Does anyone else have one, and how have you found it. I have had two now, during my different stages of diagnosis. They try there best to match you up with someone who has had the same diagnosis as you. I firstly had a lady called Anne who was from scotland and who had had dcis, but not invasive. I then had a lady called Heather who has had dcis, invasive and no node involvement. I must say I think its a really really good support idea, and just wanted to mention it just incase people didnt realise about the service.
s x