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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:
||San Francisco/SF_SEAL (Support, Education and Advocacy for Lyme)
|Contact Person for this Group:
|Contact Person Telephone:
|Contact Person E-Mail:
|State or Province:
|Regions of your state / province served by this group (i.e. south-east Pennsylvania):
||San Francisco and beyond
|Your E-Mail Address:
||We meet the third Tuesday of the month from 2-4pm at the San Francisco Main Library (30 Grove/Larkin, next to the Civic Center Muni/BART station). See the first floor Info Desk for meeting room location.
|URL For Support Group:
|We offer a combination of support group, education and advocacy for those with Lyme disease and coinfections, as well as interested others. We are in support of the ILADS guidelines for symptom recognition, testing and treatment. We also recognize the benefit of an integrated treatment approach. Meetings will generally begin with a support group go-around, followed by education/advocacy discussion. Activism will center around San Francisco. However, anyone from the Lyme community anywhere is welcome to come and participate at whatever level is personally comfortable regarding support/education/advocacy activity anywhere. Your input and creativity are welcome in personal sharing, health education and in getting the word out to the public about Lyme disease and coinfections.
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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