LLMDs in San Francisco Bay Area (or Boston)?

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Regular Member

Date Joined Nov 2008
Total Posts : 51
   Posted 8/20/2010 10:32 PM (GMT -6)   
I see an older thread, but anyone have someone they are using now?

Also what is the wait like to get in? If there is someone in Boston I can see soon...I am here for the next month before heading back to SF area...


Lynn (whose legs have wonderful shooting aching pains now. So fun to sleep like this!)

Regular Member

Date Joined Aug 2009
Total Posts : 89
   Posted 8/21/2010 7:49 AM (GMT -6)   
Hi Lynn.
I see a LLMD in Redwood City, just outside of San Fran. I actually see his nurse practitioner. My son and I have received wonderful care. Don't know if I am allowed to post names so look up Dr. H in Redwood City ;)
aka Momtomonsters

Forum Moderator

Date Joined May 2007
Total Posts : 35853
   Posted 8/22/2010 2:18 PM (GMT -6)   
Hi Lynn!
What supplements are you taking? Magnesium seems to help some of us with those legs pains, and it's not terribly expensive.
Even the mightiest oak tree was once a little nut who held it's ground!!!
May we all find peace along the journey to find healing.
"Absence of proof is not proof of absence" - Dr. Edwin Masters, great LLMD & researcher -RIP

Veteran Member

Date Joined Oct 2009
Total Posts : 699
   Posted 8/22/2010 5:20 PM (GMT -6)   
Hi Lynn. My LLMD is in Sacramento. I also know of a good one in San Francisco. What area of the SF Bay Area are you looking for?

I have Lyme; it doesn't have me.

Regular Member

Date Joined Nov 2008
Total Posts : 51
   Posted 9/3/2010 2:59 PM (GMT -6)   
So I actually found one, but man is it pricey. Its Dr S in San Francisco and I had to pay a lot of money at the time of booking. I HOPE this gets me some answers. Appt in OCT.

I am so SICK and being in severe pain.

Regular Member

Date Joined Nov 2008
Total Posts : 51
   Posted 9/3/2010 2:59 PM (GMT -6)   
And thanks everyone. I live in San jose, CA

Regular Member

Date Joined Jul 2009
Total Posts : 113
   Posted 9/3/2010 3:19 PM (GMT -6)   
I see Dr. S and I think it's definitely worth the $.

Veteran Member

Date Joined Oct 2006
Total Posts : 1458
   Posted 9/18/2010 4:45 AM (GMT -6)   
Try contacting CALDA (Calif. Lyme Dis. Assoc.) for suggestions.
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