JT2,
You didn't say whether your rad treatment was IMRT or XRT. The likelyhood of your saliva returning, at least some, is much better with IMRT.
I pretty much lost all of my saliva initially, but it has slowly returned over 3 years. It started coming back at around the one year point, and continues to improve. I still need liquids to eat, but the water bottle is not required ALL of the time like it was. I'm able to go for a 3 to 5 mile run without it. Just a piece of the dry-mouth gum.
My sense of taste gradually returned to near normal after 12 to 18 months. There are some things that still don't taste right, and I still can't tolerate spicey foods, but improvements continue.

As far as the range of motion (trismus) issues and swallowing, does your health service have a speech and swallowing therapist available?
Mine did, and her assistance was invaluable in returning to near normal. She prescribed a device called the Therabite which helped me to stretch my mouth open slowly over several months, and she also performed a swallowing study which identified where my problems were, and allowed her to prescribe a series of swallowing exercises to improve the swallowing function.

I hope this info is helpful.

Hang in there, the improvements are frustratingly slow sometimes, but things continue to get better.

Good Health,

Chuck


SCC Stage IV right tonsil T3N3M0. Dx 08/03. Clinical Trial:8 weeks Taxol, Carboplatin then Hydrea, 5FU, IMRT x's 48, SND, Iressa x 2yrs. Now 20 years out and thriving. Dealing with a Prostate cancer diagnosis now. Add a Bladder cancer diagnosis to all the fun.
It's always something
"Adversity doesn't build character, it reveals it."