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» LymeNet Flash » Questions and Discussion » Seeking a Doctor » SEEKING A LLMD IN THE LOS ANGELES AREA

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Author Topic: SEEKING A LLMD IN THE LOS ANGELES AREA
Ariel1
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Have a friend who has extreme Lyme symptoms but doctors don't think she has Lyme because she is in the West Coast. She lives in the Thousand Oaks/Ventura County area but can drive to Los Angeles. Thank you!


Ariel
Posts: 88 | From DC Metro area | Registered: Sep 2009  |  IP: Logged | Report this post to a Moderator
Robin123
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Ariel - the West coast has Lyme disease from one end to the other - it's everywhere.

Dorothy Leland has a blog, Touched by Lyme, on the CALDA website (www.lymedisease.org). She got info from over 150 Californians and where they were bitten here.

Someone will send you a doctor list soon from here.

If your friend is interested, she could ask to join CaliforniaLyme at http://health.groups.yahoo.com/group/CaliforniaLyme
to discuss and get doctor referrals.

California support groups are at www.lymedisease.org/California/California_Support_Groups.html
Posts: 13171 | From San Francisco | Registered: May 2006  |  IP: Logged | Report this post to a Moderator
Ariel1
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Robin - Thank you for this info.

I'll be sure to pass it along to my friend.

Ariel
Posts: 88 | From DC Metro area | Registered: Sep 2009  |  IP: Logged | Report this post to a Moderator
   

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