LymeNet Flash: Lyme Disease Chat Rooms

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»	LymeNet Flash » Questions and Discussion » General Support » Lyme Disease Chat Rooms

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Author

Topic: Lyme Disease Chat Rooms

TLDB
Junior Member
Member # 40686

posted

There was a topic on this forum posted a while ago in regards to the existence of Lyme Disease chat rooms.

Specifically Here: http://flash.lymenet.org/ubb/Forum3/HTML/011965.html

I wanted to add to it, but I guess the topic is closed so here is my reply if it serves as any interest or benefit to anyone.

http://www.thelymediseaseblog.com/lymechat.html

It's a 24/7 chat room site for those with Lyme Disease. You can chat with others in regards to specific Lyme Disease topics.

[group hug]

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Lyme Disease Chat Rooms

http://www.thelymediseaseblog.com/lymechat.html

Posts: 2 | From U.S. | Registered: May 2013 | IP: Logged |

Lymetoo
Moderator
Member # 743

posted

Thanks... there were some recent questions about chat rooms and the consensus was that there weren't any. So .. there are some who will be glad to know it DOES EXIST!!

The thread you found was so old that I guess it no longer works.

--------------------
--Lymetutu--
Opinions, not medical advice!

Posts: 96223 | From Texas | Registered: Feb 2001 | IP: Logged |

Carol in PA
Frequent Contributor (5K+ posts)
Member # 5338

posted

Here is the Lyme chat room that is associated with the LymeFriends site.

http://client11.addonchat.com/sc.php?id=306727

This is open all the time.
We used to have nightly chats.
Try the icons at the bottom to see what they do.

Posts: 6947 | From Lancaster, PA | Registered: Feb 2004 | IP: Logged |

Lymetoo
Moderator
Member # 743

posted

Carol.. Tracy came here a few weeks ago and said the one for Lyme friends is no longer in use.

--------------------
--Lymetutu--
Opinions, not medical advice!

Posts: 96223 | From Texas | Registered: Feb 2001 | IP: Logged |

Carol in PA
Frequent Contributor (5K+ posts)
Member # 5338

posted

As you can see, the room is there, and it works.

If you invite some other people to come in and chat with you, then it's "in use" again.

Posts: 6947 | From Lancaster, PA | Registered: Feb 2004 | IP: Logged |

HK
LymeNet Contributor
Member # 45290

posted

I'm new to chat rooms and not sure if this will go through or if I'll be in or if anyone will read this but I'm desperate for an ear so I'm trying (hopefully not in vain). My name is Pam and I'm dealing with a family of lyme victims. They seem to take turns getting symptoms and right now I'm ready to hop the fence into someone else's life. The grass has to be greener. My own lyme seems to be in check for a few years now but it's never truly gone (of course).

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Back At It

Posts: 203 | From NJ | Registered: Feb 2015 | IP: Logged |

duncan
LymeNet Contributor
Member # 46242

posted

Well, I see the chat room listed on this site, but there doesn't seem to be an operating link...

ETA: Ooops! that was just the name of this topic. Sigh. Bad brain day.

IS there a chat room??

Posts: 228 | From Unitied States | Registered: Jul 2015 | IP: Logged |

Ann-Ohio
Frequent Contributor (1K+ posts)
Member # 44364

posted

My experience with chat rooms is that trolls get on and ruin everything.

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Ann-OH

Posts: 1597 | From Ohio | Registered: Aug 2014 | IP: Logged |

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