Just wondered what everyone knows about CIN 1??

My baby sister (ok so she's almost 22 so not a baby) has just found out she has it. I just want to be able to reassure her that it isn't necessarily a major major thing.

She goes in to have an op in 3wks, I think she said they put die onto the abnormal cells and then remove some of them to test them? I'm not sure, but I think she metioned a biopsy? Or is this the same thing?