This is topic Connecticut LLMD & local Support group contacts in forum Seeking a Doctor at LymeNet Flash.

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Posted by Lisa Lyme (Member # 33537) on :
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.
Posted by hopingandpraying (Member # 9256) on :
I'm not from CT, but have some suggestions for you:

Check the online state Lyme groups at: 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.
Posted by Lymetoo (Member # 743) on :
Look on the left side of this screen. See the green area?

Click on "support groups"
Posted by Sammi (Member # 110) on :
I sent you a private message.

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