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#2750 06-11-2004 03:27 PM | Joined: Aug 2003 Posts: 1,627 Patient Advocate (1000+ posts) | | Patient Advocate (1000+ posts)
Joined: Aug 2003 Posts: 1,627 | As always, Brian makes such a good point. If I had a question and knew I could get the answer to it within minutes, I would do that rather then post on the board and wait. The "meat" of this board would go from Filet Mignon to Hamburger I fear! I still would love to talk to any of you via instant messenger if any of you have AIM or AOL. My screen name is [email protected]
SCC Left Mandible. Jaw replaced with bone from leg. Neck disection, 37 radiation treatments. Recurrence 8-28-07, stage 2, tongue. One third of tongue removed 10-4-07. 5-23-08 chemo started for tumor behind swallowing passage, Our good friend and much loved OCF member Minnie has been lost to the disease (RIP 10-29-08). We will all miss her greatly.
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#2751 06-11-2004 03:47 PM | Joined: Jun 2004 Posts: 26 Contributing Member (25+ posts) | | Contributing Member (25+ posts)
Joined: Jun 2004 Posts: 26 | I absolutely 100% agree Brian. Thanks for putting out there to see in a different way.
-Betty
Caregiver to Sister, Woodstock, VT - 3/4 tongue removed & reconstructed w/forearm 5/21/04, some in the lymph nodes, neck dissection, brachy radiation in the hospital and now going through 2nd round radiation and to add cysplatin chemo. Stage II-III.
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