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» LymeNet Flash » Questions and Discussion » Seeking a Doctor » need llmd in central CT

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Author Topic: need llmd in central CT
2young2dieMom
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Member # 25434

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Any recommendations for a llmd in the new haven area? I see Dr M but he's gotten too expensive and doesn't take insurance. I definitely have Babesia and probably many other things but I don't test positive. I was dxd with ALS in the beginning have been on every abx and ivig for 7 years. I'm doing much better!

[ 11-13-2018, 08:07 PM: Message edited by: sixgoofykids ]

--------------------
Dxd ALS 3/2010
Dxd cllinical Lyme 4/2010
Positive for Protomyxzoa but absolutely nothing else in Igenex

Posts: 415 | From central ct | Registered: Apr 2010  |  IP: Logged | Report this post to a Moderator
Bartenderbonnie
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I am sending you a pm.
Posts: 1440 | From Florida | Registered: Nov 2016  |  IP: Logged | Report this post to a Moderator
hopingandpraying
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Check the online state Lyme groups at:
https://groups.yahoo.com/neo/groups/ConnecticutLyme/info

Maybe they can help. They would know better about CT.

Some more resources for you (including Support Groups info):
http://whatislyme.com/lyme-in-connecticut/

http://www.lymenet.org/SupportGroups/UnitedStates/Connecticut/

Posts: 8366 | From Illinois | Registered: May 2006  |  IP: Logged | Report this post to a Moderator
   

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