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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
|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:
This email is for inquiries from Lyme patients only. It is not to be used
for other purposes, including marketing or promotion.
|State or Province:
|Regions of your state / province served by this group (i.e. south-east Pennsylvania):
||Vermont and adjacent regions of neighboring states.
|Your E-Mail Address:
|URL For Support Group:
|We are a growing and active group of people with Lyme, plus our families
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.
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:
Lyme Disease Network of New Jersey
907 Pebble Creek Court,
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