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» LymeNet Flash » Questions and Discussion » Seeking a Doctor » Anyone seen Dr. K, neurologist in CT?

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Author Topic: Anyone seen Dr. K, neurologist in CT?
Neville
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Member # 5890

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Hello,

I have an appointment scheduled with Dr. K late this month. I'm interested in hearing about others experience with this doctor and if they felt it was a worthwhile investment in their health. Naturally insurance is not accepted and the out-of-pocket cost is quite steep.

I have been to see many doctors including LLMD's and only found a couple to be worth my time and expense.

I have neuro-lyme with motor and sensory complications. A non-LLMD neurologist has suggested I have CIDP. I am frequently weak, numb, have neuropathic pain and itching and muscle contractions. I have reacted very poorly to antibiotic therapy in recent years.

I am travelling a great distance to see this specialist in the hopes he can suggest or facilitate a treatment that might be helpful.

Any information is appreciated.

Thank you,

Neville

** edited to remove city, please see terms of use **

[ 06-10-2011, 10:03 AM: Message edited by: sixgoofykids ]

Posts: 37 | From Kentucky USA | Registered: Jul 2004  |  IP: Logged | Report this post to a Moderator
Neville
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Member # 5890

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Thank you, Sixgoofykids.

Had no idea city names would be too disclosing.

Posts: 37 | From Kentucky USA | Registered: Jul 2004  |  IP: Logged | Report this post to a Moderator
   

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