LymeNet Flash: LLMD in Connecticut

LymeNet on Facebook

LymeNet on Twitter

Follow @LymeDiseaseNet

The Lyme Disease Network receives a commission from Amazon.com for each purchase originating from this site.

When purchasing from Amazon.com, please
click here first.

Thank you.

Dedicated to the Bachmann Family

LymeNet needs your help:
LymeNet 2020 fund drive

The Lyme Disease Network is a non-profit organization funded by individual donations.

»	LymeNet Flash » Questions and Discussion » Seeking a Doctor » LLMD in Connecticut

UBBFriend: Email this page to someone!

Author

Topic: LLMD in Connecticut

ferdinand the bull
Junior Member
Member # 32956

posted

My name is David, I'm 24 years old and have been sick for around a year and a half.

I live in Austin Texas, but I'm finding it impossible to get any referals to LLMD's in the area.

I have family in CT and can travel back and forth realitively easily, So if anyone could send me referals for CT I would greatly appreciate it.

Thanks again

David

Posts: 2 | From Austin,Texas | Registered: Jul 2011 | IP: Logged |

t9im
Frequent Contributor (1K+ posts)
Member # 25489

posted

PM sent with CT MD's

Maybe you should watch the below videos and read the article at the end. You may want to share with your close family so they will know partially what you are up against.

It's amazing there is a controversy to this insidious disease and I've found it easiest to show a couple of u tube video's on the controversy.

http://www.youtube.com/watch?v=PVPRWiukp_M

http://www.youtube.com/watch?v=8yk0C-uX9cU

If you watch this video you can see some of the miss diagnosis.

http://www.youtube.com/watch?v=3nIuIF6q8FA&feature=related

http://www.youtube.com/watch?v=V-lHDA863TM&feature=related

--------------------
Tim

Posts: 1111 | From Glastonbury, CT | Registered: Apr 2010 | IP: Logged |

littlebit27
Frequent Contributor (1K+ posts)
Member # 24477

posted

Sending you a PM.

--------------------
*Brittany Lyme Aware on FB*
http://littlebithaslyme.wordpress.com/

Posts: 2310 | From Southeast | Registered: Feb 2010 | IP: Logged |

Brian5671
Junior Member
Member # 32982

posted

same deal here...any docs in the CT area?
-
have dx of psoriatic arthritis, but have other symptoms more indicative of lyme...perhaps I'm unlucky enough to have both...thx

Posts: 2 | From Fairfield, CT | Registered: Jul 2011 | IP: Logged |

Printer-friendly view of this topic

The Lyme Disease Network is a non-profit organization funded by individual donations. If you would like to support the Network and the LymeNet system of Web services, please send your donations to:

The Lyme Disease Network of New Jersey
907 Pebble Creek Court, Pennington, NJ 08534 USA
http://www.lymenet.org/