Hi to all...

Very interesting about UT in Dallas, our surgeon was there but left it up to us on using UT doctors or one closer. Since, the Hep C, he said using our current onocologist would be fine.

Loma Linda is in the process of setting everything up. Is is normal to have second thought on treatment options? I want to throw up every minute and question myself on the really knowing the facts.

How often can a person receive treatment. Do people go through it more than once? A lot of you have had surgery first then treatment. Our doctor said it would be too disfiguring and they want to shrink it first???? Does this sound correct?

My gut feeling is to try the PBT and the regular radiation. I know he was sooooo sick during the HEP C treatment, he had to quit. His blood count and his constant vomiting was just too much. I just don't think he will make it on the traditional treatment emotionally...knowing what he went through before.

Thanks for all for your support.

Patsy