This is topic Lyme Friendly Neurologist in Seattle in forum Medical Questions at LymeNet Flash.


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Posted by NeuroEcclectic (Member # 17783) on :
 
I respect and do not post physician names on the

board, however, if there is anyone who is apart

of Lymenet in Washingston State that need a

neurologist who is not ANTILYME (LOL) feel free

to send me a message and I would be glad to

share his information.

This neurologist was so excited to learn from me

that he used my MRI studies at a major

convention for Neurologists!

Regards.
 
Posted by GiGi (Member # 259) on :
 
Would love to meet that person! Would you send me the info by e-mail, please. I found one neurologist originally in 1996, but he pulled the plugs to me and the ID involved after three months of IV Rocephin when I was still deadly ill. In retrospect I am glad that they stopped abx. I took another route, as you can tell from my other posts, and got very well. Now many years ago. Please mail me the info. And thank you.


[email protected]
 
Posted by islandgirl (Member # 5914) on :
 
I also would like the name of your neurologist, and hope you will email me the information.

I have so many lesions on my brain and can't find anyone lyme literate to give a definate opinion other than, we don't know what it is.

Even asked my llmd if Columbia could look at my MRIs....they won't, even though I said I would pay whatever to have it done.

Thanks you.
 
Posted by islandgirl (Member # 5914) on :
 
lyme brain. agaain.

Here is my email address: [email protected]
 


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