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#52311 10-15-2007 05:23 AM | Joined: Feb 2007 Posts: 1,940 "OCF across the pond" Patient Advocate (1000+ posts) | "OCF across the pond" Patient Advocate (1000+ posts) Joined: Feb 2007 Posts: 1,940 | Anniemay no one can truly answer the question you have asked but i do have very recent personal experience of this situation as do some others such as Amy.It is a very delicate subject to discuss on an open forum where people are still fighting the fight,but if you want to send me an e-mail or private message i will help where i can .I could also suggest that you read the blogs for myself and amy mine is called "walking towards the light" and amy's is a "caregivers journal" you will find them on the forum index under OCF Cancer Blogs.
I am sorry for your news
liz
Liz in the UK
Husband Robin aged 44 years Dx 8th Dec 2006 poorly differentiated SCC tongue with met to neck T1N2cM0 Surgery and Radiation.Finished TX April 2007 Recurrence June/07 died July 29th/07.
Never take your eye off the ball, it may just smack you in the mouth.
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