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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
| 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. |