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#19194 01-02-2006 09:44 PM
Joined: Nov 2005
Posts: 306
Platinum Member (300+ posts)
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Platinum Member (300+ posts)

Joined: Nov 2005
Posts: 306
Genie, Sorry to have you among us, but we are many, and we have learned alot about our kind of cancer here. There aren't any stupid qustions about cancer, or fear, or treatment - so don't hold back. Many here will identify with you and your situation, and many will reach out to you to help. Tell us more about your experience and what they are doing to help you. Tom


SCC BOT, mets to neck, T4.
From 3/03: 10wks daily multi-drug chemo,
Then daily chemo with twice daily IMRT for 12 weeks - week on, week off. No surgery. New lung primary 12/07. Searching out tx options.
#19195 01-03-2006 05:12 PM
Joined: Mar 2002
Posts: 4,912
Likes: 52
OCF Founder
Patient Advocate (old timer, 2000 posts)
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OCF Founder
Patient Advocate (old timer, 2000 posts)

Joined: Mar 2002
Posts: 4,912
Likes: 52
I have emailed genie, telling her that many people have answered her post and that if she is having trouble figuring out how to work the board, I could help her on the phone. She has not returned my email.


Brian, stage 4 oral cancer survivor. OCF Founder and Director. The first responsibility of a leader is to define reality. The last is to say thank you. In between, the leader is a servant.
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