Love your comment about your radiation oncologist. I remember I was complaining to mine about dry mouth and he said something like, "at least you're alive," which I know is true and I am grateful, but not a day goes by that I am not reminded of my cancer because my mouth and throat are so compromised even two years out. And I like my radiation oncologist, I do. But he also told me at my last check-up that for HPV+ cancers (like mine) the standard treatment will probably be reduced from 7 to 5 weeks. Good for all those coming after me; they will probably have fewer side effects. But I am stuck with the mouth I got and now this paralyzed vocal chord. Ugh. I appreciate your taking the time to share your experiences with me. -Michelle


SCC left tonsil, stage IV, HPV+, metastatic to one lymph node. Biopsy 12/23/10; tonsillectomy 1/13/11; DX 1/25/11; Peg in 1/28/11. Peg out 6/29. TX 1/31/11-3/21/11: 35 IMRT plus 3 Cisplatin. Pet-Scan 6/20/11 = CLEAR! Three years out, learning to live with the long-term side effects of radiation while reminding myself to feel blessed.