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» LymeNet Flash » Questions and Discussion » Seeking a Doctor » Connecticut LLMD & local Support group contacts

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Author Topic: Connecticut LLMD & local Support group contacts
Lisa Lyme
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Member # 33537

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Hey just double checking to see all my options. I have a llmd referral from the LDA, but want to know if there are other llmd's in CT.

Also, is there any body here who is from CT that knows of a good local support group.

--------------------
Take It Easy, Peace
Posts: 59 | From Old Lyme | Registered: Aug 2011  |  IP: Logged | Report this post to a Moderator
hopingandpraying
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I'm not from CT, but have some suggestions for you:

Check the online state Lyme groups at: http://health.groups.yahoo.com/group/Connecticutlyme

www.lyme-aware.org/connecticut.html has info for CT with several support group links on it.

I think there is a page on Facebook called Lyme and Connecticut or Lyme in Connecticut you might want to look at.
Posts: 8991 | From Illinois | Registered: May 2006  |  IP: Logged | Report this post to a Moderator
Lymetoo
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Look on the left side of this screen. See the green area?

Click on "support groups"

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--Lymetutu--
Opinions, not medical advice!
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Sammi
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I sent you a private message.
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