LymeNet Flash: Dr. K in Washington state -- Experiences?

This is topic Dr. K in Washington state -- Experiences? in forum Seeking a Doctor at LymeNet Flash.

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Posted by lolipepper (Member # 36979) on :

Hi all,

After three years with three second-rate supposed LLMD's, I am considering a pricey trip to WA to see Dr. K.

I did a search to see if I could find any posts about this but it seems most info has been shared via PM.

I am highly motivated due to progressively worsening ocular and neuro involvement -- I think I need to see the best of the best.

Any information would be much appreciated!

Posted by AuntyLynn (Member # 35938) on :

Where do you live?
There are some excellent docs on the East Coast too.

We need to protect the privacy of our LLMDS, and their patients, that's why all of this info is shared by PMs.

Posted by Lymetoo (Member # 743) on :

comments here

http://flash.lymenet.org/scripts/ultimatebb.cgi/topic/1/116205?

Posted by lolipepper (Member # 36979) on :

AuntyLynn -- I am from the east coast and I do travel back there sometimes but Washington would be easier for me since I now live in southern California.

Lymetoo, thanks very much for that -- I did see that thread, was just hoping to hear more specifics from people who have actually been under his care, rather than general comments on his overall approach (with which I am familiar) and cost.

Posted by lolipepper (Member # 36979) on :

Up for more feedback -- if anyone could PM me and tell me about their experience with Dr. K I would be very grateful!

[Smile]

Posted by Razzle (Member # 30398) on :

lolipepper,

Just sent you a PM...

Posted by lolipepper (Member # 36979) on :

Thanks again, Razzle. [Smile]

Anyone else?

Positive testimonials?....