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Welcome to The Lyme Disease Network,
a non-profit foundation dedicated to public education of
the prevention and treatment of Lyme disease and other tick-borne illnesses.

On the Internet since 1993.


LymeNet needs your help:
LymeNet Fund Drive 2020



If you would like to add or update a support group, please contact the webmaster.
Name of Support Group: Vermont Lyme Network
Contact Person for this Group: Dayle Ann and Susan, co-founders
Contact Person Telephone:  
Contact Person E-Mail: [email protected]
This email is for inquiries from Lyme patients only. It is not to be used for other purposes, including marketing or promotion.
City:  
State or Province: Vermont
Country: United States
Regions of your state / province served by this group (i.e. south-east Pennsylvania): Vermont and adjacent regions of neighboring states.
Your Name:  
Your E-Mail Address:  
Other Information:  
URL For Support Group: http://www.vermontlyme.org

Comments:
We are a growing and active group of people with Lyme, plus our families and friends.

We began as a few individuals connected to one another via email, but grew into an informal non-dues organization, with a steering committee and a coordinator. We have a website with key information about Lyme for both laypeople and the medical community, and links to important resources.

We sponsor an online support group for people with Lyme disease and other tick-borne diseases. Our online support group is active and friendly. We will do our best to help people locate Lyme-literate MDs within travel distance or who can work with your local physician. Email inquiries are welcome.

We also have a separate online group for members involved in outreach, organizing and education activities.

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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


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