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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 LDSG
|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 County and the SF Bay Area
|Your E-Mail Address:
|URL For Support Group:
|We are a new group, moving forward as of June 2004, serving a strong
regional need in the Bay Area. Please feel free to call or write us in order to meet other
patients and counselors from the Lyme Disease (LD) community. Free services which
we offer are, among others: discussion on & demographics of tick-borne illnesses
(TBIs) in California and elsewhere; connections with various phone counselors,
existing local LDSGs and sympathetic vector-borne disease research professionals;
notions about which California doctors may be the most qualified
and experienced in diagnosing and treating TBIs; info on reference articles
concerning TBIs, here and abroad.
We finally have a monthly support meeting -- for those who would
best be served by meeting in SF. Please call us and we'll gladly
share details with you about our venues, as the locations will be
variable over the next months. See you there, hopefully!
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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