MariaA
Frequent Contributor (1K+ posts)
Member # 9128
posted
Hey you's,
Lyme Chat's been kind of quiet lately, but last year it was a major source of 'support' and information for quite a few people- I'm wondering if new members even know about it: http://lymefriends.ning.com/page/lyme-chat-1
come join me there!
-------------------- Symptom Free!!! Thank you all!!!!
Tracy9
Frequent Contributor (1K+ posts)
Member # 7521
posted
Also you need a password to get in.....please email [email protected] to get a sign in name and password.
It is always busy between 12 and 2 or 3 am, but it used to be rocking starting at 7 pm. It would be nice for more of us to get together earlier. Thanks Maria!
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
| IP: Logged |
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/