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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:
||National Capital Lyme Disease Association
|Contact Person for this Group:
||Monte L Skall
|Contact Person Telephone:
|Contact Person E-Mail:
|State or Province:
||District of Colombia
|Regions of your state / province served by this group (i.e. south-east Pennsylvania):
||District of Columbia, No. Virginia & Maryland
||Monte L Skall
|Your E-Mail Address:
|URL For Support Group:
|The National Capital Lyme Disease Association meets at Sibley Hospital, Dining Rooms A and B, on the first Sunday of each month.
We have adopted a three-fold purpose.
The National Capital Lyme Disease Association also meets on the second
Thursday of each month at county libraries. See www.natcaplyme.org for
current times and locations.
SUPPORT - Build a network to share our personal trials and experiences. Network with other Lyme organizations by participation in conferences,
AWARENESS - Schedule presentations by doctors and other health professionals; alternative treatment experts; disability rights and benefits professionals. Heighten public awareness in the National Capital Area through distribution of printed material to doctors' offices, hospitals, and schools.
CURE - Contact local, state, federal and international medical and political representatives; Raise funds to support Lyme research; Host conferences/symposiums; Gain media support (TV, radio, newspapers).
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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