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» LymeNet Flash » Questions and Discussion » Seeking a Doctor » Looking for other patients of San Francisco LLMD

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Author Topic: Looking for other patients of San Francisco LLMD
EmilyT
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Member # 11632

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Hi all,

I have an upcoming appt. with Dr. S in SF, and I'm wondering what to expect. I saw a different LLMD when I lived back East but now that I'm out in California I've decided to try this doc.

His appts aren't cheap and I haven't heard too much about his methods, but I want to get the most out of my first appt. that I can...So, I'm wondering if any current or former patients of this doc can PM me and tell me a little about their experiences with treatment, etc. Thanks, I really appreciate it!

-Emily
Posts: 33 | From CA | Registered: Apr 2007  |  IP: Logged | Report this post to a Moderator
bettyg
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i'm not a patient, but check your profile for a pm from me! [Smile]
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jblral
LymeNet Contributor
Member # 8836

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This LLMD will be speaking at the upcoming conference on April 18. More info:
http://www.lymedisease.org/news/index.php

Recommend you join the CaliforniaLyme on-line support group:

http://health.groups.yahoo.com/group/CaliforniaLyme/

There are members in your area who can tell you about doctors.

Also, the California Lyme Disease Association website maintains a list of support groups throughout the state. Check for one in your area:

http://lymedisease.org/california/california_support_groups.html
Posts: 991 | From California | Registered: Feb 2006  |  IP: Logged | Report this post to a Moderator
   

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