Yes,a folder is a good idea and also an appointment diary(one in the kit). Always ask doctors for copies of pathology results.I photocopy referral letters incase they get lost.Take notes when talking to doctors cos chances are you'll forget what they said. I run a bc support group in north,west Sydney and we meet once a month.We network information and support each other.We also have a library of "stuff"like scarves,caps,wigs,etc.We are having a guest speaker next month to talk on lymphoedema.Not all support groups run the same way - ours is still evolving.Sometimes you are not ready for a group until after surgery recovery.The kit is information overload but you are on a steep learning curve and the books are fairly straightforward.Perhaps just deal with the surgery part first.Treatments after that usually depend on what your pathology results are and they come about a week after surgery.If breast cancer is caught early then the odds are in your favour.I've had it twice-each time it was early bc(2003 and 2010) and I'm fine now.You will find strength you never knew you had and you'll get through it. Tonya xx