I have the same type of cancer you have. Mine is (was) at the base of my tongue. I hope that youR situation is a little better. They had to go in through the side of my jaw (which needs a metal plate to hold secure) cut out 40% of my tongue. Next, and posssible the worse was the radiation treatments followed by kemo. What is bad about the radiation is that it affects your whole mouth making eating difficult. The porblems with the radiation is that it will affect the inside of your mouth forever. It is not something that will re-grow itself into new cells. I needed a feeding tube installed in my stomach to help me eat. I hope things are not as bad for you. I have been on liquids for 2 years now. As far as we know the cancer is still in remission. I assume that you have had a PET/SCAN.?? My surgery was done at St. Francis Hospital in Hartford, CT. I have an excellant surgen who has been doing this type of surgery for more than 20 years. If you need his name and phone, I will be happy to give it to you. You can call my cell phone at --- Message edited by CancerCompass staff: for personal protection, phone number removed. Please review CancerCompass Member Guidelines at
http://www.cancercompass.com/common/guidelines.html ---. I hope I have been of some help. Kindest Regards, Zayle