Hi everybody,
Im really interested in how you got your info at diagnosis. Was it verbal, in writing or, or as Ive heard, taped and given to you.Given the catastrophic nature of the situation, I'm really amazed at the variety of means that we were told. I for one, still feel there is so much I dont know about my own situation-its all so foreign and scary that I feel some kind of written info on your personal situation would have helped. Of course I got the helpful leaflets etc, but my own info, such as path report, treatment plan etc could form part of an important 'journey' log.
What do you think?
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