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Need LLMD in WA, ID, MN

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Posted 1/6/2013 5:23 AM (GMT 0)
I would greatly appreciate names of LLMDs in the states of WA (where I live), ID (near where I live) and MN (where I have family).  I tested positive on Band 41 Igenex 4 yrs ago and was told I didn't have Lyme with just 1 band positive.

My symptoms are getting worse and I believe I have Lyme - or at least need someone who can tell me what  they think based on testing and symptoms.

2 months ago I went to Institute/Clinic run by a renowned LLMD in Seattle area and left very disheartened for a variety of reasons. Also found out after after my 4 days of being there that if I have questions, phone calls are minimum of $125/call and emails are $90 each.  This is but part of my disappointment.

I appreciate any help anyone can give me.  Kathleen

Posted 1/6/2013 5:33 AM (GMT 0)
Hi Kathleen,

I have a couple of suggestions..one in Seattle who travels to Spokane (where I have seen her..still do. her emails are free btw.). And one in Portland. Both are more on the natural/alternative side, although one does prescribe abx. Very curious where you went in Seattle! Sorry it did not work out!!
I live in Moscow, btw.

Email me and I'd be glad to share. Nice to see someone kind of close geographically on the site!

Take care,
Nancy
Posted 1/6/2013 5:34 AM (GMT 0)
Kathleen...you will need to enable your email on the site to contact me :)
Posted 1/6/2013 5:53 AM (GMT 0)
I also know of one in Southern Oregon. Its close-ish. I can't reccomend him because I have yet to have an actual appt but if all other options fail I can give you his info :)
Posted 1/6/2013 6:03 AM (GMT 0)
Nan, I have enabled my email here - thanks for letting me know that!  I have sent you an email. Please let me know if you don't receive it. Thanks, Kathleen
Posted 1/6/2013 6:05 AM (GMT 0)
gracelynn, I would appreciate you sending me the name of the Oregon dr. Then, after you see him, I would appreciate hearing of your impressions. thanks, Kathleen
Posted 1/6/2013 3:21 PM (GMT 0)
Hi Kathleenta,
I'm sorry, but you still don't have your email enabled - did you scroll to the bottom of the page and click the submit button? That's the most common mistake made.

I also wanted to say welcome - so welcome!! smilewinkgrin Giggle!

I'm so sorry for what all you have had to go through up to this point!! Hopefully things will improve greatly soon!!

If you haven't yet, please do read through our "New to Lyme? Start here!" thread as it's packed full of important information, helpful links and pdf's, symptom lists (as Lyme rarely travels alone!!), detoxing instructions, and even a list of questions you can ask any doc that you wish to treat you for these infections!!
Posted 1/6/2013 5:20 PM (GMT 0)
Thanks for the post, traveler. I'm not sure why my email isn't enabled. When I look it shows it is. I sent you an email directly -hopefully you got it. Thanks, Kathleenta
Posted 1/6/2013 11:33 PM (GMT 0)
Yep!! I got your email, but the funny thing is when I look at your email option, it still says it's not available! LOL!!!

Anyone else? Is it just my computer?
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