WFC:
I've done some research on Amifostine, and want to pass on a concern. Amifostine is very hard on your kidneys. Almost every site makes this comment. Please make sure you are adequately hydrated (8 glasses) before treatment. And some afterward.

Also. Amifostine can be given two ways: injection (newest method)and intravenously. I also understand that all chemo drugs are hard on your veins. If you're having difficulty, ask about getting it intravenously through a PORT. A PORT is a little devise under the skin that protects your veins from the chemo.

My doctor refuses to give me Amifostine, but I don't know why. I haven't found anything negative about the drug, however, I do know people have had a difficult time tolerating it. Some people have stopped treatment and/or stopped radiation because of the side effects. Quite honestly, I'm a little confused by my doctor's reaction.

I going to a meeting on Wednesday held by a specialist in radiology. So I'll ask him, and relay the answers.

Rest and Take it Easy this Weekend
Sandyst



Sandy 56, BOT SCC Biopsy 1/21/09 Stage 3, T3NXM0.
Finished 3 cycle induction chemotherapy 4/7/09. (Chisplatin, 5-fu and Texotere). Re-staged 4/20/09,(very successful.) Will start Carboplatin/radiation 2 Gy/5 days/7 weeks (Tomotherapy) starting May 4th. Finished 6/22/09.
OCF member/supporter