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» LymeNet Flash » Questions and Discussion » Seeking a Doctor » Question about Dr S in SF, California!!!

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Author Topic: Question about Dr S in SF, California!!!
Lover11
Member
Member # 19686

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I am being very pressured to go see this doctor.

I feel uncomfortable throwing down such a large amount of money though unless I have some idea of who he is.

Does anybody have any experience with him they can share with me?

Posts: 48 | From San Francisco, CA | Registered: Mar 2009  |  IP: Logged | Report this post to a Moderator
Siciliano
Frequent Contributor (1K+ posts)
Member # 15920

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:hi:Welcome Kali, we're happy to have you visit our site. You will see there is alot of info you will find here!

You need to edit your post please, delete the city name. This is too much info to post on an open forum.

Go to the 3rd box to the right of your name, the pencil icon to delete--thank you.

If you go to the left side of the screen, 3rd one down to "support groups" you will find contact names, ph#s and these groups have first hand knowledge about llmds, they can give you valueable info. [Smile]

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I'm sorry but I am no longer accepting any private messages due to my own battle with lyme.

Posts: 3897 | From New Hampshire | Registered: Jun 2008  |  IP: Logged | Report this post to a Moderator
Siciliano
Frequent Contributor (1K+ posts)
Member # 15920

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Kali, I sent you a pm, hope it helps. Good luck. [hi]

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I'm sorry but I am no longer accepting any private messages due to my own battle with lyme.

Posts: 3897 | From New Hampshire | Registered: Jun 2008  |  IP: Logged | Report this post to a Moderator
Robin123
Moderator
Member # 9197

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Pm'ing you.
Posts: 13171 | From San Francisco | Registered: May 2006  |  IP: Logged | Report this post to a Moderator
jblral
LymeNet Contributor
Member # 8836

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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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