Seeking LLMD near Berkeley CA 94706

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Borelliana

New Member

Joined : Mar 2013

Posts : 13

Posted 3/12/2013 2:41 AM (GMT 0)

Title sez it all.
Thanx!

bluebyyou

Veteran Member

Joined : Nov 2006

Posts : 1952

Posted 3/13/2013 2:41 PM (GMT 0)

Hi Kaliornia,

If you email me, I can send you some names. I live near Boston and have never seen doctors on the West Coast, so maybe other members can give you more feedback.

Thank you

Borelliana

New Member

Joined : Mar 2013

Posts : 13

Posted 3/13/2013 7:31 PM (GMT 0)

Any Doctors on the left coast would be helpful. As an example, my Doctor said I'm not positive, and gave me her reference:

""IgG Western Blot strips which have 5 (or more) of the 10 significant
bands are considered positive for specific antibody to B. burgdorferi.
(Proceedings of the Second Conference of Lyme Disease, Dearborn,
Michigan, 1994)."

Yow! Is that scary or what? If she doesn't move-up to at least '05 thinking, I'm outta there!
I told her that IF the Medical Community had a grasp on Lymes disease, then just WHY do 70% of
the autopsies on former youngish Alzheimer patients have spirochetes in their brain tissues?

LupnerRN

Regular Member

Joined : Sep 2008

Posts : 350

Posted 3/13/2013 9:42 PM (GMT 0)

Hello, I'm in Livermore and have a list of Bay Area docs.
Email me. there's a good support group on meetups.com, the LEAPs group from that website meet at Kaiser Oakland, Moss building, every third Thursday of the month.

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