People seem to be having great difficulty getting into the chat room on Lyme Disease Audio Network, that we usually use.
Here is the other room we created before, but hadn't really used much. I suggest we all switch over to it; I will change the address on posts and email everyone.
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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disturbedme
Frequent Contributor (1K+ posts)
Member # 12346
posted
It's not working tonight...
-------------------- One can never consent to creep when one feels an impulse to soar. ~ Helen Keller
My Lyme Story Posts: 2965 | From Land of Confusion (bitten in KS, moved to PA, now living in MD) | Registered: Jun 2007
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Tracy9
Frequent Contributor (1K+ posts)
Member # 7521
posted
Changed address above to new chat room. Check it out, let's try it out for a while and see how we like it.
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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