Let me put his another way. I just started a second course of chemo-radiation therapy yesterday (hypopharyngeal squamous cell)and there doesn't seem to be a lot of information out there for two timers. I'm hoping that someone out there can share what that's been like and any long term quality of life issues they may be experiencing. My first diagnosis was in 2013 (base of tongue)and I was told this new round seems likely caused by the first treatment.

Anybody care to take a swing?