quote:

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Originally posted by mbroderick:
I am not aware of any LLMD's in West Virginia.

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Hmmmm... I got the name from:
http://www.lymediseaseassociation.org/referral/ViewName.php

The person does not have MD in front of the name like the other two results. Is it possible that it's not a doctor, or is that a requirement to be included in the database?

Thanks
Roxy
Edited to say: There aren't any support groups listed for that state either.

Edited Further: The Pittsburgh, PA area support group telephone number is disconnected. Is there a way to get an updated number?
 

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Posted by Keshvara (Member # 13599) on :
 
Hi All,

Well, Dr. P, is certainly a medical dr. I've just made an appointment with her and will report back. On a positive note, the only *new* patients she is taking are those with Lyme!!

The receptionist was lovely, answered all of my questions. Dr. P seems to be open to treating with traditional and complimentary care methods.

So.....report in July.
 

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Posted by motownlyme (Member # 11485) on :
 
I see Dr. P and I'm sending you a PM.
 

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Posted by bettyg (Member # 6147) on :
 
to those going to her already, we don't have info on her in nationwide lists,


could you send me a private message with the following info IF possible:


would you get the following IF possible from them??

we need full name
SPECIALTY
street addy
city, state

phone no.
fax no.
web site or email if possible

cost per hour for 1st visit
cost for followups

do they take insurance?
what kind?
treat by IV or ORAL?


BIG THANKS so we can help others.

i'll email it to the others w/nationwide lists!!
 

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