LymeNet Flash: need info about LLMD in CT

This is topic need info about LLMD in CT in forum Seeking a Doctor at LymeNet Flash.

To visit this topic, use this URL:
https://flash.lymenet.org/ubb/ultimatebb.php/topic/2/27540

Posted by dbwilc (Member # 49401) on :

hello,

i have an appt with Dr P in CT and was wondering about any opinions/experiences? Any info would be GREATLY appreciated...thank you so much

[ 12-06-2016, 06:22 PM: Message edited by: faithful777 ]

Posted by tickbite666 (Member # 43399) on :

He's worth the wait...

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/websites-and-support-groups-by-state/

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

Posted by HopefulNY (Member # 46070) on :

Dbwilc,
I see Dr P in CT. Had my consult and started treatment. He is so so bright ( and I have been ill for 25 years so I don't say that very often), plus he's very compassionate. He knows his Lyme, like no ones business.
He uses orals, no IVs. Very careful and doesn't only go by tests.
You're in great hands!