This is topic Info on LLND in CT in forum Seeking a Doctor at LymeNet Flash.


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Posted by aileenhome (Member # 3960) on :
 
I am at the point where I need to totally rethink my treatment.

I saw Dr I ND in CT talk about lyme on a webinar about autoimmune disease.

Has anyone experience working with him?
 
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.

Some more resources for you (including Support Groups info):
http://whatislyme.com/websites-and-support-groups-by-state/

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


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