LymeNet Flash: In need of a doctor in Ct

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»	LymeNet Flash » Questions and Discussion » Seeking a Doctor » In need of a doctor in Ct

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Author

Topic: In need of a doctor in Ct

paver
Junior Member
Member # 30349

posted

I am in search of a lyme disease doctor in Ct.I am showing alot of symptoms of the late stages of lyme. Thanks

Posts: 7 | From ct | Registered: Jan 2011 | IP: Logged |

Keebler
Honored Contributor (25K+ posts)
Member # 12673

posted

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I hope you get some good specific suggestions, in the meantime, these links may help guide your search:
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http://www.lymenet.org/SupportGroups/

Find your area Lyme SUPPORT GROUPS through LymeNet

=======================

* http://www.turnthecorner.org

TURN THE CORNER is dedicated to the support of research, education, awareness and innovative treatments for Lyme disease and other tick-borne diseases.

* http://www.turnthecorner.org/content/selection-proper-physicians

Turn the Corner Foundation - Find Lyme Literate Medical Help

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* http://www.lymediseaseassociation.org

Lyme Disease Association

* http://www.lymediseaseassociation.org/index.php?option=com_content&view=article&id=277&Itemid=368

LDA Doctor Referral System

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When you get a doctor's name, be sure to check about their being what we call ILADS-educated or ILADS-minded. Talk to your local support groups, call the doctor's office and talk with the office manager about the doctor's affiliations and experience so that you might find a "good fit" for your particular case.

More about ILADS here:

www.ilads.org

ILADS - INTERNATIONAL LYME & ASSOCIATED DISEASES SOCIETY

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(Sorry, I could not easily find the comparable group for CT - and just had to stop looking.) If you contact the NY group, they can guide you for CT, I'm sure.
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http://www.empirestatelymediseaseassociation.org

EMPIRE STATE LYME DISEASE ASSOCIATION

http://www.empirestatelymediseaseassociation.org/Lyme_Disease/support_group_meetings_empire_state_lyme.htm

Support Groups

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Great information links here:

http://www.lymedisease.org/

California - Lyme Disease Association (CALDA) is a non-profit corporation acting as the central voice for all tick-borne disease issues. An excellent website for anyone in any state.
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Posts: 48021 | From Tree House | Registered: Jul 2007 | IP: Logged |

Lymetoo
Moderator
Member # 743

posted

message sent

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--Lymetutu--
Opinions, not medical advice!

Posts: 96239 | From Texas | Registered: Feb 2001 | IP: Logged |

Nancy2
Frequent Contributor (1K+ posts)
Member # 95

posted

PM Sent!

Posts: 1487 | From New England | Registered: Oct 2000 | IP: Logged |

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

posted

Sending you aPM.

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

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

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