECT LINE plus if it's for ADULT or a child; we need age of CHILD; some llmds have AGE restrictions.

OTHER STATES will show the SPECIFIC NAME OF THEIR STATE and closest, largest city to them in SUBJECT line plus adult or child; UNDER 21; we need their age!.

http://www.mdjunction.com/forums/lyme-disease-support- forums/llmd-info/Itemid=217/func=post/do=reply

• Also, I'll need the following info in your request post:

in your llmd request, please EDIT and add more info ok.

Are you UNDER AGE 21;; if yes, I need your age shown as some of our llmds have AGE RESTRICTIONS; thanks!

how long you've been sick

if you've tested for lyme/co-infections;

which labs doing work for which specific test, etc.

did you have western blot igm/igg done by igenex?

if yes, what were the POSITIVE & INDETERMINDED numbers; NOT negatives.

thanks for understanding; just EDIT your post. you can find all by going to left MY DISCUSSIONS, click on it.

after you add more, i'll send you names ok.

just send me a PRIVATE MESSAGE left side, giving me the direct link to come to here, and i'll send you the names ok big thanks.

Betty's suggested posting guidelines:

NO ALL CAPS POSTS; they are illegible to me/other neuro folks!

Many of members have neuro lyme, and it is hard to read long solid block text and be able to comprehend; example, me, 42 yrs. neuro chronic lyme, so we are UNABLE to comprehend and read. Thank you for helping us help YOU

please post in short paragraphs like you see below or look at a few other posts, but we neuro folks need them short.

1-2 sentences MAX per paragraph and hit ENTER TWICE to doublespace between each paragraph. We've lost our comprehension skills to read solid block text.

we neuros lose our train of thought if the sentence is broken up in the middle; so please keep an ENTIRE sentence together as ONE. hugs

For easier reading, please edit your post. You can break up your longer paragraphs into smaller paragraphs. Please hit

ENTER key twice after each paragraph.

Go to left hand corner; click edit send. Then go to bottom and click SUBSCRIBE TO THIS DISCUSSION.

Thank you for posting in a manner that makes it easier for all to read and help others.

Bettyg, llmd coordinator/group leader/Iowa activist

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