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Re: Chat??

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Hi ,

The chat we were all referring too is a phone chat set up for us and paid for by the wonderful folks at the Pulmonary Fibrosis Foundation. It occurs every other Thursday at 7 Eastern, 6 Central, 5 Mountain and 4 Pacific time. The next one is on October 23. The toll free number to call is is and the pin # for the chat is 961089#.

It's a great opportunity to actually speak to others in the group and get to know folks on a different level than just the postings on the board. Hope you can join us next time!

Beth-Moderator

Fibrotic NSIP 06/06 UCTD 06/08

Chat??

Hi. I too enjoy reading everone's post and our efforts to breath easy. Lots of folks mentioned being online or the lack of people being on line for a chat. When and where is the chat? I would love to chat with you all. I don't read all of my emails, but I always read the support group postings...it helps so much. Today, my doctor says that I'm probably declining. I walked 200 less feet during the 6 min. walk. I'm going in for another heart cath in 2 wks. to see if it's the pulmonary hypertension that's worse & not the fibrosis. , welcome!Okay, time for Tracleer & bed.I thank you all for being here. Scleroderma( '92/93), PF('03),Pulm. Hypertension( '06)

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