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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 - Central Virginia Chapter
|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):
||The chapter will serve Lyme sufferers and supporters from the counties, cities and towns around Lynchburg, Roanoke, Farmville, Lovingston, Halifax County and Charlottesville
|Your E-Mail Address:
|URL For Support Group:
|The Central Virginia Chapter will meet at Central Virginia Community College, Merritt Hall - Room 5207
The Central Virginia Chapter will follow the guidelines of the National Capital Lyme & Tick-Borne Disease Association.
We are pleased to announce that Joe LeBlanc will be leading the group. Joe is a board member of the National Capital Lyme and Tick-Borne Disease Association. He has a long and impressive history of educating the public on Lyme and Tick-Borne Diseases.
Mr. LeBlanc has been researching Lyme disease since late 1994 when his wife Betty first became ill. Both he and his wife have talked to many other Lyme sufferers, not only in central Virginia but have received calls from all over the US. Joe has been on local radio and in the past has had WSET interview he and his wife in their rural country home. Interviews about their struggles with Lyme have also appeared in newspapers over several years, as well as Letters-to-the-Editor. Joe has presented Lyme information at the local Amherst Rescue Squad "Health Day".
A 3 part series on The Lyme Controversy was presented on WSET in Lynchburg. It has raised a lot of interest which prompted Joe to form a NATCAPLYME chapter to make more people aware of the difficulties facing them and their families.
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:
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