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#8874 12-03-2006 03:52 PM | Joined: Oct 2006 Posts: 248 Gold Member (200+ posts) |  Gold Member (200+ posts)
Joined: Oct 2006 Posts: 248 | Brian, I personally want to thank you for providing all of us a forum for our voices to be heard. To me it is not the 2000 posts that amaze me but the time and effort and thoughtfullness you put into all of your posts. I have been around cancer wards pretty much the last 15 yrs, and I think I've learned more from this site in just one short month. I wish you all the success in the Yrs to come you truly are an inspiration to so many. Congrats!!!!
Mark D.
Mark D. Stage 3 Nasopharynx dx10/99 T2N3M0 40xrad 2x Cisplatin 5FU. acute leuk 1998.
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#8875 12-04-2006 05:18 AM | Joined: Aug 2005 Posts: 158 Senior Member (100+ posts) | | Senior Member (100+ posts)
Joined: Aug 2005 Posts: 158 | Slightly shuffle the letters in your name and one comes up with "Brain". The dream and vision that once was born in your brain has assisted ever so many of us in "getting through it all." I shudder to think where I might be today had I not found OCF.
Thank you from the depths of my being for taking that first step that became the foundation of the Foundation. It certainly has not taken long for your idea to learn to crawl, then walk and now run like the wind, providing a dedicated place for us to learn, utilize and pass on to those who follow us, making their journey just a bit easier.
I tip my hat and applaud you for your selfless dedication to OCF. Thank you for being here when I needed you most.
Bill
No love, no friendship can cross the path of our destiny without leaving some mark on it forever. - Francois Mauriac
Thank you for leaving your mark.
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#8876 12-04-2006 05:04 PM | Joined: Jan 2006 Posts: 32 Contributing Member (25+ posts) | | Contributing Member (25+ posts)
Joined: Jan 2006 Posts: 32 | Dear Brian, like many before, I would like to thank you so so much for all th efforts that you are putting into OCF. The website is such an immense source of knowledge that we can trust. The support is just incredible. For people like me who live far from a large city centre where all the action is, OCF is just life saving. As a caregiver, I find OCF my source of energy as I often do not want to burden people who surround me and I know that people here will not be annoyed. Knowing that people are going through the same things allows me to connect to another level, I know they understand. I've become a groupie  !! Thank you again Brian Marie-Lyne
Wife of David, 44yo, SCC-BOT-R) mod. rad. ND in Jan 06. 35x standard RT from Feb-April 06. Recur on L) side same level in Sept 06 with mod rad ND. 1/48 node positive SCC + 1/48 positive micropapillary carcioma consistant with thyroid CA.
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#8877 12-05-2006 04:43 AM | Joined: Jul 2006 Posts: 388 Platinum Member (300+ posts) | | Platinum Member (300+ posts)
Joined: Jul 2006 Posts: 388 | Brian (or as Florida Bill paralettered)"Brain" -
Thanks to your endless research and caring, thorough responses and submissions, I think many of us know more than some doctors about oral cancer. This site is nothing short of phenomenal.
Warmly, JaneP
Husband: 3 SCC gum and cheek cancers 2002, 2005, 2006: surgery only. Scans clear after removal of small, well differentiated, non-invasive cancers. No radiation. 4th SCC lip diagnosed 4/13/07 - in situ, removed in biopsy. More lip removed 2/8/08 - dysplasia. 2 Biopsies 3/17/09 no cancer (lichenoids)
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