pmerv
Frequent Contributor (1K+ posts)
Member # 1504
posted
CALDA is hosting a workshop for activists, support group leaders, patient advocates, friends and family who wish to become more effective advocates for the rights of people with Lyme and other tick-borne diseases. The workshop, Lyme Action Program, will take place on Thursday, October 16, the day before the LDA and ILADS conferences. We have made an effort to keep the costs down and the program is being supported the Turn the Corner Foundation. For a preliminary schedule and application, please go to http://www.lymedisease.org/activism/lyme_events.html
-------------------- Phyllis Mervine LymeDisease.org Posts: 1808 | From Ukiah, California, USA | Registered: Aug 2001
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NP40
Frequent Contributor (1K+ posts)
Member # 6711
posted
Phyllis,
Any word on video conferencing via the net ?
Posts: 1632 | From Northern Wisconsin | Registered: Jan 2005
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13 years Lyme & Co.; Small Fiber Neuropathy; Myasthenia Gravis, Adrenal Insufficiency. On chemo for 2 1/2 years as experimental treatment for MG. Posts: 4480 | From Northeastern Connecticut | Registered: Jun 2005
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NP40
Frequent Contributor (1K+ posts)
Member # 6711
posted
Google "Internet Video conferencing sites".
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:
The
Lyme Disease Network of New Jersey 907 Pebble Creek Court,
Pennington,
NJ08534USA http://www.lymenet.org/