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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