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Need LLMD suggestions in San Francisco Bay Area

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Lyme Disease
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Posted 3/31/2016 6:38 PM (GMT -5)
Hello all,

I am in need of LLMD suggestions! I have been sick with all the traditional symptoms for months, positive for EBV and finally got Lyme results back last week, positive only for 2 bands on Western Blot, had C 57 panel run and I am extremely low.

Anyway, I am willing to travel hours by car if anyone has any great LLMD suggestions in or around the Bay Area. Thanks in advance. :)
Posted 3/31/2016 7:18 PM (GMT -5)
Welcome. I am in San Jose.

I have a list of the 5 or 6 highly regarded LLMD's in the Bay Area. You can either email me by clicking on my user name and then my email address or you can enable your email address. I believe you can do that by clicking on your user name.

We are not allowed to post dr's names on the board.
Posted 3/31/2016 10:36 PM (GMT -5)
How to enable your email address:

Go to My Profile
Go to Edit Profile
Make sure your email address is in the box
Bull's eye the Enable Email Address
Go to the bottom of the page and hit Submit

Here is a huge list of California lyme doctors:

/sites.google.com/site/lymedoctors/california
Posted 3/31/2016 10:40 PM (GMT -5)
She's taken care of.

Thanks Annette.

Careful with that google search. I know for a fact that there are dr's on that list that are not LLMD's and will say that. One is in the same office as my LLND and he is not an LLND just a great ND. I also know that there are dr's who will say they are Llmd/nd's and treat with herbals and have no idea what Houttuynia is.

There is such a need in California that dr's have added Lyme to their bio to increase their business. They attend one Ilads session and they think they are qualified. Far from it. I believe that the intent is good but the outcome of the patient concerns me.

Post Edited (jrpsf) : 3/31/2016 9:49:17 PM (GMT-6)

Posted 3/31/2016 10:49 PM (GMT -5)
Anytime Janet! <3
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