Platinum Member (300+ posts) Joined: Jun 2013 Posts: 346 Likes: 3 | Actually, what you said made sense. I forgot that another city opened a 'branch' of their hospital research stuff here in our city, and they do consultations and treatments. It's mostly for their children's programs, or was at first, so I keep forgetting they are there. But I suppose they would give doctors some of the same information and training. Still, in an area like mine, doctors would end up doing a lot of their own research and continuing education, and therefore still come to some independent conclusions. I forget they exist because when I did use that place for a second opinion, I still had to drive to the other city, but that was quite a few years ago. Wonder how it works now... hm. Probably still have to drive, to find the specialists. (We would have gone anyway, as we had a young friend in the hospital there also with cancer, so we combined it with a visit to her, which she enjoyed. And since we have three major cities within about six hours, lots of folks do drive to other places ... I can't, as I get very ill from travel, but many do. We have great doctors locally though, and getting better every day, so that helps.)
Surgery 5/31/13 Tongue lesion, right side SCC, HPV+, poorly differentiated T1N0 based on biopsy and scan Selective neck dissection 8/27/13, clear nodes 12/2/13 follow-up with concerns 12/3/13 biopsy, surgery, cancer returned 1/8/14 Port installed PEG installed Chemo and rads 2/14/14 halfway through carboplatin/taxotere and rads March '14, Tx done, port out w/ complications, PEG out in June 2017: probable trigeminal neuralgia Fall 2017: HBOT Jan 18: oral surgery
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