This may sound crazy, but nevertheless, here goes. My husband goes back for a follow-up CT scan and appointment with his surgeon in a week. This will be the first visit since finishing his radiation and chemo treatments. He is still taking all nutrition through his PEG. I am sure there are a million questions we should ask when we see the doctor, but I feel like I am not thinking of them all. Any pertinent questions we should be asking? Thanks for any input.


Caregiver to husband (age 52 at time of diagnosis)
Diagnosed with SCC right orapharynx in Aug. 2007 Stage T3N2bMx 9 of 57 nodes involved
Radical right neck dissection 9-24-07
35 IMRT & 7 chemo treatments
PEG tube still used for feedings
Finished all treatments on 12-10-07