Hi. I only just found this forum and wish I had found it early on in my treatment when I would have found it useful for myself. I had my PEG tube removed today and that feels like a closure at least for the time being. Almost 7 months on from the surgery I am feeling pretty fit and eating almost normally, albeit with a glass of water (or beer!) handy to help with the occasional mouthful that sticks.
Happy to share my own experiences here in the UK which I suspect are not so different from you guys over the big water.

If anyone is reading this shortly after a diagnosis of tongue cancer like mine, I hope you can keep a positive attitude towards the likelihood of a cure. Ok, I know its too early to know for sure if I am cured, but the treatment is over and life is a little fresher, girls a little prettier and the world a little more beautiful than it was before.
My best wishes to you all. Martin


Diagnosed Early April 2010 SCC left tongue t3n1
PEG insertion 26th April 2010
Patial glossectomy with flap from arm and left neck dissection 28th April
20 sessions of radiotherapy in June
PEG removal Today - yippee! 19th Nov