posted
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.
-------------------- Contracted LD et al, August 2000 Officially dx, February 2006 My Lyme Neuroborreliosis mimics Multiple Sclerosis. Lesions- Brain, Cervical and Thoracic spine. Posts: 123 | From Seattle, WA | Registered: Oct 2008
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GiGi
Frequent Contributor (5K+ posts)
Member # 259
posted
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.
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