Hi. I want to write an article about the patient experience of appearing before a tumour board. (We call them multi-disciplinary-panels here in New Zealand.) I've appeared in front of one twice and think that first one was one of the weirdest experiences of my life. It's like some nightmare experience of being a celebrity at a press conference.

It's gratifying to know that about 15 to 20 (?) medical professionals care about your case and make the best possible decision. But what a daunting experience it is.

I would appreciate any of your comments about the experience from a patient point of view. How did you feel? Is it all a blur?

Here in Auckland a group of head and neckers is formalising its support group and, from next year, producing a proper newsletter. I thought a range of views (anonymous) might give me useful material:)