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CT results as I move toward 7 years with stage 4

Hello all,
I am sorry I am not around as much. I still read many posts and just don't respond as I should. To any new members, I am stage 4 ( 4 lung resections, 1 liver rresection, colon, 10 months chemo, pulmonary embolism) and I am still here. The randomness and unfairness of this disease is the part that is so hard. I did get CT scan done Thursday at Stanford and it is all good with CEA below 1. No new spots. This makes it the first time since dx ( 8/06 ) that I have gone 1 year since a surgery or two. I still ski and surf, far behind my kids now.
Tonight I celebrate even though I have a cold, just drank a cold beer, smiled with the kids and wife and thought of many of you. I am still coaching and teaching and I do not have any good reason why things are going well. I do know that the long survivors on here lifted me up so thank to the survivors, thanks to their support team and safe travels to the warriors who have gone before.
Still active in the impact zone.
Love
Chip
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Thanks Chip
Thanks so much for your post Chip. I was diagnosed in Aug 2012 and after radiation/chemo and suegery thought I was cancer free only to find now that it has moved to my lymph nodes and am stage IV. I'm trying to remain positive but it has been tough so stories like yours help me believe I can be around to watch my kids grow up. Thank you so much for giving us all hope! Keep on living life to the fullest!
Thanks
Janice
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Sorry to read this, but metsPerky chick said:Thanks Chip
Thanks so much for your post Chip. I was diagnosed in Aug 2012 and after radiation/chemo and suegery thought I was cancer free only to find now that it has moved to my lymph nodes and am stage IV. I'm trying to remain positive but it has been tough so stories like yours help me believe I can be around to watch my kids grow up. Thank you so much for giving us all hope! Keep on living life to the fullest!
Thanks
Janice
Sorry to read this, but mets to only one other location isn't as bad as mets everywhere like some of us have. The best option for extended survival is surgery to remove the tumors, in conjunction with chemo (before and/or after surgery). My advice is to stay aggressive and get the tumors surgically revoved if at all possible. I'm not a candidate for surgery due to my widespread mets, so I am looking into other options, like dendritic cell vaccines.
Tedd
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