This is topic need llmd in central CT in forum Seeking a Doctor at LymeNet Flash.


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Posted by 2young2dieMom (Member # 25434) on :
 
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 ]
 
Posted by Bartenderbonnie (Member # 49177) on :
 
I am sending you a pm.
 
Posted by hopingandpraying (Member # 9256) on :
 
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/
 


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