To join the Lymphedema Online Support Group, go to the following website.
There is no charge to join, and we have approximately 300 subscribers. Many
list members say that they learn more in a few hours on the list than they
have learned in many years of running around to different doctors. Last
year, the Wall Street Journal mentioned our list and Oncolists as two good
places on the Internet to get information on lymphedema. Please feel free
to join the list yourself or to give the instructions on how to join to
anyone who might be interested.
This is another way to join the Lymphedema Online Support Group:
To subscribe to the Lymphedema Online Support Group, send an e-mail to:
Leave the subject blank. In the message, just write:
SUBSCRIBE LYMPHEDEMA yourfirstname yourlastname
Please contact me if I can help you in any way.
Listowner, Lymphedema Online Support Group
Ann's NOTE: I met Renee Kaplan at the Era of Hope Conference 2000 sponsored by the Department of Defense. She is dedicated to helping those of us with lymphedema.
|Remember we are NOT Doctors and have NO medical training.|
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