HI Again,

Thanks everyone for the good info. I guess I am pushing it. I did tell the Doc who put my tube in just Monday that I was really mad at all the Docs because I really don't think anyone prepared me for all this. Everyday i seem to get a little better and something new happens.

Someone told me the other day to take Nyquil for the mucos and that seems to help at night. Nothing really helps in the day time and it seems to be worse in the afternoon.

Minnie, how to you stand not being able to eat chocolate?? I already have a big box of Harry and David choc waiting for when i get my taste back. I really think it won't taste good tho because I tried an M&M the other day and it was awful. It seems anything creamy or cheesy tastes bad.

I called American Cancer Society this morning to check on support groups and they don't have any in the area just for head and neck. I will try a couple they gave me and see how that goes.

Thanks again to everyone out there who has been such a lot of help. God Bless you all